WO1999003984A2

WO1999003984A2 - Proteases from gram-positive organisms

Info

Publication number: WO1999003984A2
Application number: PCT/US1998/014647
Authority: WO
Inventors: David A. Estell
Original assignee: Genencor International, Inc.; Genencor International B.V.
Priority date: 1997-07-15
Filing date: 1998-07-14
Publication date: 1999-01-28
Also published as: WO1999003984A3; EP0991754A2; AU8487098A; JP2001510037A

Abstract

The present invention relates to the identification of novel serine proteases in Gram-positive microorganisms. The present invention provides the nucleic acid and amino acid sequences for the Bacillus subtilis serine proteases SP1, SP2, SP3, SP4 and SP5. The present invention also provides host cells having a mutation or deletion of part or all of the gene encoding SP1, SP2, SP3, SP4 and SP5. The present invention also provides host cells further comprising nucleic acid encoding desired heterologous proteins such as enzymes. The present invention also provides a cleaning composition comprising a serine protease of the present invention.

Description

PROTEASES FROM GRAM-POSITIVE ORGANISMS

FIELD OF THE INVENTION

The present invention relates to serine proteases derived from gram-positive microorganisms The present invention provides nucleic acid and ammo acid sequences of serine protease 1 , 2, 3, 4 and 5 identified in Bacillus The present invention also provides methods for the production of serine protease 1 , 2, 3, 4 and 5 in host cells as well as the production of heterologous proteins in a host cell having a mutation or deletion of part or all of at least one of the serine proteases of the present invention

BACKGROUND OF THE INVENTION

Gram-positive microorganisms, such as members of the group Bacillus, have been used for large-scale industrial fermentation due, in part, to their ability to secrete their fermentation products into the culture media In gram-positive bacteria, secreted proteins are exported across a cell membrane and a cell wall, and then are subsequently released into the external media usually maintaining their native conformation

Various gram-positive microorganisms are known to secrete extracellular and/or intracellular protease at some stage in their life cycles Many proteases are produced in large quantities for industrial purposes A negative aspect of the presence of proteases in gram-positive organisms is their contribution to the overall degradation of secreted heterologous or foreign proteins

The classification of proteases found in microorganisms is based on their catalytic mechanism which results in four groups the serine proteases, metalloproteases, cysteine proteases, and aspartic proteases These categories can be distinguished by their sensitivity to various inhibitors For example, the serine proteases are inhibited by phenylmethylsulfonylfluoπde (PMSF) and dnsopropylfluorophosphate (DIFP), the metalloproteases by chelating agents, the cysteine enzymes by lodoacetamide and heavy metals and the aspartic proteases by pepstatin The serine proteases have alkaline pH optima, the metalloproteases are optimally active around neutrality, and the cysteine and aspartic enzymes have acidic pH optima (Biotechnology Handbooks, Bacillus vol 2, edited by Harwood, 1989 Plenum Press, New York)

Proteolytic enzymes that are dependent upon a serine residue for catalytic activity are called serine proteases As described in Methods in Enzymology, vol 244, Academic Press, Inc 1994, page 21 , serine proteases of the family S9 have the catalytic residue triad "Ser-Asp-His with conservation of ammo acids around them SUMMARY OF THE INVENTION

The present invention relates to the unexpected discovery of five heretofore unknown or unrecognized S9 type serine proteases found in uncharacteπzed translated genomic nucleic acid sequences of Bacillus subtilis, designated herein as SP1 , SP2, SP3, SP4 and SP5 having the nucleic acid and ammo acid as shown in the Figures The present invention is based, in part, upon the presence the ammo acid triad S-D-H in the five serine proteases, as well as ammo acid conservation around the triad The present invention is also based in part upon the heretofore uncharacteπzed or unrecognized overall ammo acid relatedness that SP1 , SP2, SP3, SP4 and SP5 have with the serine protease dipeptidyl- ammo peptidase B from yeast (DAP) and with each other

The present invention provides isolated polynucleotide and ammo acid sequences for SP1 , SP2, SP3, SP4 and SP5 Due to the degeneracy of the genetic code, the present invention encompasses any nucleic acid sequence that encodes the SP1 , SP2, SP3, SP4 and SP5 deduced ammo acid sequences shown in Figures 2A-2B-Fιgure 6, respectively

The present invention encompasses ammo acid variations of B subtilis SP1 , SP2, SP3, SP4 and SP5 disclosed herein that have proteolytic activity B subtilis SP1 , SP2, SP3, SP4 and SP5, as well as proteolytically active ammo acid variations thereof, have application in cleaning compositions In one aspect of the present invention, SP1 , SP2, SP3, SP4 and SP5 obtainable from a gram-positive microorganism are produced on an industrial fermentation scale in a microbial host expression system In another aspect, isolated and purified SP1 , SP2, SP3, SP4 or SP5 obtainable from a gram-positive microorganism is used in compositions of matter intended for cleaning purposes, such as detergents Accordingly, the present invention provides a cleaning composition comprising at least one of SP1 , SP2, SP3, SP4 and SP5 obtainable from a gram-positive microorganism The serine protease may be used alone in the cleaning composition or in combination with other enzymes and/or mediators or enhancers

The production of desired heterologous proteins or polypeptides in gram-positive microorganisms may be hindered by the presence of one or more proteases which degrade the produced heterologous protein or polypeptide Therefore, the present invention also encompasses gram-positive microorganism having a mutation or deletion of part or all of the gene encoding SP1 , SP2, SP3, SP4 and/or SP5, which results in the mactivation of their proteolytic activity, either alone or in combination with deletions or mutations in other proteases, such as apr, npr, epr, mpr for example, or other proteases known to those of skill in the art In one embodiment of the present invention, the gram-positive organism is a member of the genus Bacillus In another embodiment, the Bacillus is Bacillus subtilis

In another aspect, the gram-positive microorganism host having one or more deletions or mutations in a serine protease of the present invention is further genetically engineered to produce a desired protein. In one embodiment of the present invention, the desired protein is heterologous to the gram-positive host cell. In another embodiment, the desired protein is homologous to the host cell. The present invention encompasses a gram- positive host cell having a deletion or interruption of the naturally occurring nucleic acid encoding the homologous protein, such as a protease, and having nucleic acid encoding the homologous protein or a variant thereof re-introduced in a recombinant form. In another embodiment, the host cell produces the homologous protein. Accordingly, the present invention also provides methods and expression systems for reducing degradation of heterologous or homologous proteins produced in gram-positive microorganisms comprising the steps of obtaining a Bacillus host cell comprising nucleic acid encoding said heterologous protein wherein said host cell contains a mutation or deletion in at least one of the genes encoding SP1 , SP2, SP3, SP4 and SP5; and growing said Bacillus host cell under conditions suitable for the expression of said heterologous protein. The gram-positive microorganism may be normally sporulating or non-sporulating.

The present invention provides methods for detecting gram positive microorganism homologs of B. subtilis SP1 , SP2, SP3, SP4 and SP5 that comprises hybridizing part or all of the nucleic acid encoding B. subtilis SP1, SP2, SP3, SP4 and SP5 with nucleic acid derived from gram-positive organisms, either of genomic or cDNA origin.

BRIEF DESCRIPTION OF THE DRAWINGS

Figures 1A-1C shows the DNA (SEQ ID NO:1) and deduced amino acid sequence (SEQ ID NO:2) for SP1 (YUXL).

Figure 2A-2B show an amino acid alignment between DAP (dap2_yeast) (SEQ ID NO:3) and SP1 (YUXL). For Figures 2A-2B, 3 and 4, the amino acid triad S-D-H is indicated.

Figure 3 shows an amino acid alignment between SP1 (YUXL) (SEQ ID NO:2) and SP2 (YTMA) (SEQ ID NO:5).

Figure 4 shows and amino acid alignment between SP1 (YUXL) (SEQ ID NO:2) and SP3 (YITV) (SEQ ID NO:7).

Figure 5 shows and amino acid alignment between SP1 (YUXL) (SEQ ID NO:2) and SP4 (YQKD) (SEQ ID NO:9).

Figure 6 shows and amino acid alignment between SP1 (YUXL) (SEQ ID NO:2) and SP5 (CAH) (SEQ ID NO: 10).

Figures 7A-7B shows the DNA (SEQ ID NO:4) and deduced amino acid sequence for SP2 (YTMA) (SEQ ID NO:5).

Figures 8A-8B shows the DNA (SEQ ID NO:6) and deduced amino acid sequence for SP3 (YITV) (SEQ ID NO:7).

Figures 9A-9B shows the DNA (SEQ ID NO:8) and deduced amino acid sequence for SP4 (YQKD) (SEQ ID NO:9).

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS Definitions -- As used herein, the genus Bacillus includes all members known to those of skill in the art, including but not limited to B. subtilis, B. licheniformis, B. lentus, B. brevis, B. ' stearothermophilus, B. alkalophilus, B. amyloliquefaciens, B. coagulans, B. ciculans, B. lautus and B. thuπngiensis.

RECTIFIED SHEET (RULE 91J The present invention encompasses novel SP1 , SP2, SP3, SP4 and SP5 from gram positive organisms In a preferred embodiment, the gram-positive organisms is a Bacillus In another preferred embodiment, the gram-positive organism is Bacillus subtilis As used herein, "S subtilis SP1 (YuxL) refers to the DNA and deduced am o acid sequence shown in Figures 1A-1C and Figures 2A-2B, SP2 (YtmA) refers to the DNA and deduced am o acid sequence shown in Figures 7A-7B and Figure 3, SP3 (YitV) refers to the DNA and deduced am o acid sequence shown in Figures 8A-8B and Figure 4, SP4 (YqkD) refers to the DNA and deduced ammo acid sequence shown in Figures 9A-9B and Figure 5, and SP5 (CAH) refers to the deduced ammo acid sequence shown in Figure 6 The present invention encompasses ammo acid variations of the B subtilis ammo acid sequences of SP1 , SP2, SP3, SP4 and SP5 that have proteolytic activity Such proteolytic ammo acid variants can be used in cleaning compositions

As used herein, "nucleic acid" refers to a nucleotide or polynucleotide sequence, and fragments or portions thereof, and to DNA or RNA of genomic or synthetic origin which may be double-stranded or single-stranded, whether representing the sense or antisense strand As used herein "ammo acid" refers to peptide or protein sequences or portions thereof A "polynucleotide homolog" as used herein refers to a novel gram-positive microorganism polynucleotide that has at least 80%, at least 90% and at least 95% identity to B subtilis SP1, SP2, SP3, SP4 or SP5, or which is capable of hybridizing to B subtilis SP1 , SP2, SP3, SP4 or SP5 under conditions of high stringency and which encodes an ammo acid sequence having serine protease activity

The terms "isolated" or "purified" as used herein refer to a nucleic acid or ammo acid that is removed from at least one component with which it is naturally associated

As used herein, the term "heterologous protein" refers to a protein or polypeptide that does not naturally occur in a gram-positive host cell Examples of heterologous proteins include enzymes such as hydrolases including proteases, cellulases, amylases, carbohydrases, and lipases, isomerases such as racemases, epimerases, tautomerases, or mutases, transferases, kmases and phophatases The heterologous gene may encode therapeutically significant proteins or peptides, such as growth factors, cytokines, ligands, receptors and inhibitors, as well as vaccines and antibodies The gene may encode commercially important industrial proteins or peptides, such as proteases, carbohydrases such as amylases and glucoamylases, cellulases, oxidases and lipases The gene of interest may be a naturally occurring gene, a mutated gene or a synthetic gene

The term "homologous protein" refers to a protein or polypeptide native or naturally occurring in a gram-positive host cell The invention includes host cells producing the homologous protein via recombinant DNA technology The present invention encompasses a gram-positive host cell having a deletion or interruption of the nucleic acid encoding the naturally occurring homologous protein, such as a protease, and having nucleic acid encoding the homologous protein, or a variant thereof re-introduced in a recombinant form In another embodiment, the host cell produces the homologous protein

As used herein, the term "overexpressmg" when referring to the production of a protein in a host cell means that the protein is produced in greater amounts than its production in its naturally occurring environment

As used herein, the phrase "proteolytic activity" refers to a protein that is able to hydrolyze a peptide bond Enzymes having proteolytic activity are described in Enzyme Nomenclature, 1992, edited Webb Academic Press, Inc

Detailed Description of the Preferred Embodiments

The unexpected discovery of the serine proteases SP1 , SP2, SP3, SP4 and SP5 in B subtilis provides a basis for producing host cells, expression methods and systems which can be used to prevent the degradation of recombinantly produced heterologous proteins In a preferred embodiment, the host cell is a gram-positive host cell that has a deletion or mutation in the naturally occurring serine protease said mutation resulting in the complete deletion or mactivation of the production by the host cell of the proteolytic serine protease gene product In another embodiment of the present invention, the host cell is additionally genetically engineered to produced a desired protein or polypeptide

It may also be desired to genetically engineer host cells of any type to produce a gram-positive senne protease SP1 , SP2, SP3, SP4 or SP5 Such host cells are used in large scale fermentation to produce large quantities of the serine protease which may be isolated or purified and used in cleaning products, such as detergents

I Serine Protease Nucleic Acid and Ammo Acid Seguences

The SP1 , SP2, SP3 and SP4 polynucleotides having the sequences as shown in the Figures encode the Bacillus subtilis serine SP1 , SP2, SP3, and SP4 As will be understood by the skilled artisan, due to the degeneracy of the genetic code, a variety of polynucleotides can encode the Bacillus SP1 , SP2, SP3, SP4 and SP5 The present invention encompasses all such polynucleotides

The present invention encompasses novel SP1 , SP2, SP3, SP4 and SP5 polynucleotide homologs encoding gram-positive microorganism serine proteases SP1 , SP2, SP3, SP4 and SP5, respectively, which have at least 80%, or at least 90% or at least 95% identity to β subtilis as long as the homolog encodes a protein that has proteolytic activity Gram-positive polynucleotide homologs of B subtilis SP1 , SP2, SP3, SP4 or SP5 may be obtained by standard procedures known in the art from, for example, cloned DNA (e g , a DNA "library"), genomic DNA libraries, by chemical synthesis once identified, by cDNA cloning, or by the cloning of genomic DNA, or fragments thereof, purified from a desired cell (See, for example, Sambrook et al , 1989, Molecular Cloning, A Laboratory Manual, 2d Ed , Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York, Glover, D M (ed ), 1985, DNA Cloning A Practical Approach, MRL Press, Ltd , Oxford, U K Vol I, II ) A preferred source is from genomic DNA Nucleic acid sequences derived from genomic DNA may contain regulatory regions in addition to coding regions Whatever the source, the isolated serine protease gene should be molecularly cloned into a suitable vector for propagation of the gene

In the molecular cloning of the gene from genomic DNA, DNA fragments are generated, some of which will encode the desired gene The DNA may be cleaved at specific sites using various restriction enzymes Alternatively, one may use DNAse in the presence of manganese to fragment the DNA, or the DNA can be physically sheared, as for example, by sonication

The linear DNA fragments can then be separated according to size by standard techniques, including but not limited to, agarose and polyacrylamide gel electrophoresis and column chromatography

Once the DNA fragments are generated, identification of the specific DNA fragment containing the SP1 , SP2, SP3, SP4 or SP5 may be accomplished in a number of ways For example, a B subtilis SP1 , SP2, SP3, SP4 or SP5 gene of the present invention or its specific RNA, or a fragment thereof, such as a probe or primer, may be isolated and labeled and then used in hybridization assays to detect a gram-positive SP1 , SP2, SP3, SP4 or SP5 gene (Benton, W and Davis, R , 1977, Science 196 180, Grunstein, M And Hogness, D ,

1975, Proc Natl Acad Sci USA 72 3961) Those DNA fragments sharing substantial sequence similarity to the probe will hybridize under stringent conditions

Accordingly, the present invention provides a method for the detection of gram- positive SP1 , SP2, SP3, SP4 or SP5 polynucleotide homologs which comprises hybridizing part or all of a nucleic acid sequence of B subtilis SP1 SP2, SP3, SP4 or SP5 with gram- positive microorganism nucleic acid of either genomic or cDNA origin

Also included within the scope of the present invention are gram-positive microorganism polynucleotide sequences that are capable of hybridizing to the nucleotide sequence of B subtilis SP1 , SP2, SP3, SP4 or SP5 under conditions of intermediate to maximal stringency Hybridization conditions are based on the melting temperature (Tm) of the nucleic acid binding complex, as taught in Berger and Kimmel (1987, Guide to Molecular

Cloning Techniques, Methods in Enzymology, Vol 152, Academic Press, San Diego CA) incorporated herein by reference, and confer a defined "stringency" as explained below "Maximum stringency" typically occurs at about Tm-5°C (5°C below the Tm of the probe), "high stringency" at about 5°C to 10°C below Tm, "intermediate stringency" at about 10°C to 20°C below Tm, and "low stringency" at about 20°C to 25°C below Tm As will be understood by those of skill in the art, a maximum stringency hybridization can be used to identify or detect identical polynucleotide sequences while an intermediate or low stringency hybridization can be used to identify or detect polynucleotide sequence homologs

The term "hybridization" as used herein shall include "the process by which a strand of nucleic acid joins with a complementary strand through base pairing" (Coombs J (1994) Dictionary of Biotechnology, Stockton Press, New York NY)

The process of amplification as carried out in polymerase chain reaction (PCR) technologies is described in Dieffenbach CW and GS Dveksler (1995, PCR Primer, a Laboratory Manual, Cold Spring Harbor Press, Plamview NY) A nucleic acid sequence of at least about 0 nucleotides and as many as about 60 nucleotides from B subtilis SP1 SP2, SP3, SP4 or SP5 preferably about 12 to 30 nucleotides and more preferably about 20-25 nucleotides can be used as a probe or PCR primer

The B subtilis ammo acid sequences SP1 SP2, SP3, SP4 and SP5 (shown in Figures 2A-2B through Figure 6) were identified via a FASTA search of Bacillus subtilis genomic nucleic acid sequences B subtilis SP1 (YuxL) was identified by its structural homology to the serine protease DAP classified as an S9 type serine protease, designated in Figures 2A-2B as "dap2_yeast" As shown in Figures 2A-2B, SP1 has the ammo acid dyad "S-D-H" indicated Conservation of ammo acids around each residue is noted in Figures 2A-2B through Figure 6 SP2 (YtmA), SP3 (YitV), SP4 (YqkD) and SP5 (CAH) were identified upon by their structural and overall ammo acid homology to SP1 (YuxL) SP1 and SP4 were described in Parsot and Kebayashi, respectively, but were not characterized as serine proteases or serine proteases of the S9 family

II Expression Systems

The present invention provides host cells, expression methods and systems for the enhanced production and secretion of desired heterologous or homologous proteins in gram-positive microorganisms In one embodiment, a host cell is genetically engineered to have a deletion or mutation in the gene encoding a gram-positive SP1 , SP2, SP3, SP4 or SP5 such that the respective activity is deleted In an alternative embodiment of the present invention, a gram-positive microorganism is genetically engineered to produce a serine protease of the present invention Inactivation of a gram-positive serine protease in a host cell

Producing an expression host cell incapable of producing the naturally occurring serine protease necessitates the replacement and/or inactivation of the naturally occurring gene from the genome of the host cell In a preferred embodiment, the mutation is a non- reverting mutation

One method for mutating nucleic acid encoding a gram-positive serine protease is to clone the nucleic acid or part thereof, modify the nucleic acid by site directed mutagenesis and reintroduce the mutated nucleic acid into the cell on a plasmid By homologous recombination, the mutated gene may be introduced into the chromosome In the parent host cell, the result is that the naturally occurring nucleic acid and the mutated nucleic acid are located in tandem on the chromosome After a second recombination, the modified sequence is left in the chromosome having thereby effectively introduced the mutation into the chromosomal gene for progeny of the parent host cell

Another method for inactivating the serine protease proteolytic activity is through deleting the chromosomal gene copy In a preferred embodiment the entire gene is deleted, the deletion occurring in such as way as to make reversion impossible In another preferred embodiment, a partial deletion is produced, provided that the nucleic acid sequence left in the chromosome is too short for homologous recombination with a plasmid encoded serine protease gene In another preferred embodiment, nucleic acid encoding the catalytic ammo acid residues are deleted

Deletion of the naturally occurring gram-positive microorganism serine protease can be carried out as follows A serine protease gene including its 5 and 3' regions is isolated and inserted into a cloning vector The coding region of the serine protease gene is deleted form the vector in vitro, leaving behind a sufficient amount of the 5' and 3' flanking sequences to provide for homologous recombination with the naturally occurring gene in the parent host cell The vector is then transformed into the gram-positive host cell The vector integrates into the chromosome via homologous recombination in the flanking regions This method leads to a gram-positive strain in which the protease gene has been deleted

The vector used in an integration method is preferably a plasmid A selectable marker may be included to allow for ease of identification of desired recombinant microorgansims Additionally, as will be appreciated by one of skill in the art, the vector is preferably one which can be selectively integrated into the chromosome This can be achieved by introducing an inducible origin of replication, for example, a temperature sensitive origin into the plasmid By growing the transformants at a temperature to which the origin of replication is sensitive, the replication function of the plasmid is inactivated, thereby providing a means for selection of chromosomal integrants Integrants may be selected for growth at high temperatures in the presence of the selectable marker, such as an antibiotic Integration mechanisms are described in WO 88/06623

Integration by the Campbell-type mechanism can take place in the 5' flanking region of the protease gene, resulting in a protease positive strain carrying the entire plasmid vector in the chromosome in the serine protease locus Since illegitimate recombination will give different results it will be necessary to determine whether the complete gene has been deleted, such as through nucleic acid sequencing or restriction maps

Another method of inactivating the naturally occurring serine protease gene is to mutagenize the chromosomal gene copy by transforming a gram-positive microorganism with oligonucleotides which are mutagenic Alternatively, the chromosomal serine protease gene can be replaced with a mutant gene by homologous recombination

The present invention encompasses host cells having additional protease deletions or mutations, such as deletions or mutations in apr, npr, epr, mpr and others known to those of skill in the art United States Patent 5 264,366 discloses Bacillus host cells having a deletion of apr and npr, United States Patent 5,585,253 discloses Bacillus host cells having a deletion of epr, Margot et al , 1996, Microbiology 142 3437-3444 disclose host cells having a deletion in wpr and EP patent 0369817 discloses Bacillus host cells having a deletion of mpr

III Production of Serine protease

For production of serine protease in a host cell, an expression vector comprising at least one copy of nucleic acid encoding a gram-positive microorganism SP1 , SP2, SP3, SP4 or SP5, and preferably comprising multiple copies is transformed into the host cell under conditions suitable for expression of the serine protease In accordance with the present invention, polynucleotides which encode a gram-positive microorganism SP1 , SP2, SP3, SP4 or SP5, or fragments thereof, or fusion proteins or polynucleotide homolog sequences that encode ammo acid variants of B SP1 , SP2, SP3, SP4 or SP5, may be used to generate recombinant DNA molecules that direct their expression in host cells In a preferred embodiment, the gram-positive host cell belongs to the genus Bacillus In another preferred embodiment, the gram positive host cell is B subtilis

As will be understood by those of skill in the art, it may be advantageous to produce polynucleotide sequences possessing non-naturally occurring codons Codons preferred by a particular gram-positive host cell (Murray E et al (1989) Nuc Acids Res 17 477-508) can be selected, for example, to increase the rate of expression or to produce recombinant RNA transcripts having desirable properties, such as a longer half-life, than transcripts produced from naturally occurring sequence Altered SP1 , SP2, SP3, SP4 or SP5 polynucleotide sequences which may be used in accordance with the invention include deletions, insertions or substitutions of different nucleotide residues resulting in a polynucleotide that encodes the same or a functionally equivalent SP1 , SP2, SP3, SP4 or SP5 homolog, respectively As used herein a "deletion" is defined as a change in either nucleotide or ammo acid sequence in which one or more nucleotides or am o acid residues, respectively, are absent

As used herein an "insertion" or "addition" is that change in a nucleotide or ammo acid sequence which has resulted in the addition of one or more nucleotides or ammo acid residues, respectively, as compared to the naturally occurring SP1 , SP2, SP3, SP4 or SP5

As used herein "substitution" results from the replacement of one or more nucleotides or ammo acids by different nucleotides or am o acids, respectively

The encoded protein may also show deletions, insertions or substitutions of am o acid residues which produce a silent change and result in a functionally SP1 , SP2, SP3, SP4 or SP5 variant Deliberate ammo acid substitutions may be made on the basis of similarity in polarity, charge, solubility, hydrophobicity, hydrophilicity, and/or the amphipathic nature of the residues as long as the variant retains the ability to modulate secretion For example, negatively charged am o acids include aspartic acid and glutamic acid, positively charged ammo acids include lysine and argmine, and ammo acids with uncharged polar head groups having similar hydrophilicity values include leucme, isoleucine, vahne, glycine, alanme, asparagme, glutamine, serine, threonme, phenylalanme, and tyrosme

The SP1 , SP2 SP3, SP4 or SP5 polynucleotides of the present invention may be engineered in order to modify the cloning, processing and/or expression of the gene product For example, mutations may be introduced using techniques which are well known in the art, eg, site-directed mutagenesis to insert new restriction sites, to alter glycosylation patterns or to change codon preference, for example

In one embodiment of the present invention, a gram-positive microorganism SP1 , SP2, SP3, SP4 or SP5 polynucleotide may be ligated to a heterologous sequence to encode a fusion protein A fusion protein may also be engineered to contain a cleavage site located between the serine protease nucleotide sequence and the heterologous protein sequence, so that the serine protease may be cleaved and purified away from the heterologous moiety

IV Vector Sequences

Expression vectors used in expressing the serine proteases of the present invention in gram-positive microorganisms comprise at least one promoter associated with a serine protease selected from the group consisting of SP1 , SP2, SP3, SP4 and SP5, which promoter is functional in the host cell In one embodiment of the present invention, the promoter is the wild-type promoter for the selected serine protease and in another embodiment of the present invention, the promoter is heterologous to the serine protease, but still functional in the host cell In one preferred embodiment of the present invention, nucleic acid encoding the serine protease is stably integrated into the microorganism genome

In a preferred embodiment, the expression vector contains a multiple cloning site cassette which preferably comprises at least one restriction endonuclease site unique to the vector, to facilitate ease of nucleic acid manipulation In a preferred embodiment, the vector also comprises one or more selectable markers As used herein, the term selectable marker refers to a gene capable of expression in the gram-positive host which allows for ease of selection of those hosts containing the vector Examples of such selectable markers include but are not limited to antibiotics, such as, erythromycin, actinomycin, chloramphemcol and tetracyclme

V Transformation

A variety of host cells can be used for the production of SP1 , SP2, SP3, SP4 or SP5 including bacterial, fungal, mammalian and insects cells General transformation procedures are taught in Current Protocols In Molecular Biology (vol 1 , edited by Ausubel et al , John Wiley & Sons, Inc 1987, Chapter 9) and include calcium phosphate methods, transformation using DEAE-Dextran and electroporation Plant transformation methods are taught in Rodnquez (WO 95/14099, published 26 May 1995)

In a preferred embodiment the host cell is a gram-positive microorganism and in another preferred embodiment, the host cell is Bacillus In one embodiment of the present invention, nucleic acid encoding one or more serine protease(s) of the present invention is introduced into a host cell via an expression vector capable of replicating within the host cell Suitable replicating plasmids for Bacillus are described in Molecular Biological Methods for Bacillus, Ed Harwood and Cutting, John Wiley & Sons, 1990, hereby expressly incorporated by reference, see chapter 3 on plasmids Suitable replicating plasmids for B subtilis are listed on page 92

In another embodiment nucleic acid encoding a serine protease(s) of the present invention is stably integrated into the microorganism genome Preferred host cells are gram-positive host cells Another preferred host is Bacillus Another preferred host is Bacillus subtilis Several strategies have been described in the literature for the direct cloning of DNA in Bacillus Plasmid marker rescue transformation involves the uptake of a donor plasmid by competent cells carrying a partially homologous resident plasmid (Contente et al , Plasmid 2 555-571 (1979), Haima et al , Mol Gen Genet 223 185-191 (1990), We rauch et al , J Bactenol 154(3) 1077-1087 (1983), and Weinrauch et al , J Bactenol 169(3) 1205-1211 (1987)) The incoming donor plasmid recombines with the homologous region of the resident "helper" plasmid in a process that mimics chromosomal transformation

Transformation by protoplast transformation is described for B subtilis in Chang and Cohen, (1979) Mol Gen Genet 168 111-115, for B megatenum in Vorobjeva et al , (1980) FEMS Microbiol Letters 7 261-263, for B amyloliquefaciens in Smith et al , (1986) Appl and Env Microbiol 51 634, for B thuπngiensis in Fisher et al , (1981) Arch Microbiol 139 213-217, for B sphaeπcus in McDonald (1984) J Gen Microbiol 130 203, and B larvae in Bakhiet et al , (1985) 49 577 Mann et al , (1986, Current Microbiol 13 131-135) report on transformation of Bacillus protoplasts and Holubova, (1985) Folia Microbiol 30 97) disclose methods for introducing DNA into protoplasts using DNA containing liposomes

VI Identification of Transformants

Whether a host cell has been transformed with a mutated or a naturally occurring gene encoding a gram-positive SP1 , SP2, SP3, SP4 or SP5 detection of the presence/absence of marker gene expression can suggests whether the gene of interest is present However, its expression should be confirmed For example, if the nucleic acid encoding a serine protease is inserted within a marker gene sequence, recombinant cells containing the insert can be identified by the absence of marker gene function Alternatively, a marker gene can be placed in tandem with nucleic acid encoding the serine protease under the control of a single promoter Expression of the marker gene in response to induction or selection usually indicates expression of the serine protease as well Alternatively, host cells which contain the coding sequence for a senne protease and express the protein may be identified by a variety of procedures known to those of skill in the art These procedures include, but are not limited to, DNA-DNA or DNA-RNA hybridization and protein bioassay or immunoassay techniques which include membrane- based, solution-based, or chip-based technologies for the detection and/or quantification of the nucleic acid or protein

The presence of the cysteine polynucleotide sequence can be detected by DNA- DNA or DNA-RNA hybridization or amplification using probes, portions or fragments of B subtilis SP1 , SP2, SP3, SP4 or SP5

VII Assay of Protease Activity There are various assays known to those of skill in the art for detecting and measuring protease activity There are assays based upon the release of acid-soluble peptides from casein or hemoglobin measured as absorbance at 280 nm or coloπmetπcally using the Fo n method (Bergmeyer, et al , 1984, Methods of Enzymatic Analysis vol 5, Peptidases, Protemases and their Inhibitors, Verlag Chemie, Weinheim) Other assays involve the solubihzation of chromogenic substrates (Ward, 1983, Protemases, in Microbial Enzymes and Biotechnology (W M Fogarty, ed ), Applied Science, London, pp 251-317)

VIII Secretion of Recombinant Proteins

Means for determining the levels of secretion of a heterologous or homologous protein in a gram-positive host cell and detecting secreted proteins include, using either polyclonal or monoclonal antibodies specific for the protein Examples include enzyme- linked immunosorbent assay (ELISA), radioimmunoassay (RIA) and fluorescent activated cell sorting (FACS) These and other assays are described, among other places, in Hampton R et al (1990, Serological Methods, a Laboratory Manual. APS Press, St Paul MN) and Maddox DE et al (1983, J Exp Med 158 1211)

A wide variety of labels and conjugation technigues are known by those skilled in the art and can be used in various nucleic and am o acid assays Means for producing labeled hybridization or PCR probes for detecting specific polynucleotide sequences include oligolabelmg, nick translation, end-labeling or PCR amplification using a labeled nucleotide Alternatively, the nucleotide sequence, or any portion of it, may be cloned into a vector for the production of an mRNA probe Such vectors are known in the art, are commercially available, and may be used to synthesize RNA probes in vitro by addition of an appropriate RNA polymerase such as T7, T3 or SP6 and labeled nucleotides

A number of companies such as Pharmacia Biotech (Piscataway NJ), Promega (Madison Wl), and US Biochemical Corp (Cleveland OH) supply commercial kits and protocols for these procedures Suitable reporter molecules or labels include those radionuc des, enzymes, fluorescent, chemiluminescent or chromogenic agents as well as substrates, cofactors, inhibitors, magnetic particles and the like Patents teaching the use of such labels include US Patents 3,817,837, 3,850,752, 3,939,350, 3,996,345, 4,277,437, 4,275,149 and 4,366,241 Also, recombinant immunoglobulms may be produced as shown in US Patent No 4,816,567 and incorporated herein by reference

IX Purification of Proteins

Gram positive host cells transformed with polynucleotide sequences encoding heterologous or homologous protein may be cultured under conditions suitable for the expression and recovery of the encoded protein from cell culture The protein produced by a recombinant gram-positive host cell comprising a serine protease of the present invention will be secreted into the culture media Other recombinant constructions may join the heterologous or homologous polynucleotide sequences to nucleotide sequence encoding a polypeptide domain which will facilitate purification of soluble proteins (Kroll DJ et al (1993) DNA Cell Biol 12 441-53)

Such purification facilitating domains include, but are not limited to, metal chelatmg peptides such as histidine-tryptophan modules that allow purification on immobilized metals (Porath J (1992) Protein Expr Puπf 3 263-281), protein A domains that allow purification on immobilized immunoglobuhn, and the domain utilized in the FLAGS extension/affinity purification system (Immunex Corp, Seattle WA) The inclusion of a cleavable linker sequence such as Factor XA or enterokinase (Invitrogen, San Diego CA) between the purification domain and the heterologous protein can be used to facilitate purification

X Uses of The Present Invention

Genetically Engineered Host Cells

The present invention provides genetically engineered host cells comprising preferably non-revertable mutations or deletions in the naturally occurring gene encoding one or more of SP1 , SP2, SP3, SP4 or SP5 such that the proteolytic activity is diminished or deleted altogether The host cell may contain additional protease deletions, such as deletions of the mature subtihsn protease and/or mature neutral protease disclosed in United States Patent No 5,264,366

In a preferred embodiment, the host cell is genetically engineered to produce a desired protein or polypeptide In a preferred embodiment the host cell is a Bacillus In another preferred embodiment, the host cell is a Bacillus subtilis

In an alternative embodiment, a host cell is genetically engineered to produce a gram-positive SP1 , SP2, SP3, SP4 or SP5 In a preferred embodiment, the host cell is grown under large scale fermentation conditions, the SP1 , SP2, SP3, SP4 or SP5 is isolated and/or purified and used in cleaning compositions such as detergents WO 95/10615 discloses detergent formulation A serine protease of the present invention can be useful in formulating various cleaning compositions A number of known compounds are suitable surfactants useful in compositions comprising the serine protease of the invention These include nonionic, anionic, cationic, anionic or zwitteπonic detergents, as disclosed in US 4,404,128 and US 4,261 ,868 A suitable detergent formulation is that described in Example 7 of US Patent 5,204,015 The art is familiar with the different formulations which can be used as cleaning compositions In addition, a serine protease of the present invention can be used, for example, in bar or liquid soap applications, dishcare formulations, contact lens cleaning solutions or products, peptide hydrolysis, waste treatment, textile applications, as fusion-cleavage enzymes in protein production, etc A serine protease of the present invention may provide enhanced performance in a detergent composition (as compared to another detergent protease). As used herein, enhanced performance in a detergent is defined as increasing cleaning of certain enzyme sensitive stains such as grass or blood, as determined by usual evaluation after a standard wash cycle.

A serine protease of the present invention can be formulated into known powdered and liquid detergents having pH between 6 5 and 12.0 at levels of about .01 to about 5% (preferably .1 % to .5%) by weight These detergent cleaning compositions can also include other enzymes such as known proteases, amylases, cellulases, lipases or endoglycosidases, as well as builders and stabilizers

The addition of a serine protease to conventional cleaning compositions does not create any special use limitation In other words, any temperature and pH suitable for the detergent is also suitable for the present compositions as long as the pH is within the above range, and the temperature is below the described serine protease denaturing temperature In addition, a serine protease of the present invention can be used in a cleaning composition without detergents, again either alone or in combination with builders and stabilizers.

One aspect of the invention is a composition for the treatment of a textile that includes a serine protease of the present invention. The composition can be used to treat for example silk or wool as described in publications such as RD 216,034, EP 134,267, US 4,533,359; and EP 344,259

Proteases can be included in animal feed such as part of animal feed additives as described in, for example, US 5,612,055, US 5,314,692, and US 5,147,642

Polynucleotides

A B.subt s SP1 , SP2, SP3, SP4 or SP5 polynucleotide, or any part thereof, provides the basis for detecting the presence of gram-positive microorganism polynucleotide homologs through hybridization techniques and PCR technology

Accordingly, one aspect of the present invention is to provide for nucleic acid hybridization and PCR probes which can be used to detect polynucleotide sequences, including genomic and cDNA sequences, encoding gram-positive SP1 , SP2, SP3, SP4 or SP5 or portions thereof.

The manner and method of carrying out the present invention may be more fully understood by those of skill in the art by reference to the following examples, which examples are not intended in any manner to limit the scope of the present invention or of the claims directed thereto

Example I Preparation of a Genomic library

The following example illustrates the preparation of a Bacillus genomic library

Genomic DNA from Bacillus cells is prepared as taught in Current Protocols In Molecular Biology vol 1 , edited by Ausubel et al , John Wiley & Sons, Inc 1987, chapter 2 4 1 Generally, Bacillus cells from a saturated liquid culture are lysed and the proteins removed by digestion with protemase K Cell wall debris, polysacchaπdes, and remaining proteins are removed by selective precipitation with CTAB, and high molecular weight genomic DNA is recovered from the resulting supernatant by isopropanol precipitation If exceptionally clean genomic DNA is desired, an additional step of purifying the Bacillus genomic DNA on a cesium chloride gradient is added

After obtaining purified genomic DNA, the DNA is subjected to Sau3A digestion Sau3A recognizes the 4 base pair site GATC and generates fragments compatible with several convenient phage lambda and cosmid vectors The DNA is subjected to partial digestion to increase the chance of obtaining random fragments

The partially digested Bacillus genomic DNA is subjected to size fractionation on a 1% agarose gel prior to cloning into a vector Alternatively, size fractionation on a sucrose gradient can be used The genomic DNA obtained from the size fractionation step is purified away from the agarose and ligated into a cloning vector appropriate for use in a host cell and transformed into the host cell

Example II

The following example describes the detection of gram-positive microorganism SP1 The same procedures can be used to detect SP2, SP3, SP4 or SP5

DNA derived from a gram-positive microorganism is prepared according to the methods disclosed in Current Protocols in Molecular Biology, Chap 2 or 3 The nucleic acid is subjected to hybridization and/or PCR amplification with a probe or primer derived from SP1 A preferred probe comprises the nucleic acid section encoding conserved ammo acid residues

The nucleic acid probe is labeled by combining 50 pmol of the nucleic acid and 250 mCi of [gamma ^²P] adenosme tπphosphate (Amersham Chicago IL) and T4 polynucleotide kmase (DuPont NEN®, Boston MA) The labeled probe is purified with Sephadex G-25 super fine resin column (Pharmacia) A portion containing 10/ counts per minute of each is used in a typical membrane based hybridization analysis of nucleic acid sample of either genomic or cDNA origin The DNA sample which has been subjected to restriction endonuclease digestion is fractionated on a 0.7 percent agarose gel and transferred to nylon membranes (Nytran Plus, Schleicher & Schuell, Durham NH). Hybridization is carried out for 16 hours at 40 degrees C. To remove nonspecific signals, blots are sequentially washed at room temperature under increasingly stringent conditions up to 0.1 x saline sodium citrate and 0.5% sodium dodecyl sulfate. The blots are exposed to film for several hours, the film developed and hybridization patterns are compared visually to detect polynucleotide homologs of B. subtilis SP1. The homologs are subjected to confirmatory nucleic acid sequencing. Methods for nucleic acid sequencing are well known in the art. Conventional enzymatic methods employ DNA polymerase Klenow fragment, SEQUENASE® (US Biochemical Corp, Cleveland, OH) or Taq polymerase to extend DNA chains from an oligonucleotide primer annealed to the DNA template of interest.

Various other examples and modifications of the foregoing description and examples will be apparent to a person skilled in the art after reading the disclosure without departing from the spirit and scope of the invention, and it is intended that all such examples or modifications be included within the scope of the appended claims. All publications and patents referenced herein are hereby incorporated in their entirety.

Claims

1. A gram-positive microorganism having a mutation or deletion of part or all of one or more of the genes encoding a serine protease selected from the group consisting of SP1 , SP2, SP3, SP4 and SP5 said mutation or deletion resulting in the inactivation of the SP1 , SP2, SP3, SP4 or SP5 proteolytic activity.

2. The gram-positive microorganism according to Claim 1 that is a member of the family Bacillus.

3. The microorganism according to Claim 2 wherein the member is selected from the group consisting of B. licheniformis, B. lentus, B. brevis, B. stearothermophilus, B. alkalophilus, B. amyloliquefaciens, B. coagulans, B. circulans, B. lautus and Bacillus thuringiensis.

4. The microorganism of Claim 1 wherein said microorganism is capable of expressing a heterologous protein.

5. The microorganism of Claim 4 wherein said heterologous protein is selected from the group consisting of hormone, enzyme, growth factor and cytokine.

6. The microorganism of Claim 5 wherein said heterologous protein is an enzyme.

7. The microorganism of Claim 6 wherein said enzyme is selected from the group consisting of a proteases, carbohydrases, and lipases; isomerases such as racemases, epimerases, tautomerases, or mutases; transferases, kinases and phophatases.

8. A cleaning composition comprising a serine protease selected from the group consisting of SP1, SP2, SP3, SP4 and SP5.

9. An expression vector comprising nucleic acid encoding a serine protease selected from the group consisting of SP1 , SP2, SP3, SP5 and SP5.

10. A host cell comprising an expression vector according to Claim 9

11. A method for the production of a heterologous protein in a Bacillus host cell comprising the steps of (a) obtaining a Bacillus host cell comprising nucleic acid encoding said heterologous protein wherein said host cell contains a mutation or deletion in at least one of the genes encoding serine protease 1 , serine protease 2 serine protease 3; serine protease 4 and serine protease 5.

(b) growing said Bacillus host cell under conditions suitable for the expression of said heterologous protein.

13. The method of Claim 11 wherein said Bacillus cell is selected from the group consisting of Bacillus subtilis, B. licheniformis, B. lentus, B. brevis, B. stearothermophilus, B. alkalophilus, B. amyloliquefaciens, B. coagulans, B. circulans, B. lautus and Bacillus thuringiensis.

14. The method of Claim 13 wherein said Bacillus host cell further comprises a mutation or deletion in at least one of the genes encoding apr, npr, epr, wpr and mrp.

15. A gram-positive microorganism having at mutation or deletion in at least one of the genes encoding a serine protease selected from the group consisting of serine protease 1 , serine protease 2 serine protease 3; serine protease 4 and serine protease 5.

16. The microorganism of Claim 16 further comprising a mutation or deletion in at least one of the genes encoding apr, npr, epr, wpr and mrp.