Patent Application
20110229938
The present invention provides methods for amplifying a genomic locus without the use of antibiotics. In particular, the invention relates to a method for amplifying in vivo a DNA sequence encoding a polypeptide of interest, a cell harboring multiple copies of said amplified DNA sequence, and a vector harboring a DNA construct to be used in the method. Furthermore, the present invention relates to a method of producing a polypeptide of interest e.g. an enzyme, by culturing a cell as described above.
Expression and recombinant production of exogenous polypeptides is a widely used technique. It is well known that cells can be transformed with nucleic acids encoding exogenous polypeptides of interest for expression and production of large quantities of the desired polypeptides. In some applications, the methods are used to produce vast amounts of polypeptide over what would be produced naturally by the originating organism. Indeed, expression of exogenous nucleic acid sequences, as well as over-expression of endogenous sequences have been extensively used in modern biotechnology.
Despite advances in molecular biology and protein engineering, there remains a need for new methods and compositions that increase expression levels of polypeptides in host cells.
Provided herein is a method of amplifying a genomic locus. In certain embodiments, the method may comprise: a) contacting a population of bacterial host cells with an inhibitor of an essential enzyme, where the bacterial host cells comprise a genomic locus of the structure: A1-P-M-A2, where A1 and A2 are direct repeats, P comprises a coding sequence for a polypeptide of interest, and M comprises a coding sequence for the essential enzyme, and b) selecting for cells that are resistant to the inhibitor; where cells that are resistant to the inhibitor have multiple copies of the amplification unit. The bacterial host cell may be a Bacillus sp. cell, although other bacterial cell types, e.g., Streptomyces sp., are envisioned. In some embodiments, the polypeptide of interest is a subtilisin e.g. the subtilisin of SEQ ID NO:8, or mature form thereof set forth in SEQ ID NO:12. In certain cases, the method avoids the use of antibiotic markers and antibiotics, and provides an alternative to antibiotic-based amplification systems. In certain embodiments, the essential enzyme has the amino acid sequence of an enzyme e.g. a wild-type enzyme, that is endogenous to the cell. In particular embodiments, the bacterial host cell used in the method may or may not contain an inactivated endogenous gene encoding the essential enzyme, where the inactivated gene may be at a different genomic locus to the genomic locus of structure: A1-P-M-A2. In certain cases, the essential enzyme may be alanine racemase e.g. SEQ ID NO:11, and the inhibitor may be β-chloro-D-alanine or cycloserine, although other enzyme/inhibitor combinations may be employed. In some embodiments, the amplification unit comprises the sequence set forth in SEQ ID NO:7.
The amplification unit provides for expression of the essential enzyme encoded by region M. In particular embodiments, M may comprise a coding sequence for the essential enzyme and a promoter operably linked to the coding sequence, wherein the promoter is native to the coding sequence for the essential enzyme. In certain embodiments, the coding sequence and the promoter may be endogenous to the host cell. The amplification unit also provides for expression of the protein of interest encoded by region P. In particular embodiments, the coding sequence of P may be operably linked to an endogenous or non-endogenous promoter that is present in the adjacent direct repeat (A1). In other embodiments, the promoter for P may not be present in the adjacent direct repeat. Rather, the promoter may be present in region P.
In some embodiments, the invention provides a bacterial host cell comprising a genomic locus comprising an amplification unit of the structure: A1-P-M-A2, wherein A1 and A2 are direct repeats, P comprises a coding sequence for a polypeptide of interest, and M comprises a coding sequence for an essential enzyme is also provided. In this embodiment, the amplification unit provides for significant expression of the essential enzyme. The bacterial host cell may be a Bacillus sp. cell, although other bacterial cell types, e.g., Streptomyces sp., are envisioned. In some embodiments, the polypeptide of interest is a subtilisin e.g. the subtilisin of SEQ ID NO:8, or mature form thereof set forth in SEQ ID NO:12. In certain cases, the method avoids the use of antibiotic markers and antibiotics, and provides an alternative to antibiotic-based amplification systems. In certain embodiments, the essential enzyme has the amino acid sequence of an enzyme e.g. a wild-type enzyme, that is endogenous to the cell. In particular embodiments, the bacterial host cell may or may not contain an inactivated endogenous gene encoding the essential enzyme, where the inactivated gene may be at a different genomic locus to the genomic locus of structure: A1-P-M-A2. In certain cases, the essential enzyme may be alanine racemase e.g. SEQ ID NO:11, and the inhibitor may be β-chloro-D-alanine or cycloserine, although other enzyme/inhibitor combinations may be employed. In some embodiments, the amplification unit comprises the sequence set forth in SEQ ID NO:7.
In other embodiments, the bacterial host cell of the invention comprises a genomic locus comprising multiple copies of an amplification unit of the structure: A1-P-M-A2, where A1 and A2 are direct repeats, P comprises a first coding sequence for a polypeptide of interest, and M comprises a second coding sequence of an essential enzyme. In some embodiments, the amplification unit comprises a polynucleotide sequence set forth in SEQ ID NO:7. In some embodiments, the first coding sequence is operably linked to a promoter that is present in direct repeat A1. In particular embodiments, the bacterial host cell comprises a genomic locus comprising multiple copies an amplification unit described by the formula: (A1-P-M)n-A2, where n is at least 2, A1 and A2 are direct repeats, P comprises a coding sequence for a polypeptide of interest, and M encodes an essential enzyme, where the coding sequence of M is operably linked to an endogenous or non-endogenous promoter. In one embodiment, the coding sequence of M and the promoter may be endogenous to the host cell. In some embodiments, the bacterial host cell comprises a genomic locus comprising multiple copies e.g. at least 2 copies, of the amplification unit of SEQ ID NO:7. The amplification unit provides for expression of both the polypeptide of interest e.g. a subtilisin, and the essential enzyme. In some embodiments, the expressed polypeptide of interest is subtilisin FNA set forth in SEQ ID NO:8, or mature form thereof set forth in SEQ ID NO:12, and the essential enzyme is alanine racemase set forth is SEQ ID NO:11. In a particular embodiment, the promoter operably linked to the coding sequence of P may be part of the adjacent direct repeat (A1). In another embodiment, the promoter operably linked to the coding sequence of region P is present in region P rather than in the adjacent direct repeat.
In another embodiment, the invention encompasses a bacterial cell culture that comprises growth medium and a population of bacterial host cells comprising at least one, at least 2 or more copies of the amplification unit of the structure A1-P-M-A2, wherein A1 and A2 are direct repeats, P comprises a first coding sequence for a protein of interest, and M comprises a second coding sequence of an essential enzyme. As described above, the amplification unit provides for expression of both the polypeptide of interest e.g. a subtilisin, and the essential enzyme. In some embodiments, the expressed polypeptide of interest is subtilisin FNA set forth in SEQ ID NO:8, or mature form thereof set forth in SEQ ID NO:12, and the essential enzyme is alanine racemase set forth is SEQ ID NO:11. In yet another embodiment, the bacterial cell culture may be employed in a protein production method that comprises: maintaining a culture of subject cells under conditions suitable to produce the polypeptide of interest encoded by the coding sequence. In particular embodiments, this method may further comprise recovering the polypeptide of interest from the culture medium.
Unless defined otherwise herein, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although any methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, the preferred methods and materials are described.
All patents and publications, including all sequences disclosed within such patents and publications, referred to herein are expressly incorporated by reference.
Numeric ranges are inclusive of the numbers defining the range. Unless otherwise indicated, nucleic acids are written left to right in 5′ to 3′ orientation; amino acid sequences are written left to right in amino to carboxy orientation, respectively.
The headings provided herein are not limitations of the various aspects or embodiments of the invention. Accordingly, the terms defined immediately below are more fully defined by reference to the specification as a whole.
Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Singleton, et al., DICTIONARY OF MICROBIOLOGY AND MOLECULAR BIOLOGY, 2D ED., John Wiley and Sons, New York (1994), and Hale & Markham, THE HARPER COLLINS DICTIONARY OF BIOLOGY, Harper Perennial, N.Y. (1991) provide one of skill with the general meaning of many of the terms used herein. Still, certain terms are defined below for the sake of clarity and ease of reference.
The term “recombinant” refers to a polynucleotide or polypeptide that does not naturally occur in a host cell. A recombinant molecule may contain two or more naturally-occurring sequences that are linked together in a way that does not occur naturally. A recombinant cell contains a recombinant polynucleotide or polypeptide.
The term “heterologous” refers to elements that are not normally associated with each other. For example, if a host cell produces a heterologous protein, that protein is not normally produced in that host cell. Likewise, a promoter that is operably linked to a heterologous coding sequence is a promoter that is operably linked to a coding sequence that it is not usually operably linked to in a wild-type host cell. The term “homologous”, with reference to a polynucleotide or protein, refers to a polynucleotide or protein that occurs naturally in a host cell.
The terms “protein” and “polypeptide” are used interchangeably herein.
A “signal sequence” is a sequence of amino acids present at the N-terminal portion of a protein which facilitates the secretion of the mature form of the protein from the cell. The definition of a signal sequence is a functional one. The mature form of the extracellular protein lacks the signal sequence, which is cleaved off during the secretion process.
The term “nucleic acid” encompasses DNA, RNA, single stranded or double stranded and chemical modifications thereof. The terms “nucleic acid” and “polynucleotide” are used interchangeably herein.
A “vector” refers to a polynucleotide designed to introduce nucleic acids into one or more host cells. In certain embodiments, a vector can autonomously replicate in different host cells and include: cloning vectors, expression vectors, shuttle vectors, plasmids, phage particles, cassettes and the like. In other embodiments, a vector can integrate into a host cell genome.
A “promoter” is a regulatory sequence that initiates transcription of a downstream nucleic acid.
The term “operably linked” refers to an arrangement of elements that allows them to be functionally related. For example, a promoter is operably linked to a coding sequence if it controls the transcription of the sequence.
The term “selective marker” refers to a protein capable of expression in a host that allows for ease of selection of those hosts containing an introduced nucleic acid or vector. Examples of selectable markers include, but are not limited to, antimicrobials (e.g., hygromycin, bleomycin, or chloramphenicol) and/or genes that confer a metabolic advantage, such as a nutritional advantage on the host cell.
The terms “recovered”, “isolated”, and “separated” as used herein refer to a protein, cell, nucleic acid or amino acid that is removed from at least one component with which it is naturally associated.
As used herein, the terms “transformed”, “stably transformed” and “transgenic” used in reference to a cell means the cell has a non-native (e.g., heterologous) nucleic acid sequence integrated into its genome or as an episomal plasmid that is maintained through multiple generations.
As used herein, the term “expression” refers to the process by which a polypeptide is produced based on the nucleic acid sequence of a gene. The process includes both transcription and translation.
The term “introduced” in the context of inserting a nucleic acid sequence into a cell, means “transfection”, or “transformation” or “transduction” and includes reference to the incorporation of a nucleic acid sequence into a eukaryotic or prokaryotic cell wherein the nucleic acid sequence may be incorporated into the genome of the cell (e.g., chromosome, plasmid, plastid, or mitochondrial DNA), converted into an autonomous replicon, or transiently expressed (e.g., transfected mRNA).
The term “hybridization” refers to the process by which a strand of nucleic acid joins with a complementary strand through base pairing as known in the art. A nucleic acid is considered to be “Selectively hybridizable” to a reference nucleic acid sequence if the two sequences specifically hybridize to one another under moderate to high stringency hybridization and wash conditions. Moderate and high stringency hybridization conditions are known (see, e.g., Ausubel, et al., Short Protocols in Molecular Biology, 3rd ed., Wiley & Sons 1995 and Sambrook et al., Molecular Cloning: A Laboratory Manual, Third
Edition, 2001 Cold Spring Harbor, N.Y.). One example of high stringency conditions include hybridization at about 42 C in 50% formamide, 5×SSC, 5×Denhardt's solution, 0.5% SDS and 100 ug/ml denatured carrier DNA followed by washing two times in 2×SSC and 0.5% SDS at room temperature and two additional times in 0.1×SSC and 0.5% SDS at 42° C.
A “coding sequence” is a DNA segment that encodes a polypeptide.
An “expression cassette” as used herein means a DNA construct comprising a protein-coding region that is operably linked to a suitable control sequence that is capable of effecting expression of the protein in a suitable host cell. Such control sequences may include a promoter to effect transcription, an optional operator sequence to control transcription to produce mRNA, a sequence encoding suitable ribosome binding sites on the mRNA, and enhancers and other sequences which control termination of transcription and translation.
A polypeptide or polynucleotide that is “native to the host cell” has an amino acid or nucleotide sequence that is the same as that of a polypeptide or polynucleotide that is present in an unaltered host cell. In certain instances, a cell may contain a recombinant nucleic acid containing a polynucleotide (e.g., a coding sequence) that is native to the cell. In these instances, the cell contains a recombinant nucleic acid comprising a polynucleotide having a nucleotide sequence that is also present in an unaltered version of the host cell (i.e., a host cell that does not contain any gene knockouts), at a different locus. In certain instances, a cell may contain a recombinant nucleic acid encoding a polypeptide that is native to the cell. In these instances, the cell contains a recombinant nucleic acid encoding a polypeptide having an amino acid sequence that is the same as that of a polypeptide found in an unaltered version of the host cell (i.e., a host cell that does not contain any gene knockouts). The term “endogenous” is synonymous with the term “native”.
A “native promoter”, with reference to a coding sequence that is operably linked to its native promoter, refers to a promoter of a wild type host cell that is operably linked to the coding sequence in that cell.
The term “direct repeats” refers to at least two sequence elements that are present in the same orientation and that can undergo homologous recombination in a cell. Direct repeats have identical or almost identical nucleotide sequences (e.g., at least 98% or 99% sequence identity) over at least 50 nucleotides, e.g., at least 100, at least 200 or at least 500 or more nucleotides.
The term “inhibitor” refers to a compound that reversibly inhibits an enzyme, either by competitive inhibition or non-competitive inhibition (e.g., allosterically).
The term “essential enzyme” is an enzyme that is essential for the growth of a cell.
The term “expression cassette that provides for significant expression of an essential enzyme”, refers to an expression cassette that provides for expression of the essential enzyme at a level that is more than 50% (e.g., at least 70%, at least 90% or at least 100%, up to 1000%) of the level of an endogenous essential enzyme, if the gene for the endogenous essential enzyme is wild-type (i.e., not inactivated) in the cell.
The term “alanine racemase” refers to the enzyme that catalyzes the interconversion of L-alanine and D-alanine. An alanine racemase has an activity described as EC 5.1.1.1, according to IUBMB enzyme nomenclature. The gene encoding an alanine racemase may be denoted as an “alr”, “alrA” or “dal” gene.
Other definitions of terms may appear throughout the specification.
As noted above, a method of amplifying a genomic locus is provided. Several general features of the instant method are illustrated in
The amplification unit provides for expression of the polypeptide of interest and the essential enzyme in the cell. In certain cases, region P and region M may independently comprise an expression cassette (i.e., a coding sequence operably linked to a promoter) for the polypeptide of interest and the essential enzyme, respectively. In some embodiments, the amplification unit comprises a first expression cassette for expressing the polypeptide of interest, and a second cassette for expressing the essential enzyme. In other embodiments, the coding sequence of region P may be operably linked to a promoter that is present in the adjacent direct repeat In this embodiment and as will be discussed in greater detail below, the combined nucleotide sequence of the direct repeat and coding sequence for the essential enzyme may be endogenous to the cell, i.e., found in the genome of the host cell. In a particular embodiment, the promoter operably linked to the coding sequence of region M may be endogenous or non-endogenous to that coding sequence. In a particular embodiment, the coding sequence of region M may be driven by the promoter operably linked to the coding sequence of P.
As would be readily apparent, the orientation of P and M in any of the nucleic acids described herein may be in the opposite orientation (i.e., A1-M-P-A2). In this opposite orientation and in certain embodiments, region M's coding sequence may be operably linked to a promoter in direct repeat A1. Alternatively, region M's coding sequence may be operably linked to a promoter that is present in region M.
A population of such cells is contacted with the inhibitor of the essential enzyme, and cells that are resistant to the inhibitor (i.e., cells that can grow and divide in the presence of the inhibitor to form colonies) are selected. As shown in
tccattttcttctgctatcaaaataacagactcgtgattttccaaacgag
ctttcaaaaaagcctctgccccttgcaaatcggatgcctgtctataaaatt
cccgatattggttaaacagcggcgcaatggcggccgcatctgatgtctttg
cttggcgaatgttcatcttatttcttcctccctctcaataattttttcatt
ctatcccttttctgtaaagtttatttttcagaatacttttatcatcatgct
ttgaaaaaatatcacgataatatccattgttctcacggaagcacacgcagg
tcatttgaacgaattttttcgacaggaatttgccgggactcaggagcattt
aacctaaaaaagcatgacatttcagcataatgaacatttactcatgtctat
tttcgttcttttctgtatgaaaatagttatttcgagtctctacggaaatag
cgagagatgatatacctaaatagagataaaatcatctcaaaaaaatgGGTC
TActaaaatattattccaTTTATTacaataaattcacagaatagtctttta
agtaagtctactctgaatttttttaaaaggagagggtaaagagtgagaagc
aaaaaattgtggatcagtttgctgtttgctttagcgttaatctttacgatg
gcgttcggcagcacatcctctgcccaggcggcagggaaatcaaacggggaa
aagaaatatattgtcgggtttaaacagacaatgagcacgatgagcgccgct
aagaagaaagatgtcatttctgaaaaaggcgggaaagtgcaaaagcaattc
aaatatgtagacgcagcttcagctacattaaacgaaaaagctgtaaaagaa
ttgaaaaaagacccgagcgtcgcttacgttgaagaagatcacgtagcacat
gcgtacgcgcagtccgtgccttacggcgtatcacaaattaaagcccctgct
ctgcactctcaaggctacactggatcaaatgttaaagtagcggttatcgac
agcggtatcgattcttctcatcctgatttaaaggtagcaggcggagccagc
atggttccttctgaaacaaatcctttccaagacaacaactctcacggaact
cacgttgccggcacagttgcggctcttaataactcaatcggtgtattaggc
gttgcgccaagcgcatcactttacgctgtaaaagttctcggtgctgacggt
tccggccaatacagctggatcattaacggaatcgagtgggcgatcgcaaac
aatatggacgttattaacatgagcctcggcggaccttctggttctgctgct
ttaaaagcggcagttgataaagccgttgcatccggcgtcgtagtcgttgcg
gcagccggtaacgaaggcacttccggcagctcaagcacagtgggctaccct
ggtaaatacccttctgtcattgcagtaggcgctgttgacagcagcaaccaa
agagcatctttctcaagcgtaggacctgagcttgatgtcatggcacctggc
gtatctatccaaagcacgcttcctggaaacaaatacggcgcgttgaacggt
acatcaatggcatctccgcacgttgccggagcggctgattgattattctaa
gcacccgaactggacaaacactcaagtccgcagcagtttagaaaacaccac
tacaaaacttggtgattattctactatggaaaagggctgatcaacgtacag
gcggcagctcagtaaaacataaaaaaccggccttggccccgccggtttttt
gagatacgtgggcggaaattgacttgtccgcgataaaggaaaatgtcagca
atatgaaaaaacatatcggtgaacatgtccacttgatggcagttgtgaaag
caaacgcctacgggcatggtgatgcagaaacagcaaaggctgctcttgacg
caggtgcttcatgcttggccgtggccattttggatgaagcgatttcactgc
gcaaaaagggattgaaggcgcctatattggtgcttggcgcggttcccccgg
agtatgtggcaatcgctgctgagtatgacgtgaccttaacaggttattctg
ttgaatggcttcaggaggcagcccgccacacgaaaaaaggttctcttcatt
ttcatctgaaggtcgatacggggatgaacagacttggtgtaaaaacagagg
aagaagttcagaacgtgatggcaattcttgaccgcaaccctcgtttaaagt
gcaaaggggtatttacccattttgcgacagcggatgaaaaagaaagaggct
atttcttaatgcagtttgagcgctttaaagagctgattgctccgctgccgt
taaagaatctaatggtccactgcgcgaacagcgccgctggactccggctga
aaaaaggcttttttaatgcagtcagattcggcatcggcatgtatggccttc
gcccgtctgctgacatgtcggacgagataccgtttcagctgcgtccggcat
ttaccctgcattcgacactgtcacatgtcaaactgatcagaaaaggcgaga
gcgtcagctacggagccgagtacacagcggaaaaagacacatggatcggga
cggtgcctgtaggctatgcggacggctggctccgaaaattgaaagggaccg
acatccttgtgaagggaaaacgcctgaaaattgccggccgaatttgcatgg
accaatttatggtggagctggatcaggaatatccgccgggcacaaaagtca
cattaataggccggcagggggatgaatatatttccatggatgagattgcag
gaaggctcgaaaccattaactatgaggtggcctgtacaataagttcccgtg
ttccccgtatgtttttggaaaatgggagtataatggaagtaagaaatcctt
tattgcaggtaaatataagcaattaacctaatgactggcttttataatatg
caaaataacagactcgtgattttccaaacgagctttcaaaaaagcctctgc
cccttgcaaatcggatgcctgtctataaaattcccgatattggcttaaaca
gcggcgcaatggcggccgcatctgatgtctttgcttggcgaatgttcatct
tatttcttcctccctctcaataattttttcattctatcccttttctgtaaa
gtttatttttcagaatacttttatcatcatgctttgaaaaaatatcacgat
aatatccattgttctcacggaagcacacgcaggtcatttgaacgaattttt
tcgacaggaatttgccgggactcaggagcatttaacctaaaaaagcatgac
atttcagcataatgaacatttactcatgtctattttcgttcttttctgtat
gaaaatagttatttcgagtctctacggaaatagcgagagatgatataccta
aatagagataaaatcatctcaaaaaaatgGGTCTActaaaatattattcca
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wherein repeat units A1 and A2 are shown underlined, the polynucleotide sequence encoding the protein of interest i.e. the subtilisin FNA, is shown in bolded letters, and the polynucleotide sequence encoding the essential enzyme e.g. alanine racemase, is shown in italics. Promoter sequences are shown in bolded capital letters.
Since the host cells made by the method contain more copies of the first expression cassette, the cells may produce more polypeptide of interest encoded by the first expression cassette than host cells that have a single copy of the A1-P-M-A2 amplification unit. In particular embodiments, the resultant host cells may produce at least 20%, at least 40% at least 60%, at least 80% at least 100%, at least twice, at least three times, at least four times, at least five times or at least 10 times, up to about 100 times more protein as compared to otherwise identical host cells that have a single copy of the A1-P-M-A2 amplification unit.
The concentration of the inhibitor employed in the subject methods may vary with the essential enzyme used and the potency of the inhibitor. In particular embodiments, the inhibitor may be at a concentration in the range of 1 μM to 100 mM, e.g., in the range of 5 μM to 10 mM, 20 μM to 1 mM, although inhibitor concentrations outside of these ranges are envisioned. The inhibitor may be added to a liquid culture, or may be present in solid media (e.g., agar media) upon which the bacteria are grown. As noted above, the population of cells may be subjected to several rounds of selection, with each round of selection using a successively increasing concentration of inhibitor (e.g., a successive doubling in the concentration of inhibitor).
In a particular embodiment, the amplification unit does not contain an antibiotic resistance marker, and cell selection may be done in an antibiotic-free medium.
The first and second expression cassettes, and the host cells, are described in greater detail below.
As noted above, the amplification unit provides for expression of the polypeptide of interest and of the essential enzyme. As such, the amplification unit generally contains at least two expression cassettes: a first expression cassette for the expression of the polypeptide of interest, and a second expression cassette for the expression of the essential gene. Each expression cassette contains, in operable linkage: a promoter, a coding sequence, and a terminator. In certain cases, region P of the amplification unit may comprise the first expression cassette and region M of the amplification unit may comprise the second expression cassette. In other cases and as noted above, the direct repeat adjacent to region P may contain a promoter operably linked to the coding sequence of region P. In certain cases, the contiguous nucleotide sequence of region P and the direct repeat adjacent to region P may be endogenous to the host cell (i.e., present in the genome of the host cell). In a particular embodiment, the coding sequence of region M may be operably linked to a promoter of region P.
Each expression cassette discussed herein may contain the following elements in operable linkage: a promoter, a coding sequence, and a terminator sequence, where the expression cassette is sufficient for the production of the protein in the host cell. As will be discussed in greater detail below, the coding sequence of the first expression cassette may encode a recombinant protein, e.g., a therapeutic protein or so-called “industrial enzyme”. In particular embodiments, this coding sequence may encode a protein having a signal sequence that provides for secretion of the protein from the cell. As noted above and as will be described in greater detail below, the second expression cassette provides for expression of an essential enzyme.
The choice of promoters, terminators and signal sequence, if used, largely depends on the host cell used. Host cells include Bacillus sp. host cell, Streptomyces sp. host cells, E. coli, and other bacterial host cells. As noted above, in exemplary embodiments, a Streptomyces host cell may employed, in which case the signal sequence, if used, may be a celA signal sequence. In certain cases, the celA signal sequence may be the signal sequence encoded by the S. lividans cellulase A gene, CelA, as described by Kluepfel et al. (Nature Biotechnol. 1996 14:756-759). In other exemplary embodiments in which a Bacillus host cell is employed, the signal sequence may be any sequence of amino acids that is capable of directing the fusion protein into the secretory pathway of the Bacillus host cell. In certain cases, signal sequences that may be employed include the signal sequences of proteins that are secreted from wild-type Bacillus cells. Such signal sequences include the signal sequences encoded by α-amylase, protease, e.g., aprE or subtilisin E, or β-lactamase genes. Exemplary signal sequences include, but are not limited to, the signal sequences encoded by an α-amylase gene, a subtilisin gene, a β-lactamase gene, a neutral protease gene (e.g., nprT, nprS, nprM), or a prsA gene from any suitable Bacillus species, including, but not limited to B. stearothermophilus, B. licheniformis, B. clausii, B. subtilis and B. amyloliquefaciens. In one embodiment, the signal sequence is encoded by the aprE gene of B. subtilis (as described in Appl. Microbiol. Biotechnol. 2003 62:369-73). Further signal peptides are described by Simonen and Palva (Microbiological Reviews 1993 57: 109-137), and other references.
Suitable promoters and terminators for use in Bacillus and Streptomyces host cells are known and include: the promoters and terminators of apr (alkaline protease), npr (neutral protease), amy (α-amylase) and β-lactamase genes, as well as the B. subtilis levansucrase gene (sacB), B. licheniformis alpha-amylase gene (amyL), B. stearothermophilus maltogenic amylase gene (amyM), B. amyloliquefaciens alpha-amylase gene (amyQ), B. licheniformis penicillinase gene (penP), B. subtilis xylA and xylB genes, the promoters and terminators described in WO 93/10249, WO 98/07846, and WO 99/43835. Expression cassettes for use in Streptomyces host cells can be constructed using the promoters and terminators described in Hopwood et al (Genetic Manipulation of Streptomyces: A Laboratory Manual; Cold Spring Harbor Laboratories, 1985), Hopwood et al (Regulation of Gene Expression in Antibiotic-producing Streptomyces. In Booth, I. and Higgins, C. (Eds) Symposium of the Society for General Microbiology, Regulation of Gene Expression, Cambridge University Press, 1986 pgs. 251-276), Formwald et al (Proc. Natl. Acad. Sci. 1987 84: 2130-2134), Pulido et al (Gene. 1987 56:277-82); Dehottay et al (Eur. J. Biochem. 1987 166:345-50), Taguchi (Gene. 1989 84:279-86), Schmitt-John et al (Appl. Microbiol. Biotechnol. 1992 36:493-8), Motamedi (Gene 1995 160:25-31) and Binnie (Protein Expr. Purif. 1997 11:271-8), for example. In one embodiment, the A4 promoter may be employed, which promoter is described in WO 06/054997, which is incorporated by reference herein.
In certain embodiments, either of the coding sequences may be codon optimized for expression of the polypeptide of interest in the host cell used. Since codon usage tables listing the usage of each codon in many cells are known in the art (see, e.g., Nakamura et al, Nucl. Acids Res. 2000 28: 292) or readily derivable, such nucleic acids can be readily designed giving the amino acid sequence of the proteins to be expressed.
Systems for expression of recombinant proteins in Streptomyces and Bacillus host cells are well known in the art and need not be discussed in any greater detail than that set forth above.
First Expression Cassette
A first expression may comprise a promoter and a polynucleotide encoding a protein of interest (i.e., a coding sequence), where the promoter and the polynucleotide are operably linked such that the isolated nucleic acid causes transcription of the polynucleotide and production of the protein of interest.
The encoded protein of interest may be a so called “industrial enzyme”, a therapeutic protein, a reporter protein, a food additive or a foodstuff or the like. In one embodiment, the protein of interest may be an enzyme such as a carbohydrase, such as a liquefying and saccharifying α-amylase, an alkaline α-amylase, a β-amylase, a cellulase; a dextranase, an α-glucosidase, an α-galactosidase, a glucoamylase, a hemicellulase, a pentosanase, a xylanase, an invertase, a lactase, a naringanase, a pectinase or a pullulanase; a protease such as an acid protease, an alkali protease, bromelain, ficin, a neutral protease, papain, pepsin, a peptidase, rennet, rennin, chymosin, subtilisin, thermolysin, an aspartic proteinase, or trypsin; a lipase or esterase, such as a triglyceridase, a phospholipase, a pregastric esterase, a phosphatase, a phytase, an amidase, an iminoacylase, a glutaminase, a lysozyme, or a penicillin acylase; an isomerase such as glucose isomerase; an oxidoreductase, e.g., an amino acid oxidase, a catalase, a chloroperoxidase, a glucose oxidase, a hydroxysteroid dehydrogenase or a peroxidase; a lyase such as an acetolactate decarboxylase, an aspartic β-decarboxylase, a fumarase or a histadase; a transferase such as cyclodextrin glycosyltranferase; or a ligase, for example. In particular embodiments, the protein may be an aminopeptidase, a carboxypeptidase, a chitinase, a cutinase, a deoxyribonuclease, an α-galactosidase, a β-galactosidase, a β-glucosidase, a laccase, a mannosidase, a mutanase, a pectinolytic enzyme, a polyphenoloxidase, ribonuclease or transglutaminase, for example. In particular embodiments, the protein of interest encoded by the first expression cassette is a detergent-additive protein, i.e., a protein (e.g., an enzyme) that is: a) secreted from the cell and b) to be added to laundry detergent. Exemplary detergent-additive proteins include proteases, e.g., subtilisins, α-amylases and lipases. Subtilisins, i.e., extracellular alkaline serine proteases, are of particular interest. A subtilisin may have an amino acid sequence that is found in a wild type genome (i.e., the subtilisin may be a naturally-occurring subtilisin) or may be a variant of a naturally-occurring subtilisin and thus may contain an amino acid sequence that is at least 80%, at least 90%, at least 95% or at least 98% identical to a subtilisin encoded by a wild-type genome. Exemplary subtilisins include: Alcanase® (Novozymes), FNA™ (Genencor), Savinase® (Novozymes), Purafect™ (Genencor), KAP™ (Kao), Everlase™ (Novozymes), Purafect OxP™ (Genencor), FN4™ (Genencor), BLAP S™ (Henkel), BLAP X™ (Henkel), Esperase® (Novozymes), Kannase™ (Novozymes) and Prosperase™ (Genencor). In other embodiments, the subtilisin may be subtilisin 168, subtilisin BPN', subtilisin Carlsberg, subtilisin DY, subtilisin 147 or subtilisin 309 (See e.g., EP414279B, WO89/06279 and Stahl et al., J. Bacteriol. 1984 159:811-818). In some embodiments, the subtilisin encoded by the first expression cassette is FNA VRSKKLWISLLFALALIFTMAFGSTSSAQAAGKSNGEKKYIVGFKQTMSTMSAAKKKDVI SEKGGKVQKQFKYVDAASATLNEKAVKELKKDPSVAYVEEDHVAHA YAQSVPYGVSQ IKAPALHSQGYTGSNVKVAVIDSGIDSSHPDLKVAGGASMVPSETNPFQDNNS HGTHVAGTVAALNNSIGVLGVAPSASLYAVKVLGADGSGQYSWIINGIEWAIA NNMDVINMSLGGPSGSAALKAAVDKAVASGVVVVAAAGNEGTSGSSSTVGYP GKYPSVIAVGAVDSSNQRASFSSVGPELDVMAPGVSIQSTLPGNKYGALNGTS MASPHVAGAAALILSKHPNWTNTQVRSSLENTTTKLGDSFYYGKGLINVQAA AQ (SEQ ID NO:8). The pre-pro region of the subtilisin is shown in italics, and the mature region is shown in bolded letters (SEQ ID NO:12). An example of a polynucleotide that encodes FNA is:
Exemplary subtilisins and other proteases that may be employed herein include those described in WO 99/20770; WO 99/20726; WO 99/20769; WO 89/06279; RE 34,606; U.S. Pat. No. 4,914,031; U.S. Pat. No. 4,980,288; U.S. Pat. No. 5,208,158; U.S. Pat. No. 5,310,675; U.S. Pat. No. 5,336,611; U.S. Pat. No. 5,399,283; U.S. Pat. No. 5,441,882; U.S. Pat. No. 5,482,849; U.S. Pat. No. 5,631,217; U.S. Pat. No. 5,665,587; U.S. Pat. No. 5,700,676; U.S. Pat. No. 5,741,694; U.S. Pat. No. 5,858,757; U.S. Pat. No. 5,880,080; U.S. Pat. No. 6,197,567; and U.S. Pat. No. 6,218,165. Subtilisins in general are reviewed in great detail in Siezen (Protein Sci. 1997 6:501-523), and detergent-additive subtilisins are reviewed in Bryan (Biochim Biophys. Acta 2000 1543:203-222), Maurer (Current Opinion in Biotechnology 2004 15:330-334) and Gupta (Appl Microbiol Biotechnol. 2002 59:15-32). Certain subtilisins of interest have an activity described as EC 3.4.4.16, according to IUBMB enzyme nomenclature.
In other embodiments, the protein of interest may be a therapeutic protein (i.e., a protein having a therapeutic biological activity). Examples of suitable therapeutic proteins include: erythropoietin, cytokines such as interferon-α, interferon-β, interferon-γ, interferon-o, and granulocyte-CSF, GM-CSF, coagulation factors such as factor VIII, factor IX, and human protein C, antithrombin III, thrombin, soluble IgE receptor α-chain, IgG, IgG fragments, IgG fusions, IgM, IgA, interleukins, urokinase, chymase, and urea trypsin inhibitor, IGF-binding protein, epidermal growth factor, growth hormone-releasing factor, annexin V fusion protein, angiostatin, vascular endothelial growth factor-2, myeloid progenitor inhibitory factor-1, osteoprotegerin, α-1-antitrypsin, α-feto proteins, DNase II, kringle 3 of human plasminogen, glucocerebrosidase, TNF binding protein 1, follicle stimulating hormone, cytotoxic T lymphocyte associated antigen 4-Ig, transmembrane activator and calcium modulator and cyclophilin ligand, soluble TNF receptor Fc fusion, glucagon like protein 1 and IL-2 receptor agonist. Antibody proteins, e.g., monoclonal antibodies that may be humanized, are of particular interest.
In a further embodiment, the protein of interest may be a reporter protein. Such reporter proteins may be optically detectable or colorigenic, for example. In this embodiment, the protein may be a β-galactosidase (lacZ), β-glucuronidase (GUS), luciferase, alkaline phosphatase, nopaline synthase (NOS), chloramphenicol acetyltransferase (CAT), horseradish peroxidase (HRP) or a fluorescent protein, e.g., green fluorescent protein (GFP), or a derivative thereof.
As noted above, the coding sequence may encode a fusion protein. In some of these embodiments, the fusion protein may provide for secretion of the protein of interest from the host cell in which it is expressed and, as such, may contain a signal sequence operably linked to the N-terminus of the protein of interest, where the signal sequence contains a sequence of amino acids that directs the protein to the secretory system of the host cell, resulting in secretion of the protein from the host cell into the medium in which the host cell is growing. The signal sequence is cleaved from the fusion protein prior to secretion of the protein of interest.
Second Expression Cassette
The second expression cassette provides for expression of an essential enzyme where, as noted above, an essential enzyme is required by the cell for cell growth. In particular embodiments, the essential enzyme may be conditionally essential in that it is required for cell growth only under certain conditions (e.g., in the absence of an exogenous compound that negates any loss of the essential enzyme). In certain cases, cells lacking activity of a conditionally essential enzyme (which may be made by inactivating the gene encoding the enzyme, or by contacting the cells with an inhibitor of the enzyme) may be grown in culture by adding an exogenous compound, which in certain cases may be a product of the enzyme or alternative carbon source. Thus, in certain cases, the essential enzyme employed in the second expression cassette may be an enzyme that, when absent from a cell, renders the cell auxotrophic for a specific compound or unable to utilize one or more specific carbon sources.
Examples of such essential enzyme/inhibitor combinations are known and include, for example: enzymes that are involved in amino acid synthesis and their respective inhibitors; and enzymes involved in utilization of a specific carbon source, and their respective inhibitors. Examples of such enzymes/inhibitor combinations are set forth below. Inactivation of a gene encoding an enzyme involved in the synthesis of an amino acid causes auxotrophy for that amino acid Likewise, inactivation of a gene encoding an enzyme involved in the utilization of a specific carbon source causes auxotrophy for another carbon source. The enzyme does not cleave the inhibitor. Rather, the inhibitor reversibly and specifically inhibits the catalytic activity of the enzyme, either competitively or non-competitively.
In one embodiment, the enzyme may be S-adenosyl-methionine synthetase (encoded by metE; Genbank accession no. U52812; see Yocum et al, Cloning and characterization of the metE gene encoding S-adenosylmethionine synthetase from Bacillus subtilis. J. Bacteriol. 1996 178:4604) which can be inhibited by cycloleucine (Chiang et al Molecular characterization of Plasmodium falciparum S-adenosylmethionine synthetase. Biochem J. 1999 344:571-6) as well as methionine analogs, purine analogs, 8-azaguanine and azathioprine (Berger et al Characterisation of methionine adenosyltransferase from Mycobacterium smegmatis and M. tuberculosis BMC Microbiol. 2003; 3: 12). Inactivation of the S-adenosyl-methionine synthetase gene causes methionine auxotrophy.
In another embodiment, the enzyme may be 3-isopropylmalate dehydrogenase, which catalyzes the conversion of 3-carboxy-2-hydroxy-4-methylpentanoate to 3-carboxy-4-methyl-2-oxopentanoate. This enzyme is encoded by leuB, and leuB-deficient strains are leucine auxotrophs. 3-isopropylmalate dehydrogenase can be inhibited by, for example, O-isobutenyl oxalylhydroxamate (Singh et al The High-resolution Structure of LeuB (Rv2995c) from Mycobacterium tuberculosis Journal of Molecular Biology 2005 346: Pages 1-11).
In another embodiment, the enzyme may be diaminopimelate decarboxylase, which catalyses the conversion of Meso-2,6-diaminoheptanedioate to L-lysine and is encoded by lysA. A lysA-deficient strain will be a lysine auxotroph Inhibitors of diaminopimelate decarboxylase include analogs of diaminopimelic acid including, but not limited to: Lanthionine sulfoxides, meso and LL-isomers of lanthionine sulfone, lanthionine, N-modified analogs including N-hydroxydiaminopimelate 4 and N-aminodiaminopimelate 5 (see Kelland et al J. Biol. Chem. 1986 Analogs of diaminopimelic acid as inhibitors of meso-diaminopimelate decarboxylase from Bacillus sphaericus and wheat germ 261: 13216-13223).
In another embodiment, the enzyme may be glutamyl-tRNA reductase, which catalyses the synthesis of 5-amino levulinic acid and is encoded by hemA. A hemA-deficient strain is auxotrophic for 5-amino levulinic acid or haemin. This enzyme can be inhibited by glutamycin (Schauer et al Escherichia coli Glutamyl-tRNA Reductase J. Biol. Chem. 2002 277: 48657-48663).
In a further embodiment, the enzyme may be D-alanine racemase, which catalyzes the interconversion of L-alanine and D-alanine and is encoded by alr (also known as dal). An alr deficient strain is auxotrophic for D-alanine, which is required for cell wall biosynthesis Inhibitors of D-alanine racemase include, but are not limited to, D-cycloserine, β-chloro-D-alanine and O-carbamyl-D-serine (see, e.g., Manning et al, Inhibition of Bacterial Growth by β-chloro-D-alanine PNAS1974 71: 417-421). In some embodiments, the second expression cassette comprises a polynucleotide e.g. atgagcac aaaacctttt tacagagata cgtgggcgga aattgacttg tccgcgataa aggaaaatgt cagcaatatg aaaaaacata tcggtgaaca tgtccacttg atggcagttg tgaaagcaaa cgcctacggg catggtgatg cagaaacagc aaaggctgct cttgacgcag gtgcttcatg cttggccgtg gccattttgg atgaagcgat ttcactgcgc aaaaagggat tgaaggcgcc tatattggtg cttggcgcgg ttcccccgga gtatgtggca atcgctgctg agtatgacgt gaccttaaca ggttattctg ttgaatggct tcaggaggca gcccgccaca cgaaaaaagg ttctcttcat tttcatctga aggtcgatac ggggatgaac agacttggtg taaaaacaga ggaagaagtt cagaacgtga tggcaattct tgaccgcaac cctcgtttaa agtgcaaagg ggtatttacc cattttgcga cagcggatga aaaagaaaga ggctatttct taatgcagtt tgagcgcttt aaagagctga ttgctccgct gccgttaaag aatctaatgg tccactgcgc gaacagcgcc gctggactcc ggctgaaaaa aggctttttt aatgcagtca gattcggcat cggcatgtat ggccttcgcc cgtctgctga catgtcggac gagataccgt ttcagctgcg tccggcattt accctgcatt cgacactgtc acatgtcaaa ctgatcagaa aaggcgagag cgtcagctac ggagccgagt acacagcgga aaaagacaca tggatcggga cggtgcctgt aggctatgcg gacggctggc tccgaaaatt gaaagggacc gacatccttg tgaagggaaa acgcctgaaa attgccggcc gaatttgcat ggaccaattt atggtggagc tggatcagga atatccgccg ggcacaaaag tcacattaat aggccggcag ggggatgaat atatttccat ggatgagatt gcaggaaggc tcgaaaccat taactatgag gtggcctgta caataagttc ccgtgttccc cgtatgtttt tggaaaatgg gagtataatg gaagtaagaa atcctttatt gcaggtaaat ataagcaatt aa (SEQ ID NO:10), which encodes D-alanine racemase MSTKPFYRDTWAEIDLS AIKENVSNMKKHIGEHVHLMAVVKANAYGHGDAETAK AALDAGASCLAVAILDEAISLRKKGLKAPILVLGAVPPEYVAIAAEYDVTLTGYSV EWLQEAARHTKKGSLHFHLKVDTGMNRLGVKTEEEVQNVMAILDRNPRLKCKG VFTHFATADEKERGYFLMQFERFKELIAPLPLKNLMVHCANSAAGLRLKKGFFNA VRFGIGMYGLRPSADMSDEIPFQLRPAFTLHSTLSHVKLIRKGESVSYGAEYTAEK DTWIGTVPVGYADGWLRKLKGTDILVKGKRLKIAGRICMDQFMVELDQEYPPGT KVTLIGRQGDEYISMDEIAGRLETINYEVACTISSRVPRMFLENGSIMEVRNPLLQV NISN (SEQ ID NO:11).
Other essential enzymes for which inhibitors may be used include: xylose isomerase (xylA), gluconate kinase (EC 2.7.1.12), gluconate permease (gntK or gntP), glycerol kinase, glycerol dehydrogenase, e.g., glpP, glpF, glpK, or the glpD or arabinose isomerase (araA), for example.
In particular embodiments, the second expression cassette provides for significant expression of an essential enzyme, in that the essential enzyme is produced at a level that is more than 50% (e.g., at least about 70%, at least about 90% or at least about 100%, up to at least about 1000%) of the level of an endogenous essential enzyme, if the gene for the endogenous essential enzyme is wild-type (i.e., not inactivated) in the cell.
In certain embodiments, the essential enzyme encoded by region M may be naturally-occurring in that it has the amino acid sequence of a wild-type essential enzyme. In other embodiments, the essential enzyme encoded by region M may be a variant of a naturally-occurring enzyme, e.g., may have an amino acid sequence that is at least about 80% identical to, at least about 90% identical to, at least about 95% identical to, at least about 98% identical to, or at least about 99% identical to a naturally occurring essential enzyme.
In particular embodiments, the essential enzyme may have a naturally occurring amino acid sequence and, in certain embodiments, may be endogenous to the host cell in that it has an amino acid sequence that is encoded by the genome of the host cell, prior to any inactivation mutations.
In particular embodiments, nucleotide sequence of the expression cassette (i.e., the promoter, coding sequence and terminator) may be of a gene that is endogenous to the host cell, prior to any inactivating mutations. Such a gene may be at a different genomic locus to the locus of the expression cassettes.
Although not required for practice of the instant method, the endogenous gene for the essential enzyme (i.e., a gene that is present in a host cell that does not yet contain the A1-P-M-A2 locus) may be inactivated by mutation. Methods for specifically inactivating bacterial genes, e.g., by deletion, substitution or insertion, are well known in the art.
The bacterial host cells employed herein may be gram positive or gram negative and include, but are not limited to: Bacillus sp. bacteria, e.g., Bacillus clausii, Bacillus amyloliquefaciens, Bacillus brevis, Bacillus circulans, Bacillus coagulans, Bacillus lautus, Bacillus lentus, Bacillus licheniformis, Bacillus megaterium, Bacillus stearothermophilus, Bacillus subtilis, or Bacillus thuringiensis bacteria; Streptomyces sp. bacteria, e.g., S. lividans, S. carbophilus, S. helvaticus, S. rubiginosus or S. murinus bacteria, Pseudomonas sp. bacteria and E. coli. In particular cases, the bacterial host cells may be cells of a strain that has a history of use for production of proteins that has GRAS status, i.e., a Generally Recognized as Safe, by the FDA.
B. subtilis host cells include but not limited to those described in U.S. Pat. Nos. 5,264,366 and 4,760,025 (RE 34,606), as well as 1A6 (ATCC 39085), 168 (1A01), SB19, W23, Ts85, B637, PB1753 through PB1758, PB3360, JH642, 1A243 (ATCC 39,087), ATCC 21332, ATCC 6051, MI113, DE100 (ATCC 39,094), GX4931, PBT 110, and PEP 211 strain (See e.g., Hoch et al., Genetics 1973 73:215-228; U.S. Pat. No. 4,450,235; U.S. Pat. No. 4,302,544; and EP 0134048). The use of B. subtilis as an expression host is also described by Palva et al. and others (See, Palva et al., Gene 1982 19:81-87; also see Fahnestock and Fischer, J. Bacteriol. 1986 165:796-804; and Wang et al., Gene 1988 69:39-47), for example.
In particular embodiments, the Bacillus host cell may be engineered to maximize protein expression, and, as such, may contain an inactivating alteration in at least one of the following genes, degU, degS, degR and degQ. See, Msadek et al. (J. Bacteriol. 1990 172:824-834) and Olmos et al, (Mol. Gen. Genet. 1997 253:562-567). One strain is of the species Bacillus subtilis and carries a degU32(Hy) mutation. In another embodiment, the Bacillus host cell may comprise a mutation or deletion in scoC4, (See, Caldwell et al., J. Bacteriol. 2001 183:7329-7340); spollE (See, Arigoni et al., Mol. Microbiol. 1999 31:1407-1415); oppA or another gene in the opp operon (See, Perego et al., Mol. Microbiol. 1991 5:173-185).
The bacterial cells used in the subject method may be made by inserting recombinant nucleic acid into a genome of a bacterial host cell. In particular embodiments, the cells may be made by homologous or non-homologous recombination using a method similar to established methods, such as those of Jung et al (J. Gen. Appl. Microbiol. 1998 44 107-111); Tangney et al (FEMS Microbio. Lett. 1995 125: 107-114); Petit et al (EMBO J. 1992 11:1317-1326); U.S. Pat. No. 5,733,753 and published US patent application 20070134760.
The host cell may or may not have an inactivated endogenous gene encoding the essential enzyme.
Methods of using the above-described cells are also provided. In certain embodiments, the subject methods include: culturing a population of cell to produce the protein of interest encoded by the first expression cassette. In certain embodiments and as discussed above, the protein of interest may be secreted into the culture medium. Particular embodiments of the method include the step of recovering the protein of interest from the culture medium.
The protein of interest may be recovered from growth media by any convenient method, e.g., by precipitation, centrifugation, affinity, filtration or any other method known in the art. For example, affinity chromatography (Tilbeurgh et al., (1984) FEBS Lett. 16:215); ion-exchange chromatographic methods (Goyal et al., (1991) Biores. Technol. 36:37; Fliess et al., (1983) Eur. J. Appl. Microbiol. Biotechnol. 17:314; Bhikhabhai et al., (1984) J. Appl. Biochem. 6:336; and Ellouz et al., (1987) Chromatography 396:307), including ion-exchange using materials with high resolution power (Medve et al., (1998) J. Chromatography A 808:153; hydrophobic interaction chromatography (Tomaz and Queiroz, (1999) J. Chromatography A 865:123; two-phase partitioning (Brumbauer, et al., (1999) Bioseparation 7:287); ethanol precipitation; reverse phase HPLC; chromatography on silica or on a cation-exchange resin such as DEAE; chromatofocusing; SDS-PAGE; ammonium sulfate precipitation; and gel filtration using, e.g., Sephadex G-75, may be employed. In particular embodiments, the detergent-additive protein may be used without purification from the other components the culture medium. In certain embodiments, the components of the culture medium may simply be concentrated, for example, and then used without further purification of the protein from the other components of the growth medium.
In some embodiments, a cell may be cultured under batch or continuous fermentation conditions. Classical batch fermentation methods use a closed system, where the culture medium is made prior to the beginning of the fermentation run, the medium is inoculated with the desired organism(s), and fermentation occurs without the subsequent addition of any components to the medium. In certain cases, the pH and oxygen content, but not the carbon source content, of the growth medium may be altered during batch methods. The metabolites and cell biomass of the batch system change constantly up to the time the fermentation is stopped. In a batch system, cells usually progress through a static lag phase to a high growth log phase and finally to a stationary phase where growth rate is diminished or halted. If untreated, cells in the stationary phase eventually die. In general terms, the cells in log phase produce most protein.
A variation on the standard batch system is the “fed-batch fermentation” system. In this system, nutrients (e.g., a carbon source, nitrogen source, salts, O2, or other nutrient) are only added when their concentration in culture falls below a threshold. Fed-batch systems are useful when catabolite repression is apt to inhibit the metabolism of the cells and where it is desirable to have limited amounts of nutrients in the medium. Measurement of the actual nutrient concentration in fed-batch systems is estimated on the basis of the changes of measurable factors such as pH, dissolved oxygen and the partial pressure of waste gases such as CO2. Batch and fed-batch fermentations are common and known in the art.
Continuous fermentation is an open system where a defined culture medium is added continuously to a bioreactor and an equal amount of conditioned medium is removed simultaneously for processing. Continuous fermentation generally maintains the cultures at a constant high density where cells are primarily in log phase growth.
Continuous fermentation allows for the modulation of one factor or any number of factors that affect cell growth and/or end product concentration. For example, in one embodiment, a limiting nutrient such as the carbon source or nitrogen source is maintained at a fixed rate and all other parameters are allowed to moderate. In other systems, a number of factors affecting growth can be altered continuously while the cell concentration, measured by media turbidity, is kept constant. Continuous systems strive to maintain steady state growth conditions. Thus, cell loss due to medium being drawn off may be balanced against the cell growth rate in the fermentation. Methods of modulating nutrients and growth factors for continuous fermentation processes as well as techniques for maximizing the rate of product formation are known.
The following examples are provided in order to demonstrate and further illustrate certain preferred embodiments and aspects of the present invention and are not to be construed as limiting the scope thereof.
The experimental techniques used to manipulate DNA were standard techniques within the field of molecular biology (Sambrook et al. Molecular cloning: A Laboratory Manual). Plasmids were prepared and inserts purified using Qiagen kits (Qiagen Inc.). Restriction endonucleases and other enzymes were purchased from Roche Applied Science (Indianapolis, Ind.) and used as recommended by the manufacturers. Competent B. subtilis cells were prepared as described by Ferrari E. and B. Miller (Bacillus expression: a Gram-Positive Model. In Gene Expression Systems: Using Nature for the Art of Expression. 1999. Academic Press, N.Y.).
PCR reactions were performed with Herculase enzyme (Stratagene) according to the manufacturer's instructions. The reaction contained 200 nM of each primer, 1 unit of Herculase and 200 μM of each dNTP. A PxE Thermal Cycler from Hybaid (Thermo) was used with the following cycle: denaturation at 94° C. for 3 min., followed by 30 cycle of denaturation at 94° C. for 30 s, annealing at 55° C. for 30 s and extension at 72° C. for 1 min/1 kbp to be amplified. The PCR reaction was then analyzed on 0.8% agarose e-gels from Invitrogen.
Genomic DNA was prepared using Eppendorf Phase Lock Gel tubes (Eppendorf) and their protocol.
D-alanine, D-cycloserine and β-chloro-D-alanine were obtained from Sigma.
Assays for subtilisin were carried out as previously described (Estell, D. V., Graycar, T. P., Wells, J. A. (1985) J. Biol. Chem. 260, 6518-6521) in 0.1 M Tris buffer, pH 8.6 containing 1.6 mM N-succinyl-L-Ala-L-Ala-L-Pro-L-Phe-p-nitroanilide (Vega Biochemicals). The assay measures the increase in absorbance at 410 nm/min due to release of p-nitroaniline. Assays were performed under initial rate conditions. A protease unit is defined as the amount of protease enzyme that increases the absorbance at 410 nm by 1 absorbance unit (AU) per minute of the standard solution described above at 25 C in a cuvette with 1 cm path length.
Escherichia coli MM294: endA thiA hsdR17 supE44
Bacillus subtilis strains BG2190 (alr-) and BG2189 (alr-CmR) were described by Ferrari and Yang (1985) (Isolation of an alanine racemase gene from Bacillus subtilis and its use for plasmid maintenance in B. subtilis. Biotechnology, 3, 1003-1007 [1985]).
B. subtilis strain BG3594: nprE aprE spoIIE degU32 oppA
B. subtilis strain BG3594comK: This is B. subtilis BG3594 containing a xylR-PxylA-comK construct as described in WO 02/14490, which allows this strain to be made supercompetent (i.e. greater than 1% of a cell population is transformable with chromosomal Bacillus DNA).
B. subtilis strain CP3490: This strain is B. subtilis strain BG3594comK in which alr is knocked down (same mutation as in BG2190).
B. subtilis strain CP35491: This strain is B. subtilis strain BG3594 in which alr is knocked down (same mutation as in BG2190).
B. subtilis MDT01-138: This strain is B. subtilis strain BG3594 with an amplifiable cassette of the following structure: aprE 5′-subtilisin FNA-Chloramphenicol-aprE 5′. It has been amplified to Cm25.
B. subtilis strain CP4010: This strain is B. subtilis strain BG3594 comK with an amplifiable cassette of the following structure: aprE 5′-subtilisin FNA-alr-aprE 5′. It has been amplified using β-chloro-D-alanine.
B. subtilis strain CP4020: This strain is B. subtilis strain BG3594 with an amplifiable cassette of the following structure: aprE 5′-subtilisin FNA-alr-aprE 5′. It has been amplified using β-chloro-D-alanine.
B. subtilis strain Hyperl: has an amplified cassette encoding subtilisin FNA and containing a chloramphenicol marker.
CP3591: This strain is BG3594 with one copy of subtilisin FNA behind the aprE promoter in the oppA locus (i.e., 1 copy of subtilisin total).
CP3592: This is CP3591 with one additional copy of subtilisin FNA behind the aprE promoter between the ybdL and ybdM genes (i.e., 2 copies of subtilisin total).
CP3593: This is CP3592 with one additional copy of subtilisin FNA behind the aprE promoter in the pps locus (i.e., 3 copies of subtilisin total).
CP3594: This is CP3593 with one additional copy of subtilisin FNA behind the aprE promoter in the nprE locus (i.e., 4 copies of subtilisin total).
pDALsub1 has been described in Ferrari et al. 1985. This plasmid expresses alr. (Ferrari and Yang, Biotechnology, 3, 1003-1007 [1985]).
pBSFNACm (Seq ID NO:1): this plasmid is a pBluescript derivative (Alting-Mees, M. A. and Short, J. M. pBluescript II: gene mapping vectors. Nucleic Acids Res. 17 (22), 9494 (1989)), containing f1 (IG)—the intergenic region of phage f1; rep (pMB1)—the pMB1 replicon responsible for the replication of phagemid; bla (ApR)— gene, coding for beta-lactamase that confers resistance to ampicillin; lacZ-5′-terminal part of lacZ gene encoding the N-terminal fragment of beta-galactosidase; a polypeptide expression cassette comprising aprE 5′ region, a gene coding for a subtilisin (FNA), a chloramphenicol resistance gene from pC194 with its promoter, a repeat of the aprE 5′ region. This plasmid is used to integrate the expression cassette in the 5′ aprE region.
pBSFNAalr (Seq ID NO:2): this plasmid is derivative of pBSFNACm described above. In this plasmid, B. subtilis alr gene with its own promoter replaces the chloramphenicol-resistance gene. This plasmid is used to integrate the expression cassette in the 5′ aprE region.
LB and LB agar (LA), as described in Ausubel, F. M. et al. (eds) “Current Protocols in Molecular Biology”. John Wiley and Sons, 1995. LBG 1% is LB supplemented with 10 g/L glucose. LBSM is LB agar supplemented with 1.6% skimmed milk FNII medium used to study protease production is described in WO05052146A2. Alr-strains are propagated on LB agar+100 mg/L D-alanine
When appropriate, chloramphenicol, ampicillin, cycloserine or β-chloro-D-alanine was added to the plate or the broth.
qPCR to quantify the copy number of the gene encoding the polypeptide of interest to be produced (e.g. subtilisin) was done on an ABI Prism 7000 Sequence Detection System (Applied Biosystems, Foster City, Calif.). The TaqMan Gene Expression Master Mix kit was used as instructed by the manufacturer (Applied Biosystems, Foster City, Calif.).
Strains to be tested were grown in 5 ml of LBG 1% in a 10-ml tube, at 37 C and 250 rpm. At an OD600 of ˜1, 2.5 ml of culture was used to inoculate 25 ml of FNII medium in 250-ml Erlenmeyer shake flasks. The shake flasks were incubated at 37° C. and 250 rpm, and broth samples were taken regularly to measure subtilisin activity.
In a first phase, the concentration of β-chloro-D-alanine (CDA) necessary to inhibit growth of B. subtilis was determined by plating dilutions of LB-grown strain BG3594 on LB agar plates containing different concentrations of CDA. As shown in Table 1, while BG3594 can still grow at a concentration of 20 mg/L, growth is totally inhibited at a concentration of 50 mg/L. In a second phase, pDalsubl was transformed into BG3594 to determine if overexpression of alr can restore growth on inhibitory concentrations of CDA. As shown in Table 1, the presence of the alr-expressing plasmid allows growth on all CDA concentrations tested. This result indicates that a strain containing a chromosomally-encoded expression cassette “polypeptide of interest-alr” can grow on CDA concentrations higher than 20 mg/L only if amplification occurs. Other alanine racemase inhibitors, such as cycloserine, could be used instead of CDA.
The plasmid pBSFNAalr (SEQ ID NO:2) was constructed from pBSFNACm (SEQ ID NO:1) as follows. The B. subtilis alr gene with its own promoter was PCR-amplified using chromosomal DNA as a template. Primers used were EcoRIDrdIalrF (having a DrdI site; gaagaattcg actaggttgt cttttcgtta gacatcgttt ccctttagc; SEQ ID NO:3) and SmaI-alrR (having a SmaI site; ggttcccggg ttaattgctt atatttacct gcaataaagg; SEQ ID NO:4). The PCR product was digested with DrdI/SmaI and religated with the bigger fragment of BsmI/StuI-th digested pBSFNACm. The ligation was transformed in E. coli strain MM294 and plated on carbenicillin 50 ppm. Four colonies from this transformation were inoculated in 5 ml LB+carbenicillin 50 ppm for plasmid purification. The resultant construct was called pBSFNAalr (SEQ ID NO:2).
pBSFNAalr was digested with NotI/ScaI (buffer H), producing four fragments when run on gel. Sizes of the fragments were the following: 3660-2263-1105-174. The biggest piece, containing the cassette 5′-FNA-alr-5′ was gel purified and ligated on itself. The ligation was done with the “rapid ligation” kit (Roche). The circular piece of DNA obtained was submitted to a rolling-circle reaction (Amersham kit) and transformed into competent cells of either CP3590 or CP3591 and plated on LA+1.6% skimmed milk, either BG3594 or BG3594comK and plated on LA+1.6% skimmed milk+50 ppm CDA. Strains with the correct construct would grow on those plates and show a halo due to skimmed milk clearing by the expressed protease.
The cassette can be passed in any strain by transformation with chromosomal DNA of the strains mentioned in the paragraph above and selection on CDA 50. Amplification of the cassette was done by streaking the strain on increasing amount of CDA (up to 200 ppm). Amplified strains have a bigger halo when plated on 1.6% skimmed milk, demonstrating that passing the strain on increasing amounts of CDA leads to amplification of the cassette.
Chromosomal DNA was extracted from strains CP3591, CP3592, CP3593, BG4020, BG4020 amplified and Hyperl. DNA concentration was measured and samples were diluted to the same concentration for each sample. The same amount of DNA for each strain was then used in a qPCR reaction with primers annealing to the subtilisin gene (FNA-R2; ccagtgtagc cttgagag; SEQ ID NO:5 and FNA-F2; acaatgagca cgatgagc; SEQ ID NO:6).
Strains CP3591, CP3592 and CP3593, with 1, 2 and 3 copies of the gene, respectively, were used to build a calibration curve (
Table 2 provides the counts obtained from the qPCR reactions in BG4020, BG4020-amplified and Hyperl strains. The corresponding subtilisin gene copy number was derived from the calibration curve given in
Strains to be tested were grown in 5 ml of LBG 1% in a 10-ml tube, at 37 C and 250 rpm. At an OD600 of ˜1, 2.5 ml of culture was used to inoculate 25 ml of FNII medium in 250-ml Erlenmeyer shake flasks. The shake flasks were incubated at 37° C. and 250 rpm, and broth samples were taken regularly to measure subtilisin activity. Four strains were tested in this way: BG3591 (contains one copy of the subtilisin gene, non-amplifiable), MDT01-138 (amplified using chloramphenicol), BG4020 (strain in which the cassette 5′-subtilisin-alr-5′ has been introduced), BG4020-amplified (BG4020 strains that had been restreaked on increasing concentrations of CDA). MDT01-138 is a strain isogenic to Hyperl—it contains a chloraphenicol marker gene.
The amount of subtilisin protease produced in shake flasks by each of those strains is shown in
These results show that the alr gene can be efficiently used as a non-antibiotic, non-exogenous marker for amplifying an expression cassette encoding a polypeptide of interest, and consequently producing high levels of the polypeptide of interest.
This application claims priority on U.S. Provisional Application 61/040,456 filed on Mar. 28, 2008.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/US09/38511 | 3/27/2009 | WO | 00 | 5/19/2011 |
| Number | Date | Country | |
|---|---|---|---|
| 61040456 | Mar 2008 | US |
