A novel promoter for constitutive expression, a target protein expression system containing the same, and a method for producing allulose using the same.

Abstract

To provide a novel promoter that can consistently express a target protein at a high level, and to provide a target protein expression system and a method for producing allulose, as various uses of the promoter.SOLUTION: Provided is a promoter that is composed of a specific base sequence and that regulates the expression of allulose epimerization enzyme in Corynebacterium strains. The novel promoter according to the present invention is capable of constitutively and highly expressing a target protein, particularly an enzyme, in Corynebacterium strains. As an example, the use of a recombinant Corynebacterium strain transformed with an expression vector containing the novel promoter according to the present invention makes it possible to economically mass-produce allulose epimerization enzyme and to economically mass-produce allulose from fructose.SELECTED DRAWING: None

Description

[Technical Field]

[0001] The present invention relates to a novel promoter and its use, and more particularly to a novel promoter capable of constitutively and highly expressing a target protein, a target protein expression system including the same, and a method for producing allulose using the same. [Background technology]

[0002] With the advancement of molecular biology, various mechanisms regulating gene expression have been elucidated. Gene expression refers to the series of processes that occur within cells, in which proteins are synthesized according to the code entered in the gene through transcription and translation. In particular, the transcription process is the initial stage of gene expression, and is initiated when RNA polymerase, with the help of numerous cofactors, binds to the promoter sequence located upstream of the gene. Transcription factors (TFs) are one of these cofactors and are known to bind directly to the promoter sequence. Since gene expression regulation in prokaryotes, in particular, occurs primarily at the transcription stage, researchers are continually uncovering new transcription factors and promoters.

[0003] For industrial production of foreign proteins such as enzymes, a transformant prepared by transforming a prokaryote such as E. coli with a pET-type expression vector containing the foreign protein gene is used as an expression system. Prokaryotic expression systems transformed with pET-type expression vectors generally require expensive expression inducers such as IPTG (isopropyl-β-D-thiogalactopyranoside), and have the disadvantage of requiring detailed adjustment of the inducer concentration, equipment, and expression induction time.

[0004] On the other hand, an expression system has been proposed that uses a Corynebacterium sp. strain, a GRAS (Generally Recognized As Safe) strain, as a host cell to mass-produce a cyclose epimerization enzyme (or allulose epimerization enzyme) that has the activity of converting fructose to allulose (or cyclose). Korean Patent Registration No. 10-1695830 discloses a gene expression cassette containing a nucleic acid sequence encoding a cycle epimerization enzyme (or allulose epimerization enzyme) based on a Corynebacterium strain, and a regulatory sequence operably linked upstream thereof to regulate the expression of the cycle epimerization enzyme in a Corynebacterium strain. The regulatory sequence includes a transcription promoter derived from Escherichia coli selected from the group consisting of the trc promoter, Tac1 promoter, and Tac2 promoter, or the sod promoter, which is a transcription promoter derived from Corynebacterium glutaricum. Generally, promoters contain conserved RNA polymerase binding sites, and the 5'UTR and 3'UTR sequences around the core promoter contain binding sites for transcription factors that promote or suppress the expression of various RNAs, making the gene sequence surrounding the promoter important for improving expression efficiency. The Corynebacterium strain-based cyclosporinase enzyme expression system disclosed in the prior art requires a sophisticated regulatory mechanism for bidirectional gene expression because the promoter sequence is located in a bidirectional promoter sequence in which the McrA gene and sod gene are expressed in opposite directions. This makes it unsuitable as a system for the constitutive expression of a single desired target protein.In addition, the Corynebacterium strain-based cyclase epimerization enzyme expression system disclosed in the prior art has relatively weak expression strength due to structural hindrance of the promoter or complex regulation of the promoter, making it unsuitable for mass production of cyclase. Summary of the Invention [Problem to be solved by the invention]

[0005] The present invention was developed based on the conventional technical background, and an object of the present invention is to provide a novel promoter capable of constitutively and highly expressing a target protein. Another object of the present invention is to provide a target protein expression system and a method for producing allulose as various uses of the novel promoter. [Means for solving the problem]

[0006] The inventors of the present invention constructed a promoter that eliminated bidirectionality by deleting a fragment of the bidirectional promoter region present between the McaA gene and the sod gene in the genome sequence of the Corynebacterium glutamicum ATCC 13032 strain, and confirmed that a specific promoter among these was capable of constitutively and highly expressing allulose epimerization enzyme in Corynebacterium strains, thereby completing the present invention. Furthermore, the inventors of the present invention operably linked the promoter from which bidirectionality was eliminated to a polynucleotide encoding an allulose epimerization enzyme to prepare a recombinant expression vector, and then transformed Corynebacterium glutamicum, a GRAS (Generally Recognized As Safe) strain, with the recombinant expression vector. As a result, random mutations occurred in some promoters, and it was confirmed that among the promoter variants obtained through random mutation, specific promoter variants significantly increased the expression efficiency of the allulose epimerization enzyme, thereby completing the present invention.

[0007] In order to solve the above problems, one example of the present invention provides a promoter that is composed of the base sequence of SEQ ID NO: 6 or the base sequence of SEQ ID NO: 27, and that regulates the expression of allulose epimerization enzyme in a Corynebacterium strain.

[0008] To achieve the above object, one example of the present invention provides an allulose epimerization enzyme expression cassette comprising a polynucleotide encoding the allulose epimerization enzyme and a promoter operably linked thereto, wherein the promoter is composed of the nucleotide sequence of SEQ ID NO: 6 or the nucleotide sequence of SEQ ID NO: 27.

[0009] To solve the above problems, one example of the present invention provides a recombinant expression vector into which an allulose epimerization enzyme expression cassette is inserted.

[0010] To solve the above problems, one example of the present invention provides a recombinant Corynebacterium strain, which is obtained by transforming a Corynebacterium host strain with an allulose epimerization enzyme expression cassette or a recombinant expression vector into which the expression cassette has been inserted.

[0011] To solve the above problems, one example of the present invention provides a method for producing allulose, which includes adding a recombinant Corynebacterium strain to a fructose-containing solution and reacting the mixture. [Effects of the Invention]

[0012] The novel promoter according to the present invention can constitutively and highly express a target protein, particularly an enzyme, in a Corynebacterium strain. For example, the use of a recombinant Corynebacterium strain transformed with an expression vector containing the novel promoter according to the present invention enables economical mass production of allulose epimerization enzyme or economical mass production of allulose from fructose. DETAILED DESCRIPTION OF THE INVENTION

[0013] The present invention will be specifically described below. As used herein, the term "promoter" refers to a minimal nucleic acid sequence operably linked to a target nucleotide sequence to be transcribed and regulating the transcription of the target nucleotide sequence. The promoter may also include a promoter structure sufficient to express a regulatable promoter-dependent gene that is inducible by cell-type-specific or external signals or agents, and such a structure may be located in the 5' or 3' region of the gene. The promoter includes both conserved promoters and inducible promoters. Promoter sequences can be derived from prokaryotes, eukaryotes, or viruses. In prokaryotes, a promoter is generally defined as a binding site immediately adjacent to the transcription start site where RNA polymerase binds.

[0014] The term "homology" as used herein refers to the identity of a nucleic acid sequence with a wild type or a mutant having the same activity. Homology can be compared visually or by using a readily available comparison program, and the homology between two or more sequences can be calculated as a percentage (%). Furthermore, "homology" refers to the identity of an amino acid sequence with a wild type or a mutant having the same activity.

[0015] The term "target protein" as used herein means a foreign protein that cannot normally exist in the transformed strain (or host cell) that expresses said protein.

[0016] As used herein, the term "polynucleotide" refers to any polyribonucleotide (RNA) or polydeoxyribonucleotide (DNA), whether non-modified or modified, including, but not limited to, single-stranded or double-stranded DNA, DNA that is a mixture of single-stranded and double-stranded regions, single-stranded and double-stranded RNA, RNA that is a mixture of single-stranded and double-stranded regions, or hybrid molecules thereof.

[0017] As used herein, the term "operably linked" is defined as a state in which a promoter sequence and a nucleotide sequence encoding a protein of interest are functionally linked, such that the promoter can regulate the expression of the protein of interest. For example, a promoter is operably linked to a coding sequence if it is capable of controlling the expression of the coding sequence (i.e., if the coding sequence is under the transcriptional control of the promoter), and a ribosome binding site is operably linked to a coding sequence if the ribosome binding site is positioned so as to promote translation. The coding sequence can be operably linked to a regulatory sequence in either the sense or antisense orientation.

[0018] The term "recombinant vector" as used herein is defined as a recombinant DNA prepared by cutting out a promoter mutant or a gene of interest using a restriction enzyme and inserting it into a vector.

[0019] The term "expression cassette" as used herein refers to a regulatory sequence operably linked to a nucleotide sequence to be expressed, for example, a polynucleotide sequence encoding an allulose epimerization enzyme. Thus, unlike an expression unit, an expression cassette includes not only nucleotide sequences that regulate transcription and translation, but also nucleotide sequences that are expressed as proteins as a result of transcription and translation.

[0020] The term "expression vector" as used herein is defined as a DNA sequence required for the transcription and translation of cloned DNA in a suitable host. Specifically, it refers to a genetic construct containing essential regulatory elements operably linked to an insert so that the insert is expressed when present in the cells of an individual. Expression vectors can be produced and purified using standard recombinant DNA techniques. The type of expression vector is not particularly limited, as long as it functions to express a desired gene and produce a desired protein in various prokaryotic and eukaryotic host cells. An expression vector contains at least a promoter, an initiation codon, a gene encoding the desired protein, and a stop codon terminator. Expression vectors can also appropriately contain DNA encoding a signal peptide, additional expression regulatory sequences, 5' and 3' untranslated regions of the desired gene, a selectable marker region, or a replicable unit. The selectable marker region can be an antibiotic selectable marker gene for selecting the desired vector.

[0021] The term "recombinant strain" as used herein refers to cells transformed by introducing a polynucleotide encoding one or more target proteins or an expression vector carrying the same into a host cell. Methods for introducing the expression vector into a host cell to produce a transformant include, but are not limited to, transient transfection, microinjection, transduction, cell fusion, calcium phosphate precipitation, liposome-mediated transfection, DEAE dextran-mediated transfection, polybrene-mediated transfection, electroporation, electroinjection, chemical treatments such as PEG, gene gun methods, and heat shock. Furthermore, the host cell of a recombinant strain is not particularly limited as long as it can smoothly operate the promoter present in the expression vector, and prokaryotes are preferred.

[0022] As used herein, the term "substrate" refers to any substance or compound that is converted or adapted to be converted into another compound by the action of an enzyme. The term encompasses not only single compounds but also combinations of compounds, such as solvents, mixtures, and other materials that contain at least one substrate, as well as derivatives thereof.

[0023] One aspect of the present invention relates to a novel promoter capable of constitutively and highly expressing a target protein. One example of the novel promoter of the present invention is composed of the nucleotide sequence of SEQ ID NO: 6 or SEQ ID NO: 27. The inventors of the present invention named the promoter composed of the nucleotide sequence of SEQ ID NO: 6 "Pds2" and the promoter composed of the nucleotide sequence of SEQ ID NO: 27 "Pds4." The Pds2 promoter is a promoter in which a partial fragment is deleted from the bidirectional promoter region located between the McaA gene and the sod gene in the genome sequence of a Corynebacterium glutamicum strain, eliminating bidirectionality and improving the expression efficiency of the target protein. Furthermore, the Pds4 promoter is a promoter mutant in which 6 bp from positions 195 to 200 of the Pds2 promoter is deleted and a new 3 bp is inserted, resulting from a ribosome-binding site (RBS) spacer mutation. An expression system including a promoter according to an embodiment of the present invention can constitutively express a target protein at a high level in a Corynebacterium strain. In particular, the promoter according to an embodiment of the present invention regulates the expression of allulose epimerization enzyme in a Corynebacterium strain. Therefore, the promoter Pds2 or promoter Pds4 according to an embodiment of the present invention can be used as a promoter for constitutive expression in a Corynebacterium strain. The novel promoter according to an embodiment of the present invention is composed of the nucleotide sequence of SEQ ID NO: 6 or the nucleotide sequence of SEQ ID NO: 27, but the equivalent range of the promoter is not necessarily limited thereto. For example, the equivalent range of the novel promoter according to an embodiment of the present invention includes a sequence having substantial identity to the nucleotide sequence of SEQ ID NO: 6 or the nucleotide sequence of SEQ ID NO: 27.The term "substantial identity" means that the nucleotide sequence of SEQ ID NO: 6 or the nucleotide sequence of SEQ ID NO: 27 is aligned with any other sequence to maximize correspondence, and the sequence is analyzed to determine whether the other sequence has 70% or more, 90% or more, or 98% or more sequence homology with the nucleotide sequence of SEQ ID NO: 6 or the nucleotide sequence of SEQ ID NO: 27. A person skilled in the art will readily understand that polynucleotides having the same or similar activity within the range of substantial homology can be prepared by substituting, adding, or deleting one or more bases in the nucleotide sequence of the novel promoter using recombinant DNA techniques known in the art. Such homology comparisons can be performed by calculating the percentage (%) of homology between two or more sequences using commercially available computer programs. Therefore, the equivalent range of the novel promoter according to one example of the present invention may include a base sequence having 70% or more, 80% or more, 90% or more, 95% or more, or 99% or more homology with the base sequence of SEQ ID NO: 6 or the base sequence of SEQ ID NO: 27, within the range in which the function of consistently high expression of the target protein is maintained.

[0024] One aspect of the present invention relates to a target protein expression system comprising a novel promoter, which can be used to produce allulose epimerization enzyme expression cassettes, recombinant vectors, and recombinant strains.

[0025] An allulose epimerization enzyme expression cassette according to one embodiment of the present invention comprises a polynucleotide encoding an allulose epimerization enzyme and the aforementioned promoter operably linked thereto. The promoter is preferably located upstream of the polynucleotide encoding the allulose epimerization enzyme, which is the target protein. The promoter, a component of the allulose epimerization enzyme expression cassette, is composed of the nucleotide sequence of SEQ ID NO: 6 or the nucleotide sequence of SEQ ID NO: 27. The polynucleotide encoding the allulose epimerization enzyme, a component of the allulose epimerization enzyme expression cassette, is not particularly limited in type as long as it encodes an enzyme having the activity of converting fructose to allulose. For example, the allulose epimerizing enzyme may be derived from Flavonifractor plautii, Clostridium scidens, Treponema primitia, Ensifer adhaerens, or Ruminococcus torques, and considering the activity of converting fructose to allulose, it is preferably derived from Flavonifractor plautii. Specifically, the allulose epimerizing enzyme may be composed of the amino acid sequence of SEQ ID NO: 14, the amino acid sequence of SEQ ID NO: 16, or the amino acid sequence of SEQ ID NO: 18. The allulose epimerizing enzyme composed of the amino acid sequence of SEQ ID NO: 14 is a wild-type enzyme derived from Flavonifractor plautii. The allulose epimerization enzyme consisting of the amino acid sequence of SEQ ID NO: 16 is the amino acid sequence of SEQ ID NO: 14 in which the tryptophan (Trp) at position 29 is replaced with lysine (Lys), the glycine (Gly) at position 216 is replaced with serine (Ser), and at the same time, the methionine (Met) at position 234 is replaced with isoleucine (Ile).The allulose epimerization enzyme having the amino acid sequence of SEQ ID NO: 18 is the same as the amino acid sequence of SEQ ID NO: 14, except that the tryptophan (Trp) at position 29 is replaced with lysine (Lys), the alanine (Ala) at position 77 is replaced with serine (Ser), the glycine (Gly) at position 216 is replaced with serine (Ser), and the methionine (Met) at position 234 is replaced with isoleucine (Ile). The polynucleotide encoding the allulose epimerization enzyme is not particularly limited in type, and preferably comprises the nucleotide sequence of SEQ ID NO: 15 or a nucleotide sequence having 70% or more, 80% or more, 90% or more, 95% or more, or 99% or more homology to the nucleotide sequence of SEQ ID NO: 15. The nucleotide sequence of SEQ ID NO: 15 is a polynucleotide encoding the allulose epimerization enzyme having the amino acid sequence of SEQ ID NO: 14. Furthermore, the polynucleotide encoding the allulose epimerization enzyme can be composed of the nucleotide sequence of SEQ ID NO: 17 or the nucleotide sequence of SEQ ID NO: 19. The nucleotide sequence of SEQ ID NO: 17 is a polynucleotide encoding an allulose epimerization enzyme composed of the amino acid sequence of SEQ ID NO: 16, and the nucleotide sequence of SEQ ID NO: 19 is a polynucleotide encoding an allulose epimerization enzyme composed of the amino acid sequence of SEQ ID NO: 18. The present invention relates to an allulose epimerization enzyme and a polynucleotide encoding the same, and includes the contents disclosed in Korean Patent Publication Nos. 10-1919713, 10-2187354, 10-1656063, 10-1695830, 10-2189458, 10-1539097, 10-1539096, 10-1455759, 10-1318422, and Korean Patent Publication No. 10-2023-0073739.

[0026] An allulose epimerization enzyme expression cassette according to one embodiment of the present invention may further comprise one or more sequences selected from the group consisting of a replication origin, a multicloning site (MCS) for cloning a target protein gene, a transcription termination sequence, and a selection marker. The selection marker is used to select cells transformed with the vector, and may confer a selectable phenotype, such as drug resistance, auxotrophy, resistance to cytotoxic agents, or expression of a surface protein. For example, the selection marker may be an antibiotic resistance gene marker such as a kanamycin antibiotic resistance gene or an ampicillin antibiotic resistance gene. An allulose epimerization enzyme expression cassette according to one embodiment of the present invention may preferably comprise a polynucleotide consisting of the nucleotide sequence of SEQ ID NO: 25 or a polynucleotide consisting of the nucleotide sequence of SEQ ID NO: 28. The polynucleotide consisting of the nucleotide sequence of SEQ ID NO: 25 is an expression cassette fragment in which a promoter consisting of the nucleotide sequence of SEQ ID NO: 6 and an allulose epimerization enzyme gene consisting of the nucleotide sequence of SEQ ID NO: 19 are sequentially linked. The polynucleotide consisting of the nucleotide sequence of SEQ ID NO: 28 is an expression cassette fragment in which a promoter consisting of the nucleotide sequence of SEQ ID NO: 27 and an allulose epimerization enzyme gene consisting of the nucleotide sequence of SEQ ID NO: 19 are sequentially linked.

[0027] A recombinant vector according to one embodiment of the present invention is a recombinant expression vector into which the allulose epimerization enzyme expression cassette described above has been inserted. The recombinant expression vector preferably has a structure in which a replication origin, a promoter, a polynucleotide encoding the allulose epimerization enzyme, a transcription terminator, a kanamycin resistance gene marker, etc. are sequentially linked.

[0028] A recombinant strain according to one embodiment of the present invention is a recombinant Corynebacterium strain, which is obtained by transforming a host cell with the above-mentioned allulose epimerization enzyme expression cassette or a recombinant expression vector into which the expression cassette has been inserted. The host strain used to prepare the recombinant Corynebacterium strain is not particularly limited as long as it is a Corynebacterium strain, and may be selected from the group consisting of, for example, Corynebacterium glutamicum, Corynebacterium acetoglutamicum, Corynebacterium acetoacidophilum, Corynebacterium thermoaminogenes, Corynebacterium melassecola, and Corynebacterium efficiens.

[0029] One aspect of the present invention relates to a method for producing allulose using a target protein expression system containing a novel promoter.

[0030] A method for producing allulose according to one embodiment of the present invention includes adding a recombinant Corynebacterium strain to a fructose-containing solution and reacting the strain. The fructose acts as a mechanism for the target protein expressed by the recombinant Corynebacterium strain to activate the allulose epimerization enzyme. The fructose-containing solution contains Ca to promote the activity of the allulose epimerization enzyme. 2+ , Mn 2+The reaction temperature in the method for producing allulose from fructose is 50 to 70°C, preferably 55 to 65°C, and more preferably 60 to 65°C in consideration of smooth enzyme expression in the recombinant strain, enzyme stability, and maximum activity, and the reaction pH is 6.5 to 8, preferably 6.5 to 7.5, and more preferably 6.5 to 7. In the method for producing allulose from fructose, the fructose concentration in the fructose-containing solution is not particularly limited, but in consideration of productivity and economic efficiency, it is preferably 5 to 75% (w / w), and more preferably 10 to 55% (w / w), based on the total weight of the fructose-containing solution.

[0031] The present invention will be described in more detail with reference to the following examples, which are merely intended to clearly illustrate the technical features of the present invention and are not intended to limit the scope of protection of the present invention. The present disclosure relates, for example, to the following: [Section 1] A promoter characterized by being composed of the base sequence of SEQ ID NO: 6 or the base sequence of SEQ ID NO: 27, and regulating the expression of allulose epimerization enzyme in a Corynebacterium strain. [Section 2] Item 1. An allulose epimerization enzyme expression cassette comprising a polynucleotide encoding an allulose epimerization enzyme and the promoter according to Item 1 operably linked thereto. [Section 3] Item 3. The allulose epimerization enzyme expression cassette according to Item 2, wherein the allulose epimerization enzyme is derived from Flavonifractor plautii, Clostridium scidens, Treponema primitia, Ensifer adhaerens, or Ruminococcus torques. [Section 4] Item 3. The allulose epimerization enzyme expression cassette according to Item 2, wherein the allulose epimerization enzyme is composed of the amino acid sequence of SEQ ID NO: 14, the amino acid sequence of SEQ ID NO: 16, or the amino acid sequence of SEQ ID NO: 18. [Section 5] Item 3. The allulose epimerization enzyme expression cassette according to Item 2, wherein the polynucleotide encoding the allulose epimerization enzyme is composed of the nucleotide sequence of SEQ ID NO: 15, the nucleotide sequence of SEQ ID NO: 17, or the nucleotide sequence of SEQ ID NO: 19. [Section 6] Item 2. The allulose epimerization enzyme expression cassette according to Item 2, comprising a polynucleotide consisting of the base sequence of SEQ ID NO: 25 or a polynucleotide consisting of the base sequence of SEQ ID NO: 28. [Section 7] A recombinant expression vector into which the expression cassette according to any one of Items 2 to 6 has been inserted. [Section 8] A recombinant Corynebacterium strain, wherein a host strain of the genus Corynebacterium is transformed by introducing the expression cassette according to any one of Items 2 to 6 or a recombinant expression vector into which the expression cassette has been inserted. [Section 9] Item 9. The recombinant Corynebacterium strain according to Item 8, wherein the Corynebacterium host strain is selected from the group consisting of Corynebacterium glutamicum, Corynebacterium acetoglutamicum, Corynebacterium acetoacidophilum, Corynebacterium thermoaminogenes, Corynebacterium melassecola, and Corynebacterium efficiens. [Section 10] Item 10. A method for producing allulose, comprising adding the recombinant Corynebacterium strain according to Item 9 to a fructose-containing solution and reacting the mixture. [Example]

[0032] Example 1: Amplification and isolation of promoter sequences for expression of D-allulose 3-epimerization enzyme To identify the bidirectional promoter present in Corynebacterium sp. strains, PCR was performed using the genomic DNA of Corynebacterium glutamicum ATCC 13032 as a template and the Pctrl-F and Pds-R primer sets listed in Table 1. The resulting amplified product was cloned into the pGEM T-easy vector (Promega Co., USA) and sequenced. It was confirmed to be a 336-bp polynucleotide fragment consisting of the nucleotide sequence of SEQ ID NO: 1. The promoter portion of the polynucleotide fragment consisting of the nucleotide sequence of SEQ ID NO: 1 was designated "Pctrl." The promoter Pctrl consists of the nucleotide sequence of SEQ ID NO: 2. To identify mutant promoters of the Pctrl promoter, PCR was performed using the genomic DNA of Corynebacterium glutamicum ATCC 13032 strain as a template and the Pds1-F and Pds-R primer sets, Pds2-F and Pds-R primer sets, and Pds3-F and Pds-R primer sets listed in Table 1 to amplify each mutant promoter. The resulting amplified products were cloned into the pGEM T-easy vector (Promega Co., USA) and analyzed for nucleotide sequence. The amplified product obtained using the Pds1-F and Pds-R primer sets was a 282-bp polynucleotide fragment consisting of the nucleotide sequence of SEQ ID NO: 3. The promoter portion of the polynucleotide fragment consisting of the nucleotide sequence of SEQ ID NO: 3 was designated "Pds1." The Pds1 promoter consists of the nucleotide sequence of SEQ ID NO: 4. The amplification product obtained using the Pds2-F primer and Pds-R primer set was a polynucleotide fragment having a length of 236 bp and consisting of the base sequence of SEQ ID NO:5.The promoter region of the polynucleotide fragment consisting of the nucleotide sequence of SEQ ID NO:5 was designated "Pds2." Promoter Pds2 consists of the nucleotide sequence of SEQ ID NO:6. Furthermore, the amplification product obtained using the Pds3-F and Pds-R primer sets was a 236-bp polynucleotide fragment consisting of the nucleotide sequence of SEQ ID NO:7. The promoter region of the polynucleotide fragment consisting of the nucleotide sequence of SEQ ID NO:7 was designated "Pds3." Promoter Pds3 consists of the nucleotide sequence of SEQ ID NO:8. Promoter Pctrl is a bidirectional promoter containing the intergenic region located between the McaA and sod genes in the genome sequence of the Corynebacterium glutamicum ATCC 13032 strain. Promoters Pds1, Pds2, and Pds3 are promoter mutants in which a partial sequence of promoter Pctrl is deleted around the 282-bp intergenic region. [Table 1]

[0033] Example 2: Amplification and isolation of polynucleotide sequences encoding D-allulose 3-epimerization enzymes The applicant of the present invention disclosed a wild-type D-allulose epimerization enzyme derived from Flavonifractor plautii and a polynucleotide encoding the same in Korean Patent Publication No. 10-14739180. The wild-type D-allulose epimerization enzyme is composed of the amino acid sequence of SEQ ID NO: 14, and the polynucleotide encoding it is composed of the nucleotide sequence of SEQ ID NO: 15.

[0034] Additionally, the applicant of the present invention disclosed a D-allulose epimerization enzyme mutant W29K / G216S / M234I, which has improved fructose-to-allulose conversion rate and thermal stability, and a polynucleotide encoding the same, in Korean Patent Publication No. 10-2021-0132405. The D-allulose epimerization enzyme mutant W29K / G216S / M234I is a mutant of the wild-type D-allulose epimerization enzyme derived from Flavonifractor plautii, in which tryptophan (Trp) at position 29 is substituted with lysine (Lys), glycine (Gly) at position 216 is substituted with serine (Ser), and methionine (Met) at position 234 is substituted with isoleucine (Ile). The D-allulose epimerization enzyme mutant W29K / G216S / M234I consists of the amino acid sequence of SEQ ID NO: 16, and the polynucleotide encoding it consists of the base sequence of SEQ ID NO: 17.

[0035] In addition, the applicant of the present invention disclosed, in Korean Patent Publication No. 10-2023-0073739, a D-allulose epimerization enzyme mutant W29K / A77S / G216S / M234I, which has improved fructose-to-allulose conversion rate and thermal stability, and a polynucleotide encoding the same. The D-allulose epimerization enzyme mutant W29K / A77S / G216S / M234I is a mutant of the wild-type D-allulose epimerization enzyme derived from Flavonifractor plautii, in which tryptophan (Trp) at position 29 is substituted with lysine (Lys), alanine (Als) at position 77 is substituted with serine (Ser), glycine (Gly) at position 216 is substituted with serine (Ser), and methionine (Met) at position 234 is substituted with isoleucine (Ile). The D-allulose epimerization enzyme mutant W29K / A77S / G216S / M234I consists of the amino acid sequence of SEQ ID NO: 18, and the polynucleotide encoding it consists of the nucleotide sequence of SEQ ID NO: 19.

[0036] The inventors of the present invention have designated the D-allulose epimerization enzyme mutant W29K / A77S / G216S / M234I disclosed in Korean Patent Publication No. 10-2023-0073739 as "FpDPE2." As disclosed in Korean Patent Publication No. 10-2023-0073739, a polynucleotide fragment (SEQ ID NO: 19) of the D-allulose epimerization enzyme mutant W29K / A77S / G216S / M234I was inserted into the expression vector pET28a (Novagen) to prepare the recombinant vector pET28a::FpDPE2. PCR was then performed using the recombinant vector pET28a::FpDPE2 as a template and the FpDPE2-F and FpDPE2-R primer sets listed in Table 2 below. The resulting amplification product was cloned into pGEM T-easy vector (Promega Co., USA) and analyzed for its base sequence, confirming that it was a polynucleotide fragment 921 bp in length and composed of the base sequence of SEQ ID NO: 20. [Table 2]

[0037] Example 3: Preparation of a ligated fragment of a promoter and an allulose epimerization enzyme mutant gene Using a polynucleotide fragment consisting of the nucleotide sequence of SEQ ID NO: 1 and a polynucleotide fragment consisting of the nucleotide sequence of SEQ ID NO: 20 as templates, overlap extension PCR was performed using the Pctrl-F primer listed in Table 1 and the FpDPE2-R primer set listed in Table 2 to generate an expression cassette fragment Pctrl_FpDPE2 in which the promoter Pctrl-F and the allulose epimerization enzyme gene FpDPE2 were linked. The expression cassette fragment Pctrl_FpDPE2 was cloned into the pGEM T-easy vector (Promega Co., USA), and analysis of the nucleotide sequence confirmed that it was 1,221 bp in length and contained a polynucleotide consisting of the nucleotide sequence of SEQ ID NO: 23. In addition, a polynucleotide fragment composed of the nucleotide sequence of SEQ ID NO: 3 and a polynucleotide fragment composed of the nucleotide sequence of SEQ ID NO: 20 were used as templates, and overlap extension PCR was performed using the Pds1-F primer listed in Table 1 and the FpDPE2-R primer set listed in Table 2 to create an expression cassette fragment Pds1_FpDPE2 in which the promoter Pds1 and allulose epimerization enzyme gene FpDPE2 were linked. The expression cassette fragment Pds1_FpDPE2 is a fragment containing a polynucleotide composed of the nucleotide sequence of SEQ ID NO: 24. In addition, a polynucleotide fragment composed of the nucleotide sequence of SEQ ID NO: 5 and a polynucleotide fragment composed of the nucleotide sequence of SEQ ID NO: 20 were used as templates, and overlap extension PCR was performed using the Pds2-F primer listed in Table 1 and the FpDPE2-R primer set listed in Table 2 to create an expression cassette fragment Pds2_FpDPE2 in which the promoter Pds2 and allulose epimerization enzyme gene FpDPE2 were linked. The expression cassette fragment Pds2_FpDPE2 is a fragment containing a polynucleotide consisting of the base sequence of SEQ ID NO:25.In addition, using a polynucleotide fragment composed of the nucleotide sequence of SEQ ID NO: 7 and a polynucleotide fragment composed of the nucleotide sequence of SEQ ID NO: 20 as templates, overlap extension PCR was performed using the Pds3-F primer listed in Table 1 and the FpDPE2-R primer set listed in Table 2 to produce an expression cassette fragment Pds3_FpDPE2 in which the promoter Pds3 and the allulose epimerization enzyme gene FpDPE2 are linked. The expression cassette fragment Pds3_FpDPE2 is a fragment containing a polynucleotide composed of the nucleotide sequence of SEQ ID NO: 26. Specifically, 1 pM of the primer set was added to a reaction solution containing 100 μM deoxynucleotide triphosphates (dATP, dCTP, dGTP, dTTP), and 100 ng each of the promoter and D-allulose epimerization enzyme mutant DNA fragments used as templates were mixed. PCR was performed for 25 to 30 cycles using a Thermocycler (TP600, TAKARA BIO Inc., JAPAN) in the presence of 1 unit of pfu-X DNA polymerase mixture (Bioneer).

[0038] Example 4: Construction of an expression vector for a D-allulose epimerization enzyme mutant The expression cassette fragments Pctrl_FpDPE2, Pds1_FpDPE2, Pds2_FpDPE2, and Pds3_FpDPE2 prepared in Example 3 were each digested with the restriction enzymes PstI and BamHI and ligated to the commercial plasmid expression vector pVWEx1, which contains the same restriction enzyme sites, to prepare the D-allulose epimerization enzyme mutant expression vectors pPctrl_FpDPE2, pPds1_FpDPE2, pPds2_FpDPE2, and pPds3_FpDPE2. The D-allulose epimerization enzyme mutant expression vectors were then transformed into the E. coli DH5α strain by the heat shock method (see Sambrook and Russell: Molecular Cloning), and kanamycin-resistant colonies were selected. The isolated colonies were inoculated into LB liquid medium containing kanamycin and cultured overnight at 37°C. The recombinant plasmids were extracted and sequenced, confirming that the vector sequences of the clones matched. The isolated recombinant plasmids were transformed into E. coli JM110 by the heat shock method (see Sambrook and Russell, Molecular Cloning), and kanamycin-resistant colonies were isolated.

[0039] Example 5: Construction of recombinant Corynebacterium strains expressing D-allulose epimerization enzyme mutants Colonies of the recombinant E. coli JM110 strain isolated in Example 4 were inoculated into LB liquid medium containing kanamycin and cultured overnight at 37°C. The recombinant plasmid was then extracted and transformed into a Corynebacterium glutamicum strain using the heat shock method (see Sambrook and Russell, Molecular Cloning). The transformed recombinant Corynebacterium glutamicum strain was then inoculated into 2YT solid medium containing kanamycin and cultured at 30°C for 24 hours. Colonies exhibiting kanamycin resistance were then isolated. The isolated colonies were then inoculated into 2YT liquid medium containing kanamycin and cultured at 30°C for 24 hours. The recombinant plasmid was then extracted and sequenced. As a result, random mutations were confirmed in the promoter Pds2 or allulose epimerization enzyme mutant gene sequences of some recombinant plasmids containing the promoter Pds2. The following Table 3 summarizes the random mutations that occurred in some recombinant plasmids containing the promoter Pds2. [Table 3] TIFF0007805404000004.tif117153

[0040] As shown in Table 3, in the case of the recombinant plasmid expression vectors recovered from colonies 1, 3, 4, 5, and 8, mutations occurred in the gene sequence of the allulose epimerization enzyme mutant, and it was predicted that translation to produce the desired allulose epimerization enzyme mutant would not be possible. In contrast, in the case of the recombinant plasmid expression vectors recovered from colonies 2, 6, and 7, mutations occurred in the promoter sequence, but the enzyme gene sequences were identical, and therefore it was determined that there was a possibility of expression of the desired enzyme. The mutant promoter in the recombinant plasmid expression vector recovered from colony 2 was named "Pds4," the mutant promoter in the recombinant plasmid expression vector recovered from colony 6 was named "Pds4-1," and the mutant promoter in the recombinant plasmid expression vector recovered from colony 7 was named "Pds4-2." The Pds4 promoter is composed of the nucleotide sequence of SEQ ID NO: 27. Furthermore, the recombinant plasmid expression vector recovered from colony 2 was renamed pPds4_FpDPE2, the recombinant plasmid expression vector recovered from colony 6 was renamed pPds4-1_FpDPE2, and the recombinant plasmid expression vector recovered from colony 7 was renamed pPds4-2_FpDPE2. The expression cassette fragment Pds4_FpDPE2 present in the recombinant plasmid expression vector pPds4_FpDPE2 is a fragment containing a polynucleotide composed of the nucleotide sequence of SEQ ID NO: 28.

[0041] Example 6: Measurement of the conversion rate of fructose to allulose and comparison of the strength of promoter-driven enzyme expression among recombinant Corynebacterium strains The conversion rate of fructose to allulose is proportional to the expression level of the D-allulose epimerization enzyme in the Corynebacterium strain. By measuring the conversion rate of fructose to allulose for each recombinant Corynebacterium strain, we compared the strength of the induction of enzyme expression by each promoter in the recombinant Corynebacterium strain.

[0042] To culture the recombinant Corynebacterium strain transformed with the recombinant expression vector, 100 ml of LB medium containing 50 μg / ml kanamycin was placed in a 1 L flask and inoculated with 1 ml of the recombinant Corynebacterium strain prepared in Example 5. The flask was then transferred to a shaking incubator and cultured for 14 hours at 30°C with 140 rpm shaking. The culture was then centrifuged to recover the bacterial cells. The recovered bacterial cells were then added to a 50 mM PIPES buffer solution (pH 7.0) containing 30% (w / w) fructose and 1 mM manganese sulfate (MnSO4) metal ions at a concentration of 1 mg / ml. The reaction was allowed to proceed at 62°C for a predetermined time, after which the temperature of the reaction mixture was lowered to 4°C to terminate the reaction. The mixture was then centrifuged at 16,600 × g and 4°C to recover the supernatant. The concentrations of allulose and fructose in the supernatant were then measured using high-performance liquid chromatography (HPLC), and the conversion rate of fructose to allulose was calculated from the results, which was then used as an indicator of enzyme activity.

[0043] Table 4 below summarizes the conversion rate as a function of reaction time when fructose is converted to allulose using the recombinant Corynebacterium strains prepared in the examples of the present invention. [Table 4]

[0044] As shown in Table 4, the recombinant Corynebacterium strains incorporating the Pds4 promoter and the Pds2 promoter showed higher fructose-to-allulose conversion rates than the recombinant Corynebacterium strain incorporating the Pctrl promoter. In particular, the recombinant Corynebacterium strain incorporating the Pds4 promoter showed the highest fructose-to-allulose conversion rate. These results demonstrate that the Pds4 and Pds2 promoters have a stronger enzyme expression induction effect than the Pctrl promoter. Furthermore, because the Pds4 and Pds2 promoters are in the form of a partial deletion or mutation of the Pctrl promoter in Corynebacterium strains, they are expected to not place a burden on the recombinant Corynebacterium strains and are therefore considered suitable as constitutively expressed promoters.

[0045] As described above, the present invention has been described through the above examples, but the scope of protection of the present invention is not necessarily limited thereto, and various modifications are possible within the scope of the scope and spirit of the present invention. Therefore, the scope of protection of the present invention should not be limited to the specific embodiment disclosed as the best mode, but should be interpreted as including all embodiments falling within the scope of the claims attached to the present invention.

Claims

1. An allulose epimerization enzyme expression cassette comprising a polynucleotide encoding an allulose epimerization enzyme and a promoter operably linked thereto, wherein the promoter is composed of the base sequence of SEQ ID NO: 6 or the base sequence of SEQ ID NO: 27, and regulates the expression of the allulose epimerization enzyme in a Corynebacterium strain.

2. The allulose epimerization enzyme expression cassette according to claim 1, wherein the allulose epimerization enzyme is derived from Flavonifractor plautii, Clostridium scidens, Treponema primitia, Ensifer adhaerens, or Ruminococcus torques.

3. The allulose epimerization enzyme expression cassette of claim 1, wherein the allulose epimerization enzyme is composed of the amino acid sequence of SEQ ID NO: 14, the amino acid sequence of SEQ ID NO: 16, or the amino acid sequence of SEQ ID NO:

18.

4. The allulose epimerization enzyme expression cassette of claim 1, wherein the polynucleotide encoding the allulose epimerization enzyme is composed of the base sequence of SEQ ID NO: 15, the base sequence of SEQ ID NO: 17, or the base sequence of SEQ ID NO:

19.

5. The allulose epimerization enzyme expression cassette of claim 1, comprising a polynucleotide consisting of the base sequence of SEQ ID NO: 25 or a polynucleotide consisting of the base sequence of SEQ ID NO:

28.

6. A recombinant expression vector into which the expression cassette according to any one of claims 1 to 5 has been inserted.

7. A recombinant Corynebacterium strain, wherein a host strain of the genus Corynebacterium is transformed by introducing the expression cassette according to any one of claims 1 to 5 or a recombinant expression vector into which the expression cassette has been inserted.

8. 8. The recombinant Corynebacterium strain of claim 7, wherein the Corynebacterium host strain is selected from the group consisting of Corynebacterium glutamicum, Corynebacterium acetoglutamicum, Corynebacterium acetoacidophilum, Corynebacterium thermoaminogenes, Corynebacterium melassecola, and Corynebacterium efficiens.

9. A method for producing allulose, comprising the step of adding the recombinant Corynebacterium strain of claim 8 to a fructose-containing solution and reacting the solution.

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