CN1102151C - Method for extracting and separating filiform blue-green algae water-soluble polyose and ecto-polyose - Google Patents
Method for extracting and separating filiform blue-green algae water-soluble polyose and ecto-polyose Download PDFInfo
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Abstract
The present invention relates to a high efficiency universal extraction separation method which is suitable for familiar threadlike blue algae water solubility polysaccharide and extra-cellular polysaccharide, wherein a method of extracting the water solubility polysaccharide mainly comprises the following steps of decolorizing, removing slag, extracting in hot water, depositing through using ethyl alcohol, drying in a vacuum way, etc. A method for preparing the extra-cellular polysaccharide mainly comprises the following steps of the centrifuging suction filtration, the pressure reducing concentration, the dialysis desalinization, the vacuum drying operation, etc. The acidic extra-cellular polysaccharide is obtained in cell removing culture liquid by directly using the deposition characteristic of quaternary ammonium salt. The separation and purification of the polysaccharide mainly comprises the following steps of the deproteinization, the anion-exchange chromatography, etc. The method is suitable for the familiar threadlike blue algae, such as prayer bead algae, anabena algae, microcystis algae, spirulina, mat algae, etc., wherein the polysaccharide from a plurality of kinds of prayer bead algae has strong complement activation activity and high viscosity so that the polysaccharide can be used as an immunity reinforcing agent and a thickening agent in food industry. Moreover, the method is simple and feasible without special equipment, and simultaneously, the method is suitable for industrialization production.
Description
The present invention relates to the extraction separation of little polysaccharides, particularly the extraction and separation method of filamentous cyanobacteria water-soluble polysaccharide and exocellular polysaccharide.
Blue-green algae or title cyanobacteria are the widest photosynthetic prokaryotic organism of distributed in nature, can live in seawater and the fresh water, also can live on subaerial slowly drained soil and the rock, can also appear in the environment of various very severes.Some filamentous cyanobacteria is used as the food source for a long time, is used as valuable foodstuff additive as spirulina; In China, deliver vegetables, beads algaes such as Nostoc and Nostoc commune are traditional rare delicacies, and are nutritious, have good edible and pharmaceutical use, on books such as Compendium of Material Medica and supplementary Amplifications of the Compendium of Materia Medica, be documented.Algal polysaccharides is to use maximum products and have the application and development prospect in the algae product so far, but the research to algal polysaccharides mainly concentrates on kelp so far, research to blue-green algae and other little polysaccharides is few, the domestic polysaccharide that the research of blue algae polysaccharide almost only is confined to spirulina.
Chinese patent literature: 1, the extracting method of water-soluble spirulina polyose, classification number: C08B 37/04, the applying date: 94.05.16, the day for announcing: 95.11.22, application number: 94105389, applicant: South China Normal University.This invention is a kind of extracting method of water-soluble spirulina polyose, specifically is to adopt the alkaline solution extracting, neutralizes with organic acid.2, from spirulina, extract the method and the application thereof of protein and polysaccharide, 1/14. applying date of classification number: C07K: 94.08.24, the day for announcing: 95.08.09, application number: 94112454, applicant: Shenyang Institute of Phamaceutical Industry.This invention relates to from spirulina the method for extracting protein and polysaccharide, specifically be in the time of 5-15 ℃, to soak to extract 5-20 hour, triplicate, through further extract, method such as precipitation makes protein and polysaccharide.Above binomial patent is not carried out extraction separation to exocellular polysaccharide just at water-soluble spirulina polyose.
China's non-patent literature: 1, the purification of spirulina antiradiation polysaccharide and analysis, Pang Qishen, Guo Baojiang, Ruan Jihong, Acta Biochimica et Biophysica Sinica, 1989,21:445-449.The document has reported to extract to have the method for the active water-soluble polysaccharide of radioprotective from spirulina.2, the research of the separation of spirulina maxim polysaccharide, purifying and anti-oxidation characteristics thereof, Zhou Zhigang, Liu Zhili, Liu Xuexian, Botany Gazette, 1997,39:77-81.Document report spirulina polysaccharide has the effect of significant removing hydroxy radical qiao.More than 2 pieces of documents just carried out extraction and purifying at the water-soluble polysaccharide of spirulina, exocellular polysaccharide is not studied.3, cyanobacteria polysaccharide and applied research overview thereof, Huang Zebo, Liu Yongding, biotechnology circular, 1997, the 4 phase: 26-32.The document has been introduced cyanobacteria (blue-green algae) STUDY ON POLYSACHAROSE progress and has been analyzed their potential using values, but the extraction and separation method of blue algae polysaccharide is not carried out systematic review.
External non-patent literature: 1.Polysaccharides from cyanobacteria.BertocchiC., Navarini, L., Ces*ro, A.﹠amp; Anastasio, M., Carbohydrate Polymers, 1990,12:127-153, the document is summarized cyanobacteria (blue-green algae) STUDY ON POLYSACHAROSE, has set forth the component of blue algae polysaccharide emphatically, but the extraction and separation method of blue algae polysaccharide is explained.2.Polysaccharides in desert reclamation:compositions of exocellularproteoglycan complexes produced by filamentous blue-green andunicellular green edaphic algae.Flaibani, A., Olsen, Y.﹠amp; Painter, T.J., Carbohydrate Research, 1989,190:235-238, the document is analyzed the component of a kind of beads algae (with a kind of unicell green alga) excretory exocellular polysaccharide.3.Extraction, purification and identification of polysaccharides of Spirulina (Arthrospira) platensis (Cyanophyceae), Tseng, C.T.﹠amp; Zhao.Y.Algological Studies, 1994, the 75:303-312. document is extracted and is analyzed at the water-soluble polysaccharide of spirulina.
The object of the present invention is to provide a kind of efficient general extraction and separation technology that is applicable to common filamentous cyanobacteria water-soluble polysaccharide and is secreted into the exocellular polysaccharide in the substratum, for the polysaccharide that makes full use of filamentous cyanobacteria provides a kind of convenient and practical method.
In order to realize this purpose, its main technical schemes is: extract water-soluble polysaccharide by steps such as decolouring impurity elimination, hot water extraction, ethanol sedimentation, vacuum-dryings; Extract exocellular polysaccharide by steps such as centrifugal suction filtration, concentrating under reduced pressure, dialysis desalting, vacuum-dryings; Acid exocellular polysaccharide also can directly make with quaternary salt deposit in taking off cell culture fluid; By step separation and purification water-soluble polysaccharide and exocellular polysaccharides such as deproteinated, anion-exchange chromatography, vacuum-dryings.
Use the technical program, to 19 kinds of common filamentous cyanobacterias: common beads algae (Nostoc commune, Nostoc commune), send out shape beads algae (N.flagelliforme, deliver vegetables), intend spherical beads algae (N.sphaeroides, Nostoc), beads algae (Nostoc sp.) HB856, rice field anabena (Anabaenaoryzae) HB13, fixed nitrogen anabena (A.azotica) HB686, ball spore anabena (A.sphaerica) HB1017, changeable anabena (A.variabilis) HB1058, anabena, Anabaena sp.) HB1042, anabena (Anabaena sp.) HB1105, breed pipe chain algae (Aulosirafertilissima), Microcystis aeruginosa (Microcystis spp.), split palpus algae Schizothrix sp.), little sheath algae (Microcoleus sp.), seat algae Phormidium sp.), single divergent algae (Tolypothrix sp.), fake valoniopsis pachynema Scytonema sp.), spirulina plalensis (Spirulina platensis) and spirulina maxim (S, maxima) etc. water-soluble polysaccharide and exocellular polysaccharide carry out the extraction separation test relatively, and showing has following effect:
1, this extraction and separation method is applicable to filamentous cyanobacteria;
2, can from filamentous cyanobacteria frond and nutrient solution, distinguish extraction separation water-soluble polysaccharide and exocellular polysaccharide simultaneously, make full use of its resource;
3, acid exocellular polysaccharide can directly make with quaternary salt deposit after taking off cell culture fluid making;
4, several nostoc polysaccharides have the active and very high viscosity of very strong complement activation, can be used as the thickening material in immunostimulant and the foodstuffs industry;
5, easy to operate, do not need specific installation, can be used for suitability for industrialized production.
The extraction of embodiment 1. water-soluble polysaccharides
(1) to get filamentous cyanobacteria (bright algae or dried algae) some in the decolouring impurity elimination, add the alcohol solution dipping of 80% (v/v) after the pulverizing.Dried algae is difficult for pulverizing, and can directly soak.Treat to blend again after following (2) the step water logging; The immersion amount is different different because of the blue-green algae kind, is generally every gram algae sample when soaking dried algae and adds the 20-100ml ethanolic soln.
The algae sample is with 80% ethanolic soln at room temperature after the soaked overnight.Extracted 2 hours in 50 ℃ of stirrings, filter to remove small molecules and foreign pigment.Collect the algae sample, add above-mentioned immersion and measure the above ethanolic soln of half volume and extracted again 1 hour.Filter and collect the algae sample, add absolute ethanol washing for several times, and allow ethanol volatilize naturally.
(2) the algae sample after the above-mentioned decolouring impurity elimination of hot water extraction, adding distil water is soaked overnight at room temperature.Amount of water is different different because of the blue-green algae kind, for the 10-100 of algae sample dry weight doubly: general classes adds water 10-20 doubly, and the kind that Nostoc, Nostoc commune etc. very easily absorb waters then adds water 50-100 times.
After the algae sample soaks into, stir extraction 2-3 hour down, naturally cool to room temperature, centrifugal (5000-6000g, 15-30 minute) at 80-100 ℃.Keep supernatant liquor.Algae-residue is added and is stated water consumption distilled water over half and extracted 1 hour under same temperature.Centrifugal collection supernatant liquor merges secondary raffinate.Heavy-gravity extract too as the extracting solution of Nostoc, is being difficult to can to adopt 4 layers of methods such as gauze filtered while hot to come separation and Extraction liquid and insolubles when centrifugal.
(3) concentrating under reduced pressure is evaporated to five to 1/20th of original volume with said extracted liquid under 40-50 ℃.
(4) ethanol sedimentation precipitates above-mentioned concentrated solution with ethanol, and the alcoholic acid final concentration is 80% (v/v).Filter the collecting precipitation thing, wash for several times with further decolouring impurity elimination with dehydrated alcohol, anhydrous propanone.Throw out makes Crude polysaccharides through vacuum-drying.
The preparation of embodiment 2. exocellular polysaccharides
(1) takes off nutrient solution after cell centrifugation is collected filamentous cyanobacteria, through suction filtration and cross the 0.45m porous membrane, make and take off cell culture fluid.
(2) concentrating under reduced pressure is evaporated to ten to 1/20th of original volume with the above-mentioned cell culture fluid that takes off under 40-50 ℃.
(3) earlier through dialysis (the molecular interception amount is 3500 dalton) desalination, removal small molecular weight impurity, lyophilize makes exocellular polysaccharide again with above-mentioned concentrated solution for desalination, precipitation.Or the method that above-mentioned concentrated solution is directly pressed embodiment 1 they (4) is with ethanol sedimentation, repeatedly for several times with the desalination impurity elimination, and with dehydrated alcohol, anhydrous propanone washing, vacuum-drying makes exocellular polysaccharide again.
If the acid exocellular polysaccharide of preparation can adopt the method that adds a small amount of quaternary ammonium salt directly polysaccharide to be precipitated out,, thereby make exocellular polysaccharide again through 80% (v/v) ethanolic soln, dehydrated alcohol, anhydrous propanone washing after drying from take off cell culture fluid.Added quaternary ammonium salt has bromohexadecane base TMA (TriMethylAmine) (CTAB) during the precipitation exocellular polysaccharide
Hexadecyl pyridine hydrochloride (CPC) etc., consumption is 100-200mg/L, method generally is that CTAB or CPC etc. is mixed with less than adding behind 10% the solution again, takes off cell culture fluid but also can directly be dissolved in.
The separation and purification of embodiment 3. polysaccharide
(1) Deproteinization removes the protein in the Crude polysaccharides if desired, can adopt Sevag method or proteolytic enzyme solution to carry out.If adopt the Sevag method.Generally be add with the isopyknic chloroform-propyl carbinol of polysaccharide soln (1-10%) (5: 1, v/v) mixed solution.Abundant mixing, centrifugal (1500g, 10 minutes).Get the upper strata water.After repeating for several times, add ethanol (final concentration 80%, v/v) precipitation polysaccharide.
When adopting enzymolysis process, can be respectively add stomach en-and trypsinase at 37 ± 2 ℃ of enzymolysis 1-2 hour respectively down to polysaccharide soln.Unit is different with the algae kind to be had than big-difference institute's enzyme concentration because of enzyme is lived, and reduces to meet the requirements with protein content in enzymolysis, dialysis (MWCO=3500) the back polysaccharide sample to be as the criterion (as less than 2%).
(2) the polysaccharide sample heating for dissolving of anion-exchange chromatography after with Crude polysaccharides or above-mentioned Deproteinization in distilled water (1-10mg/ml), on anion-exchange chromatography posts such as DEAE-Sepharose, carry out chromatography after crossing the 0.45m porous membrane, carry out progressively wash-out with distilled water, 1.0M and 2.0M NaCl, with phenolsulfuric acid method monitoring sugar amount, the fraction collection washings, concentrate respectively, dialysis back freeze-drying, or with ethanol sedimentation final vacuum drying.In each polysaccharide sample of gained, the water washings is a neutral polysaccharide, and the salt washings is an acidic polysaccharose.
The extraction separation and the kinematic viscosity thereof of embodiment 4. Nostoc, Nostoc commune and the natural sample complement activation of beads algae active polysaccharide such as deliver vegetables
(1) the decolouring impurity elimination get Nostoc, Nostoc commune and the air-dry natural algae sample of delivering vegetables some, be soaked in the ethanolic soln of 80% (v/v), the immersion amount is every gram algae sample 40ml ethanolic soln.At room temperature after the soaked overnight, stir extraction 2 hours in 50-C, filter, collect the algae sample, the ethanolic soln that adds with volume 80% extracted 1 hour again.Filter and collect the algae sample, add absolute ethanol washing for several times, and allow ethanol volatilize naturally.
(2) the algae sample after the above-mentioned decolouring impurity elimination of hot water extraction is with an amount of distilled water soaked overnight at room temperature.Break up with the algae sample of agitator after, add an amount of distilled water (it is 100 milliliters in every gram algae sample that secondary adds the water cumulative volume) back again and under 100*C, stir and extracted 3 hours water-swelling.While hot with 4 layers of filtered through gauze to separate Nostoc extracting solution and insolubles; But Nostoc commune and the extracting solution of delivering vegetables after naturally cooling to room temperature, adopt centrifugal (6000g, 30 minutes) method to separate, and keep supernatant liquor.Algae-residue adds with the distilled water of volume again and extracted 1 hour under same temperature, and filtered through gauze (Nostoc) or centrifugal (Nostoc commune, deliver vegetables) merge secondary raffinate.
(3) ethanol sedimentation with said extracted liquid be evaporated under 40 ℃ original volume 1/5th after, add ethanol and precipitate, the alcoholic acid final concentration is 80% (v/v).Filter the collecting precipitation thing, with dehydrated alcohol, anhydrous propanone washing for several times, make Crude polysaccharides through vacuum-drying.The Crude polysaccharides that makes so all is a floss, and color and luster is white substantially, but the slightly little yellow of Nostoc and Nostoc commune polysaccharide, the slightly grey of polysaccharide of delivering vegetables.The yield of Nostoc, Nostoc commune and the polysaccharide of delivering vegetables is respectively 40%, 30% and 17%.
(4) the refining Nostoc Crude polysaccharides heating for dissolving of getting above-mentioned filtered through gauze of Crude polysaccharides is in an amount of distilled water, and the cooling back is centrifugal, gets supernatant liquor, adopts above-mentioned ethanol sedimentation, dehydrated alcohol and anhydrous propanone washing, vacuum drying way to make with extra care.
The Crude polysaccharides heating for dissolving of getting three kinds of beads algaes is mixed with 10% the aqueous solution in distilled water, adopts Sevag method Deproteinization, promptly adds and the isopyknic chloroform-propyl carbinol of polysaccharide soln (5: 1, v/v) mixed solution, abundant mixing, centrifugal (1500g, 10 minutes), get the upper strata water.After repeating 4 times, (final concentration 80%, v/v) precipitation polysaccharide is with dehydrated alcohol, anhydrous propanone washing final vacuum drying to add ethanol.
(5) anion-exchange chromatography with polysaccharide sample heating for dissolving in distilled water (1.5mg/ml), cross 0.45m porous membrane (Acro 50A) back at DEAE-Sepharose Fast Flow post (5-40cm, Pharmacia) carry out anion-exchange chromatography on, carry out progressively wash-out with distilled water, 1.0M and 2.0M NaCl, with phenolsulfuric acid method monitoring sugar amount, the fraction collection washings, the back freeze-drying concentrates respectively, dialyses.Wherein, the polysaccharide of delivering vegetables does not detect sugared sample when carrying out wash-out with 2.0M NaCl behind this chromatography column.
(6) biological activity after testing, Zhi Bei polysaccharide (comprise Crude polysaccharides and separation and purification after polysaccharide) has very strong complement activation activity as stated above.Wherein, behind anion-exchange chromatography, the activity of acidic polysaccharose is apparently higher than neutral polysaccharide.
(7) the above-mentioned polysaccharide of kinematic viscosity has higher viscosity, and 0.1% the kinematic viscosity of above-mentioned all kinds of polysaccharide solutions under 25 ± 0.01 ℃: (a) the Nostoc Crude polysaccharides that makes through 4 layers of filtered through gauze is 4.79 centistokes.This polysaccharide is 6.61 centistokes through being dissolved in the polysaccharide that makes after distilled water, centrifugal, ethanol sedimentation, the drying, and the distilled water that this sample makes behind anion-exchange chromatography, 1M and 2M NaCl eluate are respectively 0.95,1.41,1.45 centistokes; (b) Nostoc commune Crude polysaccharides, the distilled water that makes behind anion-exchange chromatography, 1M and 2M NaCl eluate are respectively 4.16,1.76,1.18,1.12 centistokes; (c) deliver vegetables Crude polysaccharides, the distilled water that makes behind anion-exchange chromatography and 1M NaCl eluate is respectively 3.10,1.20,1.20 centistokes.
The preparation and the kinematic viscosity thereof of the outer polymkeric substance of embodiment 5. beads gonidium
(1) the Nostoc commune FACHB 261, the N.flagelliforme FACHB 838 that provide for Chinese Academy of Sciences typical case culture collection council algae kind storehouse of the culture condition Nostoc commune and the algae kind of delivering vegetables, Nostoc is an aseptic isolated algae kind from natural population.Substratum is Woods Hole MBL liquid nutrient medium (has or do not have NaNO3), and volume is 10 liters, and temperature is 28*1*C, and light intensity is 160mEm
-2S
-1, the pressurized air of logical humidification, inoculum size is 20ml (optical density(OD) is 1.0,1=750nm, optical path 5cm), cultivates altogether 18 days.
(2) nutrient solution behind the preparative centrifugation of the extracellular polymeric results beads algae is also crossed 0.45m porous membrane (Acro 50A) through suction filtration, makes and takes off cell culture fluid.Be evaporated under 40 ℃-500ml after, (MWC0=3500) dialyses with the Spectra/Por dialysis tubing, lyophilize makes extracellular polymeric.Have from above-mentioned that the ratio of isolating extracellular polymeric and biomass is respectively nitrogen and the nitrogen-free agar: Nostoc 28% and 31%; Nostoc commune 66% and 15% delivers vegetables 22% and 20%.Wherein, after testing, the extracellular polymeric sugar degree of Nostoc is lower, but the Nostoc commune and the extracellular polymeric of delivering vegetables are mainly polysaccharose substance.
(3) kinematic viscosity is under 25 ± 0.01 ℃, and the kinematic viscosity of the isolating exocellular polysaccharide aqueous solution (0.1%) is respectively from nitrogen and nitrogen-free agar are arranged: Nostoc 0.95 and 0.94 centistoke; Nostoc commune 3.45 and 1.77 centistokes; 1.01 and 1.08 centistokes of delivering vegetables.
Claims (5)
1, a kind of extracting method of filamentous cyanobacteria water-soluble polysaccharide is characterized in that being widely used in common filamentous cyanobacteria and follow these steps to order carrying out: (1) joins the dried algae of filamentous cyanobacteria into its weight 20-100 80% (volume ratio) doubly
In the ethanolic soln, soaked overnight; (2) heat to 50 ℃, stirred 2 hours, filter and collect the algae sample; (3) the above ethanolic soln of half volume extracted 1 hour again in the adding (1), filtered and collected
The algae sample; 4) add absolute ethanol washing for several times, and allow ethanol volatilize naturally; (5) add dried algae weight 10-100 distilled water doubly, at room temperature soaked overnight is stirred essence; (6) heat to 80-100 ℃, stir and extracted 2-3 hour; (7) naturally cool to room temperature, centrifugal, keep supernatant liquor; (8) in algae-residue, add water consumption distilled water over half in (5), at 80-100 ℃
Following stirring was extracted 1 hour; (9) centrifugal collection supernatant liquor; (10) supernatant liquor of merging (7) and (9) is evaporated to former under 40-50 ℃
/ 5th to 1/20th of a volume; (11) adding ethanol to its final concentration is 80% (volume ratio), filters the collecting precipitation thing; (12) for several times with dehydrated alcohol, anhydrous propanone washing; (13) vacuum-drying makes Crude polysaccharides.
2, the extracting method of a kind of filamentous cyanobacteria water-soluble polysaccharide according to claim 1 is characterized in that further comprising the separation purification method of its water-soluble polysaccharide:
(1) Deproteinization: a. organic solvent method: add and the isopyknic chloroform of 1-10 weight % filamentous cyanobacteria polysaccharide soln-propyl carbinol mixed solution, wherein the volume ratio of chloroform and propyl carbinol is 5: 1, abundant mixing, centrifugal, after getting the upper strata water and repeating for several times, add ethanol (final concentration 80%, volume ratio) precipitation polysaccharide.Or b. enzymolysis process: adding an amount of stomach en-and trypsinase, at 37 ℃ of following enzymolysis 1-2 hours, is the dialysis of 3500 dialysis membrane with the molecular interception amount;
(2) anion-exchange chromatography: with the polysaccharide sample dissolution behind filamentous cyanobacteria Crude polysaccharides or the Deproteinization in distilled water, make the polysaccharide soln that concentration is 1-10mg/ml, cross 0.45 μ porous membrane, separate with anion-exchange chromatography posts such as DEAE-Sepharose, carry out progressively wash-out with distilled water, 1.0M and 2.0M sodium-chlor, with phenolsulfuric acid method monitoring sugar amount, the fraction collection eluate, the back freeze-drying concentrates respectively, dialyses, or with ethanol sedimentation final vacuum drying, wherein the water elution thing is a neutral polysaccharide, and the eluting salt thing is an acidic polysaccharose.
3, a kind of extracting method of filamentous cyanobacteria exocellular polysaccharide, it is characterized in that being widely used in common filamentous cyanobacteria and follow these steps to order carrying out: (1) is centrifugal with the filamentous cyanobacteria culture, supernatant liquor is through suction filtration and cross 0.45 μ porous membrane, makes and takes off cell culture fluid; (2) will take off cell culture fluid and under 40-50 ℃, be evaporated to 1/10th to 1/20th of original volume; (3) be 3500 daltonian dialysis membrane dialysis with concentrated solution with the molecular interception amount; (4) lyophilize makes exocellular polysaccharide.
4, a kind of extracting method of filamentous cyanobacteria exocellular polysaccharide, it is characterized in that being widely used in common filamentous cyanobacteria and follow these steps to order carrying out: (1) is centrifugal with the filamentous cyanobacteria culture, supernatant liquor is through suction filtration and cross 0.45 μ porous membrane, makes and takes off cell culture fluid; (2) will take off cell culture fluid and under 40-50 ℃, be evaporated to 1/10th to 1/20th of original volume; (3) adding ethanol to its final concentration is 80% (volume ratio), filters the collecting precipitation thing; (4) for several times with dehydrated alcohol, anhydrous propanone washing; (5) vacuum-drying makes exocellular polysaccharide.
5,, it is characterized in that further comprising the separation purification method of exocellular polysaccharide according to the extracting method of claim 3 or 4 described a kind of filamentous cyanobacteria exocellular polysaccharides:
(1) Deproteinization: a. organic solvent method: add and the isopyknic chloroform of 1-10 weight % filamentous cyanobacteria polysaccharide soln-propyl carbinol mixed solution, wherein the volume ratio of chloroform and propyl carbinol is 5: 1, abundant mixing, centrifugal, after getting the upper strata water and repeating for several times, add ethanol (final concentration 80%, volume ratio) precipitation polysaccharide.Or b. enzymolysis process: adding an amount of stomach en-and trypsinase, at 37 ℃ of following enzymolysis 1-2 hours, is the dialysis of 3500 dialysis membrane with the molecular interception amount;
(2) anion-exchange chromatography: with the polysaccharide sample dissolution behind filamentous cyanobacteria Crude polysaccharides or the Deproteinization in distilled water, make the polysaccharide soln that concentration is 1-10mg/ml, cross 0.45 μ porous membrane, separate with anion-exchange chromatography posts such as DEAE-Sepharose, carry out progressively wash-out with distilled water, 1.0M and 2.0M sodium-chlor, with phenolsulfuric acid method monitoring sugar amount, the fraction collection eluate, the back freeze-drying concentrates respectively, dialyses, or with ethanol sedimentation final vacuum drying, wherein the water elution thing is a neutral polysaccharide, and the eluting salt thing is an acidic polysaccharose.
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Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU921500A1 (en) * | 1980-03-06 | 1982-04-23 | Тихоокеанский институт биоорганической химии Дальневосточного научного центра АН СССР | Method of producing pectine from sea grasses |
| JPS59113001A (en) * | 1982-12-20 | 1984-06-29 | Mitsubishi Acetate Co Ltd | Production of carrageenan |
| SU1116209A1 (en) * | 1983-06-22 | 1984-09-30 | Научно-Производственное Объединение Фундаментостроения "Союзспецфундаменттяжстрой" | Concrete pump |
| JPS616720A (en) * | 1984-06-20 | 1986-01-13 | Yokogawa Hokushin Electric Corp | Power supply device |
| JPH02229599A (en) * | 1989-03-01 | 1990-09-12 | Mitsubishi Electric Corp | Water treatment device |
| JPH06256208A (en) * | 1993-03-03 | 1994-09-13 | Food Design Gijutsu Kenkyu Kumiai | Immunopotentiator |
| CN1106414A (en) * | 1994-08-24 | 1995-08-09 | 沈阳医药工业研究所 | Method for extracting protein and polysaccharide from spiral algae and its use |
-
1997
- 1997-12-25 CN CN97109350A patent/CN1102151C/en not_active Expired - Fee Related
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU921500A1 (en) * | 1980-03-06 | 1982-04-23 | Тихоокеанский институт биоорганической химии Дальневосточного научного центра АН СССР | Method of producing pectine from sea grasses |
| JPS59113001A (en) * | 1982-12-20 | 1984-06-29 | Mitsubishi Acetate Co Ltd | Production of carrageenan |
| SU1116209A1 (en) * | 1983-06-22 | 1984-09-30 | Научно-Производственное Объединение Фундаментостроения "Союзспецфундаменттяжстрой" | Concrete pump |
| JPS616720A (en) * | 1984-06-20 | 1986-01-13 | Yokogawa Hokushin Electric Corp | Power supply device |
| JPH02229599A (en) * | 1989-03-01 | 1990-09-12 | Mitsubishi Electric Corp | Water treatment device |
| JPH06256208A (en) * | 1993-03-03 | 1994-09-13 | Food Design Gijutsu Kenkyu Kumiai | Immunopotentiator |
| CN1106414A (en) * | 1994-08-24 | 1995-08-09 | 沈阳医药工业研究所 | Method for extracting protein and polysaccharide from spiral algae and its use |
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