Method for producing protein of interest

Abstract

To provide a method for producing a protein of interest using a gram-positive bacterium with improved productivity.SOLUTION: A method for producing a protein of interest includes culturing a gram-positive bacterium containing a gene encoding a heterologous FK506-binding protein (FKBP) and a gene encoding the protein of interest, or mixed-culturing a gram-positive bacterium containing a gene encoding a heterologous FKBP and a gram-positive bacterium containing a gene encoding the protein of interest.SELECTED DRAWING: None

Description

[Technical field]

[0001] The present invention relates to a method for producing a target protein with improved productivity. [Background technology]

[0002] The industrial production of useful substances by microorganisms is diverse, including foods, amino acids, organic acids, nucleic acid-related substances, antibiotics, carbohydrates, lipids, proteins, etc., and their uses are also widespread, ranging from daily necessities such as foods, medicines, detergents, and cosmetics, to raw materials for various chemical products. Industrially useful host microorganisms include Escherichia coli, Bacillus subtilis, yeast, and filamentous fungi. In the industrial production of useful substances by such microorganisms, improving productivity is one of the important issues.

[0003] Proline isomerase (PPIase) is an enzyme that catalyzes the isomerization of prolyl bonds and can assist in protein folding (Non-Patent Document 1). PPIase consists of three families, namely, cyclophilin, FK506-binding protein (FKBP), and parvulin, which differ in sensitivity to inhibitors. It is known that the sequence identity of the amino acid sequences among the three PPIase families is low. PPIases from all three families are present in the periplasm of Escherichia coli. Among them, FkpA belonging to FKBP has been well studied, and it has been reported that the productivity of the target protein can be improved by increasing its expression level (Non-Patent Document 2). It has also been reported that the region of FkpA that contributes to improving the productivity of the target protein in Escherichia coli is the chaperone region on the N-terminus (Non-Patent Document 3). It has been reported that the productivity of the target protein can be improved in a cell-free system by adding PPIases from any of the three families (Patent Document 1). In the secretory production of target proteins in Gram-positive bacteria, many studies have been conducted on enhancing the expression of parbulins, including PrsA (Non-Patent Document 4).

[0004] Bacillus subtilis, a gram-positive bacterium, has PrsA as an endogenous chaperone and PPIase (Non-Patent Document 5), and it has been reported that productivity of a target protein can be improved by enhancing the expression level of PrsA (Patent Document 2, Non-Patent Documents 6 and 7). PrsA is fixed to the outer surface of the cell membrane and promotes folding of proteins transported via translocase. Proteins that are not properly folded are degraded by proteases present in the cell wall and at the cell membrane-cell membrane interface, so they must be properly folded immediately after the signal peptide is cleaved (Non-Patent Document 4).

[0005] On the other hand, the effect of FKBP on the production of target proteins in Gram-positive bacteria has not been reported. [Prior art documents] [Patent documents]

[0006] [Patent Document 1] JP 2005-253432 A [Patent Document 2] Patent No. 4202985 [Non-patent literature]

[0007] [Non-Patent Document 1] Journal of Molecular Biology, 2015, 427(7): 1609-1631 [Non-Patent Document 2] Biotechnol Prog. 2017, 33(1): 212-220 [Non-Patent Document 3] Microbial Cell Factories, 2010, volume 9, Article number: 22 [Non-Patent Document 4] Microbial Cell Factories, 2019, volume 18, Article number: 158 [Non-Patent Document 5] J Biol Chem. 2004, 279(18):19302-14 [Non-Patent Document 6] Journal of Bacteriology, 1998, 180(11): 2830-2835 [Non-Patent Document 7] Journal of Bacteriology, 2001, 183(6): 1881-1890 Summary of the Invention [Problem to be solved by the invention]

[0008] The present invention relates to providing a method for producing a target protein using a Gram-positive bacterium, typically Bacillus subtilis, with improved productivity. [Means for solving the problem]

[0009] The inventors conducted intensive research in light of the above-mentioned problems and discovered that in the production of a target protein using Gram-positive bacteria, the productivity of the target protein can be improved by expressing a specific PPIase derived from a heterologous organism in the Gram-positive bacteria.

[0010] That is, the present invention relates to the following 1) and 2). 1) A method for producing a target protein, comprising culturing a Gram-positive bacterium containing a gene encoding a heterologous FKBP and a gene encoding a target protein, or co-culturing a Gram-positive bacterium containing a gene encoding a heterologous FKBP and a Gram-positive bacterium containing a gene encoding a target protein. 2) A Gram-positive bacterium containing a gene encoding a heterologous FKBP, or a gene encoding a heterologous FKBP and a gene encoding a protein of interest. Effect of the Invention

[0011] According to the present invention, it becomes possible to efficiently produce a target protein using Gram-positive bacteria, typically Bacillus subtilis. [Brief description of the drawings]

[0012] [Figure 1] Amount of Fab produced when each PPIase was expressed in a Fab-producing Bacillus subtilis strain. [Diagram 2] Fab production amount when PrsA or FkpA was expressed in a Fab-producing Bacillus subtilis strain. [Diagram 3] The amount of Fab produced when the entire region of FkpA (FkpA), the N-terminal region (FkpA_N), or the C-terminal region (FkpA_C) of FkpA was expressed in a Fab-producing Bacillus subtilis strain. [Figure 4] The amount of Fab produced when FkpA was secreted (FkpA_p) or anchored to the cell membrane (FkpA_m) in a Fab-producing Bacillus subtilis strain. [Diagram 5] Phylogenetic tree of FKBPs. [Figure 6] HMM profile of the BCFK clade. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0013] In the present specification, the identity of a nucleotide sequence or an amino acid sequence is calculated by the Lipman-Pearson method (Science, 1985, 227:1435-1441). Specifically, it is calculated by performing an analysis using the search homology program of the genetic information processing software Genetyx-Win, with the unit size to compare (ktup) set to 2.

[0014] As used herein, "at least 80% identity" with respect to an amino acid sequence or a nucleotide sequence means identity of 80% or more, preferably 85% or more, more preferably 90% or more, even more preferably 95% or more, even more preferably 96% or more, even more preferably 97% or more, even more preferably 98% or more, and even more preferably 99% or more.

[0015] In the present specification, the "corresponding position" or "corresponding region" on an amino acid sequence or a nucleotide sequence can be determined by aligning a target sequence with a reference sequence (e.g., the amino acid sequence of SEQ ID NO: 1) so as to give maximum homology. Alignment of amino acid sequences or nucleotide sequences can be performed using known algorithms, and the procedures are known to those skilled in the art. For example, alignment can be performed using the Clustal W multiple alignment program (Nucleic Acids Res, 1994, 22:4673-4680) with default settings. Alternatively, Clustal W2 or Clustal omega, which are revised versions of Clustal W, can be used. Clustal W, Clustal W2 and Clustal omega are available, for example, on the Clustal website operated by University College Dublin ([www.clustal.org]), the European Bioinformatics Institute (EBI [www.ebi.ac.uk / index.html]), and the website of the DNA Data Bank of Japan operated by the National Institute of Genetics (DDBJ [www.ddbj.nig.ac.jp / searches-j.html]). The position of the target sequence aligned to any position of the reference sequence by the above-mentioned alignment is considered to be a "position corresponding to" the any position. In addition, a region flanked by corresponding positions or a region consisting of a corresponding motif is considered to be a corresponding region.

[0016] Those skilled in the art can further fine-tune the alignment of the amino acid sequences obtained above to optimize it. Such an optimal alignment is preferably determined taking into consideration the identity or similarity of the amino acid sequences, the frequency of gaps to be inserted, and the like. Here, the identity or similarity of the amino acid sequences refers to the ratio (%) of the number of positions at which identical or similar amino acid residues exist in both sequences when two amino acid sequences are aligned to the total number of amino acid residues. The term "similar amino acid residues" refers to amino acid residues that have similar properties in terms of polarity and charge among the 20 types of amino acids that constitute proteins, and that cause so-called conservative substitutions. Such groups of similar amino acid residues are well known to those skilled in the art, and examples thereof include, but are not limited to, arginine and lysine; glutamic acid and aspartic acid; serine and threonine; glutamine and asparagine; leucine and isoleucine.

[0017] As used herein, the term "amino acid residue" refers to the 20 types of amino acid residues constituting proteins: alanine (Ala or A), arginine (Arg or R), asparagine (Asn or N), aspartic acid (Asp or D), cysteine ​​(Cys or C), glutamine (Gln or Q), glutamic acid (Glu or E), glycine (Gly or G), histidine (His or H), isoleucine (Ile or I), leucine (Leu or L), lysine (Lys or K), methionine (Met or M), phenylalanine (Phe or F), proline (Pro or P), serine (Ser or S), threonine (Thr or T), tryptophan (Trp or W), tyrosine (Tyr or Y), and valine (Val or V).

[0018] As used herein, the term "operably linked" between a regulatory region and a gene refers to a state in which the gene and the regulatory region are linked such that the gene can be expressed under the control of the regulatory region. The procedure for "operably linked" between a gene and a regulatory region is well known to those skilled in the art.

[0019] In this specification, "upstream" and "downstream" of a gene refer to the upstream and downstream of the transcription direction of the gene. For example, "a gene located downstream of a promoter" means that the gene is present on the 3' side of the promoter in the DNA sense strand, and "upstream" of a gene means the 5' region of the gene in the DNA sense strand.

[0020] The names of the genes of Bacillus subtilis described herein are based on the Bacillus subtilis genome data published on the Internet at JAFAN: Japan Functional Analysis Network for Bacillus subtilis (BSORF DB) ([bacillus.genome.ad.jp / ], updated January 18, 2006). The gene numbers of Bacillus subtilis described herein refer to the gene numbers registered in BSORF DB.

[0021] As used herein, FK506-binding protein (FKBP) refers to an enzyme that constitutes a family of peptidylprolyl isomerases (PPIases, EC5.1.2.8) that catalyze the isomerization of prolyl bonds and can assist in protein folding. FKBP is a group of PPIase enzymes whose activity is inhibited by binding to FK506, an immune inhibitor.

[0022] As used herein, a "clade" is a grouping of sequences from a common ancestor and all descendants of that common ancestor (evolution.berkeley.edu / evolibrary / article / 0_0_0 / evo_06). Clades can be visualized as phylogenetic trees and share common characteristics. Subclades that group together within a clade in a phylogenetic tree can also share common characteristics, and sequences in one subclade are more closely related to each other than sequences in other subclades in that clade.

[0023] As used herein, the term "BCFK clade" refers to a group of sequences belonging to the FKBP family. Sequences belonging to the BCFK clade are defined as sequences having a Hidden Markov Model (HMM) score of 115 or more over the entire length of the amino acid sequence against the HMM profile shown in FIG. 6. Preferred sequences belonging to the BCFK clade are sequences having a HMM score of 150 or more over the entire length of the amino acid sequence against the HMM profile shown in FIG. 6. The HMM profile in Figure 6 was created by constructing a multiple alignment using MAFFT v7.471 with FKBP sequences belonging to the BCFK clade, and then using HMMER version 3.3.2 (http: / / hmmer.org / ) with the parameters --pnone --wnone. The Uniprot numbers of the FKBP sequences used to create the HMM profile defining the BCFK clade are shown in Table 3 below. The HMM profile can be binarized using hmmpress, and a homology search can be performed using hmmscan to calculate the HMM score of any sequence against the created HMM profile of the BCFK clade.

[0024] As used herein, the term "antibody-related molecule" refers to a protein containing an immunoglobulin or a molecular species consisting of a single domain or a combination of two or more domains selected from the domains constituting an immunoglobulin. The domains constituting an immunoglobulin include VH, CH1, CH2, and CH3, which are domains of an immunoglobulin heavy chain, and VL and CL, which are domains of an immunoglobulin light chain. An antibody-related molecule may be a monomeric protein or a multimeric protein. When an antibody-related molecule is a multimeric protein, it may be a homomultimer consisting of a single type of subunit, or a heteromultimer consisting of two or more types of subunits. Preferably, an antibody-related molecule is a molecule that contains an antigen recognition domain of an immunoglobulin and can specifically bind to a target such as a protein. Examples of antibody-related molecules include immunoglobulins such as IgG, as well as small molecule antibodies such as Fab, F(ab')2, single chain antibodies (scFv), diabodies, and variable domains of heavy chains of heavy chain antibodies (VHH).

[0025] As used herein, "Fab" refers to an antibody consisting of the VH-CH1 domain of an immunoglobulin heavy chain and the VL-CL domain of an immunoglobulin light chain.

[0026] As used herein, "VHH" refers to the variable domain of a heavy chain of a heavy chain antibody. Heavy chain antibodies have been found in camelids and cartilaginous fish such as sharks. Those derived from cartilaginous fish such as sharks are also called VNAR (single variable new antigen receptor domain antibody). The VHH in this specification is derived from, for example, camelids or sharks, preferably from camelids. VHH is a molecule capable of recognizing an antigen with a single domain, and is the smallest unit of antibody molecules found to date. The VHH produced in the present invention can contain one or more heavy chain variable domains derived from a heavy chain antibody, and the number of heavy chain variable domains contained in the VHH is not limited. The heavy chain variable domain contained in the VHH produced in the present invention may be a heavy chain variable domain derived from a natural heavy chain antibody or a modified version thereof. Furthermore, the VHH produced by the present invention may contain fragments other than the heavy chain variable domain derived from the immunoglobulin heavy chain (e.g., fragments of the constant region of a heavy chain antibody, or human-derived fragments, linker sequences, etc.), or amino acid mutations for stabilization.

[0027] In this specification, the camelid family includes Bactrian camels, dromedaries, llamas, alpacas, vicunas, guanacos, etc., and preferably includes alpacas.

[0028] The method for producing a target protein of the present invention comprises culturing a Gram-positive bacterium containing a gene encoding a heterologous FKBP and a gene encoding a target protein, or co-culturing a Gram-positive bacterium containing a gene encoding a heterologous FKBP and a Gram-positive bacterium containing a gene encoding a target protein.

[0029] In the method of the present invention, the FKBP is not particularly limited as long as it is a heterologous FKBP. Here, heterologous means a microorganism or organism classified as a species other than that to which the Gram-positive bacterium for producing the target protein belongs. As such a heterologous FKBP, from the viewpoint of improving the productivity of the target protein, a polypeptide belonging to the BCFK clade and having prolyl bond isomerization activity, a polypeptide consisting of the amino acid sequence shown in SEQ ID NO: 6, or a polypeptide consisting of an amino acid sequence having at least 80% identity with the amino acid sequence shown in SEQ ID NO: 6 and having prolyl bond isomerization activity is preferred, and a polypeptide consisting of any of the amino acid sequences shown in SEQ ID NOs: 1 to 6, or a polypeptide consisting of an amino acid sequence having at least 80% identity with the amino acid sequence shown in SEQ ID NOs: 1 to 6 and having prolyl bond isomerization activity is more preferred.

[0030] The polypeptide consisting of the amino acid sequence shown in SEQ ID NO: 6 is MJFKS derived from Methanococcus jannaschii. The polypeptide consisting of the amino acid sequence shown in SEQ ID NO: 1 is FkpA derived from Escherichia coli. The polypeptide consisting of the amino acid sequence shown in SEQ ID NO: 2 is FKBP_l derived from Lelliottia amnigena. The polypeptide consisting of the amino acid sequence shown in SEQ ID NO: 3 is FKBP_K derived from Klebsiella quasipneumoniae. The polypeptide consisting of the amino acid sequence shown in SEQ ID NO: 4 is FKBP_E derived from Erwinia sp. B116. The polypeptide consisting of the amino acid sequence shown in SEQ ID NO: 5 is FKBP_P derived from Pantoea sp. Nvir. The polypeptide consisting of the amino acid sequence shown in any one of SEQ ID NOs: 1 to 6 is a polypeptide belonging to the FKBP family and has prolyl bond isomerization activity. Among them, the polypeptide consisting of the amino acid sequence shown in any one of SEQ ID NOs: 1 to 5 is a polypeptide belonging to the BCFK clade.

[0031] "Prolyl bond isomerization activity" refers to the activity of isomerizing cis-trans prolyl bonds in proteins. Prolyl bond isomerization activity can be evaluated using a method well known in the art. For example, the activity can be determined by measuring the refolding rate of ribonuclease T1 (RNase) by the target polypeptide (Marika Vitikainen et al. Journal of Biological Chemistry, 2004, 279(18): 19302-19314).

[0032] The gene encoding the heterologous FKBP is a polynucleotide encoding the heterologous FKBP described above. As the gene encoding the heterologous FKBP, a polynucleotide consisting of the nucleotide sequence shown in SEQ ID NO: 35 encoding FkpA, a polynucleotide consisting of the nucleotide sequence shown in SEQ ID NO: 40 encoding FKBP_1, a polynucleotide consisting of the nucleotide sequence shown in SEQ ID NO: 41 encoding FKBP_K, a polynucleotide consisting of the nucleotide sequence shown in SEQ ID NO: 42 encoding FKBP_E, a polynucleotide consisting of the nucleotide sequence shown in SEQ ID NO: 43 encoding FKBP_P, a polynucleotide consisting of the nucleotide sequence shown in SEQ ID NO: 46 encoding MJFKS, or a polynucleotide consisting of a nucleotide sequence having at least 80% identity with any of the nucleotide sequences shown in SEQ ID NOs: 35, 40 to 43, and 46 and encoding a polypeptide having prolyl bond isomerization activity is preferred, and a polynucleotide consisting of any of the nucleotide sequences shown in SEQ ID NOs: 35, 40 to 43, and 46 is more preferred.

[0033] A gene encoding a heterologous FKBP can be prepared according to a conventional method. For example, a gene encoding a heterologous FKBP can be prepared by extracting genomic DNA from a microorganism or organism that naturally produces the heterologous FKBP in a conventional manner, or by extracting RNA and synthesizing cDNA by reverse transcription. For example, a gene encoding FkpA (SEQ ID NO: 35) can be prepared from Escherichia coli (NBRC 3301) or the like. The above microorganism can be purchased from a public microorganism collection. A gene encoding a heterologous FKBP into which a mutation has been introduced may be prepared by further performing site-specific mutagenesis on the gene encoding the heterologous FKBP obtained by the above procedure. Alternatively, a gene encoding a heterologous FKBP may be chemically synthesized based on the amino acid sequence of the heterologous FKBP. In addition, a gene encoding a heterologous FKBP may be codon-optimized according to the species of Gram-positive bacteria as the host cell. Information on codons used by various organisms is available from the Codon Usage Database ([www.kazusa.or.jp / codon / ]).

[0034] The gene encoding the heterologous FKBP may be operably linked to a control region. The term "control region" refers to a region that has the function of controlling the expression of a gene located downstream thereof in a cell, and preferably has the function of constitutively expressing or highly expressing the gene located downstream. More specifically, it can be defined as a region that exists upstream of the coding region of a gene and has the function of controlling the transcription of the coding region by interacting with RNA polymerase. Preferably, the control region in this specification refers to a region of about 200 to 600 nucleotides upstream of the coding region of a gene. The control region includes a transcription initiation control region and / or a translation initiation control region, or a region from the transcription initiation control region to the translation initiation control region. The transcription initiation control region is a region that includes a promoter and a transcription initiation point, and the translation initiation control region is a site corresponding to the Shine-Dalgarno (SD) sequence that forms a ribosome binding site together with an initiation codon (Shine, J., Dalgarno, L., Proc. Natl. Acad. Sci. USA., 1974, 71: 1342-1346).

[0035] Preferred examples of the control region include, but are not limited to, a control region that functions in Gram-positive bacteria, preferably bacteria of the genus Bacillus, for example, the control region of the α-amylase gene, protease gene, aprE gene, or spoVG gene derived from bacteria of the genus Bacillus, the control region of the cellulase gene of Bacillus sp. KSM-S237 strain (JP 2000-210081 A), the control region of the cellulase gene of Bacillus sp. KSM-64 strain (JP 2011-10387 A), and the control region of the kanamycin resistance gene or chloramphenicol resistance gene derived from Staphylococcus aureus (for both, see JP 2009-089708 A). More preferred examples of the control region include promoters derived from the genus Bacillus, such as the cellulase gene promoter of Bacillus sp. KSM-S237 strain (SEQ ID NO: 94), the cellulase gene promoter of Bacillus sp. KSM-64 strain (SEQ ID NO: 95), and the Bacillus subtilis spoVG gene promoter (SEQ ID NO: 96). Further, preferred control regions include promoters consisting of a nucleotide sequence having at least 90% identity with any of SEQ ID NOs: 94 to 96.

[0036] From the viewpoint of improving the productivity of the target protein, the gene encoding the heterologous FKBP is preferably operably linked to a polynucleotide encoding a secretory signal peptide (referred to as a secretory signal sequence) having the function of secreting the expressed FKBP outside the cell. A preferred example of the secretory signal sequence is a secretory signal sequence that functions in gram-positive bacteria, preferably in the genus Bacillus, such as a secretory signal sequence derived from the genus Bacillus. A preferred example of the secretory signal sequence derived from the genus Bacillus is the secretory signal sequence of the cellulase gene of Bacillus sp. KSM-S237 strain (SEQ ID NO: 97), the secretory signal sequence of the cellulase gene of Bacillus sp. KSM-64 strain (SEQ ID NO: 98), the secretory signal sequence of the amylase gene amyE of Bacillus subtilis (SEQ ID NO: 99), etc. Further examples of the secretory signal sequence derived from the genus Bacillus include a nucleotide sequence that has at least 80% identity with any of SEQ ID NOs: 97 to 99 and has the function of secreting the expressed protein outside the cell. The sequence encoding the heterologous FKBP linked to the secretory signal sequence derived from these Bacillus bacteria may or may not contain the secretory signal sequence of a native heterologous FKBP.

[0037] Thus, a gene encoding a heterologous FKBP may contain nucleotide sequences of untranslated regions (UTRs) in addition to the open reading frame (ORF). For example, the gene may contain a promoter, a secretory signal sequence, and a terminator as described above.

[0038] In the method of the present invention, the gene encoding the target protein may be a foreign gene (heterologous gene) encoding a heterologous protein, a gene encoding a protein derived from the same species introduced from the outside, or an endogenous gene encoding a protein that the host cell can naturally express. The target protein is preferably a protein having at least one prolyl bond isomerization site. Here, the prolyl bond isomerization site in the target protein is a site that can be isomerized during the production process of the target protein, i.e., a cis-prolyl bond site, and the presence or absence and / or number of cis-prolyl bond sites in the target protein can be confirmed by referring to the three-dimensional structure of the target protein obtained by X-ray crystal structure analysis. The type of the target protein is not particularly limited. Examples of the target protein include enzymes involved in the synthesis of a desired protein or a desired target substance, such as antibody-related molecules, cytokines, hormones, other physiologically active peptides, transporters, industrial enzymes such as proteases, and metabolic enzymes.

[0039] Preferably, the target protein is an antibody-related molecule, more preferably a small antibody such as Fab, ScFv, VHH, etc. More preferably, the target protein is selected from the group consisting of Fab, ScFv, and VHH, even more preferably Fab.

[0040] The gene encoding the target protein can be prepared according to a conventional method. For example, the gene encoding the target protein can be prepared by extracting genomic DNA from a microorganism or organism that naturally produces the target protein by a conventional method, or by extracting RNA and synthesizing cDNA by reverse transcription. Alternatively, the gene encoding the target protein can be chemically synthesized based on the amino acid sequence of the target protein. In addition, the gene encoding the target protein may be codon-optimized to suit the species of Gram-positive bacteria used as the host cell.

[0041] The gene encoding the target protein may be operably linked to a regulatory region. Also, the gene encoding the target protein is preferably operably linked to a secretory signal sequence that allows the expressed target protein to be secreted outside the cell. Details of the regulatory region and secretory signal are the same as those described for the gene encoding the heterologous FKBP.

[0042] The gene encoding the heterologous FKBP and the gene encoding the target protein may be introduced into the same Gram-positive bacterium, or may be introduced into different Gram-positive bacteria. When the gene encoding the heterologous FKBP and the gene encoding the target protein are introduced into different Gram-positive bacteria, the Gram-positive bacteria may be the same or different, but from the viewpoint of culture efficiency, it is preferable that they are the same. In addition, when the gene encoding the heterologous FKBP and the gene encoding the target protein are introduced into different Gram-positive bacteria, it is preferable that each gene is operably linked to a secretion signal sequence. More preferably, the gene encoding the heterologous FKBP and the gene encoding the target protein are introduced into the same Gram-positive bacterium.

[0043] The gram-positive bacteria as the host cell are not particularly limited as long as they can be used for protein production, and examples thereof include Bacillus bacteria such as Bacillus subtilis, Bacillus licheniformis, Bacillus cereus, Bacillus thuringiensis, and Bacillus amyloliquefaciens, and Clostridium bacteria such as Clostridium butyricum. Among them, Bacillus bacteria are preferred, and Bacillus subtilis is more preferred.

[0044] The Gram-positive bacteria may be a wild-type strain, or may be a mutant strain that has been mutated. For example, as a mutant strain of Bacillus subtilis, it is preferable to use a Bacillus subtilis strain that is deficient in at least one extracellular protease gene in order to effectively prevent extracellular decomposition of a protein secreted outside the cell and improve protein productivity. Here, the "deficiency" of an extracellular protease means that the activity of the extracellular protease is reduced compared to the activity of a cell that is not deficient in an extracellular protease (e.g., a wild-type strain). A cell deficient in an extracellular protease (an extracellular protease-deficient strain) can be prepared by partial or complete deletion or inactivation (so-called knockdown or knockout, etc.) of the gene for the extracellular protease in the cell. Preferably, the activity of the extracellular protease in the extracellular protease-deficient strain is reduced to 50% or less, more preferably 25% or less, compared to the wild-type strain. The extracellular protease gene deleted in the extracellular protease-deficient Bacillus subtilis strain is preferably at least one gene, more preferably three genes, and even more preferably all genes selected from the group consisting of aprE (BSORF DB gene number: BG10190), epr (BG10561), wprA (BG11846), mpr (BG10690), nprB (BG10691), bpr (BG10233), nprE (BG10448), vpr (BG10591) and aprX (BG12567). A preferred example of such a Bacillus subtilis mutant strain is the extracellular protease-deficient Bacillus subtilis strain Dpr9 (see Japanese Patent No. 4485341). Furthermore, the Bacillus subtilis mutant strain may be one in which a sigma factor such as sigF has been deleted (see Japanese Patent No. 4336082), or recA involved in homologous recombination activity has been deleted (see Japanese Patent No. 6088282), etc. A Bacillus subtilis mutant strain in which one or both of sigF and recA have been deleted in the Dpr9 strain may also be used.

[0045] The introduction of a gene encoding a heterologous FKBP, a gene encoding a target protein, or a gene encoding a heterologous FKBP and a gene encoding a target protein into a Gram-positive bacterium as a host cell can be carried out according to a standard method. For example, a gene encoding a heterologous FKBP can be incorporated into the genome of a host Gram-positive bacterial cell by introducing a gene encoding a heterologous FKBP or a vector containing the gene into the host Gram-positive bacterial cell. A gene encoding a target protein can be incorporated into the genome of a host Gram-positive bacterial cell by introducing a gene encoding a target protein or a vector containing the gene into the host Gram-positive bacterial cell. A gene encoding a heterologous FKBP and a gene encoding a target protein can be incorporated into the genome of a host Gram-positive bacterial cell by introducing a gene encoding a heterologous FKBP or a vector containing the gene and a gene encoding a target protein or a vector containing the gene, or a vector containing both a gene encoding a heterologous FKBP and a gene encoding a target protein into the host Gram-positive bacterial cell. Alternatively, an expression vector containing a gene encoding a heterologous FKBP, an expression vector containing a gene encoding a protein of interest, an expression vector containing a gene encoding a heterologous FKBP and an expression vector containing a gene encoding a protein of interest, or an expression vector containing both a gene encoding a heterologous FKBP and a gene encoding a protein of interest may be introduced into a host Gram-positive bacterial cell. When two types of genes or vectors are introduced into the same host cell, the order of introduction is not limited, and either may be introduced first, or they may be introduced simultaneously.

[0046] To introduce a gene or vector into a Gram-positive bacterial cell, known transformation techniques such as the competent cell method, electroporation, protoplast method, particle gun method, and PEG method can be applied.

[0047] A vector containing a gene encoding a heterologous FKBP, a vector containing a gene encoding a target protein, or a vector containing a gene encoding a heterologous FKBP and a gene encoding a target protein can be constructed by inserting and linking the gene encoding the heterologous FKBP and / or the gene encoding the target protein, and, if necessary, a control region or a secretion signal sequence, into any vector by a conventional method. The type of the vector is not particularly limited, and may be any vector such as a plasmid, a phage, a phagemid, a cosmid, a virus, a YAC vector, or a shuttle vector. Furthermore, the vector is preferably a vector that can be amplified in a host cell, and more preferably an expression vector. Examples of preferred vectors include, but are not limited to, shuttle vectors such as pHA3040SP64, pHSP64R or pASP64 (Japanese Patent No. 3492935), pHY300PLK (an expression vector capable of transforming both Escherichia coli and Bacillus subtilis; Jpn J Genet, 1985, 60:235-243), pHY-S237 (JP Patent Publication No. 2014-158430), and pAC3 (Nucleic Acids Res, 1988, 16:8732); and plasmids usable for transformation of Bacillus bacteria such as pUB110 (J Bacteriol, 1978, 134:318-329) and pTA10607 (Plasmid, 1987, 18:8-15). Plasmids derived from E. coli (e.g., pET22b(+), pBR322, pBR325, pUC57, pUC118, pUC119, pUC18, pUC19, pBluescript, etc.) can also be used.

[0048] In the method of the present invention, the gram-positive bacteria containing a gene encoding a heterologous FKBP and a gene encoding a target protein obtained by the above-mentioned procedure are cultured, or the gram-positive bacteria containing a gene encoding a heterologous FKBP and the gram-positive bacteria containing a gene encoding a target protein are co-cultured. The gram-positive bacteria may be cultured according to a general method for culturing gram-positive bacteria. For example, a medium for culturing gram-positive bacteria contains a carbon source and a nitrogen source necessary for the growth of the bacteria. Examples of carbon sources include glucose, dextran, soluble starch, sucrose, and methanol. Examples of nitrogen sources include ammonium salts, nitrates, amino acids, corn steep liquor, peptone, casein, meat extract, soybean meal, and potato extract. If necessary, the medium may contain other nutrients, such as inorganic salts (e.g., sodium chloride, calcium chloride, sodium dihydrogen phosphate, and magnesium chloride), vitamins, and antibiotics (e.g., tetracycline, neomycin, kanamycin, spectinomycin, and erythromycin). Culture conditions, such as temperature, aeration and agitation conditions, medium pH, and culture time, can be appropriately selected depending on the bacterial species, characteristics, culture scale, etc.

[0049] By culturing the Gram-positive bacteria, the target protein is expressed in the cells of the Gram-positive bacteria. Furthermore, when the gene encoding the target protein is linked to a polynucleotide encoding a secretory signal peptide, the expressed target protein is secreted outside the cells. The target protein produced by the method of the present invention can be recovered from the culture medium by using a general method used for protein purification, such as cell disruption, centrifugation, ammonium sulfate precipitation, gel chromatography, ion exchange chromatography, affinity chromatography, etc., alone or in appropriate combination.

[0050] According to the method of the present invention, as shown in the Examples described below, by expressing a heterologous FKBP during expression of a target protein in a Gram-positive bacterium, the productivity of the target protein is greatly improved compared to the case of expression of the target protein alone. Furthermore, the productivity of the target protein is greatly improved compared to the case of coexisting PrsA (Patent Document 2, Non-Patent Documents 5 and 6), which has been reported to contribute to improving the productivity of the target protein in Bacillus subtilis during expression of the target protein in a Gram-positive bacterium. In this way, the method of the present invention can efficiently produce a target protein with high productivity using a Gram-positive bacterium, and realizes a reduction in the time and cost required for the production of the target protein.

[0051] Furthermore, by secreting and expressing a heterologous FKBP during expression of a target protein in a Gram-positive bacterium, the productivity of the target protein is significantly improved compared to when the heterologous FKBP is expressed in a state where it is anchored to the cell membrane. It is known that proteins produced in Bacillus subtilis are folded in the vicinity of the cell membrane (Non-Patent Document 4 mentioned above), so it was completely unexpected that the productivity of the target protein is improved when an FKBP capable of assisting protein folding is secreted and expressed not in the vicinity of the cell membrane.

[0052] The present invention also includes the following substances, manufacturing methods, uses, methods, etc. as exemplary embodiments, but the present invention is not limited to these embodiments.

[0053] [1] A method for producing a target protein, comprising culturing a Gram-positive bacterium containing a gene encoding a heterologous FKBP and a gene encoding a target protein, or co-culturing a Gram-positive bacterium containing a gene encoding a heterologous FKBP and a Gram-positive bacterium containing a gene encoding a target protein, preferably comprising culturing a Gram-positive bacterium containing a gene encoding a heterologous FKBP and a gene encoding a target protein. [2] A method for improving productivity of a target protein, comprising culturing a Gram-positive bacterium containing a gene encoding a heterologous FKBP and a gene encoding a target protein, or co-culturing a Gram-positive bacterium containing a gene encoding a heterologous FKBP and a Gram-positive bacterium containing a gene encoding a target protein, preferably comprising culturing a Gram-positive bacterium containing a gene encoding a heterologous FKBP and a gene encoding a target protein. [3] The method according to [1] or [2], wherein the heterologous FKBP is a polypeptide belonging to the BCFK clade and having prolyl bond isomerization activity, a polypeptide consisting of the amino acid sequence shown in SEQ ID NO: 6, or a polypeptide consisting of an amino acid sequence having at least 80% identity to the amino acid sequence shown in SEQ ID NO: 6 and having prolyl bond isomerization activity, preferably a polypeptide belonging to the BCFK clade and having prolyl bond isomerization activity or a polypeptide consisting of the amino acid sequence shown in SEQ ID NO: 6. [4] The method according to [1] or [2], wherein the heterologous FKBP is a polypeptide consisting of an amino acid sequence shown in any one of SEQ ID NOs: 1 to 6, or a polypeptide consisting of an amino acid sequence having at least 80% identity to the amino acid sequence shown in any one of SEQ ID NOs: 1 to 6 and having prolyl bond isomerization activity, preferably a polypeptide consisting of an amino acid sequence shown in any one of SEQ ID NOs: 1 to 6. [5] The method according to [1] or [2], wherein the gene encoding the heterologous FKBP is a polynucleotide consisting of a nucleotide sequence shown in any one of SEQ ID NOs: 35, 40 to 43, and 46, or a polynucleotide having at least 80% identity to the nucleotide sequence shown in any one of SEQ ID NOs: 35, 40 to 43, and 46 and encoding a polypeptide having prolyl bond isomerization activity, preferably a polynucleotide consisting of a nucleotide sequence shown in any one of SEQ ID NOs: 35, 40 to 43, and 46. [6] The method according to any one of [1] to [5], wherein the gene encoding the heterologous FKBP is operably linked to a polynucleotide encoding a secretory signal peptide. [7] The method according to any one of [1] to [6], wherein the Gram-positive bacterium is a bacterium of the genus Bacillus, and is preferably Bacillus subtilis or a mutant strain thereof. [8] The method according to any one of [1] to [6], wherein the Gram-positive bacterium is a Bacillus subtilis bacterium in which at least one extracellular protease gene has been deleted or inactivated, preferably a Bacillus subtilis bacterium in which at least one extracellular protease gene selected from the group consisting of aprE, epr, wprA, mpr, nprB, bpr, nprE, vpr, and aprX has been deleted or inactivated, and more preferably a Bacillus subtilis bacterium in which aprE, epr, wprA, mpr, nprB, bpr, nprE, vpr, and aprX have been deleted or inactivated. [9] The method according to any one of [1] to [8], wherein the target protein has at least one prolyl bond isomerization site.

[10] The method according to any one of [1] to [9], wherein the target protein is an antibody-related molecule, preferably selected from the group consisting of Fab, ScFv, and VHH, and more preferably Fab.

[11] The method according to any one of [1] to

[10] , further comprising recovering the target protein from the culture.

[0054]

[12] A Gram-positive bacterium containing a gene encoding a heterologous FKBP, or a gene encoding a heterologous FKBP and a gene encoding a target protein.

[13] The gram-positive bacterium according to

[12] , wherein the heterologous FKBP is a polypeptide belonging to the BCFK clade and having prolyl bond isomerization activity, a polypeptide consisting of the amino acid sequence shown in SEQ ID NO: 6, or a polypeptide consisting of an amino acid sequence having at least 80% identity to the amino acid sequence shown in SEQ ID NO: 6 and having prolyl bond isomerization activity, preferably a polypeptide belonging to the BCFK clade and having prolyl bond isomerization activity or a polypeptide consisting of the amino acid sequence shown in SEQ ID NO: 6.

[14] The gram-positive bacterium according to

[12] , wherein the heterologous FKBP is a polypeptide consisting of an amino acid sequence shown in any one of SEQ ID NOs: 1 to 6, or a polypeptide consisting of an amino acid sequence having at least 80% identity to the amino acid sequence shown in any one of SEQ ID NOs: 1 to 6 and having prolyl bond isomerization activity, preferably a polypeptide consisting of an amino acid sequence shown in any one of SEQ ID NOs: 1 to 6.

[15] The gram-positive bacterium according to

[12] , wherein the gene encoding the heterologous FKBP is a polynucleotide consisting of a nucleotide sequence shown in any one of SEQ ID NOs: 35, 40 to 43, and 46, or a polynucleotide having at least 80% identity to the nucleotide sequence shown in any one of SEQ ID NOs: 35, 40 to 43, and 46 and encoding a polypeptide having prolyl bond isomerization activity, preferably a polynucleotide consisting of a nucleotide sequence shown in any one of SEQ ID NOs: 35, 40 to 43, and 46.

[16] The Gram-positive bacterium according to any one of

[12] to

[15] , wherein a gene encoding the heterologous FKBP is operably linked to a polynucleotide encoding a secretory signal peptide.

[17] The Gram-positive bacterium according to any one of

[12] to

[16] , which is a bacterium of the genus Bacillus, preferably Bacillus subtilis or a mutant thereof.

[18] The Gram-positive bacterium according to any one of

[12] to

[16] , which is a Bacillus subtilis bacterium in which at least one extracellular protease gene has been deleted or inactivated, preferably a Bacillus subtilis bacterium in which at least one extracellular protease gene selected from the group consisting of aprE, epr, wprA, mpr, nprB, bpr, nprE, vpr, and aprX has been deleted or inactivated, and more preferably aprE, epr, wprA, mpr, nprB, bpr, nprE, vpr, and aprX has been deleted or inactivated.

[19] The Gram-positive bacterium according to any one of

[12] to

[18] , wherein the target protein has at least one prolyl bond isomerization site.

[20] The Gram-positive bacterium according to any one of

[12] to

[19] , wherein the target protein is an antibody-related molecule, preferably selected from the group consisting of Fab, ScFv and VHH, and more preferably Fab. EXAMPLES

[0055] The present invention will be described in more detail below with reference to examples, although the technical scope of the present invention is not limited to these examples.

[0056] Materials and Methods (1) Host strain The host Bacillus subtilis used was a derivative of Bacillus subtilis strain 168. A sigF gene-deficient strain (Dpr9ΔsigF) was prepared from the extracellular protease-deficient Bacillus subtilis strain Dpr9 (see Japanese Patent No. 4485341, deficient in extracellular proteases epr, wprA, mpr, nprB, bpr, nprE, vpr, aprE, and aprX) according to the method described in Japanese Patent No. 4336082.

[0057] (2) Culture medium LB medium: 1% Bacto TM Tryptone, 0.5% Bacto TM Yeast Extract, 1% sodium chloride. 1.5% agar was added to the plate medium. Tetracycline (50 ppm) was added as necessary. DM3 medium: 1% CMC (Kanto Chemical), 0.5% Bacto TM Casamino Acids, 0.5% Bacto TM Yeast Extract, 8.1% disodium succinate 6H2O, 0.35% dipotassium hydrogen phosphate, 0.15% potassium dihydrogen phosphate, 0.5% glucose, 20 mM magnesium chloride, 0.01% BSA, 50 ppm tetracycline. 1% agar was added to the plate medium. 2×L-mal medium: 2% Bacto TM Tryptone, 1% Bacto TMYeast Extract, 1% Sodium Chloride, 7.5% Maltose Monohydrate, 7.5 ppm Manganese Sulfate, 15 ppm Tetracycline.

[0058] Example 1. Increased protein production by expression of PPIase 1-1. Construction of plasmid for expressing PPIase The plasmid sequence was amplified by PCR using the primer set of SEQ ID NO: 7 and SEQ ID NO: 8 and PrimeSTAR Max DNA polymerase (TaKaRa) with the recombinant plasmid pHY-S237 (JP Patent Publication No. 2014-158430) prepared based on pHY300PLK as a template. The promoter DNA derived from the spoVG gene was amplified by PCR using the primer set of SEQ ID NO: 9 and SEQ ID NO: 10 with the genome of the 168 strain as a template. The obtained promoter DNA was incorporated into the plasmid sequence using the In-Fusion HD Cloning Kit (Takara). The cellulase sequence was removed from the obtained plasmid sequence by PCR using the primer set of SEQ ID NO: 11 and SEQ ID NO: 12. The plasmid sequence was amplified by PCR using the primer set of SEQ ID NO: 11 and SEQ ID NO: 13 with the obtained plasmid as a template. The secretion signal DNA was amplified by PCR using the primer set of SEQ ID NO: 14 and SEQ ID NO: 15 with the genome of the 168 strain as a template. The obtained secretion signal DNA was incorporated into a plasmid sequence using the In-Fusion HD Cloning Kit (Takara) to construct a plasmid for expressing PPIase.

[0059] 1-2.Design of plasmid for expressing PPIase The plasmid sequence was amplified by PCR using the primer set of SEQ ID NO: 11 and SEQ ID NO: 13 and PrimeSTAR Max DNA polymerase (TaKaRa) with the PPIase expression plasmid constructed in 1-1 as a template. The DNA encoding PrsA shown in SEQ ID NO: 18 was amplified by PCR using the primer set of SEQ ID NO: 16 and SEQ ID NO: 17 with the genome of strain 168 as a template (SEQ ID NO: 19). The obtained DNA encoding PrsA was integrated into the plasmid sequence using In-Fusion HD Cloning Kit (Takara) to obtain a plasmid for PrsA expression. The plasmid sequence was amplified by PCR using the primer set of SEQ ID NO: 13 and SEQ ID NO: 20 and PrimeSTAR Max DNA polymerase (TaKaRa) with the PPIase expression plasmid constructed in 1-1 as a template. Using the genome of Escherichia coli DH5α as a template, DNAs encoding SurA (SEQ ID NO:29), PpiA (SEQ ID NO:30), Tig (SEQ ID NO:31), and FkpA (SEQ ID NO:1) were amplified by PCR using primer sets of SEQ ID NO:21 and SEQ ID NO:22, SEQ ID NO:23 and SEQ ID NO:24, SEQ ID NO:25 and SEQ ID NO:26, and SEQ ID NO:27 and SEQ ID NO:28 (SEQ ID NO:32 to 35). The obtained DNAs encoding PPIase were incorporated into a plasmid sequence using In-Fusion HD Cloning Kit (Takara) to obtain plasmids for expressing SurA, PpiA, Tig, and FkpA, respectively. The nucleotide sequences shown in SEQ ID NOs: 40 to 48, which encode the amino acid sequences of FKBP_l (sequence number 2), FKBP_K (sequence number 3), FKBP_E (sequence number 4), FKBP_P (sequence number 5), FKBP2 (sequence number 36), FK153 (sequence number 37), MJFKS (sequence number 6), FKBP52 (sequence number 38), and CyP40 (sequence number 39), were synthesized by GenPlus cloning from Genescript Inc., by incorporating them between the regions shown in SEQ ID NOs: 49 and 50 of the PPIase expression plasmid constructed in 1-1, to obtain plasmids for expression of FKBP_l, FKBP_K, FKBP_E, FKBP_P, FKBP2, FK153, MJFKS, FKBP52, and CyP40, respectively.

[0060] 1-3. Construction of Fab expression strains The genome of strain 168 was used as a template, and a DNA fragment (A) containing the ybdO gene region and a DNA fragment (B) containing the ybxG gene region were amplified by PCR using the primer sets of SEQ ID NO: 51 and SEQ ID NO: 52, and SEQ ID NO: 53 and SEQ ID NO: 54. The chloramphenicol resistance gene region (C) was amplified by PCR using the primer set of SEQ ID NO: 55 and SEQ ID NO: 56, using the plasmid pC194 DNA as a template. Fab_c (Certolizumab Fab) consisting of the heavy chain and light chain shown in SEQ ID NO: 57 and SEQ ID NO: 58, which can be expressed in an operon, was synthesized by incorporating the base sequence shown in SEQ ID NO: 59, which can be expressed in an operon, between the regions shown in SEQ ID NO: 60 and SEQ ID NO: 50 of the PPIase expression plasmid constructed in 1-1 by GenPlus cloning of Genescript, Inc., to obtain a Fab_c expression plasmid. A DNA fragment (D) containing the Fab_c expression region was amplified by PCR using the primer set of SEQ ID NO: 61 and SEQ ID NO: 62, using the Fab_c expression plasmid as a template. The above four fragments (A), (B), (C), and (D) were mixed as a template, and SOE-PCR was performed using a primer set of SEQ ID NO: 51 and SEQ ID NO: 54 to ligate the four fragments and obtain a DNA fragment for genome integration of the Fab_c expression region. The obtained DNA fragment for genome integration of the Fab_c expression region was transformed into Bacillus subtilis Dpr9ΔsigF strain by the competent cell method. After transformation, colonies grown on LB agar medium containing chloramphenicol (10 μg / mL) were isolated as transformants. The strain obtained in this manner was named a Fab_c production strain.

[0061] 1-4. Introduction of PPIase expression plasmid into Bacillus subtilis The PPlase expression plasmid constructed in 1-2 was introduced into the Fab_c production strain by the protoplast method described below. Bacillus subtilis stocked in glycerol was inoculated into 1 mL of LB liquid medium and cultured overnight at 30°C and 210 rpm with shaking. The next day, 10 μL of this culture was inoculated into a new 1 mL of LB liquid medium and cultured at 37°C and 210 rpm with shaking for about 2 hours. This culture was collected in a 1.5 mL tube and centrifuged at 1,2000 rpm for 5 minutes. The pellet from which the supernatant was removed was suspended in 500 μL of SMMP containing 4 mg / mL of Lysozyme (SIGMA) and incubated at 37°C for 1 hour. Next, the mixture was centrifuged at 3,500 rpm for 10 minutes, and the pellet from which the supernatant was removed was suspended in 400 μL of SMMP. 33 μL of this suspension was mixed with various plasmids, and 100 μL of 40% PEG was added and vortexed. To this solution, 350 μL of SMMP was added, mixed by inversion, and shaken at 30° C. and 210 rpm for 1 hour. The entire amount was then spread onto a DM3 agar medium plate and incubated at 30° C. for 2 to 3 days.

[0062] 1-5.Fab production The recombinant Bacillus subtilis prepared in 1-4 was inoculated into 500 μL of LB medium containing 50 ppm tetracycline and cultured overnight at 30°C in a 96-well plate to prepare a preculture solution. The preculture solution was inoculated at 1% into 800 μL of 2×L-mal medium containing 15 ppm tetracycline and cultured in a 96-well plate at 30°C for 72 hours. At the end of the culture, the mixture was centrifuged at 4°C, 3000 rpm, and 20 minutes, and the supernatant was collected.

[0063] 1-6. Quantification of Fab production by ELISA 100 μL of 1 μg / mL TNF-α (Wako) was added to each well of an F96 Cert.Maxisorp Nunc-Immuno™ Plate (Thermo Fisher Scientific), sealed, and left to stand overnight at 4°C. After removing the TNF-α that was not adsorbed to the well, 200 μL of PBST (PBS containing 0.1% (v / v) Tween 20) was added and immediately removed. This washing procedure was performed three times. PBST containing 2% skim milk was added and incubated at room temperature for 1 hour. After removing the PBST containing skim milk, 200 μL of PBST was added and immediately removed. This washing procedure was performed three times. The culture supernatant collected in 1-5 was diluted 50-fold with PBST, and further diluted 10-fold with PBST containing 2% skim milk. The same dilution procedure was performed for the dilution series of Certolizumab Recombinant Human Monoclonal Antibody (Invitrogen). 100 μL of the diluted solution was added to each well with TNF-α immobilized, and incubated at room temperature for 1 hour. After removing the diluted solution, 200 μL of PBST was added and immediately removed. This washing procedure was performed three times. Goat anti-Human IgG (H+L) Secondary Antibody, HRP (Invitrogen) was used as the detection antibody. The detection antibody was diluted 1 / 5,000 with PBST. 100 μL of the detection antibody was added to each well, and incubated at room temperature for 1 hour. After removing the detection antibody, 200 μL of PBST was added and immediately removed. This washing procedure was performed three times. The color-developing substrate was prepared by dissolving OPD tablets (Thermo Fisher Scientific) in Stable Peroxide Substrate Buffer (Thermo Fisher Scientific). 100 μL of the color-developing substrate was added to each well, and incubated for 10 minutes in the dark. After adding 100 μL of 0.5 mol / L sulfuric acid, the absorbance at 490 nm was measured using a microplate reader.The amount of Fab_c produced was calculated based on the dilution series concentration of Certolizumab Recombinant Human Monoclonal Antibody (Invitrogen), and the relative value to that of the Fab_c producing strain into which pHY300PLK had been introduced was shown (Figure 1). As a result, it was confirmed that the amount of Fab_c produced was significantly improved in the Fab_c producing strain harboring the plasmids for expressing FkpA, FKBP_l, FKBP_K, FKBP_E, FKBP_P, and MJFKS. The amount of Fab_c produced was reduced in the Fab_c producing strain harboring the plasmid for expressing PrsA, an endogenous factor of Bacillus subtilis. Fab_c has a prolyl bond isomerization site, specifically, a cis-type prolyl bond.

[0064] 1-7. Confirmation of Fab production by Western blotting The culture supernatant obtained in 1-5 was mixed with an equal volume of Laemmli Sample Buffer (BIO-RAD), and then heat-treated at 99°C for 5 minutes to prepare a sample. TM Mini-PROTEAN TGX TMPrecast Gel (BIO-RAD) was used. 5 μL of sample was applied to each well and electrophoresed at 210 V for 5 minutes. Precision Plus Blue standard (BIO-RAD) was used as a molecular weight marker, and Certolizumab Recombinant Human Monoclonal Antibody (Invitrogen) was also electrophoresed simultaneously as a standard. Proteins were transferred from SDS-PAGE gel to a PVDF membrane using Trans-Blot Turbo Mini PVDF Transfer Packs (BIO-RAD) and Trans-Blot Turbo System (BIO-RAD). Goat anti-Human IgG (H+L) Secondary Antibody, HRP (Invitrogen) was used as the antibody, and iBind Western System (Invitrogen) was used for antibody reaction. Target proteins were detected using 1-Step Ultra TMB-Blotting Solution (Thermo Scientific) (Figure 2). As with the ELISA quantification shown in 1-6, it was confirmed that the productivity of the Fab_c producing strain harboring the FkpA expression plasmid was higher than that of the Fab_c producing strain into which pHY300PLK had been introduced. It was also confirmed that the productivity of the Fab_c producing strain harboring the PrsA expression plasmid was lower than that of the Fab_c producing strain into which pHY300PLK had been introduced.

[0065] Example 2: Verification of domains necessary for high productivity 2-1. Design of plasmids for expressing each domain Using the FkpA expression plasmid constructed in 1-2 as a template, the C-terminal or N-terminal region of FkpA was removed by PCR using the primer sets of sequence numbers 63 and 64, and sequence numbers 65 and 66, and PrimeSTAR Max DNA polymerase (TaKaRa), to obtain an FkpA_N expression plasmid expressing the N-terminal region of FkpA (sequence number 67) and an FkpA_C expression plasmid expressing the C-terminal region (sequence number 68), respectively.

[0066] 2-2. Introduction of PPIase expression plasmid into Bacillus subtilis The plasmids for expressing each domain constructed in 2-1 were introduced into the Fab_c producing strain by the protoplast method shown in 1-4.

[0067] 2-3.Fab production The recombinant Bacillus subtilis prepared in 2-2 was inoculated into 500 μL of LB medium containing 50 ppm tetracycline and cultured overnight at 30°C in a 96-well plate to prepare a preculture solution. The preculture solution was inoculated at 1% into 800 μL of 2×L-mal medium containing 15 ppm tetracycline and cultured in a 96-well plate at 30°C for 72 hours. At the end of the culture, the mixture was centrifuged at 4°C, 3000 rpm, and 20 minutes, and the supernatant was collected.

[0068] 2-4. Quantification of Fab production by ELISA The amount of Fab_c produced was quantified by the ELISA method shown in 1-6. The amount of Fab_c produced was calculated based on the dilution series concentration of Certolizumab Recombinant Human Monoclonal Antibody (Invitrogen), and the relative value to the Fab_c producing strain into which pHY300PLK had been introduced is shown (Figure 3). As a result, it was confirmed that in order to obtain a significant productivity improvement effect in the Bacillus subtilis production system, it is necessary to express both the N-terminal and C-terminal regions of FkpA.

[0069] Example 3: Verification of the effect of increasing protein production depending on the location of PPIase 3-1. Construction of Fab expression plasmid The plasmid sequence was amplified by PCR using the primer set of SEQ ID NO: 7 and SEQ ID NO: 8 and PrimeSTAR Max DNA polymerase (TaKaRa) with the recombinant plasmid pHY-S237 (JP Patent Publication No. 2014-158430) prepared based on pHY300PLK as a template. The promoter DNA derived from the spoVG gene was amplified by PCR using the primer set of SEQ ID NO: 9 and SEQ ID NO: 10 with the genome of the 168 strain as a template. The obtained promoter DNA was incorporated into the plasmid sequence using the In-Fusion HD Cloning Kit (Takara). The plasmid sequence was amplified by PCR using the primer set of SEQ ID NO: 11 and SEQ ID NO: 13 with the obtained plasmid as a template. The base sequence shown in SEQ ID NO: 71, which can express Fab_l (Fab against lysozyme) consisting of heavy chain and light chain shown in SEQ ID NO: 69 and SEQ ID NO: 70 in an operon, was artificially synthesized at Thermo Fisher Scientific, and incorporated into the plasmid sequence using the In-Fusion HD Cloning Kit (Takara) to construct a plasmid for expressing Fab_l.

[0070] 3-2. Construction of PPIase-expressing strain Using the genome of strain 168 as a template, a DNA fragment containing the bglP gene region (A), a DNA fragment containing the yxxE gene region (B), and a promoter DNA derived from the spoVG gene (C) were amplified by PCR using primer sets of SEQ ID NO: 72 and SEQ ID NO: 73, SEQ ID NO: 74 and SEQ ID NO: 75, and SEQ ID NO: 76 and SEQ ID NO: 77. Using plasmid pC194 DNA as a template, a chloramphenicol resistance gene region (D) was amplified by PCR using a primer set of SEQ ID NO: 55 and SEQ ID NO: 56. Using the genome of E. coli DH5α as a template, a DNA encoding FkpA linked to a secretion signal or a signal for anchoring a protein on a membrane was amplified by PCR using primer sets of SEQ ID NO: 78 and SEQ ID NO: 79, and SEQ ID NO: 79 and SEQ ID NO: 80 (E)(E'). The above five fragments (A)(B)(C)(D)(E) or (A)(B)(C)(D)(E') were mixed as a template, and SOE-PCR was performed using a primer set of SEQ ID NO: 72 and SEQ ID NO: 75 to obtain a DNA fragment for genome integration that expresses FkpA by secreting or anchoring it to a membrane by linking the five fragments. The obtained DNA fragment for genome integration was used to transform Bacillus subtilis Dpr9ΔsigF strain by the competent cell method. After transformation, colonies that grew on LB agar medium containing chloramphenicol (10 μg / mL) were isolated as transformants. The strain thus obtained that could secrete and express FkpA was named FkpA_p strain, and the strain that could express FkpA by anchoring it to a membrane was named FkpA_m strain.

[0071] 3-3. Introduction of Fab expression plasmid into Bacillus subtilis The Fab_l expression plasmid constructed in 3-1 was introduced into the FkpA_p and FkpA_m strains by the protoplast method described in 1-4.

[0072] 3-4.Fab production The recombinant Bacillus subtilis prepared in 3-3 was inoculated into 500 μL of LB medium containing 50 ppm tetracycline and cultured overnight at 30°C in a 96-well plate to prepare a preculture solution. The preculture solution was inoculated at 1% into 800 μL of 2×L-mal medium containing 15 ppm tetracycline and cultured in a 96-well plate at 30°C for 72 hours. At the end of the culture, the mixture was centrifuged at 4°C, 3000 rpm, and 20 minutes, and the supernatant was collected.

[0073] 3-5. Quantification of Fab production by ELISA 100 μL of 100 μg / mL Lysozyme, from Egg White (Wako) was added to each well of F96 Cert.Maxisorp Nunc-Immuno (trademark) Plate (Thermo Fisher Scientific), and after sealing, it was left to stand overnight at 4 ° C. After removing Lysozyme that was not adsorbed to the well, 200 μL of PBST (PBS containing 0.1% (v / v) Tween 20) was added and immediately removed. This washing operation was performed three times. PBST containing 2% skim milk was added and incubated at room temperature for 1 hour. After removing PBST containing skim milk, 200 μL of PBST was added and immediately removed. This washing operation was performed three times. The culture supernatant collected in 3-4 was diluted 10 times with PBST containing 2% skim milk. 100 μL of the diluted solution was added to each well where Lysozyme was immobilized, and incubated at room temperature for 1 hour. After removing the diluted solution, 200 μL of PBST was added and immediately removed. This washing procedure was performed three times. Mouse IgG Fab Antibody:HRP (biovalley) was used as the detection antibody. The detection antibody was diluted 1 / 5,000 with PBST. 100 μL of the detection antibody was added to each well and incubated at room temperature for 1 hour. After removing the detection antibody, 200 μL of PBST was added and immediately removed. This washing procedure was performed three times. The color-developing substrate was prepared by dissolving OPD tablets (Thermo Fisher Scientific) in Stable Peroxide Substrate Buffer (Thermo Fisher Scientific). 100 μL of the color-developing substrate was added to each well and incubated for 20 minutes in the dark. After adding 100 μL of 0.5 mol / L sulfuric acid, the absorbance at 490 nm was measured using a Microplate Reader. The absorbance obtained is shown as a relative value to that of the strain in which the Fab_l expression plasmid was introduced into Dpr9ΔsigF (Figure 4). As a result, it became clear that, although it is known that B. subtilis folds proteins near the cell membrane, secreting FkpA rather than expressing it by anchoring it to the membrane contributes to high production of the target protein.In addition, Fab_l has a prolyl bond isomerization site, specifically, a cis-type prolyl bond.

[0074] Example 4 Increased protein production by expression of PPIase 4-1. Construction of plasmid for expressing RNaseT1 The base sequence shown in sequence number 101, which encodes the amino acid sequence of RNaseT1 (sequence number 100), was synthesized by Genescript's GenPlus cloning, by incorporating it between the regions shown in sequence numbers 49 and 50 of the PPIase expression plasmid constructed in 1-1, to obtain an RNaseT1 expression plasmid.

[0075] 4-2.Introduction of RNaseT1 expression plasmid into PPlase expression strain The RNaseT1 expression plasmid was introduced into the Bacillus subtilis Dpr9ΔsigF strain and the FkpA_p strain constructed in 3-2 by the protoplast method described in 1-4.

[0076] 4-3.RNaseT1 production The recombinant Bacillus subtilis prepared in 4-2 was inoculated into 500 μL of LB medium containing 50 ppm tetracycline and cultured overnight at 30°C in a 96-well plate to prepare a preculture solution. The preculture solution was inoculated at 1% into 800 μL of 2×L-mal medium containing 15 ppm tetracycline and cultured in a 96-well plate at 30°C for 72 hours. At the end of the culture, the mixture was centrifuged at 4°C, 3000 rpm, and 20 minutes, and the supernatant was collected.

[0077] 4-4. Quantification of RNase T1 production by SDS-PAGE The culture supernatant collected in 4-3 was mixed with equal amounts of Laemmli Sample Buffer (BIO-RAD) and then heated at 99°C for 5 minutes to prepare the sample. Mini-PROTEIN TGX Stain-Free (BIO-RAD) was used for the gel. 5 μL of sample was applied to each well and electrophoresed at 210 V for 25 minutes. Precision Plus protein Unstained standard (BIO-RAD) was used as the molecular weight marker. Protein bands were detected using a ChemiDoc MP Imaging System. The detected proteins were quantified using a calibration curve created based on a lysozyme preparation (Sigma-Aldrich) (Table 1). As a result, it was confirmed that the production of RNase T1 was greatly improved by the expression of PPIase. RNase T1 has a prolyl bond isomerization site, specifically, a cis-type prolyl bond.

[0078] [Table 1]

[0079] Reference Example 1 Identification of PPIase sequences belonging to the BCFK clade using HMM profiles Phylogenetic analysis of FKBP Phylogenetic analysis was performed using the sequence group obtained by adding the FkpA sequence shown in SEQ ID NO: 81 to the FKBP sequence group registered as the seed sequence of the PF00254 family in Pfam shown in Table 2. After constructing a multiple alignment using the default parameters of MAFFT v7.471, conserved regions were extracted using trimAl v1.4.rev15, and an evolutionary model was selected using ModelTest-NG v0.1.7. IQ-TREE multicore version 2.0.3 was used for the phylogenetic analysis, and the evolutionary model was specified as LG+G4+F. The phylogenetic tree visualized using Figtree (http: / / tree.bio.ed.ac.uk / software / FigTree / ) is shown in Figure 5. The Uniprot numbers of the FKBP sequences belonging to the BCFK clade in Figure 5 are shown in Table 3.

[0080] [Table 2]

[0081] [Table 3]

[0082] (2) Identification of FKBP sequences belonging to the BCFK clade The file BCFK.fasta was prepared by compiling the FKBP sequences belonging to the BCFK clade shown in Table 3 in Fasta format. A multiple alignment was constructed using MAFFT v7.471 with the command mafft --auto BCFK_mafft.fasta>BCFK.fasta. Next, the HMM profile shown in Figure 6 was created using HMMER version 3.3.2 with the command hmmbuild --pnone --wnone BCFK_mafft.hmm BCFK_mafft.fasta, and the profile was binarized using the command hmmpress BCFK_mafft.hmm. The file No_BCFK.Fasta was prepared by compiling the FKBP sequences not belonging to the BCFK clade from the FKBP sequences in Table 2 in Fasta format. By executing the command hmmscan --tblout BCFK.tblout BCFK_mafft.hmm No_BCFK.Fasta, a homology search was performed for FKBP sequences that were not included in the BCFK clade against the HMM profile that defines the BCFK clade. As a result, it was confirmed that all sequences that were not included in the BCFK clade had an HMM score of 112.3 or less. Next, a file Express_PPIase.Fasta was prepared that summarized the PPIase (PrsA, FkpA, FKBP_l, FKBP_K, FKBP_E, FKBP_P, MJFKS, SurA, PpiA, Tig, FKBP2, FK153, FKBP52, CyP40) sequences represented by SEQ ID NO: 18, 81 to 93 in Fasta format. A homology search of the PPIase sequence described in Example 1 was performed against the HMM profile defining the BCFK clade by executing the command hmmscan --tblout BCFK.tblout BCFK_mafft.hmm Express_PPIase.Fasta. Sequences with no homology were given an HMM score of 0. The results are shown in Table 4. FkpA, FKBP_l, FKBP_K, FKBP_E, and FKBP_P, which showed high productivity improvement effects in 1-6 of Example 1, have HMM scores of 150 or more, and can be said to be FKBP sequences belonging to the BCFK clade.In this manner, it is possible to confirm whether any PPIase sequence belongs to the BCFK clade.

[0083] [Table 4]

Claims

1. A method for producing a target protein, comprising culturing a Gram-positive bacterium containing a gene encoding a heterologous FK506 binding protein (FKBP) and a gene encoding a target protein, or co-culturing a Gram-positive bacterium containing a gene encoding a heterologous FKBP and a Gram-positive bacterium containing a gene encoding a target protein.

2. The method of claim 1, wherein the heterologous FKBP is a polypeptide belonging to the BCFK clade and having prolyl bond isomerization activity, a polypeptide consisting of the amino acid sequence shown in SEQ ID NO: 6, or a polypeptide consisting of an amino acid sequence having at least 80% identity to the amino acid sequence shown in SEQ ID NO: 6 and having prolyl bond isomerization activity.

3. The method according to claim 1, wherein the heterologous FKBP is a polypeptide consisting of an amino acid sequence shown in any one of SEQ ID NOs: 1 to 6, or a polypeptide consisting of an amino acid sequence having at least 80% identity to an amino acid sequence shown in any one of SEQ ID NOs: 1 to 6 and having prolyl bond isomerization activity.

4. The method of claim 1 , wherein the gene encoding the heterologous FKBP is operably linked to a polynucleotide encoding a secretory signal peptide.

5. The method of claim 1 , wherein the Gram-positive bacterium is Bacillus subtilis or a mutant thereof.

6. 2. The method of claim 1, wherein the Gram-positive bacterium is Bacillus subtilis in which at least one extracellular protease gene has been deleted or inactivated.

7. The method according to any one of claims 1 to 6, wherein the target protein has at least one prolyl bond isomerization site.

8. The method according to any one of claims 1 to 6, wherein the target protein is an antibody-related molecule.

9. The method according to any one of claims 1 to 6, wherein the target protein is a Fab.

10. A Gram-positive bacterium comprising a gene encoding a heterologous FKBP, or a gene encoding a heterologous FKBP and a gene encoding a protein of interest.

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