CN1433473A - Modification of polysaccharide containing materials - Google Patents

Modification of polysaccharide containing materials Download PDF

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Publication number
CN1433473A
CN1433473A CN00818140A CN00818140A CN1433473A CN 1433473 A CN1433473 A CN 1433473A CN 00818140 A CN00818140 A CN 00818140A CN 00818140 A CN00818140 A CN 00818140A CN 1433473 A CN1433473 A CN 1433473A
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Prior art keywords
binding domains
polysaccharide
polysaccharide binding
composition
covalent coupling
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CN00818140A
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CN1329516C (en
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I·莱维
A·努斯诺维奇
O·肖塞尤
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Yissum Research Development Co of Hebrew University of Jerusalem
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CBD Technologies Ltd
Yissum Research Development Co of Hebrew University of Jerusalem
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
    • C08B37/0006—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
    • C08B37/0024—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid beta-D-Glucans; (beta-1,3)-D-Glucans, e.g. paramylon, coriolan, sclerotan, pachyman, callose, scleroglucan, schizophyllan, laminaran, lentinan or curdlan; (beta-1,6)-D-Glucans, e.g. pustulan; (beta-1,4)-D-Glucans; (beta-1,3)(beta-1,4)-D-Glucans, e.g. lichenan; Derivatives thereof
    • C08B37/0027—2-Acetamido-2-deoxy-beta-glucans; Derivatives thereof
    • C08B37/003—Chitin, i.e. 2-acetamido-2-deoxy-(beta-1,4)-D-glucan or N-acetyl-beta-1,4-D-glucosamine; Chitosan, i.e. deacetylated product of chitin or (beta-1,4)-D-glucosamine; Derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B15/00—Preparation of other cellulose derivatives or modified cellulose, e.g. complexes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B15/00—Preparation of other cellulose derivatives or modified cellulose, e.g. complexes
    • C08B15/10—Crosslinking of cellulose
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B31/00—Preparation of derivatives of starch
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14—Hydrolases (3)
    • C12N9/24—Hydrolases (3) acting on glycosyl compounds (3.2)
    • C12N9/2402—Hydrolases (3) acting on glycosyl compounds (3.2) hydrolysing O- and S- glycosyl compounds (3.2.1)
    • C12N9/2405—Glucanases
    • C12N9/2434—Glucanases acting on beta-1,4-glucosidic bonds
    • C12N9/2437—Cellulases (3.2.1.4; 3.2.1.74; 3.2.1.91; 3.2.1.150)
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Y—ENZYMES
    • C12Y302/00—Hydrolases acting on glycosyl compounds, i.e. glycosylases (3.2)
    • C12Y302/01—Glycosidases, i.e. enzymes hydrolysing O- and S-glycosyl compounds (3.2.1)
    • C12Y302/01004—Cellulase (3.2.1.4), i.e. endo-1,4-beta-glucanase
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/01—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
    • D06M15/15—Proteins or derivatives thereof
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
    • D06M16/003—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic with enzymes or microorganisms
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
    • D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
    • D21C9/001—Modification of pulp properties
    • D21C9/002—Modification of pulp properties by chemical means; preparation of dewatered pulp, e.g. in sheet or bulk form, containing special additives
    • D21C9/005—Modification of pulp properties by chemical means; preparation of dewatered pulp, e.g. in sheet or bulk form, containing special additives organic compounds
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/005—Microorganisms or enzymes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Materials Engineering (AREA)
  • Polymers & Plastics (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Microbiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Molecular Biology (AREA)
  • Genetics & Genomics (AREA)
  • Zoology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Textile Engineering (AREA)
  • General Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Biotechnology (AREA)
  • Peptides Or Proteins (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Paper (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Compounds Of Unknown Constitution (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)

Abstract

The present inventio provides compositions for cross-linking and/or modifying the properties of polysaccharide containing materials. Methods for cross-linking polysaccharide containing materials include the step of treating polysaccharide structures with a PBD fusion protein. Properties of polysaccharide containing materials can be functionalized by treatment with PBD fusion proteins comprising a functional moiety. Polysaccharide containing materials such as paper and textiles with increased wet strengths and/or elasticity are described.

Description

Contain the modification of polysaccharide material
Invention field and background of invention
The present invention relates to be used to change the method and composition of structural performance, chemical property, physicals and the mechanical property of polysaccharide material, described method and composition uses the biological linking agent based on the biological composition of the poly structure of the polysaccharide binding domains that merges with biological entities or chemical entities or be connected and gained.Example of the present invention is to use cellulose binding domain (CBD) fusion rotein, cellulose binding domain-A albumen-Ab mixture or the S-peptide-cellulose binding domain-S-albumen syzygy that contains two cellulose binding domains, to strengthen the mechanical property of tissue paper, filter paper and cotton yarn, for example wet tenacity.
Polysaccharide is the ubiquitous stable structure component of finding at occurring in nature.Many biological utilisation polysaccharide provide 3D shape and surface tissue as the structured material inside and outside the cell.The structural integrity that derives from the polysaccharide of natural origin usually keeps after separation of polysaccharides, makes and can use it for various commercial purposes.Polysaccharide has also adopted the synthetic commercial purpose that is used for of synthesis method because of its ideal physicals.In both cases, derive from or the polysaccharide (for example Mierocrystalline cellulose) in synthetic or non-synthetic source comprises the starting material that are used for various commercially important product (for example paper pulp and textile fibres).
Papermaking process comprises four key steps traditionally: form the aq suspension of cellulosic fibre, be commonly referred to paper pulp; Various processing materials and paper are strengthened in material (for example strongthener and/or applying glue material) the adding paper pulp; Copy paper, the suspension by cast gained on shaped fibers leaches most of water, and with described fiber drying, forms required cellulose net; And behind described paper preliminarily dried, described net is carried out aftertreatment, and think that the paper of gained provides various desired characteristic, comprise that surface applications applying glue material is to improve the dry strength of paper.Those additives that are applied to paper pulp in aqueous slurry are called as wet end additive, comprising: retention aid, to keep fines and filler, for example alum, polymine, cationic starch etc.; Flocculating aids (drainageaids), for example polymine; Defoamer; With resin or additive, for example microfibre and absorbent filler.Other wet end additive comprises wet tenacity and the polymkeric substance of dry strength, for example cationic poly aryl amides and poly-(the acid amides amine/epoxy chloropropane) of adding to improve paper.Also add starch, guar gum and polyacrylamide, to improve dry strength.Sometimes add sizing agent, to give the hydrophilic fibre cellulose fiber with hydrophobic property.These medicaments are used for making the paper that is used for fluid container (for example breast or juice), dixie cup and need prevents the surface of the use ink printing that ink spreads.This class sizing agent comprises gum rosin, wax emulsion and the nearest fibrin reaction glue that derives from pine tree.Behind the described scraps of paper of preliminarily dried, by spraying coating, kapillary sorption coating, dip coated, print roll coating etc., additive is applied to paper, be commonly referred to the cadre and add.Poly-(vinyl alcohol), ACRYLIC EMULSION or vinyl-acetic ester emulsion, starch, sizing agent, polyurethane(s) and SBR latex add in the cadre usually.
The main products of paper industry is corrugation sandwich layer (corrugating medium), promptly is used for the middle layer fluting board of corrugated containers.Starch accounts for the 2-5% of fluting board gross weight.Use various technology to come the wet tenacity of this improvement corrugation sandwich layer, comprised for example formaldehyde resin of applied chemistry linking agent, or using hydrophobic material wax for example.Yet,, thereby stopped in paper, adding this compounds basically or with this compounds treatment paper because these compounds have disadvantageous effect to the recyclability of treated paper.The more expensive raw material of other technology utilization of using is semi-chemical pulp for example, so that increase the weight and the intensity of every square of rice paper.This a kind of method in back causes the expense of starting material and production process itself to increase.
The same with papermaking, cellulose materials (for example cotton fibre) is processed into fabric also relates to several steps: fiber spinning is become yarn; By yarn weaving woven fabrics or knitted fabrics and follow-up pre-treatment, dyeing and housekeeping operation.Woven product are principal modes of fabric knitting.Generally starching in stock tank of yarn is dewatered on steam cans then, makes yarn be configured as the sheet yarn, and the sheet yarn is divided into single thread through yarn-distributing rod with the sheet yarn.Use yarn weaving then, promptly between a series of warp thread, weave by weft yarn.What pre-treatment was included is destarch, kiering and bleaching step by step.In this industry, also use a step to unite the technology of scouringing and bleaching.
With all cpds as the slurry of warp thread, with broken yarn during preventing to weave.Good yarn slurry is that the film that forms sufficient intensity thinks that the yarn of starching provides protection but can not cause the slurry of broken yarn under serous coat by force.Before weaving, slurry is placed on the warp thread, for yarn provides intensity and protection yarn protected from wear.The traditional slurry that contains cotton generally comprises membrane-forming agent (for example starch, starch derivative, polyvinyl alcohol, vibrin, wax, acrylate copolymer and multipolymer and salt thereof), wetting agent, static inhibitor and combination thereof.Traditional aathermoset resin system (perhaps after fixing or Procuring) causes the reduction of cellulosic fibre embrittlement and its microtexture unit's flowability, causes wearability, breaking tenacity and the tearing resistance usually to be subjected to grievous injury.Wearability reduces 75-85% usually, and breaking tenacity reduces 50-60%, and tearing resistance reduces about 50%.In addition, if the yarn of cellulose fiber then is difficult to make the complete destarch of sizing with above-mentioned traditional method starching.Even the complete destarch of sizing, destarch process also are complicated or expensive.
Recently, free of contamination demand becomes more and more important to realize destarch in a simple procedure.Therefore, valuable is that exploitation is used to contain polysaccharide material (for example paper or textiles), reduces or avoid using the additive of potential poisonous and its application of expensive and time-consuming chemical cross-linking agent.
Pertinent literature:
The binding domains that Din etc. (1991) Bio/Technology 9:1096-1099 has described with the bacteria cellulose enzyme destroys cellulosic fibre.Kim etc. (1993, Protein Science 2:348-356) have described a kind of S-of having peptide carrier, one and have had the oligopeptides transcribed spacer of protease recognition sequence and the recombination fusion protein of a tilactase target.Shpigel etc. (1999) Biotech.Bioeng.65:17-23 has described Heparinase I (deriving from heparin Flavobacterium (Flavobacterium the heparinum)) Expression of Fusion Protein that N-terminal or C-terminal with the CBD of C.cellulovorans merge.
The United States Patent (USP) of Kilburn etc. discloses the preparation and the application of described fusion rotein aspect polypeptide immobilization and purifying of the fusion rotein that comprises a cellulase substrate land for the 5th, 137, No. 819.The United States Patent (USP) of Kilburn etc. discloses non-albumen chemical part for the 5th, 928, No. 917 and has had the conjugate of the polypeptide of cellulose binding.Conjugated protein and the conjugate of polysaccharide has description in No. the 5th, 962,289, the United States Patent (USP) of Kilburn etc.The United States Patent (USP) of Gilkes etc. discloses for the 5th, 821, No. 358 with the binding domains of polysaccharidase and/or the method and composition of catalyst structure domain modified polysaccharide structure (for example cotton fibre and ramee).
The United States Patent (USP) of Shoseyov etc. discloses a kind of CBD and the described CBD and second proteic fusion product that crystalline cellulose and chitin is had high-affinity for the 5th, 837, No. 814.Also disclose the application of described CBD and described fusion product, comprised useful for drug delivery, affine separation and diagnostic techniques.Also referring to No. the 5th, 496,934, No. the 5th, 719,044, United States Patent (USP), United States Patent (USP) and the U.S.5 of Shoseyov etc., 856,201, the content of each patent all is attached to herein by reference.
B.B.Spence Encyclopedia of Polymer Science and Technology, second edition, Wiley-Interscience, the 10th volume, 761-786 page or leaf, New York (1987) have provided the summary of relevant paper with additive effectiveness.
Brief summary of the invention
The present invention relates to use the composition that comprises at least one polysaccharide binding domains to make polymeric material or crosslinked and/or functionalized composition and the method for polysaccharide material.Composition of the present invention comprises polysaccharide binding domains (PBD) fusion rotein, PBD coupling agent unit, PBD functional moiety and the polysaccharide of modifying with these compositions.PBD of the present invention coupling agent unit comprises one, two or more PBD, and each PBD can both combine with a polysaccharide independently, also can randomly be included in the one or more joint units of link coupled between the described PBD.Described method comprises the step that polysaccharide structures is contacted with the PBD fusion rotein of q.s, makes its contact conditions and duration of contact the one or more characteristics be enough to modify the polysaccharide material that contains a kind of polysaccharide structures.Described method and composition can be applicable to the polysaccharide material that contains of manufacturing machine performance, chemical property, electric property and/or physicals change.
According to one aspect of the present invention, provide a kind of manufacturing to have the method that contains polysaccharide material of at least a desired structure characteristic, chemical property, physicals, electric property and/or mechanical property, said method comprising the steps of: make polysaccharide structures that contains polysaccharide material and the composition that contains the polysaccharide binding domains described polysaccharide structures is worked into described contain in the polysaccharide material before, during and/or contact afterwards, thereby make the described polysaccharide material that contains with desired structure characteristic, chemical property, physicals, electric property and/or mechanical property.
According to another aspect of the present invention, provide a kind of topic to state composition, described composition comprises: a kind of polysaccharide material that contains that comprises polysaccharide structures; With a kind of composition that contains the polysaccharide binding domains, described composition is treated to combine with the described polysaccharide structures that contains polysaccharide material, for the described polysaccharide material that contains provides at least a required structural performance, chemical property, physicals, electric property and/or mechanical property.
According to the further feature of the following preferred embodiment of the invention, the described polysaccharide structures that contains polysaccharide material is worked into described contain in the polysaccharide material before, realize described polysaccharide structures is contacted with the described polysaccharide binding domains composition that contains.
According to the further feature of described preferred embodiment, the described polysaccharide structures that contains polysaccharide material is worked into described contain in the polysaccharide material during, realize described polysaccharide structures is contacted with the described polysaccharide binding domains composition that contains.
According to the further feature of described preferred embodiment, the described polysaccharide structures that contains polysaccharide material is worked into described contain in the polysaccharide material after, realize described polysaccharide structures is contacted with the described polysaccharide binding domains composition that contains.
According to the further feature of described preferred embodiment, the described polysaccharide material that contains is selected from paper, textiles, yarn and fiber.
According to the further feature of described preferred embodiment, described structural performance is selected from crosslinked, the described predetermined gathering and the described predetermined surface reticulate pattern that contains polysaccharide material that contains the polysaccharide structures of polysaccharide material of predeterminated level between the described polysaccharide structures that contains polysaccharide material.
According to the further feature of described preferred embodiment, described chemical property is selected from predetermined hydrophobicity, predetermined wetting ability, predetermined wetting properties, predetermined chemical reactivity, predetermined photochemical reaction, predetermined functionality and predetermined surface tension.
According to the further feature of described preferred embodiment, described physicals is selected from predetermined strain under predetermined Young's modulus, the maximum load, predetermined breaking point energy, predetermined water-absorbent, predetermined swelling property and predetermined toughness.
According to the further feature of described preferred embodiment, described electric property is selected from predetermined surface charge and predetermined electroconductibility.
According to the further feature of described preferred embodiment, described mechanical property is selected from predetermined tensile strength, predetermined shearing resistance, predetermined wearability, predetermined frictional coefficient, predetermined elasticity and predetermined wet tenacity.
According to the further feature of described preferred embodiment, describedly contain the other polysaccharide binding domains that polysaccharide binding domains composition comprises a polysaccharide binding domains and at least one and its covalent coupling.
According to the further feature of described preferred embodiment, described contain polysaccharide binding domains composition comprise a polysaccharide binding domains and with another protein of its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the hydrophobic group that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the hydrophilic radical that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the biological part retinal diseases that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the enzyme that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the chemical reaction group that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the chemical light reactive group that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the lipase that polysaccharide binding domains composition comprises a polysaccharide binding domains and one and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the laccase that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain A albumen-antibody that polysaccharide binding domains composition comprises a polysaccharide binding domains and one and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the peptide that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the polypeptide that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain hydrocarbon or the hydrocarbon derivative that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the derivative of fatty acid that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the electrically charged part that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the ion part that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the silicon bound fraction that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, the described polysaccharide binding domains composition that contains comprises that a polysaccharide binding domains and one combine part with the polymkeric substance of its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the metal that polysaccharide binding domains composition comprises a polysaccharide binding domains and a kind of and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the metallothionein(MT) sample albumen that polysaccharide binding domains composition comprises a polysaccharide binding domains and one and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the ferritin that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the melts combine part that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the bacterium siderophore that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the metallothionein(MT) that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the sulfydryl that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the aldehyde that polysaccharide binding domains composition comprises a polysaccharide binding domains and one and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the maleimide that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the hydrazides that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the epoxide that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the carbodiimide that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, describedly contain the triazobenzene that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
According to the further feature of described preferred embodiment, the described polysaccharide binding domains composition that contains comprises a polysaccharide binding domains, and described polysaccharide binding domains is a cellulose binding domain.
According to the further feature of described preferred embodiment, the described polysaccharide binding domains composition that contains comprises a polysaccharide binding domains, and described polysaccharide binding domains is the starch binding domains.
According to the further feature of described preferred embodiment, described contain polysaccharide binding domains composition comprise one can with Mierocrystalline cellulose bonded polysaccharide binding domains.
According to the further feature of described preferred embodiment, described contain polysaccharide binding domains composition comprise one can with starch bonded polysaccharide binding domains.
According to the further feature of described preferred embodiment, described contain polysaccharide binding domains composition comprise one can with chitin bonded polysaccharide binding domains.
According to the further feature of described preferred embodiment, the described polysaccharide binding domains composition that contains comprises a polysaccharide binding domains, and described polysaccharide binding domains is the dextran binding domains, β-1 for example, 3-dextran binding domains.
According to the further feature of described preferred embodiment, the described polysaccharide binding domains composition that contains comprises a polysaccharide binding domains, and described polysaccharide binding domains comprises that the suis dextran is in conjunction with tumor-necrosis factor glycoproteins.
According to another aspect of the present invention, provide a kind of topic to state composition, described composition comprises: a kind of polysaccharide material that contains that comprises polysaccharide structures; Contain polysaccharide binding domains composition with a kind for the treatment of with the described described polysaccharide structures bonded that contains polysaccharide material, describedly contain the polysaccharide binding domains that polysaccharide binding domains composition comprises at least two covalent couplings, form and make the described crosslinked polysaccharide binding domains coupling agent of polysaccharide structures that contains polysaccharide material.
Provide a kind of topic to state composition more on the one hand according to of the present invention, described composition comprises: a kind of polysaccharide material that contains that comprises polysaccharide structures; Treat and the described described polysaccharide binding domains composition that contains of polysaccharide structures bonded that contains polysaccharide material with a kind of, describedly contain the functionalized moiety that polysaccharide binding domains composition comprises at least one polysaccharide binding domains and and its covalent coupling, described at least one polysaccharide binding domains is connected described functionalized moiety with the described described polysaccharide structures that contains polysaccharide material.
According to another aspect of the present invention, provide a kind of topic to state composition, described composition comprises: a kind of polysaccharide material that contains that comprises polysaccharide structures; Contain polysaccharide binding domains composition with a kind for the treatment of with the described described polysaccharide structures bonded that contains polysaccharide material, describedly contain the hydrophobic parts that polysaccharide binding domains composition comprises at least one polysaccharide binding domains and and its covalent coupling, described at least one polysaccharide binding domains is connected described hydrophobic parts with the described described polysaccharide structures that contains polysaccharide material.
Provide a kind of topic to state composition more on the one hand according to of the present invention, described composition comprises: a kind of polysaccharide material that contains that comprises polysaccharide structures; Contain polysaccharide binding domains composition with a kind for the treatment of with the described described polysaccharide structures bonded that contains polysaccharide material, describedly contain the hydrophilic parts that polysaccharide binding domains composition comprises at least one polysaccharide binding domains and and its covalent coupling, described at least one polysaccharide binding domains is connected described hydrophilic parts with the described described polysaccharide structures that contains polysaccharide material.
According to another aspect of the present invention, provide a kind of topic to state composition, described composition comprises: a kind of polysaccharide material that contains that comprises polysaccharide structures; Contain polysaccharide binding domains composition with a kind for the treatment of with the described described polysaccharide structures bonded that contains polysaccharide material, describedly contain the chemical reactivity part that polysaccharide binding domains composition comprises at least one polysaccharide binding domains and and its covalent coupling, described at least one polysaccharide binding domains is connected described chemical reactivity part with the described described polysaccharide structures that contains polysaccharide material.
According to another aspect of the present invention, provide a kind of topic to state composition, described composition comprises: a kind of polysaccharide material that contains that comprises polysaccharide structures; Contain polysaccharide binding domains composition with a kind for the treatment of with the described described polysaccharide structures bonded that contains polysaccharide material, describedly contain the photochemical reaction part that polysaccharide binding domains composition comprises at least one polysaccharide binding domains and and its covalent coupling, described at least one polysaccharide binding domains is connected described photochemical reaction part with the described described polysaccharide structures that contains polysaccharide material.
According to another aspect of the present invention, provide a kind of topic to state composition, described composition comprises a polysaccharide binding domains coupling agent, and described coupling agent comprises the polysaccharide binding domains of at least two covalent couplings.
Provide a kind of nucleic acid construct more on the one hand according to of the present invention, described nucleic acid construct comprises the polynucleotide of encoding fusion protein, and described fusion rotein comprises at least two polysaccharide binding domainss.Preferably, described nucleic acid construct also comprises the other polynucleotide of at least one at least one joint peptide of encoding, described at least two the polysaccharide binding domainss of described joint peptide coupling.
According to another aspect of the present invention, provide a kind of manufacturing to contain the method for polysaccharide material, the described polysaccharide material that contains has at least a required structural performance, chemical property, physicals, electric property and/or mechanical property, said method comprising the steps of: make the polysaccharide structures that contains polysaccharide material and polysaccharide binding domains described polysaccharide structures is worked into described contain in the polysaccharide material during and/or contact afterwards, and, thereby make the described desired structure characteristic that has after this with at least one part or group covalency and the coupling of described polysaccharide binding domains, chemical property, physicals, electric property and/or mechanical property contain polysaccharide material.
The present invention has successfully overcome the shortcoming of present known structure by being provided for making the good method and the reagent that contain polysaccharide structures material (for example paper and textiles).
The accompanying drawing summary
At this only by embodiment and the present invention is described with reference to the drawings.Now specifically referring to the details of accompanying drawing, what emphasize is, shown detail is as an example, only is used for illustrative ground and discusses the preferred embodiments of the invention, its objective is provide think the most useful the easiest description of understanding the principle of the invention and notion aspect.At this on the one hand, do not spend strength to show than basic comprehension more detailed CONSTRUCTED SPECIFICATION of the present invention essential to the invention, described description combines with accompanying drawing, makes about how specific implementation several forms of the present invention are conspicuous for those skilled in the art in practice.
Figure 1A is the graphic explanation of pET-CBD plasmid.
Figure 1B-1C has shown nucleotide sequence (SEQ ID NO:1) and the aminoacid sequence (SEQ ID NO:2) of CBDclos.
Fig. 1 D is illustrating of pET-CBD-180.
Fig. 1 E-G has shown nucleotide sequence (SEQ ID NO:3) and aminoacid sequence (SEQ ID NO:4) and the restriction endonuclease recognition site of CBD-180.
Fig. 2 A is the illustrating of pET-CCP-180 of containing the CBD that meets the fusion of frame ground with it of copy CBD-180 and a copy.
Fig. 2 B-E has shown nucleotide sequence (SEQ IDNO:5) and the aminoacid sequence (SEQ ID NO:6) and the restriction endonuclease recognition site of CCP (cellulose crosslinked albumen).
Fig. 3 A is the graphic explanation of pET-ProtA-CBD.
Fig. 3 B-G has shown nucleotide sequence (SEQ ID NO:7) and the aminoacid sequence (SEQ ID NO:8) of ProtA-CBD.
Fig. 4 A is the graphic explanation of pET29-Spep-CBD-Sprot.
Fig. 4 B-G has shown nucleotide sequence (SEQ ID NO:9) and the aminoacid sequence (SEQ ID NO:10) of Spep-CBD-Sprot.
The graphic explanation per molecule of Fig. 5 A has the cellulose crosslinked albumen of two cellulose binding domains.
The cellulose crosslinked albumen of the graphic explanatory view 5A of Fig. 5 B, one of them cellulose binding domain combines with the first paradigmatic structure unit, and second cellulose binding domain combines with the second paradigmatic structure unit.
CBD coupling agent unit that belongs to class of the graphic explanation of Fig. 6.
Each embodiment of the respectively graphic explanation CBD of Fig. 7 A-C coupling agent unit.Fig. 7 A has shown a kind of CBD coupling agent unit, and it has: by a pair of terminal CBD that a joint unit connects, described joint unit comprise a pair of respectively with a CBD link coupled starch binding domains; With a starch part, described starch part and the coupling of two starch binding domainss.Fig. 7 B has shown a kind of CBD coupling agent unit, and it has: by a pair of terminal CBD that a joint unit connects, described joint unit comprises a plurality of CBD, and each CBD is by a JUN/FOS bridge and an adjacent CBD coupling.Fig. 7 C has shown the CBD coupling agent unit with a pair of terminal CBD that is partly connected by a large protein.
The graphic explanation of Fig. 8 has at least one CBD and a connected functional moiety's (FM) CBD functional moiety (CBDC).
The graphic explanation CBD of Fig. 9 A-C coupling agent unit can interact and the bonded variety of way with paradigmatic structure unit.
Figure 10 A-D is a bar graph, shows that respectively contrast, CBD handle and Young's modulus, the strain under the maximum load, breaking point energy and the toughness of the paper slip that CCP handles.
The graphic explanation of Figure 11 is used for handling with experimental preparation the yarn coating device of yarn.
Figure 12 A-B is a bar graph, shows that respectively contrast, CCP handle, ProtA-CBD handles and the Young's modulus of the yarn that Ab-ProtA-CBD handles and the strain under the maximum load.
Figure 13 is a photo, has shown the S-albumen-expression of results of CBD-S-peptide (SCS) in intestinal bacteria.Protein label (1 road) is induced e. coli total protein (2 road) before with IPTG, induces e. coli total protein (3 road) afterwards and contains the proteic inclusion body of SCS (4 road) with IPTG.
Figure 14 has shown the Young's modulus figure that handles Whatman paper result with CBD, CCP or SCS.All are measured all under 23 ℃, 65% relative humidity and carry out.
Figure 15 has shown the breaking point energy through the Whatman paper of CBD, CCP and SCS processing.All are measured all under 23 ℃, 65% relative humidity and carry out.
Figure 16 has shown the toughness result through the Whatman paper of CBD, CCP and SCS processing.All are measured all under 23 ℃, 65% relative humidity and carry out.
Figure 17 has shown the stress of Whatman paper under maximum load through CBD, CCP and SCS processing.All are measured all under 23 ℃, 65% relative humidity and carry out.
Figure 18 has shown the typical stress and strain relation curve of the preliminary shaping Whatman paper of handling with CBD or CCP.All are measured all under the constant rate of deformation (deformation rate) of 23 ℃, 65% relative humidity and 20mm/min and carry out.Square-contrast; Circle-2.5mg/ml CBD; Trilateral-2.5mg/ml CCP.
Figure l9 has shown the absorbent time of the preliminary shaping Whatman paper of handling with the CBD of different concns or CCP.All measurements are all carried out at 23 ℃.Draw distilled water (10 μ l) and place on the treated paper, to measure the time (contrast-solid strip of hypersorption second; The CBD-band of pointing with the finger or gesticulate; The hollow band of CCP-).
Figure 20 shows the time lapse photo that water absorbs on the preliminary shaping Whatman paper that CCP handles.Water droplet (every 20 μ l) is dripped on the paper that CCP handles, and every 25ms takes pictures.Water with take first frame (A) before paper contacts.After the B-E frame is photographed 2,4,6 and 8 minutes respectively.Contact back 25ms with paper at undressed paper photographs last frame (F) at water.Manifest the absorption of water with light contact angle meter (optical contact angle meter).
Detailed description of the preferred embodiments
According to the present invention, be provided for changing the method and composition of polysaccharide material surface property, chemical property, electric property and mechanical property.
Before in detail explaining at least one embodiment of the present invention, should be appreciated that application of the present invention is not limited to following description or details that embodiment exemplified.The present invention can implement other embodiment in every way.Should be appreciated that also wording used herein and term are in order to describe, should not to be considered to restrictive.
For example the polysaccharide structures of fiber and long filament described structure is worked into contain in the polysaccharide material during or afterwards, with containing the PBD compositions-treated, thereby make described polysaccharide structures and/or its product (for example textiles and paper) crosslinked and/or functionalized.Contain the PBD composition as omnipotent biological linking agent, its structure can change, and to adapt to the required result who contains the polysaccharide finished product, for example elasticity or hydrophobicity strengthen.Described biological linking agent is a polyprotein, contain at least one PBD (for example cellulose binding domain), described PBD merges with one or more biological entities or chemical entities or is connected (" merging or connection "=covalent coupling), and the magnitude range of described biological entities or chemical entities is that hundreds of dalton are to millions of dalton.Described biological entities generally is one or more second protein.Described second protein can be another kind of PBD, for example cellulose binding domain or starch binding domains or functionalized PBD, for example with hydrophobic grouping or enzyme bonded PBD, described enzyme especially can improve or quicken the described polysaccharide structures of polysaccharide finished product and/or the enzyme of characteristic processing, for example lipase or the laccase of containing.Perhaps, described second protein can be a kind of non-PBD albumen, for example A albumen-antibody complex.
In order to prepare the modified polysaccharide material that contains, make polysaccharide structures during being worked into it in polysaccharide material or afterwards, contact with the biological linking agent of capacity, its contact conditions and time are enough to change one or more performances of the polysaccharide material that contains described polysaccharide structures.As an example, applying glue or starching step that need not be traditional during cellulosic fibre being processed as paper or cotton is processed as yarn, or in conjunction with traditional applying glue or starching step, can make the polysaccharide structures gathering and/or make polysaccharide structures (for example polysaccharide fiber and long filament) crosslinked with described PBD fusion rotein, so that strengthen described structure from the wet tenacity during processing and/or the wet tenacity that contains polysaccharide material of manufacturing.Preferably, handle, substitute traditional applying glue or starching step with the PBD fusion rotein.Yet, in some applications, can usefully these two kinds of methods for example be combined with amylan and starch-containing protein-bonded PBD fusion rotein, so that described starch and described fiber are crosslinked.In addition, the PBD that comprises the functional moiety can be used for have hydrophobic part (for example derivative of fatty acid or hydrophobic amino acid sequence) for example to contain polysaccharide material (for example cellulose matrix) functionalized, contain the wetting properties of polysaccharide material (for example paper) with reduction.
The invention provides the several advantages that are better than for example being used for the commercial papers and the existing processing polysaccharide structures method of weaving processing.By handle the suitable polysaccharide material (for example cellulosic fibre) that contains with biological linking agent, can obtain with undressed material and/or compare the product of mechanical property improvement (for example intensity and wearing quality enhancing) with the material that the strongthener of non-PBD fusion rotein is handled.In addition, in the manufacturing of fluting board, can or shaping stage or size application stage before or after use described PBD reagent, to strengthen the wet tenacity of described paper.If use at shaping stage, then it provides enough wet tenacitys, makes to remove the applying glue step.Because can save in the paper conversion used machine about 1/3rd machine,, and significantly reduce the papermaking cost so this has not only saved the time.Opposite with chemical cross-linking agent and hydrophobic material, the applying biological linking agent has also improved the recyclability of the paper product that uses this method manufacturing.
Another advantage of the present invention is: in the forming step of papermaking, many fiber fines lose because passing forming net.And described PBD reagent is retained in them in the paper pulp, causes the rate of recovery of raw material higher.In addition, in last procedure of processing of making corrugated containers, use alkaline glue, so that described fluting board is incorporated on the wallboard.With strong alkaline condition wash-out PBD molecule, this has strengthened the ability of the described paper of described alkaline glue penetration.
Poly PBD fusion rotein of the present invention has two kinds of basic building blocks-a kind of PBD and a kind of second albumen, and wherein said second albumen can yes or no PBD.PBD comprises aminoacid sequence with polysaccharide (for example Mierocrystalline cellulose) or contain protein or the peptide that described PBS combines the polymkeric substance of polysaccharide substrate fundamental structural unit, described polysaccharide substrate comprises or skeleton sugar and/or terminal sugar and described sugar itself, comprises monose and disaccharide.The definition of PBD comprises mutant, varient of naturally occurring PBD etc., and unique requirement is them and contain the polysaccharide substrate and combine.PBD can reversible with the substrate polysaccharide or irreversibly combine, and described substrate can be natural or synthetic.The PBD fusion rotein can be the protein molecule with a plurality of polysaccharide binding domainss, and described polysaccharide binding domains can derive from identical or different polysaccharidase or scaffolding protein, and they can combine with identical or different polysaccharide.When having a plurality of PBD, they preferably occupy the different structure territory in the described PBD fusion rotein, and can play a role independently of each other.Term CBD is meant and can derives from the structural domain that participates in Mierocrystalline cellulose bonded natural protein, or refer to isolating aminoacid sequence or its fragment (referring to (1988) J.Biol.Chem.263:10401-10407 such as (1993) J.Bacteriol.175:5762-5768 such as for example Goldstein and Gilkes, the content of these two documents is attached to herein by reference) of self and Mierocrystalline cellulose bonded native protein.PBD and CBD can be natural, synthetic or partial synthesis.
Described polysaccharide binding domains comprises and comprises the polysaccharidase polysaccharide binding domains, that be with or without catalytic capability, can adopt in the multiple technologies that comprise biological chemistry and/or gene engineering any to obtain.Therefore, they can pass through proteolysis (referring to for example Gilkes etc., J.Biol.Chem (1988) 213:10401-10407) or by adopting technology well known by persons skilled in the art to obtain by genetic manipulation (for example random mutation, site-directed mutagenesis or DNA reorganize (DNAshuffling)).Utilize site-directed mutagenesis, can carry out mutagenesis, with suppressing or blocking-up catalytic activity but do not disturb aminoacid replacement in conjunction with polysaccharide to the specific amino acids relevant with described polysaccharidase catalytic activity.For example, in CenA, can replace the aspartic acid in site 283.A kind of like this method produces and the quite similar aminoacid sequence of original polysaccharide sequence effectively, but the functional domain that contains described catalytic activity is modified to become and do not had function owing to mutagenesis or biological chemistry; Binding domains reservation function only.Can in the aminoacid sequence of various PBD, replace, insert or lack one or more predetermined amino-acid residues, so that anomaly or mutant PBD to be provided.Can carry out the aminoacid replacement in PBD albumen or the peptide sequence with based on the similarity of the polarity of for example target amino acid residue, electric charge, hydrophobicity, wetting ability etc. or the reasonable manner of difference.Usually the amino acid whose characteristic of all that see in protein (for example polarity and hydrophobicity) is well-known in the art, and the technology that changes (sudden change) aminoacid sequence specifically also is well-known.The anomaly of gained or mutant PBD are considered to belong to scope of the present invention.Can replace, insert and/or lack, have multiple required character the to provide anomaly PBD of (for example being used for specific the crosslinked or functionalized of polysaccharide material that contain).
Only can use aminoacid sequence, but not have the complete polysaccharide sequence of specific sudden change or modification corresponding to described polysaccharide binding domains.In this case, by described polysaccharidase is cut into functional domain, obtain PBD.For example, make isolating polysaccharide, described protein is cut into two or more fragments that constitute by functional domain through protease treatment.Sometimes, described polysaccharide contains a specific protease site.For example, muck cellulomonas cartae (C.fini) endoglucanase A (CenA) contains one by the PT frame of conformation specific muck cellulomonas cartae proteolytic enzyme cutting.The product of this reaction is polysaccharide binding domains and the polysaccharidase catalyst structure domain with a PT sequence.If described polysaccharidase by highly sequence-specific proteolytic enzyme cutting, does not then make it stand the lower protease treatment of specificity, can separate described active fragments by chromatogram and other peptide purification technology well known by persons skilled in the art.
Other technology that can be used for obtaining binding domains comprises the application amino acid sequence information, produces the probe that is used for clones coding polysaccharidase or the protein-bonded dna sequence dna of polysaccharide.These cloned sequences can be used for producing the deletion mutant of polysaccharide binding domains of only encoding.On the contrary, if the protein-bonded cDNA sequence of polysaccharidase or polysaccharide is known, then can adopt the data of biological chemistry, amino acid and dna sequence dna, the position of coming the basis and the sequence homology of other polysaccharidase to predict described polysaccharide binding domains, the concrete dna sequence dna that makes up corresponding to described polysaccharide binding domains.It is known in the art being used for the protein-bonded technology of separating polyose enzyme gene and polysaccharide, comprise synthetic, from genomic dna, separate, from cDNA preparation or their combination.Can comprise gene fusion, phage display, DNA reorganization and at random or site-directed mutagenesis in order to other technology that obtains the polysaccharide binding domains.The various technology that are used for genetic manipulation are well-known, comprise restriction, digestion, excision, connection, vitro mutagenesis, primer repair, utilize joint and connector etc. (referring to Molecular Cloning:A Laboratory Manual second edition, Sambrook etc. (writing), Cold Spring Harbor Laboratory Press, NY, (1989), the document is attached to herein by reference).Can obtain the proteic nucleic acid of code book invention PBD from the RNA of separation and purification or by genomic clone.Can use technology well-known in the art, preparation or cDNA library or genomic library, flat and can in described library, use and the basic complementary probe of arbitrary part of described encoding sequence, screen specific PBD nucleotide sequence.Perhaps, cDNA or genomic dna can be used as template, adopt suitable Oligonucleolide primers to carry out the PCR clone.Can select full-length clone, promptly contain those clones of the proteic complete encoding sequence of required PBD, come construction of expression vector, perhaps overlapping cDNA can be linked together, form complete encoding sequence or its required part, for example binding domains.Perhaps, can adopt solid phase technique well known in the art, by the chemosynthesis DNA of composite coding PBD wholly or in part.
Described PBD can obtain from multiple source, comprises and can be applicable to oligosaccharides bonded enzyme of the present invention.In following table 5, listed and one or more solubilities/those binding domainss of insoluble polysaccharide bonded, comprise soluble glucan α, β and/or mix all binding domainss that key has affinity.The N1 cellulose binding domain that derives from muck cellulomonas cartae endoglucanase CenC combines with one of soluble cellulose carbohydrate (cellosaccharides) and known and any soluble polysaccharide bonded one group's protein.In addition, listed among the 1-4 at table and contained the β-1 that infers, the proteinic example (table 1) of 3-dextran binding domains; Contain the protein (Cpl superfamily) (table 2) of suis dextran in conjunction with tumor-necrosis factor glycoproteins; Enzyme (table 3) with chitin binding domains; With starch binding domains (table 4).Comprise cellulose binding domain albumen (for example by biting cellulose binding domain albumen (Shoseyov etc., PCT/US94/04132)) that fiber clostridium (Clostridium cellulovorans) produces at interior scaffolding protein, also can be in order to preparation PBP.Several fungies comprise that mould (the Trichodenma species) of wood and other fungi also produce the polysaccharidase that can isolate PBP.
Table 1
Contain and infer β-1, the proteinic general introduction of 3-dextran binding domains
Source (bacterial strain) protein registration number Ref. 1
Type i
Bacillus circulans (B.circulans) WL-12) GLCAl P23903/M34503/JQ0420 1
Bacillus circulans (IAM 1165) BglH JN0772/D17519/S67033 2
Type II
Actinomycesa lmadurae (Actinomadura sp.) is XynII U08894 3 (FC7)
Arthrobacter (Arthrobacter sp.) is GLCI D23668 9 (YCWD3)
Molten xanthine strategic point Salmonella (O.xanthineolytica) GLC P22222/M60826/A39094 4
The rotten rare bacillus of slag (R.faecitabidus) is RPI Q05308/A45053/D10753 5a (YLM-50), b
Castor-oil plant (R.communis) Ricin A12892 6
Shallow Streptomyces glaucoviolaceus (S.lividans) (1326) XlnA P26514/M64551/JS07986 7
T.tridentatus FactorGa D16622 8B.: bacillus (Bacillus), O.: Oerskovia (Oerskovia), R.faecitabidus: the rotten rare bacillus (Rarobacterfaecitabidus) of slag, R.communis: castor-oil plant (Ricinus Communis), S.: streptomyces (Streptomyces), T.: limulus (Tachypleus) (limulus polyphemus) 1Reference: 1) Yahata et al. (1990) Gene 86,113-1172) Yamamoto et al. (1993) Biosci.Biotechnol.Biochem.57,1518-15253) Harpin et al. (1994) EMBL Data Library4) Shen et al. (1991) J.Biol. Chem.266,1058-10635a) Shimoi et al. (1992) J.Biol.Chem.267,25189-251955b) Shimoi et al. (1992) J.Biochem 110,608-6136) Horn et al. (1989) Patent A128927) Shareck et al. (1991) Gene 107,75-828) Seki et al. (1994) J.Biol.Chem.269,1370-13749) Watanabe et al. (1993) EMBL Data Library
Table 2
Contain the general introduction source protein registration number Ref. of suis dextran in conjunction with the protein (Cpl superfamily) of tumor-necrosis factor glycoproteins 2Fine hair (cousin) streptococcus (S.downei (sobrinus)) is (Ingbritt) GBP M30945/A37184 6 Streptococcus mutans (GS-5) GTF-B A33128 7 Streptococcus mutans (GS-5) GTF-B P08987/M17361/B33135 8 Streptococcus mutans GTF-B of GTF-I D13858 1 fine hair (cousin) streptococcus (MFe28) GTF-I P11001/M17391 2 fine hairs (cousin) streptococcus (MFe28) GTF-S P29336/M30943/A41483 3 fine hairs (cousin) streptococcus (6715) GTF-I P27470/D90216/A38175 4 fine hairs (cousin) streptococcus DEI L34406 5 Streptococcus mutans (S.mutants) (0MZ176)3 '-ORF P05427/C33135 8 Streptococcus mutans, (GS-5) GTF-C P13470/M17361/M22054 9 Streptococcus mutans, (GS-5) GTF-C not available 10 Streptococcus mutans, (GS-5) GTF-D M29296/A45866 11 streptococcus-salivariuses, (S.salivarius) GTF-J A44811/S22726/S28809 12
Z11873/M64111 streptococcus salivarius GTF-K S22737/S22727/Z11872 13 streptococcus salivariuses (ATCC25975) GTF-L L35495 14 streptococcus salivariuses (ATCC25975) GTF-M L35928 14 streptococcus pneumonias (S.pneumoniae) R6 LytA P06653/A25634/M13812 15 streptococcus pneumonia PspA A41971/M74122 16 bacteriophage HB-3 HBL P32762/M34652 17 bacteriophage Cp-l CPL-1 P15057/J03586/A31086 18 bacteriophage Cp-9 CPL-9 P19386/M34780/JQ0438 19 phage E J-1 EJL A42936 20 clostridium difficiles (C.difficile) (VPI 10463) ToxA P16154/A37052/M30307 21
X51797/S08638 clostridium difficile (BARTS W1) ToxA A60991/X17194 22 clostridium difficiles (VPI 10463) ToxB P18177/X53138/X60984 23,24
S10317 clostridium difficile (1470) ToxB S44271/Z23277 25,26 Nuo Shi clostridium (C.novyi) a-toxin S44272/Z23280 27 Nuo Shi clostridium a-toxin Z48636 28 clostridium acetobutylicums (C.acetobutylicum) are CspA S49255/Z37723 29 clostridium acetobutylicums (NCIB8052) CspB Z50008 30 clostridium acetobutylicums (NCIB8052) CspC Z50033 30 clostridium acetobutylicums (NCIB8052) CspD Z50009 30 (NCIB8052)2Reference: 1) Sato et al. (1993) DNA sequence4,19-272) Ferreti et al. (1987) J.Bacteriol.169,4271-42783) Gilmore et al. (1990) J.Infect.Immun.58,2452-24584) Abo et al. (1991) J.Bacterial.173,989-9965) Sun et al. (1994) J.Bacteriol.176,7213-72226) Banas et al. (1990) J.Infect.Immun.58,667-6737) Shiroza et al. (1990) Protein Sequence Database8) Shiroza et al. (1987) J.Bacteriol.169,4263-42709) Ueda et al. (1988) Gene 69,101-10910) Russel (1990) Arch.Oral.Biol.35,53-5811) Honda et al. (1990) J.Gen.Microbiol.136,209-210512) Giffard et al. (1991) J.Gen. Microbil.137,2577-259313) Jacques (1992) EMBL Data Library14) Simpson et al. (1995) J.Infect.Immun.63,609-62115) Gargia et al. (1986) Gene 43,265-27216) Yother et al. (1992) J.Bacteriol.174,601-60917) Romero et al. (1990) J.Bacteriol.172,5064-507018) Garcia et al. (1988) Proc Natl.Acad.Sci, USA 85,914-91819) Garcia et al. (1990) Gene 86,81-8820) Diaz et al. (1992) J.Bacteriol.174,5516-552521) Dove et al. (1990) J.Infect.Immun.58,480-48822) Wren et al. (1990) FEMS Microbol.Lett.70,1-623) Barroso et a. (1990) Nucleic Acids.Res.18,4004-400424) von Eichel-Streiber et al. (1992) Mol.Gen.Genet.233,260-26825) Sartinger et al. (1993) EMBL Data Library26) von Eichel-Streiber et al. (1995) Mol.Microbiol.In Press27) Hofmann et al. (1993) EMBL Data Library28) Hofmann et al. (1995) Mol.Gen Genet.In Press29) Sanchez et al. (1994) EMBL Data Library30) Sanchez et al. (1995) EMBL Data Library
One of can be in many ways, identify and screening has interesting binding characteristic and specific new PBP that described mode comprises: spectrum (titration) method, for example the NMR spectrography (Zhu etc. (1995) Biochemistry 34:; Gehring etc. (1991) Biochemistry 30:5524-5531), UV differential spectrum method (Beishaw etc. (1993) Eur.J.Biochem.211:717-724), fluorescence (titration) spectrography (Miller etc. (1983) J.Biol.Chem.258:13665-13672), UV or fluorescence stop-flow analysis ((1985) Eur.J.Biochem.149:141-415 such as De Boeck); Affine method, for example affinity electrophoresis on immobilization monose or oligosaccharides (Mimura etc. (1992) J.Chronmatography 597:345-350) or affinity chromatography; Precipitation or aggegation analysis comprise nephelometric analysis (Knibbs etc. (1993) J.Biol.Chem.14940-14947); Competitive inhibition is measured (being with or without quantitative IC50 measures); And various physical methods or physico-chemical process, comprise differential scanning or isothermal titration calorimetry (Sigurskjold etc. (1992) J.Biol.Chem.267:8371-8376; Sigurskjold etc. (1994) Eur.J.Biol.225:133-141) or use hot CD or fluorescent spectrometry to exist or do not exist the comparative protein stability under the situation to measure (melt (melts)) at oligosaccharides.
Generally speaking, described PBP and oligosaccharides bonded Ka at least in weak antibody-antigen extracts (antibody-antigen extraction) scope, promptly 10 -3, preferably 10 -4, most preferably 10 -6If described PBP is heat release or heat absorption with combining of described oligosaccharides, then respectively at a lower temperature bonded increase or the temperature regulation that is reduced to during the polysaccharide structures processing provides a kind of means.
Table 3
3Reference: 1) Udea et al. (1994) J.Ferment.Bioeng.78,205-2112) Watanabe et al. (1990) J.Biol.Chem.265,15659-165653) Watanabe et al. (1992) J.Bacteriol.174,408-4144) Gleave et al. (1994) EMBL Data Library5) Sidhu et al. (1994) J.Biol.Chem.269,20167-201716) Jones et al. (1986) EMBO J.5,467-4737) Sitrit et al. (1994) EMBL Data Library8) Tsujibo et al. (1993) J.Bacteriol.175 Genbank entry only9), 176-18110) Yanai et al. (1992) J.Bacteriol.174,7398-740611) Pauley (1994) EMBL Data Library12) Kuranda et al. (1991) J.Biol.Chem.266,19758-1976713) van Damme et al. (1992) EMBL Data Library14) Broekaert et al. (1992) Biochemistry 31,4308-431415) de Bolle et al. (1993) Plant Mol.Physiol.22,1187-119016) Samac et al. (1990) Plant Physiol.93,907-91417) Potter et al. (1993) Mol.Plant Microbe Interact.6,680-68518) Buchanan-Wollaston (1995) EMBL Data Library19) Hamel et al. (1993) Plant Physiol.101,1403-140320) Broekaert et al. (1990) Proc.Natl.Acad.Sci.USA 87,7633-763721) Lee et al. (1991) J.Biol.Chem. 266,15944-1594822) Leah et al. (1994) Plant Physiol.6,579-58923) Danhash et al. (1993) Plant Mol.Biol.22 1017-102924) Ponstein et al. (1994) Plant Physiol.104,109-11825) Meins et al. (1991) Patent EP0418695-Al26) van Buuren et al. (1992) Mol.Gen.Genet.232,460-46927) Shinshi et al. (1990) Plant Mol.Biol.14,357-36828) Comellisen et al. (1991) Patent EP0440304-A229) Fukuda et al. (1991) Plant Mol.Biol.16,1-1030) Yun et al. (1994) EMBL Data Library31) Kim et al. (1994) Biosci.Biotechnol.Biochem.58,1164-116632) Nishizawa et al. (1993) Mol. Gen. Genet. 241,1-1033) Nishizawa et al. (1991) Plant Sci 76,211-21834) Huang et al. (1991) Plant Mol. Biol.16,479-48035) Zhu et al. (1991) Mol. Gen. Genet.226,289-29636) Muthukrishhnan et al. (1993) EMBL Data Library37) Vad et al. (1993) Plant Sci 92 Xu (1995) EMBL Data Library38), 69-7939) Chang et al. (1994) EMBL Data Library40) Davis et al. (1991) Plant Mol. Biol.17,631-63941) Clarke et al. (1994) Plant Mol. Biol. 25,799-81542) Broglie et al. (1989) Plant Cell 1,599-60743) Broglie et al. (1986) Proc. Natl.acad.Sci.USA 83,6820-682444) Lucas et al. (1985) FEBS Lett.193,208-21045) Hedrick et al. (1988) Plant Physiol.86,182-18646) Roberts et al. (1994) EMBL Data LibraryI.47) Vamagami et al. (1994) Biosci.Biotechnol.Biochem.58,322-32948) Beerhues et al. (1994) Plant Mol.Biol.24,353-36749) Stanford et al. (1989) Mol.Gen.Genet.215,200-20850) Liao et al. (1993) EMBL Data Library51) Smith et al. (1989) Plant Mol.Biol.13,601-60352) Wright et al. (1989) J.Mol.Evol.28,327-33653) Wright et al. (1984) Biochemistry23,280-28754) Raikhel et al. (1987) Proc.Natl.acad.Sci.USA 84,6745-674955) Hajela et al. (1993) EMBL Data Library56) Lerner et al. (1992) J.Biol.Chem.267,11085-1109157) Vo et al. (1995) EMBL Data Library
Table 4
General introduction source (bacterial strain) enzyme registration number Ref. that contains the enzyme of starch binding domains 4Aspergillus awamori (A.awarori) is (T21) AMYG S73370 3 aspergillus nigers-Aspergillus awamori AMYG1/G2 P04064/A90986/A29166/X00712/ of AMYG P23176/D00427/ JT0479 1,2 aspergillus niger (A.niger) (var.Kawachi)
X00548 4，5，6
K02465 7,8,9 aspergillus oryzaes (A.oryzae) AMYG (GLAA) P36914/JQ1346/D01035/S75274/
D01108 10,11A.Shirousamii AMYG (GLA) P22832/JQ0607/D10460 12 genus bacillus (B1018) AMY aP17692/M33302/D90112/S09196 13 bacillus (TS-23) α-AMY U22045 14 bacillus (1-1) CGT P31746/S26399 15 bacillus (6.63) CGT P31747/X66106/S21532 16 bacillus (17-1) CGT P30921/M28053/A37208 17 bacillus (38-2) CGT P09121/M19880/D00129/S24193 18; 19 ( 1011 ) CGT P05618/A26678/M17366 20 ( DSM5850 ) CGT A18991 21 ( KC201 ) CGT D13068 15,22 ( B.cereus ) ( SPOII ) β-AMY A48961/P36924/S54911 23 ( 8 ) CGT P30920/X68326/S23674 24 ( 251 ) CGT X78145 25 ( B.licheniformis ) CGTA P14014/X15752/S15920 26 ( B.macerans ) ( IFO 3490 ) CGTM ( CDG1 ) P04830/X5904/S31281 27 ( IAM 1243 ) CGT M1277 28 CGT ( CDG2 ) P31835/S26589 29B.ohbensis CGT P27036/D90243 30 ( B.stearothermophilus ) AMYMbP19531/M36539/S28784 31 bacstearothermophiluses (NO2) CGT P31797/X59042/S26588/X59043/
X59404/S31284 32 sieve ear photovoltaicing leather bacteria (C.rolfsii) (AHU 9627) AMYG2 D49448 33 dictyostelium discoideums (D.discoideum) ORF S15693/X51947 34H.grisea (var.thermoidea) GLA1 M89475 35H.resinae (ATCC20495) GAMP Q03045/X68143/X67708/S31422/
S33908 36-38 Klebsiella pneumonia (K.pneumoniae) is (74-OR23-1A) GLA-1 P14804/X67291/S13711/S13710/ of CGT P08704/M15264/A29023 39 Neurospora crassas (N.crassa) (M5A1)
S36364 40,41 Pseudomonas saccharophilas (P.saccharophila) are MTA (IAM1504) cP22963/X16732/S05667 42 pseudomonass (KO-8940) AMF-1 dD10769/JS0631/D01143 43 Pseudomonas stutzeris (P.stutzeri) are AMYP (MO-19) cP13507/M24516/A32803 44 streptomyces griseuses, (S.griseus), (IMRU 3570) AMY P30270/X57568/S14063 45 mud streptomycetes, (S.limosus), (S.albidoflavus) AML P09794/M18244/B28391 46 Streptomyces violaceus, (S.violaceus), (S.venezuela) AML P22998/M25263/JS0101 47, (ATCC15068) Th.curvata, (CCM 3352) TAM eP29750/X59159/JH0638 48 heat are produced the hot anaerobic bacillus(cillus anaerobicus) of sulphur (Th.thermosulfurogenes) fAMYA P26827/X54654/X54982/ (DSM3896/EM1) S17298/S37706 49 heat are produced the hot anaerobic bacillus(cillus anaerobicus) AMYB of sulphur P19584/M22471/A31389 50 (ATCC33743) aGive birth to starch digestion amylase, bProduce maltogenic alpha-amylase enzyme, cThe amylase of generation maltotetrose (1,4-α-maltotetrose lytic enzyme, dGenerate the amylase of Fructus Hordei Germinatus pentose, eThermally-stabilised α-Dian Fenmei, fBefore be called Clostridium thermosulfurigenes (Clostridiumthermosulfurogenes), AMYG, GAM and GLA: glucoamylase, AMY or AML: α-Dian Fenmei, CGT: beta-cyclodextrin glycosyltransferase or ring maltodextrin dextran based transferase (glucanotransferase), ORF: open reading-frame (ORF).A: Aspergillus (Asperillus), B.: bacillus, C.: corticium (Corticium), D.: dictyostelium (Dictiostelium), H.grisea:Humicola grisea, H.resinea:Hormoconis resinae (Amorphotheca resinae), K.: Klebsiella (Klebsiella), N.: neurospora (Neurospora), S.: streptomyces (Streptomyces), Th.curvata: crooked high temperature Zymomonas mobilis (Thermomonospora curvata), Th.: hot anaerobic bacillus(cillus anaerobicus) belongs to (Thermoanaerobacter). 4Reference: 1) Hayashida et al. (1989) Agric.Biol.Chem.53,135-1412) Hayashida et al. (1989) Agric.Biol.Chem.53,923-9293) Zhong et al. (1994) Wei Sheng Wu Hseuh Pao 34,184-1904) Boel et al. (1984) EMBO J.3,1097-11025) Boel et al. (1984) EMBO J.3,1581-15836) Svensson et al. (1986) Eur.J.Biochem.154,497-5027) SVensson et al. (1983) Carlsberg Res.Commun.48,529-5448) Nunberg et al. (1984) Mol.Cell.Biol.4,2306-23159) Flwer et al. (1990) Curr.Genet.18,537-54510) Hata et al. (1991) Agric.biol.Chem.55,941-94911) Hata et al. (1991) Gene 108,145-15012) Shibuya et al. (1990) Agric.Biol.Chem.54,1905-191413) Itkor et al. (1990) Biochem.Biophys.res.Commuun.166,630-63614) Lin et al. (1995) EMBL Data Library15) Schimd et al. (1988) Proceedings of the fourth Internationalsymposium on cyclodextrins.Huber, O.and Szejtli, J.Eds.pp71-76.Kluwer, Academic Publishers.16) Kaneko et al. (1989) J.Gen.Microbiol.135 Akhmetzjanov (1992) EMBL Data Library17), 3447-345718) Kaneko et al. (1988) J.Gen.Microbiol.134,97-10519) Hamamoto et al. (1987) Agric.Biol.Chem.51,2019-202220) Kimura et al. (1987) J.Bacteriol.169,4399-440221) Patent WO9114770-A122) Kitamoto et al. (1992) J.Ferment.Bioeng.74,345-35123) Nanmori et al. (1993) Appl.Environ Microbiol.59,623-62724) Nitschke et al. (1990) Appl.Microbial.Biotechnol.33,542-54625) Lawson et al. (1994) J.Mol.Biol.236,590-56026) Hill et al. (1990) Nucleids Acicds Res.18,199-19927) Fujiwara et al. (1992) Appl.Environ Microbiol.58,4016-402528) Takano et al. (1986) J.Bacteriol.166,1118-112229) Sugimoto et al.Patent N UK216990230) Sin et al. (1991) Appl.Microbiol.Biotechnol.35,600-60531) Didericksen et al. (1988) FEMS Microbiol.Lett.56,53-6032) Fujiwara et al. (1992) Appl.Environ.Microbiol.58,4016-402533) Nagasaka et al. (1995) EMBL Data Library34) Maniak et al. (1990) Nucleic Acids Res.18,3211-321735) Berka et al. (1992) EMBL Data Library36) Joutsjoki et al. (1992) FEMS Microbiol.Lett.78,237-24437) Vainio et al. (1993) Curr.Genet.24,38-4438) Fagerstrom et al. (1990) J.Gen.Microbiol.136,913-92039) Binder et al. (1986) Gene 47,269-27740) Stone et al. (1989) Curr.Genet.24,205-21141) Koh-Laur et al. (1989) Enzym.Microb.Technol.11,692-69542) Zhoe et al. (1989) FEBS Lett.255,37-4143) Shida et al. (1991) Biosci.Biotechnol.Biochem.56,76-8044) Fujita et al. (1989) J.Bacteriol.171,1333-133945) Vigal et al. (1991) Mol.Gen.Genet.225,278-28846) Long et al. (1987) J.Bacteriol.169,5745-575447) Virolle et al. (1988) Gene74,321-33448) Petricek et al. (1992) Gene112,77-8349) Bahl et al. (1991) Appl.Environ.Microbiol.57,1554-155950) Kitamoto et al. (1988) J.Bacteriol.170,5848-5854
Table 5
The source integrated structure domain discovery of polysaccharide binding domains has the protein cellulose binding domains of binding domains 1Beta-glucanase (avicelase, the CMC enzyme,
Cellodextrin enzyme)
Exoglucanase or cellobiohydrolase
Mierocrystalline cellulose is conjugated protein
Zytase
Mix zytase/dextranase
Esterase
Chitinase
Beta-1,3-glucanase
β-1, and 3-(β-1,4-)-dextranase
(β-) mannase
Beta-glucosidase enzyme/tilactase
Cellulose synthase (not confirming) starch/maltodextrin binding domains α-Dian Fenmei 2,3
Beta-amylase 4,5
Starch debranching enzyme
Glucoamylase 6,7
Cyclodextrin glucosyltransferase 8-10
(ring maltodextrin dextran based transferase)
Maltodextrin is conjugated protein 11Dextran binding domains (streptococcus) glycosyltransferase 12
Sucrose:glucan alpha1 (not confirming)
Clostridial toxin 13,14
Glucoamylase 6
Glucan-binding protein beta-glucan binding domains beta-1,3-glucanase 15,16
β-1,3-(β-1,4)-dextranase (not confirming) 17
β-1,3-glucan-binding protein chitin binding domains chitinase
The chitobiose enzyme
Chitin is conjugated protein
(also referring to cellulose binding domain)
Hevein 1Gilkes et al., Adv.Microbiol Reviews, (1991) 303-315. 2S gaard et al., J.Biol.Chem. (1993) 268:22480. 3Weselake et al., Cereal Chem. (1983) 60:98. 4Svensson et al., J. (1989) 264:309. 5Jespersen et al., J. (1991) 280:51. 6Belshaw et al., Eur.J.Biochem. (1993) 211:717. 7Sigurskjold et al., Eur.J.Biochem. (1994) 225:133. 8Villette et al., Biotechnol.Appl. Biochem. (1992) 16:57. 9Fukada et al., Biosci.Biotechnol.Biochem. (1992) 56:556. 10Lawson et al., J.Mol.Biol. (1994) 236:590. 14Von Eichel-Streiber et al., Mol.Gen Genet. (1992) 233:260. 15Klebl et al., J.Bacteriol. (1989) 171:6259. 16Watanabe et al., J.Bacteriol. (1992) 174:186. 17Duvic et al., J.Biol.Chem. (1990): 9327.
Known many CBD, CBD is divided at least 12 families, according to the planned use of CBD, can be with any family wherein as the CBD source.The I of family only contains the CBD of fungal enzyme.Most CBD in all the other 11 families derive from bacterium.The CBD of Liao Xieing is those CBD that belong to the I of family, II, III and IV the most, and the mean length of its CBD is respectively 36,105,150 and 150 amino acid.Some CBD among the I of family, II, III and the IV has been accredited as and has comprised a plurality of antiparallel beta sheets that are folded into meat jelly web-like Folding bucket.The CBD of the I of family, II and III both combined with amorphous cellulose, combine with crystalline cellulose again, and the CBD of the IV of family combined with amorphous cellulose, but did not combine with crystalline cellulose.The CBD of the IV of family only combines with soluble cellulose derivative and cell-oligosaccharide.Combine with similar affinity with chitin bonded CBD with crystalline cellulose, its binding constant is in the micro-molar concentration scope.The CBD of the I of family reversibly combines with Mierocrystalline cellulose, and the CBD of II of family and III it seems irreversibly combination under non-sex change condition.Preferred CBD comprises can derive from those following CBD: bacterial strain (N.R.Gilkes etc., (1988) J.Biol.Chem.263:10401-10407 of belonging to muck cellulomonas cartae (Cellulomonas fimi), Trichodermareesei and M.Bispora; N.R.Gilkes etc., (1991), Microbiol.Rev.55:303-315); Derive from cellulose enzyme gene (Whittle etc. (1982) the Gene 17:139-145 of muck cellulomonas cartae; Gilkes etc. (1984) J.Gen.Microbiol.130:1377-1384); Derive from the exoglucanase (Cex) of muck cellulomonas cartae and endoglucanase (CenA) with and sequence (Wong etc. (1986) the Gene 44:315-324 of gene cex and cenA; (1986) Gene 44:325-330 such as O ' Neill); Get autophagy fiber clostridial 17KD (peptide) CBD, by description (1992) (Proc.Natl.Acad Sci.89:3483-3487) such as Shoseyov.The recombinant forms of this CBD shows the strong affinity (Goldstein etc. (1993) J.Bacteriol.175:5762-5768) to Mierocrystalline cellulose and chitin.
The DNA construct of the DNA of at least one funtion part by will comprising coding polysaccharidase or the protein-bonded polysaccharide of polysaccharide land is transformed in the host cell, also can prepare PBD albumen.Described PBD dna sequence dna can be expressed in host cell (perhaps being eukaryotic cell, perhaps is prokaryotic cell prokaryocyte).To express then with isolating PBD and put together with other PBD and/or one or more functionalized albumen.
Under arbitrary these situations, described isolating polysaccharide binding domains is generally all enough pure, getting rid of the polysaccharidase catalytic activity, unless this is the desired characteristic of the fusion rotein planned.The catalytic activity of preferred this preparation is lower than the catalytic activity of the crude extract that derives from the cell of expressing described polysaccharidase.More preferably described catalytic activity is lower than reflection the stoichiometry of 1 function catalyst structure domain of per 1000 function binding domainss.In order to test the activity of required expression product, can for example from solution, remove described binding domains of inferring by combining and show with Microcrystalline Cellulose (for example Avicel (Microcrystalline Cellulose)), the combination of measuring PBD is active.Can easily from described Mierocrystalline cellulose, provide required active polypeptide with highly purified isolated in form.Will be used for the purifying (Gilkes etc. of natural cellulose enzyme with combining of Avicel, J.Biol.Chem. (1984) 259:10455-10459), the purifying (Owolabi etc., Appl.Environ.Microbiol. (1988) 54:518-523) that also is used for the plain enzyme of recombinant fiber.
Second basic building block of poly PBD fusion rotein is a kind of protein, described protein can be with as second kind of identical or different PBD of the PBD of first member.Therefore, described poly fusion rotein can be by a pair of nucleotide sequence coded dimerization PBD fusion rotein that meets the connection of frame ground, every kind of nucleotide sequence coded a kind of PBD, this is well-known in the art (referring to the United States Patent (USP) the 5th of for example Shoseyov etc., 856, No. 201 and United States Patent (USP) the 5th, 837, No. 814, these two documents all are attached to herein by reference).Fig. 5 A has shown a kind of example of PBD fusion rotein, and wherein said first albumen and second albumen all are CBD, thereby forms a kind of dimerization CBD, and wherein said CBD can identical (homologous dimerization CBD) or difference (allos dimerization CBD).Fig. 5 B has shown the cellulose crosslinked proteic application of Fig. 5 A, and one of them cellulose binding domain combines with first kind of paradigmatic structure unit, and second cellulose binding domain combines with second kind of paradigmatic structure unit.The graphic CBD coupling agent unit that a genus class has been described of Fig. 6, described unit comprises a pair of CBD that connects by a joint unit.
On the other hand, described second member can be a kind of PBD, and described PBD randomly comprises one or more functionalized groups.So-called functionalized group is meant the functional group that can change one or more performances that contain polysaccharide material.Generally speaking, described functionalized group is a kind of protein or peptide, and for example silicon binding peptide, polymkeric substance are in conjunction with peptide or melts combine peptide (Ljungquist etc., (1989) Eur.J.Biochem.86:563-569; Spanner etc., (1995) Bone 17:161-165; Slice etc. (1990) J.Biol.Chem.265:256-263; Pessi etc. (1993) Nature 362:367-369).Other example of functionalized polypeptide comprises: the starch binding domains, and the crosslinked instrument that provides of polysaccharide fiber and starch molecule is provided for it; Described starch can be the endogenous component of described fiber, or can be used as the sizing agent application.The starch binding domains can derive from for example Aspergillus glucoamylase (Chen etc. (1991), Gene 99:121-126).Equally, as the stromatin of second polypeptide high molecular weight glutenin (HMWG) for example, can make polysaccharide and gluten molecule crosslinked by utilization.About concrete application, described functionalized group also can comprise chemical group, for example one or more sulfydryls, chromophore, dyestuff, reactive group (for example aldehyde, maleimide, hydrazides, epoxide, carbodiimide) or photoresponse base (for example with PBD bonded triazobenzene).Make method that various chemical entities and PBD put together at United States Patent (USP) the 5th, 962, description is arranged in No. 289, this patent all is attached to herein by reference.
First member of described PBD fusion rotein can randomly be connected with described second member by a joint unit.The joint unit of PBD coupling agent unit can comprise various natural or synthetic molecules, comprises biological polymer (for example protein, polypeptide or polysaccharide) and synthetic polymer (for example acrylate copolymer) and stromatin high molecular weight glutenin.The example of joint unit's peptide or protein ingredient comprises JUN albumen and FOS albumen (referring to, (1989) Science 243:1695-1699 such as Gentz for example); Starch binding domains (SBD) (referring to (1991) Gene 99:121-126 such as for example Chen) and S-peptide or S-albumen (referring to (1993) Protein Science2:348-356 such as for example Kim).Part is according to the planned use of fusion rotein, and first polypeptide in the fusion rotein can directly be connected by peptide bond or bigger joint unit with second polypeptide (or a plurality of first polypeptide and/or second polypeptide).Fig. 8 illustrates a kind of CBD coupling agent unit (CU by name in the figure), and described coupling agent unit has one the one CBD, the 2nd CBD are connected described first and second CBD with one joint unit (LU).Though it is terminal that a described CBD and the 2nd CBD are depicted as in Fig. 8, and is positioned at the reverse direction of described joint unit, considered other number and the layout of CBD and joint unit, these are within the scope of the present invention.Can comprise covalent linkage, ionic linkage, hydrophobic bond, hydrogen bond, protein translation and protein expression by the combination of a kind of method or the whole bag of tricks, joint unit can be connected with each PBD of PBD coupling agent unit.
The polysaccharide fraction of joint unit can be not by the PBD combination or to hang down affinity by PBD bonded polysaccharide.An example of this polysaccharide is a starch.In addition, the joint unit of PBD coupling agent unit can be one or more polysaccharide binding domainss except that PBD.As an example, Fig. 7 A has shown a kind of CBD coupling agent unit, described coupling agent unit has a pair of terminal CBD that connects by coupling agent unit, described CBD coupling agent unit comprise one with one the one CBD link coupled first starch binding domains, one and one the 2nd CBD link coupled second starch binding domains and one and described first starch binding domains and the described second starch binding domains link coupled starch part.
The joint unit of PBD coupling agent unit also can comprise one or more PBD.As an example, Fig. 7 B has shown a kind of CBD coupling agent unit, described coupling agent unit has a pair of terminal CBD that comprises coupling agent unit's connection of a plurality of CBD by, and each CBD of wherein said joint unit is by a JUN/FOS bridge (referring to (1989) Science 243:1695-1699 such as for example Gentz) and adjacent C BD coupling.Fig. 7 C has shown a kind of CBD coupling agent unit, described CBD coupling agent unit has a pair of terminal CBD that connects by a coupling agent unit that comprises a peptide or protein portion, and described peptide or protein portion are with Mierocrystalline cellulose or related polymer debond or only combine to hang down affinity.The size of the peptide of coupling agent unit or protein component (for example joint albumen) can not wait to being higher than 1 megadalton for hundreds of dalton.As an example, the joint unit shown in Fig. 7 C can be several amino acid whose small peptides or big relatively joint albumen (for example HMWG).
Can chemical preparation or reorganization preparation poly PBD fusion rotein.For example, can on himself, produce polysaccharide land or its a plurality of districts, be purified, adopt technology well known by persons skilled in the art then, it is connected with second protein chemistry that has or do not have functionalized group.The method that protein is puted together comprises the external chemical reaction of puting together, and with the modified polysaccharide binding domains, this can combine with described structural domain or with polysaccharide matrix or carry out when polysaccharide matrix is removed.Example comprises that using the glutaraldehyde that Reichlin describes in Methods of Enzymology (1980) 70:159-165 puts together method.When the polysaccharide binding domains was combined with described matrix, the advantage that it provides was the real and matrix bonded site of protection, and stays other residue and the reaction of described second section, described second section or a kind of the 2nd PBD, or a kind of functionalized albumen.If described chemical part causes weakening in conjunction with the ability of polysaccharide substrate with combining of polysaccharide binding domains, the reaction method that the described polysaccharide matrix of then best service requirements exists is to keep the binding characteristic of described structural domain.
On the other hand, the preparation poly PBD fusion rotein of can recombinating.For the preparation PBD fusion rotein of recombinating, make up the recombinant expression vector that to express the PBD fusion rotein with the nucleotide sequence of the described PBD fusion rotein component of encoding.Generally speaking, transcribe and translate adjusting information if the nucleotide sequence that nucleic acid construct contains contains with proteinic nucleotide coding sequence effectively is connected, then this nucleic acid construct can be expressed described protein." effectively connection " is meant a kind of like this connection, and wherein said adjusting dna sequence dna and dna sequence dna ways of connecting to be expressed make and allow to transcribe and translate.The fragment of coding polysaccharide binding domains and the DNA of described second polysaccharide binding domains of coding or functionalized polypeptide are connected, make the nucleic acid of the described PBD of coding link together with the coding described second proteinic nucleic acid, it is complete causing the described PBD and the described second proteinic associating open reading-frame (ORF), allows to take place the translation of complete PBD fusion rotein.If described PBD fusion rotein has a protein coupling agent unit, then described nucleotide sequence is effectively inserted PBD encoding sequence described in the described expression construct and encode between the described second proteinic sequence.Then can be so that the various modes of expression to be provided, the connection DNA of gained is operated.
The carrier that is used for nucleic acid amplification all is well-known in the art with the carrier that is used for expression of nucleic acid.Various parameters are depended in the selection of appropriate carrier, and function (for example amplification or express), the DNA that comprises plan inserts the concrete host cell that segmental size and described carrier will transform.Those skilled in the art can utilize various expression vector/host systems to come recombinant expressed PBD albumen and PBD fusion rotein.This type systematic comprises microorganism, for example the bacterium that transforms with the recombinant phage dna that contains required PBD encoding sequence, plasmid DNA or cosmid DNA expression vector; Yeast with the recombinant yeast expression vector conversion that contains required PBD encoding sequence; Insect cell system with the recombinant virus expression vector that contains required PBD encoding sequence (for example baculovirus) infection; With the recombinant virus expression vector that contains required PBD encoding sequence (cauliflower mosaic virus (CaMV) for example; Tobacco mosaic virus (TMV) (TMV)) infects or with the recombinant plasmid expression vector that contains required PBD encoding sequence (for example Ti-plasmids) plant transformed cell system; Or, comprise engineered to contain or to stablize (for example CHO/dhfr, the CHO/ glutamine synthetase) of amplification or the clone (for example mouse cell line) of a plurality of PBD nucleic acid copies that instability increases in double minute chromosome with recombinant virus expression vector (for example adenovirus or vaccinia virus) infected animals cell system.
Contain one or more above listed components and comprise the structure of the appropriate carrier of required encoding sequence and control sequence, use the standard interconnection technique.Isolating plasmid or nucleic acid fragment are cut, prune (tailor) and be connected with the form that produces required plasmid needs again (referring to Current Protocols in Molecular Biology, the 1-III volume, Ausubel, R.M. write (1994)).In order to prove conclusively correct sequence in the DNA construct (for example plasmid),, and suitably select successful transformant by microbiotic (for example penbritin) resistance with connection mixture transformed into escherichia coli strain X 1-1 and DH52.Preparation is from the plasmid of described transformant, analyzes and/or checks order (referring to for example Messing etc., Nucleic Acids Res.9:309 (1981) by restriction; Maxam etc., Methods in Enzymology 65:499 (1980)).Generally speaking, expression vector can effectively duplicate in host cell, makes described host cell accumulate the expression vector of many copies, and then synthetic high-caliber target protein.Expression cassette can be included in the dubbing system, in suitable cell host, keeping with episome, and perhaps under it can be incorporated into situation in the host genome, can described dubbing system and described expression cassette is provided.
In case obtained the DNA of coding PBD fusion rotein, then be placed in the carrier that can in host cell, duplicate, or utilize technology to make its in-vitro multiplication such as PCR or long range PCR.Replicating vector can comprise plasmid, phage, virus, clay, artificial chromosome etc.The ideal carrier comprises being used in goal gene is carried out the carrier of mutagenesis or is used in host cell the carrier of expressing goal gene.The technology of long range PCR makes the big construct of in-vitro multiplication become possibility, makes that the propagation of the modification (for example mutagenesis or add expression signal) of goal gene and gained construct can be fully in external generation, and need not to use replicating vector or host cell.
About the PBD Expression of Fusion Protein, functional transcribing with the DNA of translation initiation with the described PBD fusion rotein of terminator and coding effectively is connected.The expression of described fusion rotein coding region can be external or carry out in host cell.Transcribe with translation initiation and terminator and derive from the various non-property exhausted source, comprise DNA to be expressed, knownly can or suspect the gene that in required system, to express, expression vector, chemosynthesis or from the native gene seat in the host cell.
For example place the expression vector that is designed for external application, and add rabbit reticulocyte lysate and cofactor, finish vivoexpression by coding region with described PBD fusion rotein; The amino acid that can add if desired, mark.This vivoexpression carrier can be provided in some or all essential in system for use in carrying expression signal.These methods are well-known in the art, and the component of this system can obtain on market.Fusion rotein that then can the direct analysis reaction mixture is for example analyzed in conjunction with activity by measuring it, perhaps can purifying institute synthetic fusion rotein, analyze then.
Expression in host cell can realize with instantaneous mode or stationary mode.Can transient expression take place by the construct that contains the expression signal that function is arranged in host cell that is imported, but described construct do not duplicate, and seldom be incorporated in the host cell, perhaps wherein host cell is not in the propagation.By inducing the activity of the adjustment type promotor that effectively is connected with goal gene, also can realize transient expression, though that this induction type system usually shows the basal expression level is low.By import can be incorporated in the host genome or in host cell the construct of self-replicating, can realize stably express.Utilization is positioned at the selective marker of expression construct or with the selective marker of expression construct transfection, the stably express of goal gene is selected, and selects to express the cell of described mark then.When stably express causes owing to integrating, then the integration of construct can take place in host genome at random, perhaps can utilize to contain and come directed with host genome homologous district to be enough to make the construct with the recombining, orienting of host gene seat.Under the situation of construct target native gene seat, can provide all or some transcribes and translate regulatory region by described native gene seat.
When the expression that needs the PBD fusion rotein at the source biology increases, can adopt several method.The extra gene of the described PBD fusion rotein of coding can be imported in the host living beings.For example also can be by using stronger promotor, remove unstable sequence by disappearance information from host genome from mRNA or from coded protein,, increase expression (United States Patent (USP) the 4th perhaps by stabilizing sequences is added among the mRNA, 910, No. 141).
Expression vector and cloning vector generally contain the promotor of being discerned by host living beings and effectively being connected with coding desired polypeptides or proteinic nucleic acid.Promotor is to be positioned at structure gene upstream from start codon (5 ') (general about 100-1000bp in initiator codon) and to control the non-translated sequence of transcribing and translating with its specific nucleic acid sequence that effectively is connected (nucleotide sequence of the PBD fusion rotein of for example encoding).
Promotor generally is divided into two classes: induction type and composing type.Inducible promoter is some variation (for example exist or lack a kind of nutrient substance or variation of temperature) and start the promotor of transcribing of improving the standard of the nucleic acid that is subjected to its control in the response culture condition.Many promotors by various potential host cell identification are well-known in the art.From the nucleic acid of source, take out described promotor by Restriction Enzyme digestion, and the encoding sequence of described isolating promoter sequence with described fusion rotein added in the carrier, described promotor can be connected effectively with the nucleic acid of encoding said fusion protein.Described promotor can be synthetic, semisynthetic, natural (for host cell) promoter sequence, perhaps can use allos (for host cell) promotor to instruct the amplification and/or the expression of described fusion rotein.The promotor that is fit to use with prokaryotic hosts is well-known in the art (referring to (1978) Nature275:615 such as for example Chang; Goeddel etc. (1979) Nature 281:544; Goeddel (1980) Nucleic AcidsRes.8:4057; EPO application publication number 36,776; With (1983) Proc.Natl.Acad.Sci.80:21-25 such as H.de Boer).The nucleotide sequence of this class promotor generally is known, thereby the joint or the connector that make the technician to utilize any required restriction site is provided, it effectively is connected (referring to Siebenlist etc., (1980) Cell20:269) with the nucleotide sequence of encoding fusion protein.
The promotor that is used for bacterial system also contains Shine-Dalgamo (S.D.) sequence that effectively is connected with the nucleic acid of the described PBD of coding.For bacterium, illustrative transcriptional regulatory district or promotor comprise lac promotor, a λ left side and right promotor, trp and lac promotor, tac promotor etc.The transcriptional regulatory district can additionally comprise the adjusting sequence of the expression time (for example expression product in existence or shortage nutrient substance or the growth medium, temperature etc.) that allows to regulate institute's fusion gene.For example, can be with the adjusting sequence that comprises phage PL promotor, phage OL operator gene and responsive to temperature type repressor, by the expression of temperature regulation fusion gene.Realize adjusting by the interaction between described repressor and the described operator gene to promotor.The expression vector that is used for prokaryotic host cell also can contain the necessary sequence of Transcription Termination or stable mRNA.Under the situation that has some inductor (for example for metallothionein promoter, being zine ion and cadmium ion), can increase expression from some promotor.By this way, can control described PBD Expression of Fusion Protein.The ability that control is expressed may be important, for example when described PBD fusion rotein when being deadly for host cell.
When host cell is yeast, be provided at function arranged in the yeast cell transcribe and translate the district, especially transcribe and translate the district from host species.The transcription initiation regulatory region for example can derive from: the gene of glycolytic pathway, such as alcoholdehydrogenase, glyceraldehyde-3-phosphate dehydrogenase (GPD), phosphoglucose isomerase, phosphoglyceric kinase etc.; But or regulatory gene, for example acid phosphatase, Sumylact L, metallothionein(MT), glucoamylase etc.Under specific occasions, composing type is transcribed or the still concrete efficient, the ability that strong promoter is connected with the control region that provides induction type to transcribe from different promoters, the easy degree of structure or the like of the induction type promotor transcribing, be connected with the purpose open reading-frame (ORF) as required, can use in the multiple adjusting sequence any.What be worth paying special attention to is the promotor that is activated in the presence of semi-lactosi.Semi-lactosi inducible promoter (GALl, GAL7 and GALl0) has been widely used in yeast high-level modulated save land marking protein (Lue etc., Mol.Cell.Biol. the 7th volume, the 3446th page, 1987; Johnson, Microbiol.Rev. the 51st volume, the 458th page, 1987).Activate from transcribing by GAL4 albumen of GAL promotor, GAL4 albumen combines with promoter region, and when having semi-lactosi activated transcription.Under the situation that lacks semi-lactosi, antagonist GAL80 combines with GAL4, stops the GAL4 activated transcription.Add semi-lactosi and prevent that GAL80 from suppressing the activation that is caused by GAL4.
Have been found that the translation initiation codon ATG expression of nucleotide sequence influence in yeast cell on every side.If the expression of required polypeptide in yeast is poor, then can modify the nucleotide sequence of foreign gene, make it comprise effective yeast translation initiation sequence, to obtain best genetic expression.For example, in yeast belong (Saccharomyces), this can meet the fusion of frame ground by gene that expression efficiency is low and endogenous yeast belong gene (the preferably gene of high level expression, for example lactase gene), described gene is carried out site-directed mutagenesis finish.The terminator can derive from 3 ' district of the gene that obtains described initiator, perhaps derives from different genes.Known many terminators, and find that they are from identical and not belong to together among the various hosts with species be gratifying.The selection of terminator more is to consider convenience usually, rather than because any specific characteristic is selected the terminator.Described terminator preferably derives from yeast genes, particularly yeast belong, Schizosaccharomyces (Schizosaccharomyces), Candida (Candida) or genus kluyveromyces (Kluyveromyces) gene.There is function in 3 ' district of also known two kinds of mammalian genes χ Interferon, rabbit and α 2 interferon genes in yeast.
In some cases, may it is desirable to provide the structure gene upstream and with the in-frame signal sequence of described structure gene (secretion leader sequence), this guarantees the secretion of institute's fusion gene.Illustrative secretion leader sequence comprises the secretion leader sequence of penicillinase, immunoglobulin (Ig), TXi Baoshouti, outer membrane protein etc.By merging, chimeric polyeptides can be secreted in the substratum with correct frame.
Can use standard technique, the construct that will comprise described fusion rotein encoding sequence imports in the host cell.These technology comprise conversion, protoplastis fusion, lipofection, transfection, transduction, joint, infection, particle gun impact, electroporation, microinjection, scraping or goal gene are imported any other method of host cell.Operable conversion method comprises that lithium acetate transforms (Methods in Enzymology, the 194th volume, 186-187 page or leaf, 1991).The whole bag of tricks that is used for the conversion of prokaryotic organism and eukaryote or cytogenetics is well-known in the art (referring to (1972) Proc.Natl.Acad.Sci. (USA) 69:2110 such as for example Cohen; With CurrentProtocols in Molecular Biology, referring to above).Can be with above-mentioned expression vector of the present invention or cloning vector transfection or more preferably transformed host cell, transformant can be cultivated in conventional nutritional medium, described substratum can suitably be revised, with the gene of evoked promoter, selection transformant or required PBD of amplification coding or PBD fusion rotein.So-called " conversion " be meant nucleic acid imported in the biology, makes described nucleic acid can or duplicate or duplicate by being incorporated in the host living beings genome as extra-chromosomal element.
Described topic is stated the expression construct that the host will have at least one copy, can have two or more, and this depends on that described gene is to be incorporated in the genome to increase, and still is present on the extra-chromosomal element and has a plurality of copy numbers.When described topic is stated the host and is yeast, can use the yeast plasmid carrier of four main types: yeast integrative plasmid (YIp), yeast replicating plasmid (YRp), yeast centromeric plasmid (YCp) and yeast episomal plasmid (YEp).YIp lacks the yeast replication orgin, must breed as the element of integrating in the yeast genes group.YRp has the autonomously replicating sequence in karyomit(e) source, breeds with the unstable divergence type plasmid of medium copy number (20-40) self-replicating type.The existing replication orgin of YCp has CEN sequence again, stablizes divergence type plasmid propagation as low copy number (10-20) self-replicating type.YEp has a replication orgin from yeast 2 μ plasmids, breeds as the irregular divergence type plasmid of high copy number self-replicating type.Select by keeping, can guarantee in yeast, to exist described plasmid according to the mark on the described plasmid.What be worth special concern is yeast vector pYES2 (a kind of YEp plasmid, can derive from Invitrogen, give uridylic prototroph and provide GALl semi-lactosi inducible promoter for expression), pRS425-pGl (a kind of YEp plasmid, derive from doctor T.H.Chang, molecular genetics assistant professor, Ohio State University, contain a composing type GPD promotor, and give leucine prototroph) and pYX424 (a kind of YEp plasmid, have a composing type TPl promotor, and give leucine prototroph; Alber and Kawasaki (1982) J.Mol.﹠amp; Appl.Genetics1:419).
By selecting, can identify transformed host cell according to the mark that contains on the importing construct.Perhaps, independent mark construct can be imported with required construct, many transformation technologies can import many dna moleculars in the host cell.Usually, according in the ability of selecting to grow on the substratum, select transforming the host.Select substratum can add microbiotic or lack unconverted host the grow necessary factor, for example nutrient substance or somatomedin.A kind of marker gene that is this imported can be given antibiotics resistance, or coding essential growth factor or enzyme, and allows to grow on the selection substratum when expressing in the conversion host.When can or directly or during the expressed labelled protein of indirect detection, also can transform host's selection.Labelled protein can single expression, perhaps as expressing with the proteic syzygy of another kind.Can detect described labelled protein according to the enzymic activity of labelled protein; For example beta galactosidase enzyme can be converted into substrate X-gal coloured product, and luciferase can be converted into fluorescein luminous product.Can be according to it luminous or decorative features come certification mark albumen; For example, when with blue light illumination, can detect the green fluorescent protein (GFP) of Victoria jellyfish (Aequorea victoria) fluorescence.Can come certification mark albumen or the molecular marker on the target protein for example with antibody.Expressing the cell of described labelled protein or sign can for example select by estimating, and for example perhaps utilizes FACS or selects with the technology of antibody elutriation.About the selection of yeast conversion body, can use any mark that in yeast, works.It is desirable to, what considered is to the resistance of kantlex and aminoglycoside G418 and the ability of growing at the substratum that lacks uridylic, leucine, Methionin or tryptophane.
In case fusion gene is imported in the suitable host, then can allow the host grow to be used for evoked promoter, to select conventional nutritional medium when suitable (make amendment) the described fusion gene of expression of transformant or amplification gene.Being used for production polypeptide of the present invention or proteinic prokaryotic cell prokaryocyte can cultivate in suitable medium, generally speaking, described substratum is as at (1989) Bacterial Media in Molecular Cloning such as Sambrook (Nolan, C. write), Cold SpringHarbor Laboratory Press, NY, the substratum of A.1-4 describing in the page or leaf, the document is attached to herein by reference.When the described product of secretion, can collect nutritional medium, by separating described product with the polysaccharide matrix combination.When product was retained in the host cell, harvested cell with its cracking, separated described product, and by combining purifying with the polysaccharide substrate.In order to produce active protein, may must allow described protein refolding.Select to regulate institute's insertion sequence expression or modify and process the host cell strain of described gene product with required ad hoc fashion.Term " host cell " can be defined as those cells that can express purpose PBD albumen or PBD fusion rotein.Host cell can comprise prokaryotic cell prokaryocyte (bacterium) and eukaryotic cell (mammalian cell, yeast cell, insect cell, vegetable cell etc.).Modification of protein product (for example phosphorylation) and processing (for example cutting) may be important for described proteic function.Different host cells has the distinctive or specific mechanism of expressed albumen being translated post-treatment usually.Can select suitable clone or host system, to guarantee the correct modification and the processing of expressed PBD albumen or PBD fusion rotein.As an example, described recombinant products can have wild-type or other glycosylation by glycosylation or not by glycosylation.Glycosylated amount depends in part on the sequence of particular peptide and the biology that is used for producing.Therefore, in Bacillus coli cells, express described product, produce not glycosylated product, and, generally cause degree of glycosylation to be lower than the degree of glycosylation of in mammalian cell, expressing described product at the expressed in insect cells product.In yeast, express, may cause glycosylation too much.Preferably, described host cell should be secreted the proteolytic ferment of minimum quantity.When expression will be carried out, do not contain the potential glycosylation site in the preferably described construct in eucaryon host (for example plant or Mammals).
Can or at prokaryotic host cell or in eukaryotic host cell, carry out the production of PBD fusion rotein.Interested prokaryotic cell prokaryocyte comprises Escherichia (Eschericia), bacillus (Bacillus), lactobacillus (Lactobacillus), cyanobacteria genus (Cyanobacteria) etc.Being worth the prokaryotic cell prokaryocyte that is used to clone and express the PBD fusion rotein of special concern is coli strain BL2 (DE3) PLYS.Eukaryotic cell comprises mammalian cell (for example cell of lactescent animal), birds cell (for example chicken cell) and is suitable for other cell of genetic manipulation, comprises insect cell, fungal cell, vegetable cell and alga cells.Can cultivate described cell, or as a part or whole part of host living beings (comprising animal) and form described cell.Virus and phage also can be used from described cell one and produce the PBD fusion rotein, especially for transgenosis, cell targeting and selection.The example of host animal comprises mouse, rat, rabbit, chicken, quail, turkey, ox, sheep, pig, goat, yak etc., and these animals are suitable for being used for the genetic manipulation and the clone of rapid amplifying transgene expression colony.About animal, by modifying described generegulation district, can change described PBD fusion rotein encoding sequence in target cell device, tissue and body fluid, to express, for example in the milk of host animal, express.
The example of host microorganism comprises yeast saccharomyces cerevisiae, saccharomyces carlsbergensis (Saccharomycescarlsbergensis) or other yeast, for example Candida, genus kluyveromyces or other fungi, for example filamentous fungus such as Aspergillus, neurospora, Penicillium (Penicillium) etc.The desired characteristics of host microorganism is that for example it characterizes on genetics well, and can be used to use super-high density to ferment the described product of high level expression.
About in birds species (for example chicken, turkey, quail and duck) and cell, producing the PBD fusion rotein, can nucleotide sequence transfered cell by the PBD fusion rotein of will encoding according to methods known in the art in, carry out transgenosis.Transgenic animal if desired then can be carried the PBD fusion rotein genetically modified carrier of encoding for embryonic pleuripotent stem cell provides, and allow it grow to be adult animals (United States Patent (USP) the 5th, 162, No. 215; Ono etc. (1996) ComparativeBiochemistry and Physiology A 113 (3): 287-292; WO 9612793; WO9606160).In most of the cases, modify described transgenosis to express high-caliber PBD fusion rotein.Can be for example by be provided at function arranged in the birds cell transcribe and/or translate regulatory region (for example instructing expression promoter in as yolk) in particular organization and egg part, modify described transgenosis.Described generegulation district can derive from various sources, comprises chick anemia virus or avian leukosis viruses or birds gene (for example chicken ovalbumin gene).
Utilization has the genetically modified rhabdovirus expression vector of PBD fusion rotein, can produce the PBD fusion rotein in insect cell.Rhabdovirus expression vector can derive from several commercial source, for example Clonetech.About above-mentioned other expression system, can suitable transcribe and translate regulatory region and conform to by what make described polypeptid coding sequence and select to be used for specific end use, can regulate described PBD fusion rotein transgene expression time, degree and activity.Be worth special concern be can be under previously selected growth conditions derivative promoter region.For example, in the genome of transgenes encoding sequence, its regulatory region and/or the cell that transgenosis imported, import responsive to temperature type and/or the sudden change of metabolite effect type, can be used for this purpose.
Transformed host cell is grown under the conditions suitable of required net result being suitable for.For host cell grown in culture, usually described condition is optimized, to reach the maximum or most economical yield of PBD fusion rotein.The culture medium condition that can optimize comprises: the interpolation of carbon source, nitrogenous source, substrate, add substrate final concentration, the keeping of vegetative period, pH, density and the selection when adding form, aerobic or anaerobic growth, growth temperature, inductor, inducing temperature, the vegetative period when inducing, the results of substrate.Select substratum to cultivate such as for example the most handy purpose of zymic microorganism, described substratum comprises that Yeast protein peptone meat soup (YPD) and minimum medium (contain amino acid, yeast nitrogenous base and ammonium sulfate, and lack the component that is used to select, for example uridylic).It is desirable to, at first substrate to be added is dissolved in the ethanol.In case of necessity, can be for example by comprising or adding semi-lactosi and induce expression from the GAL promotor, induce the expression of desired polypeptides.
Can realize expression in the host animal cell with instantaneous mode or stationary mode equally.Can pass through currently known methods, for example infect or lipofection realization transient expression, it can be repeated, with the construct that imported (referring to Ebert, PCT Publication Specification WO 94/05782) of keeping required expression level.Stable expression can realize by construct being incorporated into produce transgenic animal in the host genome.Can for example pass through the construct microinjection in the protokaryon of zygote, or by transfection, retroviral infection or other technology importing construct, thereby described construct importing can be developed into adult animals or joins the intravital clone of adult animals (United States Patent (USP) the 4th, 873, No. 191; United States Patent (USP) the 5th, 530, No. 177; United States Patent (USP) the 5th, 565, No. 362; United States Patent (USP) the 5th, 366, No. 894; Wilmut etc. (1997) Nature385:810).Recombinant eggs or embryo are transferred to (United States Patent (USP) the 4th, 873, No. 191 in surrogate mother's body; United States Patent (USP) the 5th, 530, No. 177; United States Patent (USP) the 5th, 565, No. 362; United States Patent (USP) the 5th, 366, No. 894; Wilmut etc. (referring to above)).
After the birth, for example detect the construct that is imported by PCR or southern blotting technique method according to importing marker gene (for example hair color) or with blood, breast or tissue sample, or by immunoassay or enzymatic determination to detect expressed albumen or by the product of its generation, identify transgenic animal (United States Patent (USP) the 4th, 873, No. 191; United States Patent (USP) the 5th, 530, No. 177; United States Patent (USP) the 5th, 565, No. 362; United States Patent (USP) the 5th, 366, No. 894; Wilmut etc. (referring to above)).The transgenic animal of gained can be genetically modified fully, or mosaic, only have described transgenosis in an one cell subsets.By karyocyte and stoning ovum being merged, subsequently it transferred to the appearance of the cloning of mammalian animal method that realizes in surrogate mother's body, make and behind " person of foundation " animal that obtains to comprise the construct that imports or cell, to carry out quick and production on a large scale; And before this, must there be described transgenosis (Wilmut etc. (referring to above)) in system in the kind of the animal that is used for breeding.
Expression in the described host animal provides some effect, is under the situation of domestic animal described host especially.In order in the body fluid that from host animal, obtains easily (for example breast), to produce the PBD fusion rotein, can in from the mammary gland cell of female host, express described transgenosis.Can make described transgenosis be applicable to expression, make described transgenosis be retained in the mammary gland cell or be secreted into the Ruzhong, form the PBD fusion rotein (PCT Publication Specification WO95/24488) that is positioned the Ruzhong.Can regulate sequence with specificity, the adjusting sequence of ox alpha-lactalbumin, alpha-casein, beta-casein, χ-casein, κ-casein, beta-lactoglobulin or whey acidic protein for example, make and express orientation, in mammary tissue, to express, perhaps can randomly comprise one or more introns and/or secretory signal sequence (United States Patent (USP) the 5th, 530, No. 177; No. the 5th, 565,362, the United States Patent (USP) of Rosen; No. the 5th, 366,894, the United States Patent (USP) of Clark etc.; The PCT Publication Specification WO 95/23868 of Garner etc.).If essential purifying then adopts the substrate polysaccharide, by the affinity chromatography described PBD fusion rotein of purifying easily.
When application is of the present invention, contact time enough by making polysaccharide structures with the described PBD fusion rotein of capacity, to be issued to required modification, use PBD fusion rotein modified polysaccharide structure in conditions such as suitable reagent, temperature.Generally the modification condition is optimized, with the Km, the Vmax that reach described PBD and kcat and other biochemical parameter optimal pH for example.The interaction of described PBD and substrate is generally extremely quick.In order to reach required effect, then must assess various concentration and/or the treatment time and/or the treatment temp of the PBD fusion rotein that reaches required effect.Used condition is definite by rule of thumb, and based on the requirement to used PBD fusion rotein and required net result.As an example, the representative condition that comprises the PBD fusion rotein of the PBD that derives from endoglucanase comprises that the concentration of mM phosphoric acid salt pH7.0, PBD is generally the about 0.1-10mg/ml of every 25mg cellulosic fibre (for example cotton).Temperature is generally about 20-37 ℃, preferably about 25 ℃.Treatment time is not waited from 5 minutes to 12 hours, though can use the long treatment time, as long as polysaccharide structures is without prejudice.Generally speaking, suitable is leniently to stir the mixture, and handles with the homogeneous that promotes described structure.After handling described structure,, be used to prepare final product then, for example paper or textiles with described structure drying.Perhaps or in addition, consider similarly, can handle the finished product for example paper or textiles with PBD to the above.
Can adopt mensuration, detect the inhibition end product that may during modifying processing, form, and detect the intermediary of generation during handling or final ideal performance modification process or speed of reaction.For example, may it is desirable to make fiber not exclusively crosslinked.On the contrary, may to obtain to have polysaccharide structures, for example obtain the lower yarn of rigidity that is used to weave preferably in certain intermediate point termination reaction owing to the incomplete crosslinked caused ideal performance of described structure.Those skilled in the art become known for assessing many objective tests that described PBD handles, and comprise strain, breaking point energy and toughness under Young's modulus, the maximum load.
The modified types of the polysaccharide structures that is reached depends in part on the proteinic character that merges with described binding domains at least.Modify with PBD, be defined as the variation of (can the be detected) polysaccharide structures that can observe.The gathering that this comprises described polysaccharide structures causes the change that can observe, and for example wet tenacity increases, for example variation of hydrophobicity, wetting ability, wetting properties, surface texture etc. of surface property.The electric property that contains polysaccharide material that can change comprises surface charge (plus or minus) and electroconductibility.The chemical property that contains polysaccharide material that can change comprises various chemistry and photochemical reaction chemical group is incorporated into the described at least surface that contains polysaccharide material.The mechanical property that contains polysaccharide material that can change comprises tensile strength, shearing resistance, wearability, frictional coefficient and elasticity.As an example, when described polysaccharide structures is Mierocrystalline cellulose, can make cellulosic fibre crosslinked with reagent or the composition that per molecule has two or more CBD.Fig. 9 A-C illustrates some method, a CBD coupling agent unit of the present invention is interacted with a paradigmatic structure unit of polysaccharide also combine with it.Fig. 9 A illustrates, CBD coupling agent unit have one with first paradigmatic structure unit's bonded the one CBD and with one second paradigmatic structure unit's bonded the 2nd CBD.Can expect to have under the situation of joint unit of highly flexible in use at least, a CBD of CBD coupling agent unit and the 2nd CBD can combine with same paradigmatic structure unit.Fig. 9 B has shown a CBD coupling agent unit with a flexible joint unit, and a wherein said CBD and the 2nd CBD combine with a paradigmatic structure unit.Fig. 9 C illustrates and can be how makes a plurality of paradigmatic structure units crosslinked to form the three dimensional polymeric web material with a plurality of CBD coupling agent unit.Like this, can form the aggregate of thread polysaccharide, for example cellulosic filaments.Pass through the crosslinked materials such as paper of CBD coupling agent unit, cotton yarn and cotton fabric (woven fabrics and nonwoven fabric) by what cellulose materials constituted, can change mechanical property, for example Young's modulus.The crosslinked of cellulose materials can carry out in each stage of cellulose-containing material manufacturing.For example, with regard to paper product, can handle cellulosic fibre with CBD coupling agent unit composition by each at paper-making process in stage, carry out crosslinked, the perhaps paper product that can be shaped with CBD coupling agent processed in units.Equally, can make cotton yarn or cotton fabric crosslinked with CBD coupling agent unit composition, with yarn or the cotton fabric that surface property and/or mechanical property improvement are provided.
By handling polysaccharide structures or contain polysaccharide material, can obtain to have the type material of various new physicals, electric property, chemical property and mechanical property with the PBD fusion rotein that comprises the functional moiety.Fig. 8 illustrates a kind of CBD functionalized moiety, and this part comprises at least one CBD and a functional moiety who is attached thereto (FM).Described functional moiety can be any in the number of chemical kind, comprising: hydrophobic parts, for example hydrophobic amino acid sequence or peptide or derivative of fatty acid; To reduce wetting properties and the tolerance of the described material of enhanced to humidity and water be provided; Hydrophilic parts; Electrically charged or ion part; The silicon bound fraction; Polymkeric substance is in conjunction with part; Metal or melts combine part are to provide and the combining of metal substrates (example of metal binding protein comprises the metal binding protein (1993) Nature 362:367-369 such as (for example) Pessi of bacterium siderophore, metallothionein(MT) and metallothionein(MT) sample albumen (Slice etc. (1990) J.Biol.Chem.265:256-263), ferritin (Spanner etc. (1995) Bone 17:161-165) and design); The chemical reaction base; The photochemical reaction base; Or sulfydryl.Chemical reaction base of the present invention can comprise for example aldehyde, maleimide, hydrazides, epoxide or carbodiimide.Photochemical reaction base of the present invention can comprise triazobenzene.
Equally, can provide hydrophobicity for cellulosic fibre or by the product that cellulosic fibre is made with composition with a hydrophobic parts (for example hydrophobicity polypeptide, long chain hydrocarbon or hydrocarbon derivative).The wetting properties that hydrophobicity causes being made material by modified cellulosic fibre reduces, and causes described material having wearing quality enhancing under the situation of water indirectly.On the other hand, the crosslinked wet tenacity of described material that directly causes of cellulosic fibre strengthens.For simplicity, this paper is not the wet tenacity that is used for comprising this class material specially about the mentioning of intensity of paper or other cellulose-containing material.
The type of the polysaccharide material that can modify with present method changes.Example comprises the paper product of Wood products, derived from cellulosic fiber and derives from cotton or the product of ramie (for example yarn or fabric).Term " paper " comprises flap and the molded product of being made by the combination of fibrous cellulosic materials and cellulose materials and synthetic materials.The example of paper comprises tissue paper, paper in the office, newsprinting paper, fluting board, tissue, laminated paper and cardboard paper.Are meant term " polysaccharide material " or " containing polysaccharide material " and comprise at least a polysaccharide, generally comprise the material of quite a large amount of at least a polysaccharide (for example Mierocrystalline cellulose or chitin).
Containing the CBD composition also can be applicable in the paper-making process.According to the present invention, different steps that can be in paper-making process is with containing CBD compositions-treated cellulose materials.For example, can handle at shaping stage or in size application stage.By CBD cross-linked composition (for example CBD coupling agent unit composition or cellulose crosslinked (fusion) albumen (CCP)) is added in the cellulosic fibre suspension, handle at the shaping stage of papermaking.Preferably, shaping stage or before it with containing CBD compositions-treated cellulose materials.Can the functional moiety be connected, put together with CBD or coupling No. the 5th, 962,289, United States Patent (USP) (also referring to for example) according to above being connected to form the described method of CBD coupling agent unit (Fig. 4 A-G, 5A-B) about joint unit and CBD.
When checking following non-limiting example, other purpose of the present invention, advantage and new feature will become apparent to those skilled in the art.In addition, above-described and the claimed various embodiments of the present invention of following claims one joint and aspect in any, in following examples, can find the support of experiment.
Embodiment
With reference now to following examples,, these embodiment have illustrated the present invention with above description with non-limiting way.
Generally speaking, used laboratory method comprises molecule, biological chemistry, microbiology and recombinant DNA technology among nomenclature used herein and the present invention.This class technology has sufficient explanation in the literature.Referring to (1989) such as for example " Molecular Cloning:A Laboratory Manual " Sambrook; " Current Protocols in Molecular Biology " I-III rolls up Ausubel, and R.M. writes (1994); Ausubel etc., " Current Protocols in Molecular Biology ", John Wiley and Sons, Baltimore, Maryland (1989); Perbal, " A PracticalGuide to Molecular Cloning ", John Wiley ﹠amp; Sons, New York (1988); Waston etc., " Recombinant DNA ", Scientific American Books, New York; Birren etc. (writing) " Genome Analysis:A Laboratory Manual Series ", 1-4 volume, Cold Spring Harbor Laboratory Press, New York (1998); United States Patent (USP) the 4th, 666, No. 828, the 4th, 683, No. 202, the 4th, 801, No. 531, the 5th, 192, No. 659 and the 5th, 272, the methodology of describing in No. 057; " Cell Biology:A Laboratory Handbook ", I-III rolls up Cellis, and J.E. writes (1994); " Culture of Animal Cells-A Manual ofBasic Technique " Freshney, Wiley-Liss, N.Y. (1994), the third edition; " CurrentProtocols in Immunology " I-III volume Coligan J.E. writes (1994); Stites etc. (writing), " Basic and Clinical Immunology " (the 8th edition), Appleton ﹠amp; Lange, Norwalk, CT (1994); Mishell and Shiigi (writing), " Selected Methods inCellular Immunology ", W.H.Freeman and Co., New York (1980); Available immunoassay have been described widely, referring to No. the 3rd, 791,932, United States Patent (USP) for example, the 3rd in described patent and scientific literature, 839, No. 153, the 3rd, 850, No. 752, the 3rd, 850, No. 578, the 3rd, 853, No. 987, the 3rd, 867, No. 517, the 3rd, 879, No. 262, the 3rd, 901, No. 654, the 3rd, 935, No. 074, the 3rd, 984, No. 533, the 3rd, 996, No. 345, the 4th, 034, No. 074, the 4th, 098, No. 876, the 4th, 879, No. 219, the 5th, 011, No. 771 and the 5th, 281, No. 521; " Oligonucleotide Synthesis " Gait, M.J. writes (1984); " Nucleic AcidHybridization " Hames, B.D. and Higgins S.J. write (1985); " Transcriptionand Translation " Hames, B.D. and Higgins S.J. write (1984); " Animal CellCulture " Freshney, R.I. writes (1986); " Immobilized Cells and Enzymes " IRL Press, (1986); " A Practical Guide to Molecular Cloning " Perbal, B., (1984) and " Methods in Enzymology " 1-317 volume, Academic Press; " PCRProtocols:A Guide To Methods And Applications ", Academic Press, SanDiego, CA (1990); Marshak etc., " Strategies for Protein Purification andCharacterization-A Laboratory Course Manual " CSHL Press (1996); All above-mentioned documents all are attached to herein by reference, all describe as this paper.Other general reference is provided in presents.Think that method wherein is well-known in the art, it is for convenience of the reader that these methods are provided.Wherein contained all information all is attached to herein by reference.
The preservation of biomaterial
Intestinal bacteria pET-CBD is preserved in American type culture collection (ATCC) on April 12nd, 1993,10801 Universty Boulevard, and M, VA 20110-2209, preserving number are 75444.
Embodiment 1
The structure of CBD and cbd fusion protein and expression
The content of following United States Patent (USP) discloses the structure and the expression of various CBD and cbd fusion protein, and the content of these patents is attached to herein by reference: the United States Patent (USP) the 5th, 496 of Shoseyov etc., No. 934, No. the 5th, 670,623, United States Patent (USP), United States Patent (USP) the 5th, 719, No. 044, No. the 5th, 738,984, United States Patent (USP), United States Patent (USP) the 5th, 837, No. the 5th, 856,201, No. 814 and United States Patent (USP); No. the 5th, 962,289, No. the 5th, 928,917, No. the 5th, 137,819, the United States Patent (USP) of Kilburn etc., No. the 5th, 202,247, United States Patent (USP), No. the 5th, 340,731, United States Patent (USP), United States Patent (USP) and United States Patent (USP); And No. the 5th, 821,358, the United States Patent (USP) of Gilkes etc.
1.1 bite the structure and the expression of fiber clostridial cellulose binding domain (CBDclos):
M.A.Goldstein etc. (1993) (J.Bacteriol.175:5762-5768) have described the structure of the cellulose binding domain of biting the conjugated protein A of fiber clostridium Mierocrystalline cellulose and containing the pET-CBD plasmid (referring to the overexpression among the intestinal bacteria BL12 (DE3) of Figure 1A-C).Also referring to United States Patent (USP) the 5th, 496, No. the 5th, 719,044, No. 934 and United States Patent (USP), these two patents all are attached to herein by reference.
1.2 the structure of CCP-180 and expression:
From pET-CBD (Figure 1A-C, M.A.Goldstein etc. (1993) J.Bacteriol.175:5762-5768) and pET-CBD-180 (Fig. 1 D-E, E.Shpigel etc. (1999) Biotech.Bioeng.65:17-23) makes up pET-CCP-180 (Fig. 2 A-E), and with NcoI and BamHI digestion pET-CBD and pET-CBD-180, with the dna fragmentation of gained respectively 1.2% with 0.6% sepharose on separate.(Qiagen, Inc California) extract the 500bp fragment of pET-CBD and the 5Kb fragment of pET-CBD-180 from gel, connect described two kinds of fragments to extract test kit with the Qiaex dna gel.To connect mixture and be transformed in the intestinal bacteria XLl-blue competent cell, be transformed into then in the expressive host e. coli bl21 (DE3).Contain the positive colony called after pET-CCP-180 that meets two CBD that merge on frame ground, and through the order-checking conclusive evidence.About the described method of CBDclos, carry out the expression of CCP-180 as (1993) J.Bacteriol.175:5762-5768 such as M.A.Goldstein.
1.3 the clone of A albumen-CBD and expression:
With cbpA gene (Shoseyov etc., (992) Proc.Natl.Acad.Sci.USA 89:3483-3487) as template, after containing the primer A (N-terminal primer) in an EcoRI site: 5 '-GGGGGAATTCCATGGCAGCGACAT-3 ' (SEQ ID NO:11) and contain a terminator codon, use meets the primer B (C-terminal primer) in a BamHI site: 5 '-GGGGGATCCTATGGTGCT-3 ' (SEQ ID N0:12), through pcr amplification CBD.Design described primer, make can with described 500bp dna fragmentation through the EcoRI/BamHI forced cloning in plasmid pRIT2, meet the fusion of frame ground with the C-terminal of A protein gene.Described in PCR condition such as the following document: Innis etc., PCR Protocols:A Guide to Methods ﹠amp; Applications.Innis etc. write, Academic Press, San Diego, 1990), and make following modification: in reaction mixture, use 2ng template DNA and 1mM MgCl 2With thermal control instrument (M﹠amp able to programme; J Research, Inc.) react.Write (1989) Molecular Cloning:A Laboratory Manual according to Sambrook etc., the method for Cold Spring HarborLaboratory Press is carried out the standard DNA operation.
With EcoRI and BamHI digestion pcr amplification product, (Qiagen Inc.) isolates the 500bp dna fragmentation of expection from 1.5% sepharose with the Qiaex gel extraction kit.With the T4 ligase enzyme EcoRI/BamHI fragment is connected among the pRIT2 that digests in advance with EcoRI/BamHI.With connecting mixture transformed into escherichia coli bacterial strain 2097 competent cells, containing selection conversion bacterium colony on the LB agar plate of 100mg/L penbritin.Containing target DNA inserts segmental successful construct and is named as pRIT2-CBD.
Prot A-CBD is cloned among the overexpression carrier pET3d (F.Studier etc., (1986) J.Mol.Biol.189:113-130) of T7 mediation.With pRIT2-CBD as template, with following primer through the terminal primer of pcr amplification Prot A-CBD:C: (i.e. 5 '-GGGGGGATCCTATGGTGCT-3 ' SEQ ID NO:12) as mentioned above; With N-terminal primer: 5 '-GGGGGGTACCATGGAACAACGC-3 ' (SEQ ID NO:13), this primer contains an initiation site in the NcoI site.Partly digest the PCR product with NcoI.With the DNA that BamHI digestion is reclaimed, the 1.3Kb dna fragmentation is cloned among the pET3d.With connecting mixture transformed into escherichia coli XLl-Blue competent cell, containing selection conversion bacterium colony on the LB agar plate of 100mg/L penbritin.Containing described DNA inserts segmental successful construct and is named as pET-ProtA-CBD (Fig. 3 A-G).PET-ProtA-CBD is transformed in e. coli bl21 (DE3) competent cell.As Nilsson etc., (1985), EMBO is J.4:1075-1080 described, carries out described Expression of Fusion Protein.All cells is all grown among the LB that shakes 40ml volume in the bottle under 250rpm, is supplemented with the 50mg/L penbritin among the described LB, contains the overnight culture inoculation of the intestinal bacteria 2097 of pRIT2-CBD with 400 μ l.Culture is grown under 30 ℃ temperature, until reaching O.D. 600nmBe 0.4.Temperature is risen to 42 ℃ then and reach 45 minutes, and then reduce to 37 ℃ and reach 2 hours.
In having the e. coli bl21 of pET-ProtA-CBD (DE3), obtain the overexpression of ProtA-CBD.By at the M9 minimum medium (0.65Na that contains 50 μ g/ml penbritins 2HPO 4, 0.3% KH 2PO 4, 0.255 NaCl, 0.5% NH 4Cl, 20% glucose, 2mMMgSO 4, 0.1mM CaCl 2With the 1mM vitamin) the described cell of incubated overnight, the preparation inoculum.With inoculum the TB substratum that contains 100 μ g/ml penbritins (1.2% microbial culture with tryptone, 2.4% microbial culture with yeast extract paste, 0.4% (v/v) glycerine, 0.17MKH 2PO 4With 0.72 M K 2HPO 4) with after the dilution in 1: 50, allow cell grow to O.D. in 37 ℃ 600nmBe 1.5, after this add 0.5mM isopropyl ss-D-sulfo-galactopyranoside (IPTG).Allow cell in 37 ℃ of regrowths 4 hours.With 2, centrifugal 10 minutes harvested cells of 000g.
1.4 the purifying of ProtA-CBD:
The concentration of cell with 0.1g/ml is suspended among 50mM Tris/HCl, the 10mM EDTA pH8, with RANNIE High-Voltage Experimentation chamber homogenizer (MINI/LAB 8.30H type) smudge cells.Suspension is centrifugal, be that 1 of 5mg/ml goes up on the clear liquid sample to Mierocrystalline cellulose (Avicel 200 Sigma) post (2.6 * 32cm) with protein concentration.This post PBS (15mM phosphoric acid buffer, 150mM NaCl, 3mM KCl, pH7.4) balance.Flow velocity with 5ml/min washs this post, and the absorbancy under 280nm is lower than 0.05.With 50mM Tris/NaOH pH value of solution 12.5 wash-out ProtA-CBD.The ProtA-CBD that wash-out is gone out uses the HCl titration to pH8 immediately, freeze-drying then.According to the method (U.K.Laemmli (1970) Nature 227:680-685) of Laemmli, analyzing e. coli total protein (at last sample to the cellulose column) on 12.5% SDS-PAGE and from the peak (ProtA-CBD) of described cellulose column wash-out.The ProtA-CBD peak demonstrates the band of a treaty 45kD.
Embodiment 2
The measurement of treated (CBD modifies) material and the unprocessed mechanical property of materials
With universal testing-machine (Figure 11, Instron, High Wycombe, UK) interface type 1011 measurement series mechanical propertys, sampling rate (Sample rate): 10 pts/sec, pinblock speed (Crosshead speed): 5mm/min.All are measured all under 23 ℃ and 65% relative humidity and carry out.
2.1 Young's modulus:
Modulus in tension is that Young's modulus is a key property of material.The relatively little power that Young's modulus can be defined as loosely with unlikely irreversible expanded material makes material extend required power with elastic type (regime).
2.2 the processing of paper:
By dipping in the solution that is respectively 2.5mg/ml and 2.0mg/ml in CBDclos, CCP, Prot-A-CBD, Ab-ProtA-CBD concentration in 20mM Tris alkali pH7 10 minutes, handle tissue paper rectangle paper slip (size: 45mm * 10mm * 0.1mm).Control treatment was also flooded 10 minutes in 20mM Tris alkali pH7 solution.Behind dipping, from liquid, take out treated paper slip and contrast paper slip, drying is 2 days under vacuum.
2.3 the result that paper is handled:
2.3.1 Young's modulus:
In Figure 10 A, provided the Young's modulus value of contrast pattern, CBDclos processing pattern and CCP-180 processing pattern.The Young's modulus of the paper of handling with CBD is significantly greater than the Young's modulus of contrast (unprocessed) paper.With the Young's modulus of CCP treatment paper even greater than the Young's modulus of CBD treatment paper.These results show, with CBD or use the CCP treatment paper, have changed at least a mechanical property of described paper.More particularly, compare, use or CBD or CCP treatment paper, cause the tensile strength of treated paper to increase (according to the Young's modulus pH-value determination pH) with unprocessed paper.
2.3.2 the strain under the maximum load:
In Figure 10 B, shown and shown that CBDclos handles pattern and CCP-180 handles pattern strained result under maximum load.Compare with control value, perhaps CBD handles or CCP handles and do not cause that strained significantly changes under the maximum load.These results show, can its elasticity of remarkably influenced with CBD or CCP treatment paper.
2.3.3 breaking point energy:
In Figure 10 C, shown and shown that CBD or CCP-180 handle the result of pattern breaking point energy.The breaking point of CBD treatment paper can be basic identical with contrast.Yet the paper of handling with crosslinking protein CCP-180 demonstrates compared with the control that breaking point can significantly increase.
2.3.4 toughness:
In Figure 10 D, shown and shown that CBD and CCP handle pattern flexible result.The toughness of CBD treatment paper is basic identical with contrast.Yet the paper of handling with CCP demonstrates once more compared with the control that toughness significantly increases.
2.4 yarn treatment:
The cotton yarn that is used for the research is the two yarn fibers (34/2) of 100% low grey cotton of T.P.U. (twisting count of per inch).Yarn diameter is 0.5mm, and the weight of unit length is 0.8mg/cm.In every kind of processing, utilize the special yarn treatment instrument (YTA) of type known in the art, sample of yarn is immersed in the protein soln.Figure 11 illustrates described yarn treatment machine.This machine comprises a thread wheel, reel, first groove A, second groove B and an engine that is connected with reel.Thread wheel and reel can exchange, thereby allow yarn again by groove A and groove B.Engine can move with various selected velocities, thereby allows to measure the dipping time of sample of yarn.The length of yarn can connect between thread wheel and reel, by making the liquid of yarn by containing among groove A and the groove B, can make yarn move to reel from thread wheel.Like this, can make yarn immerse a kind of liquid (two groove in exist) or time of Da Teding in two kinds of different liqs.
Multistage (lengths of) cotton yarn (3-4 rice) is wound on the thread wheel of YTA, and an end of yarn is connected to reel, and yarn advances by groove A and groove B by engine.The dipping time of yarn is about 45 seconds.
Above-mentioned cotton yarn is handled as follows:
(i) handle with CCP-180: yarn fibers is immersed in (groove A) CCP-180 solution (1mg/ml is in 20mM Tris alkali pH8).
(ii) handle and (the CBD-PA yarn fibers is immersed in (groove A) CBD-PA solution (0.75mg/ml is in 20mM Tris alkali pH8), then washing (groove B) (dipping time 45 seconds) in 1 * TBS with A albumen-CBD.
(iii) use the dual processing of A PROTEIN C BD and antibody: yarn fibers is immersed in (groove A) CBD-PA solution (0.75mg/ml is in 20mM Tris alkali pH8), and in 1 * TBS, wash (groove B) (dipping time 45 seconds).With reel and thread wheel exchange, yarn is immersed in (groove A) antiserum(antisera) solution (0.75mg IgG/ml) then, and washing (groove B) in 1 * TBS.
(iv) contrast: will reach 45 seconds among yarn fibers immersion (groove A) 20mM Tris alkali pH8.
After the processing, with all three kinds of treated samples with contrasted in drying at room temperature a few hours.
2.5 yarn treatment result:
2.5.1 Young's modulus:
The sample of yarn that control yarn sample, CCP-180 handle, the sample of yarn of A albumen-CBD processing and the Young's modulus value of the sample of yarn that Ab-A albumen-CBD handles in Figure 12 A, have been provided.The Young's modulus value of the yarn of handling with CCP-180 and Ab-A albumen-CBD is significantly higher than the Young's modulus value of contrast (unprocessed) yarn.These data show, compared with the control, handle yarn with Ab-A albumen-CBD and CCP, cause the tensile strength (according to the Young's modulus pH-value determination pH) of treated yarn to strengthen.What is interesting is that the Young's modulus value comparison of the yarn of handling with CBD-PA is much lower according to the Young's modulus value of yarn.Though be not wishing to be bound by theory, the possible explanation that the Young's modulus of the yarn that CBD-PA handles reduces is that CBD-PA makes cellulosic fibre loose (referring to No. the 5th, 821,358, United States Patent (USP) for example, its content is attached to herein by reference).
2.5.2 strain under the maximum load:
In Figure 12 B, shown and shown the sample of yarn strained result under maximum load who handles with CCP-180, CBD-PA and CBD-PA-Ab.Compared with the control, the yarn that usefulness or CCP-180 or CBD-PA-Ab handle, strain value is lower under its maximum load, thereby shows that these processing make the elasticity of yarn be lower than the elasticity of contrast.Strain value and contrast is similar under the maximum load of the yarn of handling with CBD-PA.
Embodiment 3
Material functionalized
3.1 filtration medium is functionalized to remove the heavy metal kind from liquid:
By with a CBD and functional moiety's (for example metal binding protein) coupling that heavy metal is had affinity, prepare CBD functional moiety (referring to for example Fig. 9 A-C).The substrate (for example cotton fibre) that comprises cellulose materials is handled with described CBD functional moiety, its treatment condition (pH, temperature, ionic concn etc.) make CBD functional moiety's CBD component combine with substrate, thereby described substrate is functionalized by described melts combine functional moiety, thereby melts combine substrate or filtration medium are provided.Make the liquid flow that contains the excessive levels heavy metal by described melts combine filtration medium, thereby make the concentration of heavy metal described in the described liquid flow reduce to nontoxic level widely.
3.2 cellulosic fibre is functionalized to make the package paper product that wetting properties reduces:
By with a CBD and hydrophobic functional moiety's coupling, prepare the CBD functional moiety.The hydrophobic functional moiety of the described CBD of cellulose fiber Wesy who is applicable to papermaking handles, its treatment condition (pH, temperature, ionic concn etc.) make CBD functional moiety's CBD component combine with described cellulosic fibre, thereby the cellulosic fibre that is connected with hydrophobic part is provided.Paper by described treated cellulosic fibre manufacturing is hydrophobic, thereby water-fast.
In an alternate embodiment, before or after the paper drying that will produce by (not functionalized) cellulosic fibre that is untreated, described paper is functionalized with the hydrophobic parts that a kind of CBD connects.The paper of handling with described CBD hydrophobicity functional moiety is hydrophobic, thereby water-fast.
3.3 cellulosic fibre is functionalized to make wetting properties enhanced tissue paper:
By with a CBD and the coupling of a hydrophilic functional part, prepare the CBD functional moiety.Before first drying stage of paper-making process or second drying stage or afterwards, with described CBD hydrophilic functional partially disposed (functionalized) tissue paper.Tissue paper with described CBD hydrophilic functional partially disposed is hydrophilic, and the absorption that demonstrates water and waterborne liquid strengthens.
Embodiment 4
Express S-albumen-CBD-S-peptide (SSC)
Figure 13 has shown the result of SCS at expression in escherichia coli.2 roads show with IPTG induces e. coli protein before, and 3 roads show with IPTG induces e. coli total protein afterwards, and the demonstration of 4 roads contains the proteic inclusion body of described SCS.
Embodiment 5
Handle preliminary shaping paper with CBD, CCP or SCS
Figure 14 has shown the Young's modulus figure that handles Whatman paper result with CBD, CCP or SCS.Notice, with institute to some extent the CBD of test concentrations or CCP handle Whatman paper, all cause the Young's modulus increase.
Figure 15 has shown the breaking point energy through the Whatman paper of CBD, CCP or SCS processing.Notice that the CCP that uses 2.5mg/ml concentration causes breaking point can increase about 30%.In addition, with institute's SCS processing of test concentrations to some extent, cause breaking point to increase.
Figure 16 has shown the toughness result through the Whatman paper of CBD, CCP or SCS processing.Notice that the CCP that uses 2.5mg/ml concentration causes toughness to increase about 40%.In addition, with institute to some extent the SCS of test concentrations handle, cause the toughness increase.
Figure 17 has shown the stress of Whatman paper under maximum load through CBD, CCP or SCS processing.Notice that all of being tested are handled and all caused stress increase under the maximum load.CCP with 2.5mg/ml concentration obtains the most significant effect.The increase of stress shows that paper intensity increases under the maximum load.
In another group experiment, measure CBD and CCP influence to preliminary shaping Whatman paper.
(Whatman, Maidstone, rectangle scraps of paper England) immerse the solution that contains 2.5mg/ml CBD or CCP, and (20mMTris alkali reaches 10 minutes in pH7) with No. 1 Whatman paper of 40 * 10mm, thick 0.18mm.Sample was 65% relative humidity, 23 ℃ dry 24 hours down then.The final moisture content of described paper is 3.2%.According to the international standard method of inspection that is used for paper and cardboard tensile property (ISO 1924-2) assessment mechanical property.Treated paper anti-open check with Instron generic inspection instrument (Universal Testing Machine) (UTM) 1011 types (HighWycombe UK) carries out with stretch mode.(Canton MA), makes and can suitably clamp at the anti-experimental session of opening for the clip of screw tightening, Instron Corp. with tension clamp about the rectangular paper insertion.All are measured all under 23 ℃, 65% relative humidity and carry out with constant rate of deformation 20mm/min.Measured tensile property comprises the elongation and the energy absorption of stress when breaking, the strain when breaking, breaking point.According to Hayden, W., Moffatt, W.G. and Wulff, J.Mechanical Behavior.1-22 (Johan Wiley ﹠amp; Sons, Inc., NY; 1956) and Dufresne, A., Cavaille, J.Y. and Vignon, M.R.Mechanical behavior of sheetsprepared from sugar beet cellulose microfibrils.J.Appl.Polym.Sci.64, the described method of 1185-1194 (1996) is carried out all calculating.
According to formula 1 computed stress (σ):
σ=F/S (1) wherein F is the load that applies, and S is a cross section.S remains unchanged definite by the cumulative volume of supposing sample, therefore:
S=S 0* l 0/ l (2) is S wherein 0Cross section when being zero.Can determine strain (ε) according to following formula:
ε=ln (l/l 0) (3) l wherein 0With l be respectively the length of inspection period and the length zero time.This data allow counter stress and strain curve relation to map, and being calculated as follows of Young's modulus (E):
E＝Δσ/Δε (4)
Below Bao Dao numerical value is the mean value of at least 15 measurements.
Figure 18 has shown the typical stress and strain relation curve of the preliminary shaping Whatman paper of handling with CBD or CCP.The deformational behavior of treated paper under institute's applying load can be derived according to stress-strain curve.Under 0.02 strain at the most, observing has linear relationship between stress and strain.Yet,, find to have nonlinear relationship being higher than under 0.02 the strain.As ise apparent from FIG. 18, tension stress increases to CBD from contrast respectively and increases to CCP then.The tensile strength value ratio of the CCP treatment paper paper that is untreated is high about 40%, and is higher by 14% than CBD treatment paper.The strength ratio of the CBD treatment paper paper that is untreated is high by about 25%.In two kinds of processing, described difference all is significant (table 6) on the statistics.
Table 6
Contrast CBD CCP
The stress when 2.5mg/ml 2.5mg/ml breaks (MPa) 7.4 c9.2 b10.5 aStrain when breaking (%) 10.4 b11.7 Ab15.5 aYoung's modulus (MPa) *183.3 b197.2 Ab214.5 aEnergy (10 when breaking 3J/m 3) 0.208 c0.254 b0.418 a *Young's modulus is calculated with 3% distortion.Connect after in the delegation that target numerical value has significant difference, p=0.0l on the different letter.
The variation of paper breaking strain also is a significance.In the paper of handling with CCP, breaking strain increases about 50% for the paper that is untreated.The effect of CBD is obviously lower, only causes increasing by 12%.With CBD or CCP treatment paper, produce the lower paper of fragility.In table 1, summed up the Young's modulus of the treated paper that the initial slope by stress-strain curve (being deformed into linearity until 3%) draws.Use the CCP treatment paper, cause its Young's modulus to increase by 17%, and the CBD processing causes only increasing by 7.5%.By the area under computed stress-strain curve, determine energy absorption, in table 6, summed up described result.The tendency that observes in the data of tensile strength is applicable to energy absorption; Yet its size is bigger.The comparison of the energy absorption of CCP treatment paper is according to high about 100%, and the energy absorption of CBD treatment paper only high 23%.Its CBD of the numeric ratio of CCP treatment paper handles corresponding object height about 64%.In all parameters of being tested, the effect of CCP is significant statistically, and with the CBD processing significance,statistical (table 6) is only arranged aspect stress and the energy absorption when breaking.
Figure 19 has shown the absorbent time of the preliminary shaping Whatman paper of handling with the CBD of different concns or CCP.Figure 20 shows the time lapse photo that water absorbs on the preliminary shaping Whatman paper of handling with CCP.Draw distilled water (10 μ l), be placed on the described treated paper, to measure the required time of hypersorption second.(KSVInstruments, Helsinki Finland) manifest the absorption of water also to use light contact angle meter CAM20009.A water is dripped on the pattern, take pictures with the time lapse of 20ms.When water contacts back 25ms with paper, take first frame.In the paper that is untreated, soak time was less than 1 second.The absorbent time of CBD treatment paper and CCP treatment paper increases with the increase of protein content.When using CCP with the concentration of 2.5mg/ml, (CCP is 580 seconds to high 2 orders of magnitude of paper that absorbent time is handled than the CBD with same concentration, CBD is 5 seconds by contrast), than low at least 3 orders of magnitude of height (CCP is 580 seconds, contrasts by contrast less than 1 second) that are untreated.
Manifest the kinetics that drops in the water on the CCP treatment paper with light contact angle meter (CAM).Water droplet contacted with the paper that is untreated after Figure 20 (photo F) had described 25ms.Obviously, water is absorbed in the paper immediately after contact.(picture A-E) has further been described absorption and relation passing time between of CCP treatment paper to water droplet to Figure 20.In preceding 2 minutes, do not detect absorption, contact angle keeps＞90 °.After 4 minutes, just observe and be absorbed in the paper.Even after 8 minutes, water is not also absorbed by paper fully.After 10 minutes, just observe and absorbed (Figure 19) in the paper fully.
Embodiment 6
Before the shaping stage of paper-making process, make the fiber fines cellulose fiber crosslinked
By at least two CBD are connected preparation CBD coupling agent unit composition or reagent with a joint unit.The suspension that makes the cellulosic fibre that comprises the fiber fines cellulose fiber that passes forming net (filter (filter)) leading to of significant quantity is handled described suspension by before the forming net with described CBD coupling agent unit composition.The CBD coupling agent unit of CDB coupling agent unit composition is cross-linked to form a plurality of three-dimensional fiber cellulose fiber aggregates with described fiber fines cellulose fiber.By after the forming net, described filter has kept the three-dimensional aggregate of cellulosic fibre at treated suspension, thereby guarantees that raw material (cellulosic fibre) rate of recovery improves greatly.
Above result proves, can prepare the PBD fusion rotein that comprises dual or the dimerization PBD (fusion product of two CBD for example, for example cellulose crosslinked albumen (CCP)), CBD and the proteic fusion product of A and S peptide-CBD-S albumen syzygy, and can come the modified polysaccharide structure with them.
People will appreciate that, have described some feature of the present invention so that understand in different embodiments, and described feature also can provide with combination in one embodiment.On the contrary, for for simplicity, described different characteristics of the present invention in one embodiment, these features also can separately provide or provide in any suitable subgroup mode of closing.
Though be described in conjunction with a specific embodiment thereof the present invention, obviously, many replacement schemes, modifications and variations are conspicuous for those skilled in the art.Therefore, the present invention will comprise all these class replacement schemes, the modifications and variations in the spirit and scope that belong to appended claims.All publications, patent and the patent application mentioned in this specification sheets all are attached to herein by reference, and its degree specifically and individually indicates by reference as each independent publication, patent or patent application and is attached to herein.In addition, any reference among the application quotes as proof or identifies and should not be interpreted as admitting that this reference can be used as prior art of the present invention.
Sequence table＜110〉Levy, Ilan
Shoseyov，Oded
Nussinovitch; Amos＜120〉contain the modification of polysaccharide material＜130〉00/20910＜140〉60/166; 38960/164,140＜141〉1999-11-181999-11-08＜160〉13＜170〉PatentIn version 3.0＜210〉1＜211〉507＜212〉DNA＜213〉Clostridium cellulovorans＜400〉1ccatggcagc gacatcatca atgtcagttg aattttacaa ctctaacaaa tcagcacaaa 60caaactcaat tacaccaata atcaaaatta ctaacacatc tgacagtgat ttaaatttaa 120atgacgtaaa agttagatat tattacacaa gtgatggtac acaaggacaa actttctggt 180gtgaccatgc tggtgcatta ttaggaaata gctatgttga taacactagc aaagtgacag 240caaacttcgt taaagaaaca gcaagcccaa catcaaccta tgatacatat gttgaatttg 300gatttgcaag cggacgagct actcttaaaa aaggacaatt tataactatt caaggaagaa 360taacaaaatc agactggtca aactacactc aaacaaatga ctattcattt gatgcaagta 420gttcaacacc agttgtaaat ccaaaagtta caggatatat aggtggagct aaagtacttg 480gtacagcacc ataggatcca gatgtac 507＜210〉2＜211〉163＜212〉PRT＜213〉Clostridium cellulovorans＜400〉2Met Ala Ala Thr Ser Ser Met Ser Val Glu Phe Tyr Asn Ser Asn Lys1 5 10 15Ser Ala Gln Thr Asn Ser Ile Thr Pro Ile Ile Lys Ile Thr Asn Thr
20 25 30Ser?Asp?Ser?Asp?Leu?Asn?Leu?Asn?Asp?Val?Lys?Val?Arg?Tyr?Tyr?Tyr
35 40 45Thr?Ser?Asp?Gly?Thr?Gln?Gly?Gln?Thr?Phe?Trp?Cys?Asp?His?Ala?Gly
50 55 60Ala?Leu?Leu?Gly?Asn?Ser?Tyr?Val?Asp?Asn?Thr?Ser?Lys?Val?Thr?Ala65 70 75 80Asn?Phe?Val?Lys?Glu?Thr?Ala?Ser?Pro?Thr?Ser?Thr?Tyr?Asp?Thr?Tyr
85 90 95Val?Glu?Phe?Gly?Phe?Ala?Ser?Gly?Arg?Ala?Thr?Leu?Lys?Lys?Gly?Gln
100 105 110Phe?Ile?Thr?Ile?Gln?Gly?Arg?Ile?Thr?Lys?Ser?Asp?Trp?Ser?Asn?Tyr
115 120 125Thr?Gln?Thr?Asn?Asp?Tyr?Ser?Phe?Asp?Ala?Ser?Ser?Ser?Thr?Pro?Val
130 135 140Val?Asn?Pro?Lys?Val?Thr?Gly?Tyr?Ile?Gly?Gly?Ala?Lys?Val?Leu?Gly145 150 155 160Thr?Ala?Pro<210>3<211>573<212>DNA<213>Clostridium?cellulovorans<400>3ccatgtcagt?tgaattctac?aactctaaca?aatcagcaca?aacaaactca?attacaccaa 60taatcaaaat?tactaacaca?tctgacagtg?atttaaattt?aaatgacgta?aaagttagat 120attattacac?aagtgatggt?acacaaggac?aaactttctg?gtgtgaccat?gctggtgcat 180tattaggaaa?tagctatgtt?gataacacta?gcaaagtgac?agcaaacttc?gttaaagaaa 240cagcaagccc?aacatcaacc?tatgatacat?atgttgaatt?tggatttgca?agcggacgag 300ctactcttaa?aaaaggacaa?tttataacta?ttcaaggaag?aataacaaaa?tcagactggt 360caaactacac?tcaaacaaat?gactattcat?ttgatgcaag?tagttcaaca?ccagttgtaa 420atccaaaagt?tacaggatat?ataggtggag?ctaaagtact?tggtacagca?ccaggtccag 480atgtaccatc?ttcaataatt?aatcctactt?ctgcaacatt?tgatcccggt?accatggcta 540gcatgactgg?tggacagcaa?atgggtcgga?tcc 573<210>4<211>190<212>PRT<213>Clostridium?cellulovorans<400>4Met?Ser?Val?Glu?Phe?Tyr?Asn?Ser?Asn?Lys?Ser?Ala?Gln?Thr?Asn?Ser1 5 10 15Ile?Thr?Pro?Ile?Ile?Lys?Ile?Thr?Asn?Thr?Ser?Asp?Ser?Asp?Leu?Asn
20 25 30Leu?Asn?Asp?Val?Lys?Val?Arg?Tyr?Tyr?Tyr?Thr?Ser?Asp?Gly?Thr?Gln
35 40 45Gly?Gln?Thr?Phe?Trp?Cys?Asp?His?Ala?Gly?Ala?Leu?Leu?Gly?Asn?Ser
50 55 60Tyr?Val?Asp?Asn?Thr?Ser?Lys?Val?Thr?Ala?Asn?Phe?Val?Lys?Glu?Thr65 70 75 80Ala?Ser?Pro?Thr?Ser?Thr?Tyr?Asp?Thr?Tyr?Val?Glu?Phe?Gly?Phe?Ala
85 90 95Ser?Gly?Arg?Ala?Thr?Leu?Lys?Lys?Gly?Gln?Phe?Ile?Thr?Ile?Gln?Gly
100 105 110Arg?Ile?Thr?Lys?Ser?Asp?Trp?Ser?Asn?Tyr?Thr?Gln?Thr?Asn?Asp?Tyr
115 120 125Ser?Phe?Asp?Ala?Ser?Ser?Ser?Thr?Pro?Val?Val?Asn?Pro?Lys?Val?Thr
130 135 140Gly?Tyr?Ile?Gly?Gly?Ala?Lys?Val?Leu?Gly?Thr?Ala?Pro?Gly?Pro?Asp145 150 155 160Val?Pro?Ser?Ser?Ile?Ile?Asn?Pro?Thr?Ser?Ala?Thr?Phe?Asp?Pro?Gly
165 170 175Thr?Met?Ala?Ser?Met?Thr?Gly?Gly?Gln?Gln?Met?Gly?Arg?Ile
180 185 190<210>5<211>1030<212>DNA<213>Clostridium?cellulovorans<400>5ccatgtcagt?tgaattctac?aactctaaca?aatcagcaca?aacaaactca?attacaccaa 60taatcaaaat?tactaacaca?tctgacagtg?atttaaattt?aaatgacgta?aaagttagat 120attattacac?aagtgatggt?acacaaggac?aaactttctg?gtgtgaccat?gctggtgcat 180tattaggaaa?tagctatgtt?gataacacta?gcaaagtgac?agcaaacttc?gttaaagaaa 240cagcaagccc?aacatcaacc?tatgatacat?atgttgaatt?tggatttgca?agcggacgag 300ctactcttaa?aaaaggacaa?tttataacta?ttcaaggaag?aataacaaaa?tcagactggt 360caaactacac?tcaaacaaat?gactattcat?ttgatgcaag?tagttcaaca?ccagttgtaa 420atccaaaagt?tacaggatat?ataggtggag?ctaaagtact?tggtacagca?ccaggtccag 480atgtaccatc?ttcaataatt?aatcctactt?ctgcaacatt?tgatcccggt?accatggcag 540cgacatcatc?aatgtcagtt?gaattttaca?actctaacaa?atcagcacaa?acaaactcaa 600ttacaccaat?aatcaaaatt?actaacacat?ctgacagtga?tttaaattta?aatgacgtaa 660aagttagata?ttattacaca?agtgatggta?cacaaggaca?aactttctgg?tgtgaccatg 720ctggtgcatt?attaggaaat?agctatgttg?ataacactag?caaagtgaca?gcaaacttcg 780ttaaagaaac?agcaagccca?acatcaacct?atgatacata?tgttgaattt?ggatttgcaa 840gcggacgagc?tactcttaaa?aaaggacaat?ttataactat?tcaaggaaga?ataacaaaat 900cagactggtc?aaactacact?caaacaaatg?actattcatt?tgatgcaagt?agttcaacac 960cagttgtaaa?tccaaaagtt?acaggatata?taggtggagc?taaagtactt?ggtacagcac 1020cataggatcc 1030<210>6<211>340<212>PRT<213>Clostridium?cellulovorans<400>6Met?Set?Val?Glu?Phe?Tyr?Asn?Ser?Asn?Lys?Ser?Ala?Gln?Thr?Asn?Ser1 5 10 15lle?Thr?Pro?Ile?Ile?Lys?Ile?Thr?Asn?Thr?Sar?Asp?Ser?Asp?Leu?Asn
20 26 30Leu?Asn?Asp?Val?Lys?Val?Arg?Tyr?Tyr?Tyr?Thr?Ser?Asp?Gly?Thr?Gln
35 40 45Gly?Gln?Thr?Phe?Trp?Cys?Asp?His?Ala?Gly?Ala?Leu?Leu?Gly?Asn?Ser
50 55 60Tyr?Val?Asp?Asn?Thr?Ser?Lys?Val?Thr?Ala?Asn?Phe?Val?Lys?Glu?Thr65 70 75 80Ala?Ser?Pro?Thr?Ser?Thr?Tyr?Asp?Thr?Tyr?Val?Glu?Phe?Gly?Phe?Ala
85 90 95Ser?Gly?Arg?Ala?Thr?Leu?Lys?Lys?Gly?Gln?Phe?Ile?Thr?Ile?Gln?Gly
100 105 110Arg?Ile?Thr?Lys?Ser?Asp?Trp?Ser?Asn?Tyr?Thr?Gln?Thr?Asn?Asp?Tyr
115 120 125Ser?Phe?Asp?Ala?Ser?Ser?Ser?Thr?Pro?Val?Val?Asn?Pro?Lys?Val?Thr
130 135 140Gly?Tyr?Ile?Gly?Gly?Ala?Lys?Val?Leu?Gly?Thr?Ala?Pro?Gly?Pro?Asp145 150 155 160Val?Pro?Ser?Ser?Ile?Ile?Asn?Pro?Thr?Ser?Ala?Thr?Phe?Asp?Pro?Gly
165 170 175Thr?Met?Ala?Ala?Thr?Ser?Ser?Met?Ser?Val?Glu?Phe?Tyr?Asn?Ser?Asn
180 185 190Lys?Ser?Ala?Gln?Thr?Asn?Ser?Ile?Thr?Pro?Ile?Ile?Lys?Ile?Thr?Asn
195 200 205Thr?Ser?Asp?Ser?Asp?Leu?Asn?Leu?Asn?Asp?Val?Lys?Val?Arg?Tyr?Tyr
210 215 220Tyr?Thr?Ser?Asp?Gly?Thr?Gln?Gly?Gln?Thr?Phe?Trp?Cys?Asp?His?Ala225 230 235 240Gly?Ala?Leu?Leu?Gly?Asn?Ser?Tyr?Val?Asp?Asn?Thr?Ser?Lys?Val?Thr
245 250 255Ala?Asn?Phe?Val?Lys?Glu?Thr?Ala?Ser?Pro?Thr?Ser?Thr?Tyr?Asp?Thr
260 265 270Tyr?Val?Glu?Phe?Gly?Phe?Ala?Ser?Gly?Arg?Ala?Thr?Leu?Lys?Lys?Gly
275 280 285Gln?Phe?Ile?Thr?Ile?Gln?Gly?Arg?Ile?Thr?Lys?Ser?Asp?Trp?Ser?Asn
290 295 300Tyr?Thr?Gln?Thr?Asn?Asp?Tyr?Ser?Phe?Asp?Ala?Ser?Ser?Ser?Thr?Pro305 310 315 320Val?Val?Asn?Pro?Lys?Val?Thr?Gly?Tyr?Ile?Gly?Gly?Ala?Lys?Val?Leu
325 330 335Gly?Thr?Ala?Pro
340＜210〉7＜211〉1288＜212〉DNA＜213〉＜220〉＜221〉misc_feature＜222〉 ( 3 ) .. ( 791 )＜223〉pRIT2T＜220〉＜221〉misc feature＜222〉 ( 795 ) .. ( 1280 )＜223〉cbpA＜400〉7ccatggaaca acgcataacc ctgaaagaag cttgggatca acgcaatggt tttatccaaa 60gccttaaaga tgatccaagc caaagtgcta acgttttagg tgaagctcaa aaacttaatg 120actctcaagc tccaaaagct gatgcgcaac aaaataactt caacaaagat caacaaagcg 180ccttctatga aatcttgaac atgcctaact taaacgaagc gcaacgtaac ggcttcattc 240aaagtcttaa agacgaccca agccaaagca ctaacgtttt aggtgaagct aaaaaattaa 300acgaatctca agcaccgaaa gctgataaca atttcaacaa agaacaacaa aatgctttct 360atgaaatctt gaatatgcct aacttaaacg aagaacaacg caatggtttc atccaaagct 420taaaagatga cccaagccaa agtgctaacc tattgtcaga agctaaaaag ttaaatgaat 480ctcaagcacc gaaagcggat aacaaattca acaaagaaca acaaaatgct ttctatgaaa 540tcttacattt acctaactta aacgaagaac aacgcaatgg tttcatccaa agcctaaaag 600atgacccaag ccaaagcgct aaccttttag cagaagctaa aaagctaaat gatgctcaag 660caccaaaagc tgacaacaaa ttcaacaaag aacaacaaaa tgctttctat gaaattttac 720atttacctaa cttaactgaa gaacaacgta acggcttcat ccaaagcctt aaagacgatc 780cggggaattc catggcagcg acatcatcaa tgtcagttga attttacaac tctaacaaat 840cagcacaaac aaactcaatt acaccaataa tcaaaattac taacacatct gacagtgatt 900taaatttaaa tgacgtaaaa gttagatatt attacacaag tgatggtaca caaggacaaa 960ctttctggtg tgaccatgct ggtgcattat taggaaatag ctatgttgat aacactagca 1020aagtgacagc aaacttcgtt aaagaaacag caagcccaac atcaacctat gatacatatg 1080ttgaatttgg atttgcaagc ggacgagcta ctcttaaaaa aggacaattt ataactattc 1140aaggaagaat aacaaaatca gactggtcaa actacactca aacaaatgac tattcatttg 1200atgcaagtag ttcaacacca gttgtaaatc caaaagttac aggatatata ggtggagcta 1260aagtacttgg tacagcacca taggatcc 1288＜210〉8＜211〉426＜212〉PRT＜213〉＜220〉＜221〉misc_feature＜222〉 ( 1 ) .. ( 263 )＜223〉A＜220〉＜221〉misc feature＜222〉 ( 265 ) .. ( 426 )＜223〉CBPA＜400〉8Met Glu Gln Arg Ile Thr Leu Lys Glu Ala Trp Asp Gln Arg Asn Glyl 5 10 15Phe Ile Gln Ser Leu Lys Asp Asp Pro Ser Gln Ser Ala Asn Val Leu
20 25 30Gly?Glu?Ala?Gln?Lys?Leu?Asn?Asp?Ser?Gln?Ala?Pro?Lys?Ala?Asp?Ala
35 40 45Gln?Gln?Asn?Asn?Phe?Asn?Lys?Asp?Gln?Gln?Ser?Ala?Phe?Tyr?Glu?Ile
50 55 60Leu?Asn?Met?Pro?Asn?Leu?Asn?Glu?Ala?Gln?Arg?Asn?Gly?Phe?Ile?Gln65 70 75 80Set?Leu?Lys?Asp?Asp?Pro?Ser?Gln?Ser?Thr?Asn?Val?Leu?Gly?Glu?Ala
85 90 95Lys?Lys?Leu?Asn?Glu?Ser?Gln?Ala?Pro?Lys?Ala?Asp?Asn?Ash?Phe?Asn
100 105 110Lys?Glu?Gln?Gln?Asn?Ala?Phe?Tyr?Glu?Ile?Leu?Asn?Met?Pro?Asn?Leu
115 120 125Asn?Glu?Glu?Gln?Arg?Asn?Gly?Phe?Ile?Gln?Ser?Leu?Lys?Asp?Asp?Pro
130 135 140Set?Gln?Ser?Ala?Asn?Leu?Leu?Ser?Glu?Ala?Lys?Lys?Leu?Asn?Glu?Set145 150 155 160Gln?Ala?Pro?Lys?Ala?Asp?Asn?Lys?Phe?Asn?Lys?Glu?Gln?Gln?Asn?Ala
165 170 175Phe?Tyr?Glu?Ile?Leu?His?Leu?Pro?Asn?Leu?Asn?Glu?Glu?Gln?Arg?Asn
180 185 190Gly?Phe?Ile?Gln?Ser?Leu?Lys?Asp?Asp?Pro?Ser?Gln?Ser?Ala?Asn?Leu
195 200 205Leu?Ala?Glu?Ala?Lys?Lys?Leu?Asn?Asp?Ala?Gln?Ala?Pro?Lys?Ala?Asp
210 215 220Asn?Lys?Phe?Asn?Lys?Glu?Gln?Gln?Asn?Ala?Phe?Tyr?Glu?Ile?Leu?His225 230 235 240Leu?Pro?Asn?Leu?Thr?Glu?Glu?Gln?Arg?Asn?Gly?Phe?Ile?Gln?Ser?Leu
245 250 255Lys?Asp?Asp?Pro?Gly?Asn?Ser?Met?Ala?Ala?Thr?Ser?Ser?Met?Ser?Val
260 265 270Glu?Phe?Tyr?Asn?Ser?Asn?Lys?Ser?Ala?Gln?Thr?Asn?Ser?Ile?Thr?Pro
275 280 285Ile?Ile?Lys?Ile?Thr?Asn?Thr?Ser?Asp?Ser?Asp?Leu?Asn?Leu?Asn?Asp
290 295 300Val?Lys?Val?Arg?Tyr?Tyr?Tyr?Thr?Ser?Asp?Gly?Thr?Gln?Gly?Gln?Thr305 310 315 320Phe?Trp?Cys?Asp?His?Ala?Gly?Ala?Leu?Leu?Gly?Asn?Ser?Tyr?Val?Asp
325 330 335Asn?Thr?Ser?Lys?Val?Thr?Ala?Asn?Phe?Val?Lys?Glu?Thr?Ala?Ser?Pro
340 345 350Thr?Ser?Thr?Tyr?Asp?Thr?Tyr?Val?Glu?Phe?Gly?Phe?Ala?Set?Gly?Arg
355 360 365Ala?Thr?Leu?Lys?Lys?Gly?Gln?Phe?Ile?Thr?Ile?Gln?Gly?Arg?Ile?Thr
370 375 380Lys?Ser?Asp?Trp?Ser?Asn?Tyr?Thr?Gln?Thr?Asn?Asp?Tyr?Ser?Phe?Asp385 390 395 400Ala?Ser?Ser?Ser?Thr?Pro?Val?Val?Asn?Pro?Lys?Val?Thr?Gly?Tyr?Ile
405 410 415Gly?Gly?Ala?Lys?Val?Leu?Gly?Thr?Ala?Pro
420 425＜210〉9＜211〉984＜212〉DNA＜213〉＜220〉＜221〉misc_feature＜222〉 ( 68 ) .. ( 624 )＜223〉Clostridium cellulovorans＜220〉＜221〉misc_feature＜222〉 ( 652 ) .. ( 981 )＜223〉＜400〉9catatgaaag aaaccgctgc tgctaaattc gaacgccagc acatggacag cccagatctg 60ggtaccctgg tgccacgcgg ttccatggca gcgacatcat caatgtcagt tgaattttac 120aactctaaca aatcagcaca aacaaactca attacaccaa taatcaaaat tactaacaca 180tctgacagtg atttaaattt aaatgacgta aaagttagat attattacac aagtgatggt 240acacaaggac aaactttctg gtgtgaccat gctggtgcat tattaggaaa tagctatgtt 300gataacacta gcaaagtgac agcaaacttc gttaaagaaa cagcaagccc aacatcaacc 360tatgatacat atgttgaatt tggatttgca agcggacgag ctactcttaa aaaaggacaa 420tttataacta ttcaaggaag aataacaaaa tcagactggt caaactacac tcaaacaaat 480gactattcat ttgatgcaag tagttcaaca ccagttgtaa atccaaaagt tacaggatat 540ataggtggag ctaaagtact tggtacagca ccaggtccag atgtaccatc ttcaataatt 600aatcctactt ctgcaacatt tgatcccggt accatgggtc ctcctcctgg aagcacttcc 660gctgccagca gctccaacta ttgcaaccag atgatgaaga gccggaacct gaccaaagat 720cgatgcaagc cagtgaacac ctttgtgcac gagtccctgg ctgatgtcca ggccgtgtgc 780tcccagaaaa atgttgcctg caagaatggg cagaccaatt gctaccagag ctactccacc 840atgagcatca ccgactgccg tgagaccggc agctccaagt accccaactg tgcctacaag 900accacccagg cgaataaaca catcattgtg gcttgtgagg gaaacccgta cgtgccagtc 960cacttcgacg cttcagtgta gatc 984＜210〉10＜211〉326＜212〉PRT＜213〉＜220〉＜221〉misc_feature＜222〉 ( 30 ) .. ( 208 )＜223〉Clostridium cellulovorans＜220〉＜221〉misc_feature＜222〉 ( 226 ) .. ( 326 )＜223〉＜400〉10His Met Lys Glu Thr Ala Ala Ala Lys Phe Glu Arg Gln His Met Asp1 5 l0 15Ser Pro Asp Leu Gly Thr Leu Val Pro Arg Gly Ser Met Ala Ala Thr
20 25 30Ser?Ser?Met?Ser?Val?Glu?Phe?Tyr?Asn?Ser?Asn?Lys?Ser?Ala?Gln?Thr
35 40 45Asn?Ser?Ile?Thr?Pro?Ile?Ile?Lys?Ile?Thr?Asn?Thr?Ser?Asp?Ser?Asp
50 55 60Leu?Asn?Leu?Asn?Asp?Val?Lys?Val?Arg?Tyr?Tyr?Tyr?Thr?Ser?Asp?Gly65 70 75 80Thr?Gln?Gly?Gln?Thr?Phe?Trp?Cys?Asp?His?Ala?Gly?Ala?Leu?Leu?Gly
85 90 95Asn?Ser?Tyr?Val?Asp?Asn?Thr?Ser?Lys?Val?Thr?Ala?Asn?Phe?Val?Lys
100 105 110Glu?Thr?Ala?Ser?Pro?Thr?Ser?Thr?Tyr?Asp?Thr?Tyr?Val?Glu?Phc?Gly
115 120 125Phe?Ala?Ser?Gly?Arg?Ala?Thr?Leu?Lys?Lys?Gly?Gln?Phe?Ile?Thr?Ile
130 135 140Gln?Gly?Arg?Ile?Thr?Lys?Ser?Asp?Trp?Ser?Asn?Tyr?Thr?Gln?Thr?Asn145 150 155 160Asp?Tyr?Ser?Phe?Asp?Ala?Ser?Ser?Ser?Thr?Pro?Val?Val?Asn?Pro?Lys
165 170 175Val?Thr?Gly?Tyr?Ile?Gly?Gly?Ala?Lys?Val?Leu?Gly?Thr?Ala?Pro?Gly
180 185 190Pro?Asp?Val?Pro?Ser?Ser?Ile?Ile?Asn?Pro?Thr?Ser?Ala?Thr?Phe?Asp
195 200 205Pro?Gly?Thr?Met?Gly?Pro?Pro?Pro?Gly?Ser?Thr?Ser?Ala?Ala?Ser?Ser
210 215 220Ser?Asn?Tyr?Cys?Asn?Gln?Met?Met?Lys?Ser?Arg?Asn?Leu?Thr?Lys?Asp225 230 235 240Arg?Cys?Lys?Pro?Val?Asn?Thr?Phe?Val?His?Glu?Ser?Leu?Ala?Asp?Val
245 250 255Gln?Ala?Val?Cys?Ser?Gln?Lys?Asn?Val?Ala?Cys?Lys?Asn?Gly?Gln?Thr
260 265 270Asn?Cys?Tyr?Gln?Ser?Tyr?Ser?Thr?Met?Ser?Ile?Thr?Asp?Cys?Arg?Glu
275 280 285Thr?Gly?Set?Ser?Lys?Tyr?Pro?Asn?Cys?Ala?Tyr?Lys?Thr?Thr?Gln?Ala
290 295 300Asn?Lys?His?lle?Ile?Val?Ala?Cys?Glu?Gly?Asn?Pro?Tyr?Val?Pro?Val305 310 315 320His?Phe?Asp?Ala?Ser?Val
325＜210〉11＜211〉24＜212〉DNA＜213〉synthetic oligonucleotide;＜400〉11gggggaattc catggcagcg acat 24＜210〉12＜211〉18＜212〉DNA＜213〉synthetic oligonucleotide;＜400〉12gggggatcct atggtgct 18＜210〉13＜211〉22＜212〉DNA＜213〉synthetic oligonucleotide;＜400〉13ggggggtacc atggaacaac gc 22

Claims (105)

1. a manufacturing has the method that contains polysaccharide material of at least a desired structure characteristic, chemical property, physicals, electric property and/or mechanical property, said method comprising the steps of: make the described polysaccharide structures that contains polysaccharide material and the composition that contains the polysaccharide binding domains described polysaccharide structures is worked into described contain in the polysaccharide material before, during and/or contact afterwards, thereby make the described polysaccharide material that contains with desired structure characteristic, chemical property, physicals, electric property and/or mechanical property.
2. the process of claim 1 wherein the described described polysaccharide structures that contains polysaccharide material is worked into described contain in the polysaccharide material before, realize described polysaccharide structures is contacted with the described polysaccharide binding domains composition that contains.
3. the process of claim 1 wherein the described described polysaccharide structures that contains polysaccharide material is worked into described contain in the polysaccharide material during, realize described polysaccharide structures is contacted with the described polysaccharide binding domains composition that contains.
4. the process of claim 1 wherein the described described polysaccharide structures that contains polysaccharide material is worked into described contain in the polysaccharide material after, realize described polysaccharide structures is contacted with the described polysaccharide binding domains composition that contains.
5. the process of claim 1 wherein that the described polysaccharide material that contains is selected from paper, textiles, yarn and fiber.
6. the process of claim 1 wherein that described structural performance is selected from crosslinked, the described predetermined gathering and the described predetermined surface reticulate pattern that contains polysaccharide material that contains the polysaccharide structures of polysaccharide material of predeterminated level between the described polysaccharide structures that contains polysaccharide material.
7. the process of claim 1 wherein that described chemical property is selected from predetermined hydrophobicity, predetermined wetting ability, predetermined wetting properties, predetermined chemical reactivity, predetermined photochemical reaction, predetermined functionality and predetermined surface tension.
8. the process of claim 1 wherein that described physicals is selected from predetermined strain under predetermined Young's modulus, the maximum load, predetermined breaking point energy, predetermined water-absorbent, predetermined swelling property and predetermined toughness.
9. the process of claim 1 wherein that described electric property is selected from predetermined surface charge and predetermined electroconductibility.
10. the process of claim 1 wherein that described mechanical property is selected from predetermined tensile strength, predetermined shearing resistance, predetermined wearability, predetermined frictional coefficient, predetermined elasticity and predetermined wet tenacity.
11. the process of claim 1 wherein the described other polysaccharide binding domains that polysaccharide binding domains composition comprises a polysaccharide binding domains and at least one and its covalent coupling that contains.
12. the process of claim 1 wherein described contain polysaccharide binding domains composition comprise a polysaccharide binding domains and with another protein of its covalent coupling.
13. the process of claim 1 wherein the described hydrophobic group that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
14. the process of claim 1 wherein the described hydrophilic radical that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
15. the process of claim 1 wherein the described biological part retinal diseases that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
16. the process of claim 1 wherein the described enzyme that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
17. the process of claim 1 wherein the described chemical reaction group that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
18. the process of claim 1 wherein the described chemical light reactive group that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
19. the process of claim 1 wherein the described lipase that polysaccharide binding domains composition comprises a polysaccharide binding domains and one and its covalent coupling that contains.
20. the process of claim 1 wherein the described laccase that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
21. the process of claim 1 wherein the described A albumen-antibody that polysaccharide binding domains composition comprises a polysaccharide binding domains and one and its covalent coupling that contains.
22. the process of claim 1 wherein the described peptide that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
23. the process of claim 1 wherein the described polypeptide that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
24. the process of claim 1 wherein described hydrocarbon or the hydrocarbon derivative that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contain.
25. the process of claim 1 wherein the described derivative of fatty acid that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
26. the process of claim 1 wherein the described electrically charged part that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
27. the process of claim 1 wherein the described ion part that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
28. the process of claim 1 wherein the described silicon bound fraction that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
29. the process of claim 1 wherein that the described polysaccharide binding domains composition that contains comprises that a polysaccharide binding domains and one combine part with the polymkeric substance of its covalent coupling.
30. the process of claim 1 wherein the described metal that polysaccharide binding domains composition comprises a polysaccharide binding domains and a kind of and its covalent coupling that contains.
31. the process of claim 1 wherein the described metallothionein(MT) sample albumen that polysaccharide binding domains composition comprises a polysaccharide binding domains and one and its covalent coupling that contains.
32. the process of claim 1 wherein the described ferritin that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
33. the process of claim 1 wherein the described melts combine part that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
34. the process of claim 1 wherein the described bacterium siderophore that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
35. the process of claim 1 wherein the described metallothionein(MT) that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
36. the process of claim 1 wherein the described sulfydryl that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
37. the process of claim 1 wherein the described aldehyde that polysaccharide binding domains composition comprises a polysaccharide binding domains and one and its covalent coupling that contains.
38. the process of claim 1 wherein the described maleimide that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
39. the process of claim 1 wherein the described hydrazides that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
40. the process of claim 1 wherein the described epoxide that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
41. the process of claim 1 wherein the described carbodiimide that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
42. the process of claim 1 wherein the described triazobenzene that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling that contains.
43. the process of claim 1 wherein that the described polysaccharide binding domains composition that contains comprises a polysaccharide binding domains, described polysaccharide binding domains is a cellulose binding domain.
44. the process of claim 1 wherein that the described polysaccharide binding domains composition that contains comprises a polysaccharide binding domains, described polysaccharide binding domains is the starch binding domains.
45. the process of claim 1 wherein described contain polysaccharide binding domains composition comprise one can with Mierocrystalline cellulose bonded polysaccharide binding domains.
46. the process of claim 1 wherein described contain polysaccharide binding domains composition comprise one can with starch bonded polysaccharide binding domains.
47. the process of claim 1 wherein described contain polysaccharide binding domains composition comprise one can with chitin bonded polysaccharide binding domains.
48. the process of claim 1 wherein that the described polysaccharide binding domains composition that contains comprises a polysaccharide binding domains, described polysaccharide binding domains is the dextran binding domains.
49. the process of claim 1 wherein that the described polysaccharide binding domains composition that contains comprises a polysaccharide binding domains, described polysaccharide binding domains comprises that the suis dextran is in conjunction with tumor-necrosis factor glycoproteins.
50. a topic is stated composition, described composition comprises:
A kind of polysaccharide material that contains that comprises polysaccharide structures; With
A kind for the treatment of contains polysaccharide binding domains composition with the described described polysaccharide structures bonded that contains polysaccharide material, for the described polysaccharide material that contains provides at least a required structural performance, chemical property, physicals, electric property and/or mechanical property.
51. the topic of claim 50 is stated composition, the wherein said polysaccharide material that contains is selected from paper, textiles, yarn and fiber.
52. the topic of claim 50 is stated composition, wherein said structural performance is selected from crosslinked, the described predetermined gathering and the described predetermined surface reticulate pattern that contains polysaccharide material that contains the polysaccharide structures of polysaccharide material of predeterminated level between the described polysaccharide structures that contains polysaccharide material.
53. the topic of claim 50 is stated composition, wherein said chemical property is selected from predetermined hydrophobicity, predetermined wetting ability, predetermined wetting properties, predetermined chemical reactivity, predetermined photochemical reaction, predetermined functionality and predetermined surface tension.
54. the topic of claim 50 is stated composition, wherein said physicals is selected from predetermined strain under predetermined Young's modulus, the maximum load, predetermined breaking point energy, predetermined water-absorbent, predetermined swelling property and predetermined toughness.
55. the topic of claim 50 is stated composition, wherein said electric property is selected from predetermined surface charge and predetermined electroconductibility.
56. the topic of claim 50 is stated composition, wherein said mechanical property is selected from predetermined tensile strength, predetermined shearing resistance, predetermined wearability, predetermined frictional coefficient, predetermined elasticity and predetermined wet tenacity.
57. the topic of claim 50 is stated composition, wherein saidly contains the other polysaccharide binding domains that polysaccharide binding domains composition comprises a polysaccharide binding domains and at least one and its covalent coupling.
58. the topic of claim 50 is stated composition, wherein said contain polysaccharide binding domains composition comprise a polysaccharide binding domains and with another protein of its covalent coupling.
59. the topic of claim 50 is stated composition, wherein saidly contains the hydrophobic group that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
60. the topic of claim 50 is stated composition, wherein saidly contains the hydrophilic radical that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
61. the topic of claim 50 is stated composition, wherein saidly contains the biological part retinal diseases that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
62. the topic of claim 50 is stated composition, wherein saidly contains the enzyme that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
63. the topic of claim 50 is stated composition, wherein saidly contains the chemical reaction group that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
64. the topic of claim 50 is stated composition, wherein saidly contains the chemical light reactive group that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
65. the topic of claim 50 is stated composition, wherein saidly contains the lipase that polysaccharide binding domains composition comprises a polysaccharide binding domains and one and its covalent coupling.
66. the topic of claim 50 is stated composition, wherein saidly contains the laccase that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
67. the topic of claim 50 is stated composition, wherein saidly contains A albumen-antibody that polysaccharide binding domains composition comprises a polysaccharide binding domains and one and its covalent coupling.
68. the topic of claim 50 is stated composition, wherein saidly contains the peptide that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
69. the topic of claim 50 is stated composition, wherein saidly contains the polypeptide that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
70. the topic of claim 50 is stated composition, wherein saidly contains hydrocarbon or the hydrocarbon derivative that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
71. the topic of claim 50 is stated composition, wherein saidly contains the derivative of fatty acid that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
72. the topic of claim 50 is stated composition, wherein saidly contains the electrically charged part that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
73. the topic of claim 50 is stated composition, wherein saidly contains the ion part that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
74. the topic of claim 50 is stated composition, wherein saidly contains the silicon bound fraction that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
75. the topic of claim 50 is stated composition, the wherein said polysaccharide binding domains composition that contains comprises that a polysaccharide binding domains and one combine part with the polymkeric substance of its covalent coupling.
76. the topic of claim 50 is stated composition, wherein saidly contains the metal that polysaccharide binding domains composition comprises a polysaccharide binding domains and a kind of and its covalent coupling.
77. the topic of claim 50 is stated composition, wherein saidly contains the metallothionein(MT) sample albumen that polysaccharide binding domains composition comprises a polysaccharide binding domains and one and its covalent coupling.
78. the topic of claim 50 is stated composition, wherein saidly contains the ferritin that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
79. the topic of claim 50 is stated composition, wherein saidly contains the melts combine part that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
80. the topic of claim 50 is stated composition, wherein saidly contains the bacterium siderophore that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
81. the topic of claim 50 is stated composition, wherein saidly contains the metallothionein(MT) that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
82. the topic of claim 50 is stated composition, wherein saidly contains the sulfydryl that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
83. the topic of claim 50 is stated composition, wherein saidly contains the aldehyde that polysaccharide binding domains composition comprises a polysaccharide binding domains and one and its covalent coupling.
84. the topic of claim 50 is stated composition, wherein saidly contains the maleimide that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
85. the topic of claim 50 is stated composition, wherein saidly contains the hydrazides that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
86. the topic of claim 50 is stated composition, wherein saidly contains the epoxide that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
87. the topic of claim 50 is stated composition, wherein saidly contains the carbodiimide that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
88. the topic of claim 50 is stated composition, wherein saidly contains the triazobenzene that polysaccharide binding domains composition comprises a polysaccharide binding domains and and its covalent coupling.
89. the topic of claim 50 is stated composition, the wherein said polysaccharide binding domains composition that contains comprises a polysaccharide binding domains, and described polysaccharide binding domains is a cellulose binding domain.
90. the topic of claim 50 is stated composition, the wherein said polysaccharide binding domains composition that contains comprises a polysaccharide binding domains, and described polysaccharide binding domains is the starch binding domains.
91. the topic of claim 50 is stated composition, wherein said contain polysaccharide binding domains composition comprise one can with Mierocrystalline cellulose bonded polysaccharide binding domains.
92. the topic of claim 50 is stated composition, wherein said contain polysaccharide binding domains composition comprise one can with starch bonded polysaccharide binding domains.
93. the topic of claim 50 is stated composition, wherein said contain polysaccharide binding domains composition comprise one can with chitin bonded polysaccharide binding domains.
94. the topic of claim 50 is stated composition, the wherein said polysaccharide binding domains composition that contains comprises a polysaccharide binding domains, and described polysaccharide binding domains is the dextran binding domains.
95. the topic of claim 50 is stated composition, the wherein said polysaccharide binding domains composition that contains comprises a polysaccharide binding domains, and described polysaccharide binding domains comprises that the suis dextran is in conjunction with tumor-necrosis factor glycoproteins.
96. a topic is stated composition, described composition comprises:
A kind of polysaccharide material that contains that comprises polysaccharide structures; With
A kind for the treatment of contains polysaccharide binding domains composition with the described described polysaccharide structures bonded that contains polysaccharide material, describedly contain the polysaccharide binding domains that polysaccharide binding domains composition comprises at least two covalent couplings, form and make the described crosslinked polysaccharide binding domains coupling agent of described polysaccharide structures that contains polysaccharide material.
97. a topic is stated composition, described composition comprises:
A kind of polysaccharide material that contains that comprises polysaccharide structures; With
A kind for the treatment of contains polysaccharide binding domains composition with the described described polysaccharide structures bonded that contains polysaccharide material, describedly contain the functionalized moiety that polysaccharide binding domains composition comprises at least one polysaccharide binding domains and and its covalent coupling, described at least one polysaccharide binding domains is connected described functionalized moiety with the described described polysaccharide structures that contains polysaccharide material.
98. a topic is stated composition, described composition comprises:
A kind of polysaccharide material that contains that comprises polysaccharide structures; With
A kind for the treatment of contains polysaccharide binding domains composition with the described described polysaccharide structures bonded that contains polysaccharide material, describedly contain the hydrophobic parts that polysaccharide binding domains composition comprises at least one polysaccharide binding domains and and its covalent coupling, described at least one polysaccharide binding domains is connected described hydrophobic parts with the described described polysaccharide structures that contains polysaccharide material.
99. a topic is stated composition, described composition comprises:
A kind of polysaccharide material that contains that comprises polysaccharide structures; With
A kind for the treatment of contains polysaccharide binding domains composition with the described described polysaccharide structures bonded that contains polysaccharide material, describedly contain the hydrophilic parts that polysaccharide binding domains composition comprises at least one polysaccharide binding domains and and its covalent coupling, described at least one polysaccharide binding domains is connected described hydrophilic parts with the described described polysaccharide structures that contains polysaccharide material.
100. a topic is stated composition, described composition comprises:
A kind of polysaccharide material that contains that comprises polysaccharide structures; With
A kind for the treatment of contains polysaccharide binding domains composition with the described described polysaccharide structures bonded that contains polysaccharide material, describedly contain the chemical reactivity part that polysaccharide binding domains composition comprises at least one polysaccharide binding domains and and its covalent coupling, described at least one polysaccharide binding domains is connected described chemical reactivity part with the described described polysaccharide structures that contains polysaccharide material.
101. a topic is stated composition, described composition comprises:
A kind of polysaccharide material that contains that comprises polysaccharide structures; With
A kind for the treatment of contains polysaccharide binding domains composition with the described described polysaccharide structures bonded that contains polysaccharide material, describedly contain the photochemical reaction part that polysaccharide binding domains composition comprises at least one polysaccharide binding domains and and its covalent coupling, described at least one polysaccharide binding domains is connected described photochemical reaction part with the described described polysaccharide structures that contains polysaccharide material.
102. a topic is stated composition, described composition comprises a polysaccharide binding domains coupling agent, and described coupling agent comprises the polysaccharide binding domains of at least two covalent couplings.
103. a nucleic acid construct, described nucleic acid construct comprises the polynucleotide of encoding fusion protein, and described fusion rotein comprises at least two polysaccharide binding domainss.
104. the nucleic acid construct of claim 103, described nucleic acid construct also comprise the other polynucleotide of at least one at least one joint peptide of encoding, described at least two the polysaccharide binding domainss of described joint peptide coupling.
105. a manufacturing has at least a desired structure characteristic, chemical property, physicals, the method that contains polysaccharide material of electric property and/or mechanical property, said method comprising the steps of: make the described polysaccharide structures that contains polysaccharide material and polysaccharide binding domains described polysaccharide structures is worked into described contain in the polysaccharide material during and/or contact afterwards, and, thereby make the described desired structure characteristic that has after this with at least one part or group covalency and the coupling of described polysaccharide binding domains, chemical property, physicals, electric property and/or mechanical property contain polysaccharide material.
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110776571A (en) * 2019-11-04 2020-02-11 福建省中医药研究院(福建省青草药开发服务中心） Metallothionein fusion protein construction, rapid preparation of immobilized carrier and application of metallothionein fusion protein construction and immobilized carrier in heavy metal ion removal

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU776069B2 (en) * 1999-11-08 2004-08-26 Yissum Research Development Company Of The Hebrew University Of Jerusalem Process and composition for preparing a lignocellulose-based product, and the product obtained by the process
GB2376017A (en) * 2000-12-20 2002-12-04 Unilever Plc Cellulose binding domain conjugates linked or coupled to a polysaccharide backbone
FI116198B (en) 2001-07-16 2005-10-14 Valtion Teknillinen A method for immobilizing polypeptides
GB0425102D0 (en) 2004-11-15 2004-12-15 Ciba Spec Chem Water Treat Ltd Polymeric compositions and methods of employing them in papermaking processes
JP4880615B2 (en) * 2004-12-23 2012-02-22 ダウ・コーニング・コーポレイション Crosslinkable saccharide-siloxane compositions and network structures, coatings and articles formed therefrom
CN101171386B (en) * 2005-05-04 2011-11-16 诺维信北美公司 Chlorine dioxide treatment composition and method
EP2001908A2 (en) * 2006-04-06 2008-12-17 Institut Français du Pétrole Fusion proteins between plant cell-wall degrading enzymes and a swollenin, and their uses
GB0609477D0 (en) * 2006-05-12 2006-06-21 Ciba Sc Holding Ag Process for making paper and paperboard
WO2008067591A1 (en) * 2006-12-04 2008-06-12 Innovative Purification Technologies Pty Ltd Protein particles
JP2011504374A (en) * 2007-11-26 2011-02-10 イッサム リサーチ ディベロップメント カンパニー オブ ザ ヘブリュー ユニバーシティー オブ エルサレム リミテッド Composition comprising fibrous polypeptide and polysaccharide
WO2009078438A1 (en) * 2007-12-17 2009-06-25 Osaka University Microbe complex
EP2307554B1 (en) * 2008-07-29 2013-06-26 DSM IP Assets B.V. Process for oxidizing lignocellulosic material employing a Marasmius scorodonius peroxidase
US10557153B2 (en) * 2008-08-11 2020-02-11 Dsm Ip Assets B.V. Degradation of lignocellulosic material
US9066894B2 (en) 2008-09-12 2015-06-30 University Court Of The University Of St. Andrews Carbohydrate binding molecules
WO2010065908A2 (en) * 2008-12-05 2010-06-10 Catchmark Jeffrey M Degradable biomolecule compositions
MX2011009084A (en) 2009-03-06 2012-01-25 Biopolymer Technologies Ltd Protein-containing foams, manufacture and use thereof.
CN102439056B (en) * 2009-03-06 2016-01-13 生物高聚物技术有限公司 Emulsion containing albumen and tackiness agent and their manufacture and purposes
FR2948132B1 (en) * 2009-07-20 2011-08-26 Inst Francais Textile & Habillement ASSOCIATION OF NATURAL CATIONIC AND ANIONIC PRODUCTS AS BINDER FOR TEXTILE SUPPORT
WO2011047047A2 (en) * 2009-10-13 2011-04-21 The Penn State Research Foundation Composites containing polypeptides attached to polysaccharides and molecules
CN101736583B (en) * 2009-12-18 2012-07-25 东华大学 Method for preparing chitin size modified by biological enzyme method
WO2011156380A2 (en) * 2010-06-07 2011-12-15 Biopolymer Technologies, Ltd. Protein-containing adhesives, and manufacture and use thereof
CN102310451A (en) * 2010-07-06 2012-01-11 郭明辉 Wood fiber plate prepared on basis of laccase mediator system activation
BR112013012692B1 (en) * 2010-11-23 2020-03-17 Ecohelix Ab METHOD FOR INCREASING THE MOLECULAR WEIGHT OF WOOD MANANAS AND XYLANS THAT UNDERSTAND AROMATIC PORTIONS
US9109047B2 (en) * 2011-02-03 2015-08-18 Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd High molecular ordered fibrilar structures, method for their preparation and uses thereof
EP2751132B1 (en) 2011-09-01 2022-11-30 Yissum Research Development Company of the Hebrew University of Jerusalem Ltd. Adhesive biopolymers and uses thereof
CA3075143C (en) 2011-09-09 2023-03-28 Evertree Protein-containing adhesives, and manufacture and use thereof
SI2753633T1 (en) * 2011-09-09 2017-05-31 Evertree Protein-containing adhesives, and manufacture and use thereof
EP2880116B1 (en) 2012-07-30 2020-02-05 Evertree Protein adhesives containing an anhydride, carboxylic acid, and/or carboxylate salt compound and their use
RU2621116C2 (en) * 2013-01-24 2017-05-31 ДЖОРДЖИЯ-ПЭСИФИК КЕМИКАЛЗ ЭлЭлСи Composition comprising water-repellent agents and stabilizing agents and methods for their manufacturing and application
US10059650B2 (en) 2013-06-14 2018-08-28 Yale University Systems and methods for the depolymerization of a biopolymer
US10202517B2 (en) 2013-07-26 2019-02-12 The Penn State Research Foundation Polymer compositions and coatings

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3037992C2 (en) * 1980-10-08 1983-04-21 Gesellschaft für Biotechnologische Forschung mbH (GBF), 3300 Braunschweig Process for the production of a binder for wood-based materials
US4340673A (en) * 1980-11-07 1982-07-20 Merck & Co., Inc. Process of producing modified glucans as anti-caries agent
US5340731A (en) * 1988-07-08 1994-08-23 University Of British Columbia Method of preparing a B-1,4 glycan matrix containing a bound fusion protein
US5137819A (en) * 1988-07-08 1992-08-11 University Of British Columbia Cellulose binding fusion proteins for immobilization and purification of polypeptides
JP3681750B2 (en) * 1992-10-06 2005-08-10 ノボザイムス アクティーゼルスカブ Cellulase variant
US5496934A (en) * 1993-04-14 1996-03-05 Yissum Research Development Company Of The Hebrew University Of Jerusalem Nucleic acids encoding a cellulose binding domain
BR9407752A (en) * 1993-10-04 1997-03-04 Novo Nordisk As Preparation of enzyme detergent additive detergent composition process for the treatment of lignocellulosic fibers
WO1996003546A1 (en) * 1994-07-26 1996-02-08 Novo Nordisk A/S Process for preparing a lignocellulose-based product, and product obtainable by the process
CA2231858A1 (en) * 1995-11-08 1997-05-15 Novo Nordisk A/S Process for preparing a lignocellulose-based product, and product obtainable by the process
US5874308A (en) * 1996-01-16 1999-02-23 University Of British Columbia Compositions and methods for modulating cell proliferation using growth factor-polysaccharide binding fusion proteins
WO1997028243A1 (en) * 1996-01-29 1997-08-07 Novo Nordisk A/S Process for removal or bleaching of soiling or stains from cellulosic fabric
AU1438397A (en) * 1996-01-29 1997-08-22 Novo Nordisk A/S Process for desizing cellulosic fabric
US5763385A (en) * 1996-05-14 1998-06-09 Genencor International, Inc. Modified α-amylases having altered calcium binding properties
ATE386799T1 (en) * 1996-10-28 2008-03-15 Novozymes As EXTRACELLULAR EXPRESSION OF CELLULOSE BINDING DOMAIN (CBD) USING BACILLUS
WO1999051808A1 (en) * 1998-04-03 1999-10-14 Novo Nordisk A/S Treatment of denim fabric with a pectolytic enzyme
AU776069B2 (en) * 1999-11-08 2004-08-26 Yissum Research Development Company Of The Hebrew University Of Jerusalem Process and composition for preparing a lignocellulose-based product, and the product obtained by the process

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110776571A (en) * 2019-11-04 2020-02-11 福建省中医药研究院(福建省青草药开发服务中心） Metallothionein fusion protein construction, rapid preparation of immobilized carrier and application of metallothionein fusion protein construction and immobilized carrier in heavy metal ion removal
CN110776571B (en) * 2019-11-04 2021-08-10 福建省中医药研究院(福建省青草药开发服务中心） Metallothionein fusion protein construction, rapid preparation of immobilized carrier and application of metallothionein fusion protein construction and immobilized carrier in heavy metal ion removal

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