Patent Application
20150159183
This application claims the benefit of Korean Patent Application No. 10-2013-0151708, filed on Dec. 6, 2013, in the Korean Intellectual Property Office, the disclosure of which is incorporated herein in its entirety by reference.
Incorporated by reference in its entirety herein is a computer-readable nucleotide/amino acid sequence listing submitted herewith and identified as follows: One 91,634 bytes ASCII (Text) file named “716723_ST25.TXT,” created Dec. 3, 2014.
1. Field
The present disclosure relates to a yeast cell with inactivated or depressed pyruvate carboxylase and a method of producing lactate using the yeast cell.
2. Description of the Related Art
Lactate is an organic acid that is broadly used in various industrial fields, such as food, pharmaceutics, chemicals, and electronics. Lactate is colorless, odorless, and a low-volatile material that dissolves well in water. Lactate is non-toxic to the human body and thus may be used as a flavor agent, a taste agent, or a preserving agent. Also, lactate is an environment-friendly alternative polymer material and a raw material of a polylactic acid (PLA) that is biodegradable plastic.
PLA is a polyester-based resin that is produced by ring-open polymerizing a dimer, i.e., lactide, which has been converted from lactic acid and may be variously processed into a film, sheet, fiber, plastic, etc. Thus, demands for PLA as bioplastic have recently increased to broadly replace conventional typical petrochemical plastic, such as polyethylene (PE), polypropylene (PP), polyethylene terephthalate (PET), or polystylene (PS).
In addition, lactate includes both a hydroxyl group and a carboxyl group at the same time and thus is highly reactive. Accordingly, lactate is easily converted into an industrially important compound, such as lactate ester, acetaldehyde, or propyleneglycol, and thus has received attention as an alternative chemical material of the next generation in chemical industry.
Currently, lactate is produced by an industrially petrochemical synthesis process and a biotechnological fermentation process. The petrochemical synthesis process is performed by oxidizing ethylene derived from crude oil, preparing lactonitrile through addition of hydrogen cyanide after acetaldehyde, purifying by distillation, and hydrolyzing by using chloric acid or phosphoric acid. Also, the biotechnological fermentation process is used to manufacture lactate from a reproducible carbon hydrate, such as, starch, sucrose, maltose, glucose, fructose, or xylose, as a substrate.
Therefore, a strain for efficiently producing lactate and a lactate production method using the strain are needed.
Provided is a genetically engineered yeast cell with an improved ability of producing lactate, wherein the yeast cell has reduced pyruvate to oxaloacetate conversion activity.
Provided is a method of producing lactate by using the yeast cell, and a method of preparing a yeast cell with improved ability to produce lactate.
Additional aspects will be set forth in part in the description which follows and, in part, will be apparent from the description, or may be learned by practice of the presented embodiments.
These and/or other aspects will become apparent and more readily appreciated from the following description of the embodiments, taken in conjunction with the accompanying drawings in which:
Reference will now be made in detail to embodiments, examples of which are illustrated in the accompanying drawings, wherein like reference numerals refer to the like elements throughout. In this regard, the present embodiments may have different forms and should not be construed as being limited to the descriptions set forth herein. Accordingly, the embodiments are merely described below, by referring to the figures, to explain aspects of the present description. As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items. Expressions such as “at least one of,” when preceding a list of elements, modify the entire list of elements and do not modify the individual elements of the list.
According to an aspect of the present invention, provided is a yeast cell comprising an inactivated or reduced ability to convert pyruvate into oxaloacetate. As used herein, the term “lactate” denotes “a lactic acid” or a salt thereof.
As used herein, the term “activity increase”, “enzyme activity increase”, “increased activity”, or “increased enzyme activity” denotes that a cell or an enzyme has an increased activity level compared to an activity level of a comparable cell of the same type or the original enzyme. For example, an enzyme conversion activity from a substrate to a product with respect to a corresponding enzyme may be at least about 5%, at least about 10%, at least about 15%, at least about 20%, at least about 30%, at least about 50%, at least about 60%, at least about 70%, or at least about 100% increased compared to the same biochemical conversion activity of an enzyme produced by a parent cell. A cell having an increased enzyme activity of an enzyme may be confirmed by using any method commonly known in the art.
The term “parent cell” refers to an original cell, for example, a non-engineered cell of the same type as an engineered yeast cell. With respect to a particular genetic modification, the “parent cell” can be a cell that lacks the particular genetic modification, but is identical in all other respects. Thus, a parent cell can be a cell used as starting material to produce a genetically engineered yeast cell having a reduced, inactivated, or depressed activity of a given protein (e.g., a protein having a sequence identity of about 95% or more to a polypeptide that converts pyruvate to oxaloacetate).
Meanwhile, as used herein, an “inactivated” or “depressed” or “reduced” activity of a cell enzyme or a polypeptide, or an enzyme or cell having an activity that is “inactivated” or “depressed” or “reduced” denotes a cell, an isolated enzyme, or a polypeptide having an activity that is lower than an activity measured in a cell of the comparable cell of the same type or the original enzyme, or having no activity. For example, an enzyme conversion activity from a substrate to a product with respect to a corresponding enzyme may be about 20% or more, about 30% or more, about 40% or more, about 50% or more, about 55% or more, about 60% or more, about 70% or more, about 75% or more, about 80% or more, about 85% or more, about 90% or more, about 95% or more, or about 100% reduced than the biochemical conversion activity by an enzyme produced by a parent cell. The cells having reduced activity of the enzyme may be confirmed by using a commonly known method in the art. As used herein, the term “inactivation” may refer to generating a gene that is not expressed at all or a gene encoding a gene product that has no activity even when it is expressed. The term “depression” or “reduction” may refer to generating a gene whose expression level is reduced lower than that of a non-engineered yeast cell, or a gene which encodes a protein with decreased activity although it is expressed.
Also, activity of a cell, polypeptide, or enzyme may be reduced due to deletion or disruption of a gene encoding the polypeptide or enzyme. As used herein, the “deletion” or “disruption” of the gene includes mutation or deletion of the gene or a regulatory region of the gene (e.g., operator, promoter or terminator regions of the gene), or a part thereof, sufficient to disrupt or delete gene function or the expression of a functional gene product. Mutations may include substitutions, insertions, and deletions of one or more bases in the gene or its regulator regions. As a result, the gene is not expressed or has a reduced amount of expression, or the activity of the encoded protein or enzyme is reduced or eliminated. The deletion or disruption of the gene may be accomplished by any suitable genetic engineering technique, such as homologous recombination, mutagenesis, or molecular evolution. When a cell includes a plurality of copies of the same gene or at least two different polypeptide paralogs, at least one gene may be deleted or disrupted.
As used herein, a cell that is not genetically engineered may include a parent cell or a wild-type cell from which a yeast cell comprising an inactivated or reduced ability to convert pyruvate into oxaloacetate is derived by genetic manipulation. The inactivation, depression or reduction of the enzyme may be due to mutation (substitution, addition (insertion) or deletion mutation) of a part of a gene, or deletion of the whole gene. Addition (insertion), substitution, or deletion mutation may be of at least one base group to a gene that encodes the enzyme. The inactivation, depression, reduction may be achieved by gene manipulation such as homogenous recombination, mutation generation, or molecule evolution. When a cell includes a plurality of the same genes or at least two different polypeptide paralogous genes, one or more genes may be inactivated or depressed. The inactivation, depression, reduction may be performed by transforming a vector including some sequences of the gene to a cell, and allowing the sequences to homogeneously recombine with an endogenous gene by culturing the cell, and then by selecting the homogenously recombined cell by using a selection marker.
An activity of the enzyme may be depressed or reduced due to modification of an expression control sequence of a gene, amplification of an expression-decrease related gene, deletion of an expression-increase related gene, or decreased copy number of a gene. The expression control sequence may include an induction promoter, a transcription promotion factor, or a transcription terminator. The modification of an expression control sequence of a gene may include replacing a promoter of a parent cell with a promoter having a low level of expression compared to that of the parent cell. The yeast cell may include a promoter with a low level of expression compared to that of the parent cell.
As used herein, the term “gene” refers to a nucleic acid segment expressing a specific protein, and the gene may or may not include a regulatory sequence of a 5′-non coding sequence and a 3′-non coding sequence.
As used herein, the term “sequence identity” of a nucleic acid or a polypeptide refers to a degree of similarity (i.e. homology) of base groups or amino acid residues between two aligned sequences, when the two sequences are aligned to match each other as possible, at corresponding positions. The sequence identity is a value that is measured by aligning to an optimum state and comparing the two sequences at a particular comparing region, wherein a part of the sequence within the particular comparing region may be added or deleted compared to a reference sequence. A sequence identity percentage may be calculated, for example, by 1) comparing the two sequences aligned within the whole comparing region to an optimum 2) obtaining the number of matched locations by determining the number of locations represented by the same amino acids of nucleic acids in both of the sequences, 3) dividing the number of the matched locations by the total number of the locations within the comparing region (i.e., a range size), and 4) obtaining a percentage of the sequence identity by multiplying 100 to the result. The sequence identity percent may be determined by using a common sequence comparing program, for example, BLASTN or BLASTP (NCBI), CLC Main Workbench (CLC bio), or MegAlign™ (DNASTAR Inc).
In confirming many different polypeptides or polynucleotides having the same or similar function or activity, sequence identities at several levels may be used. For example, the sequence identities may be about 50% or greater, about 55% or greater, about 60% or greater, about 65% or greater, about 70% or greater, about 75% or greater, about 80% or greater, about 85% or greater, about 90% or greater, about 95% or greater, about 96% or greater, about 97% or greater, about 98% or greater, about 99% or greater, or 100%.
The yeast cell may have an improved ability of producing lactate. The yeast cell with an improved lactate productivity refers to a yeast cell with an increased lactate productivity compared to that of a parent cell.
Also, the yeast cell may be ascomycota. The ascomycota may be saccharomycetacease. The saccharomycetaceae may be Saccharomyces genus, Kluyveromyces genus, Candida genus, Pichia genus, Issatchenkia genus, Debaryomyces genus, Zygosaccharomyces genus, Shizosaccharomyces genus, or Saccharomycopsis genus. The Saccharomyces genus may be, for example, S. cerevisiae, S. bayanus, S. boulardii, S. bulderi, S. cariocanus, S. cariocus, S. chevalieri, S. dairenensis, S. ellipsoideus, S. eubayanus, S. exiguus, S. florentinus, S. kluyveri, S. martiniae, S. monacensis, S. norbensis, S. paradoxus, S. pastorianus, S. spencerorum, S. turicensis, S. unisporus, S. uvarum, or S. zonatus. The Kluyveromyces genus may be Kluyveromyces lactis, Kluyveromyces marxianus, or Kluyveromyces thermotolerans. The Candida genus may be Candida glabrata, Candida boidinii, Candida magnolia, Candida methanosorbosa, Candida sonorensis, or Candida utilis. The Pichia genus may be Pichia stipitis. The Issatchenkia genus may be Issatchenkia orientalis. The Debaryomyces genus may be Debaryomyces hansenii. The Zygosaccharomyces genus may be Zygosaccharomyces bailli or Zygosaccharomyces rouxii. The Shizosaccharomyces genus may be S. cryophilus, S. japonicus, S. octosporus, or S. pombe.
Also, the enzyme cell may include a mutant enzyme cell for producing a desired produce, such as lactate, as well as a natural enzyme cell. The mutant enzyme cell may have resistance with respect to, for example, uracil, sulfurguanidine, sulfathiazole, azaserine, trimethoprim, or monofluoroacetate.
The polypeptide capable of converting pyruvate to oxalate may catalyze reactions, such as magnesium-ATP dependent carboxylation from pyruvate to oxaloacetate and biotin-dependent carboxylation. The polypeptide may convert pyruvate into oxaloacetate when one ATP is consumed. The polypeptide may be an enzyme that is classified as EC 6.4.1.1. The polypeptide may be two pyruvate carboxylase isoenzymes (PYC1 and PYC2) among enzymes of Saccharomyces genus. The polypeptide capable of converting pyruvate to oxaloacetate may have an amino acid sequence having about 50% or more, about 70% or more, about 80% or more, about 90% or more, about 95% or more, about 96% or more, about 97% or more, about 98% or more, about 99% or more, or about 100% or more of a sequence identity with an amino acid sequence of SEQ ID NO: 1 (GenBank ID: NP—011453.1) and/or SEQ ID NO: 2(GenBank ID: NP—009777.1). The two pyruvate carboxylase isoenzymes may be encoded by different genes. Each of the genes may have a nucleotide sequence of SEQ ID NO: 3 (GI Number: 6321376) and/or SEQ ID NO: 4 (GI Number: 63196950). The gene may be PYC1 or PYC2 that encodes a pyruvate carboxylase (PYC). The modification of an expression control sequence of a gene of PYC1, PYC2, or a combination thereof may be performed by replacing promoters PPYC1 and PPYC2 of a parent cell with promoters having a lower expression level than those of the parent cell. The promoters may be operably connected to the coding region of the polypeptide converting pyruvate to oxalate. The promoters having a low expression level may be, for example, a LEUM promoter (Pleum), a cyc1 promoter (Pcyc1), or a mutant thereof. Also, the promoters having a lower expression level than those of the promoters of a parent cell, PPYC1 and PPYC2, may be, for example, TEF1, a GPC promoter, or a GAL promoter.
In the yeast cell, an activity of a polypeptide capable of converting pyuruvate to acetaldehyde, a polypeptide capable of converting lactate to pyruvate, a polypeptide capable of converting dehydroxyacetone phosphate (DHAP) to glycerol-3-phosphate, an external mitochondrial NADH dehydrogenase, or a combination may be inactivated or depressed. The yeast cell may comprise a deletion or disruption mutation of a gene encoding a polypeptide that converts pyruvate to acetaldehyde, a gene encoding a polypeptide that converts lactate to pyruvate, a gene encoding a polypeptide that converts dehydroxyacetone phosphate (DHAP) to glycerol-3-phosphate, a gene encoding an external mitochondria NADH dehydrogenase, or a combination thereof.
In the yeast cell, an activity of a polypeptide capable of converting pyruvate to acetaldehyde may be inactivated or depressed. The polypeptide converting pyruvate to acetaldehyde may belong to EC 4.1.1.1. The polypeptide capable of converting pyruvate to acetaldehyde may have an amino acid sequence having about 50% or more, about 70% or more, about 80% or more, about 90% or more, about 95% or more, about 96% or more, about 97% or more, about 98% or more, about 99% or more, or about 100% or more of a sequence identity with an amino acid sequence of SEQ ID NO: 5. A gene that encodes the polypeptide capable of converting pyruvate to acetaldehyde may be pdc1 or pdc2 that encodes a pyruvate decarboxylase (PDC). For example, the gene that encodes the polypeptide capable of converting pyruvate to acetaldehyde may have a nucleotide sequence of SEQ ID NO: 6. The activity of the polypeptide may be reduced due to a mutation (addition, substitution, or deletion or one or more bases) in the gene, or deletion of all or part of the gene. For example, the activity of the polypeptide may be reduced due to a deletion or disruption mutation of a gene encoding a polypeptide that converts pyruvate to acetaldehyde.
The yeast cell may have an inactivated or depressed activity of a polypeptide capable of converting lactate to pyruvate. The polypeptide capable of converting lactate to pyruvate may be a cytochrome c-dependent enzyme. The polypeptide capable of converting lactate to pyruvate may be a lactate cytochrome-c oxydoreductase (CYB2). The lactate cytochrome c-oxydoreductase may be an enzyme that is classified as EC 1.1.2.4 acting on D-lactate or EC 1.1.2.3 acting on L-lactate. The polypeptide capable of converting lactate to pyruvate may include an amino acid sequence having about 50% or more, about 70% or more, about 80% or more, about 90% or more, about 95% or more, about 96% or more, about 97% or more, about 98% or more, about 99% or more, or about 100% or more sequence identity with an amino acid sequence of SEQ ID NO: 7. The gene that encodes the polypeptide capable of converting lactate to pyruvate may have a nucleotide sequence of SEQ ID NO: 8. The activity of the polypeptide may be reduced due to a mutation (addition, substitution, or deletion or one or more bases) in the gene, or deletion of all or part of the gene. For example, the activity of the polypeptide may be reduced due to a deletion or disruption mutation of a gene encoding a polypeptide that converts lactate to pyruvate.
In the yeast cell, the activity of a polypeptide capable of converting DHAP to glycerol-3-phosphate may be inactivated or depressed. The polypeptide capable of converting DHAP to glycerol-phosphate may be an enzyme catalyzing reduction of DHAP to glycerol-3-phosphate by using oxidation of NAD(P)H to NAD(P)+. The enzyme may belong to EC 1.1.1.8. The polypeptide may be cytosolic glycerol-3-phosphate dehydrogenase (GPD1). The polypeptide capable of converting DHAP to glycerol-3-phosphate may include an amino acid sequence having about 50% or more, about 70% or more, about 80% or more, about 90% or more, about 95% or more, about 96% or more, about 97% or more, about 98% or more, about 99% or more, or about 100% or more sequence identity with an amino acid sequence SEQ ID NO: 9. The gene that encodes the polypeptide capable of converting DHAP to glycerol-3-phosphate may have a nucleotide sequence of SEQ ID NO: 10. The gene may be GPD1 that encodes a glycerol-3-phosphate dehydrogenase. The activity of the polypeptide may be reduced due to a mutation (addition, substitution, or deletion or one or more bases) in the gene, or deletion of all or part of the gene. For example, the activity of the polypeptide may be reduced due to a deletion or disruption mutation of a gene encoding a polypeptide that converts dehydroxyacetone phosphate (DHAP) to glycerol-3-phosphate.
In the yeast cell, an activity of the external mitochondrial NADH dehydrogenase may be inactivated or depressed. The external mitochondrial NADH dehydrogenase may be an enzyme that is classified as EC. 1.6.5.9 or EC. 1.6.5.3. The NADH dehydrogenase may be type II NADH:ubiquinone oxidoreductase. The NADH dehydrogenase may be located on an outer surface of an inner mitochondrial membrane facing the cytoplasm. The NADH dehydrogenase may be an enzyme that catalyzes oxidation of cytosolic NADH to NAD+. The NADH dehydrogenase may re-oxidize the cytosolic NADH formed therefrom. The NADH dehydrogenase may provide the cytosolic NADH to a mitochondrial respiratory chain. The NADH dehydrogenase may be NDE1, NDE2, or a combination thereof. The NADH dehydrogenase may be different from an internal mitochondrial NADH dehydrogenase, NDI1, that is located and functions inside the mitochondria. The NDE1 and NDE2 may each have an amino acid sequence having about 50% or more, about 70% or more, about 80% or more, about 90% or more, about 95% or more, about 96% or more, about 97% or more, about 98% or more, about 99% or more, or about 100% or more sequence identity with an amino acid sequence SEQ ID NO: 11 or 12. A gene encoding NDE1 and a gene encoding NDE2 may each have a nucleotide sequence of SEQ ID NO: 13 or 14. The activity of the polypeptide may be reduced due to a mutation (addition, substitution, or deletion or one or more bases) in the gene, or deletion of all or part of the gene. For example, the activity of the polypeptide may be reduced due to a deletion or disruption mutation of a gene encoding an external mitochondria NADH dehydrogenase.
In the yeast cell, an activity of the polypeptide capable of converting pyruvate to lactate may increase. In the yeast cell, the lactate dehydrogenase activity converting pyruvate to lactate may be increased due to an increased expression of lactate dehydrogenase converting pyruvate to lactate.
The increased LDH expression may be caused by introduction of a gene encoding a lactate dehydrogenase. The gene may be an exogenous gene. The exogenous gene may be homologous or heterologous. The exogenous gene that encodes a lactate dehydrogenase may be introduced at a downstream position of a promoter enabling expression of a gene that encodes a lactate dehydrogenase. Also, a polynucleotide that encodes a lactate dehydrogenase (also, referred to as “LDH”) may be included in a genome of a yeast cell. When a polynucleotide encoding LDH functions for production of active proteins in a cell, the polynucleotide is considered “functional” in a cell. A yeast cell including the polynucleotide encoding L-LDH or D-LDH may produce a L-lactate enantiomer, a D-lactate enantiomer, or a salt thereof.
The copy number of the gene encoding LDH may increase due to the introduced gene that encodes LDH.
The yeast cell may include a gene that encodes one lactate dehydrogenase or multiple genes that encode 1 to 10 copies of lactate dehydrogenase. The multiple genes may encode, for example, 1 to 8, 1 to 5, 1 to 4, or 1 to 3 copies of lactate dehydrogenase. When the yeast cell includes the genes encoding multiple copies of lactate dehydrogenase, each of the genes may be a copy of the same gene or may include a copy of a gene that encodes at least two different lactate dehydrogenases. Multiple copies of a gene encoding exogenous lactate dehydrogenase may be included in the same locus or in multiple loci within a host cell's genome. The exogenous lactate dehydrogenase may have a better activity than an endogenous lactate dehydrogenase of a yeast cell.
The gene encoding lactate dehydrogenase may be derived from bacteria, yeast, fungi, mammals, or reptiles. The gene may be a polynucleotide that encodes at least one lactate dehydrogenase selected from Pelodiscus sinensis japonicus, Ornithorhynchus anatinus, Tursiops truncatus, Rattus norvegicus, and Xenopus laevis. A lactate dehydrogenase derived from Pelodiscus sinensis japonicas, a lactate dehydrogenase derived from Ornithorhynchus anatinus, a lactate dehydrogenase derived from Tursiops truncatus, a lactate dehydrogenase derived from Rattus norvegicus, and a lactate dehydrogenase derived from Xenopus laevis may, each respectively, have amino acid sequences having about 50% or more, 60% or more, 70% or more, 80% or more, 90% or more, 95% or more, 96% or more, 97% or more, 98% or more, 99% or more, or 100% of sequence identity with amino acid sequences of SEQ ID NO: 15, 16, 17, and 18. A gene that encodes the lactate dehydrogenase may have a nucleotide sequence of SEQ ID NO: 19.
The polynucleotide encoding lactate dehydrogenase may be expressed from a vector including lactate dehydrogenase derived from bacteria, yeast, fungus, mammals, or reptiles. The vector may include a replication origin, a promoter, a polynucleotide encoding a lactate dehydrogenase, and a terminator. The replication origin may include a yeast autonomous replication sequence (ARS). The yeast ARS may be stabilized by a yeast centrometric sequence (CEN). The promoter may be selected from the group consisting of a CYC promoter, a TEF promoter, a GPD promoter, and an ADH promoter. The CYC promoter, TEF promoter, GPD promoter, ADH promoter, and CCW12 promoter may have, each respectively, nucleotide sequences of SEQ ID NO: 21, 22, 23, 24, and 73. The terminator may be selected from the group consisting of phosphoglycerate kinase 1 (PGK1), cytochrome c transcription (CYC1), and GAL1. The CYC1 terminator may have a nucleotide sequence of SEQ ID NO: 25. The vector may further include a selection marker.
In the yeast cell, an activity of a polypeptide capable of converting pyruvate to oxaloacetate is depressed. The depression of the activity of a polypeptide may be caused by replacement of an expression control sequence of a gene encoding the polypeptide with a promoter having a low level of expression compared to that of the parent cell, an inactivated or depressed activity of a gene that encodes the polypeptide capable of converting pyruvate to acetaldehyde, a gene that encodes the polypeptide capable of converting lactate to pyruvate, a gene that encodes the polypeptide capable of converting DHAP to glycerol-3-phosphate, a gene that converts the polypeptide capable of converting external mitochondrial NADH dehydrogenase, or a combination, or introduction of a gene that encodes the polypeptide capable of converting pyruvate to lactate into the yeast cell. The polypeptide capable of converting pyruvate to oxaloacetate may be a pyruvate carboxylase 1 (PYC1), a pyruvate carboxylase 2 (PYC2), or a combination thereof.
In the yeast cell, an activity of the polypeptide capable of converting pyruvate to oxaloacetate is inactivated or depressed. The depression of an activity of PYC2, which is one of polypeptides converting pyruvate to oxaloacetate, may be caused by replacement of an expression control sequence of a gene encoding the polypeptide with a promoter having a low level of expression compared to that of the parent cell. The inactivation of the activity of PYC2 may be caused by substitution, addition, or deletion of a part of or the whole gene encoding the polypeptide, an inactivated or depressed activity of a gene that encodes the polypeptide capable of converting pyruvate to acetaldehyde, a gene that encodes the polypeptide capable of converting lactate to pyruvate, a gene that encodes the polypeptide capable of converting DHAP to glycerol-3-phosphate, a gene that converts the polypeptide capable of converting external mitochondrial NADH dehydrogenase, or a combination, or introduction of a gene that encodes the polypeptide capable of converting pyruvate to lactate into the yeast cell.
The yeast cell may produce lactate at a yield that is about 4.5 to about 15%, about 5 to about 15%, about 6 to about 15%, about 7.5 to about 15%, about 8 to about 15%, about 8 to about 14%, or about 8 to about 13.8% or more increased than that of the parent cell, in which an activity of the polypeptide capable of converting pyruvate to oxaloacetate is not inactivated or depressed. Also, the yeast cell may produce lactate at a yield of about 45.5 to about 51% or more, or about 45.5% to about 50.5%, which is a ratio of an amount of consumed glucose to an amount of produced lactate.
According to another embodiment of the present invention, provided is a method of preparing lacate, wherein the method includes culturing the yeast cell described above in a cell culture medium, whereby the yeast cell produces lactate, and collecting lactate from the culture.
The culturing may be performed in a carbon source, for example, a medium containing glucose. The medium used in the culturing of a yeast cell may be a common medium suitable for growth of a host cell such as a minimal or composite medium containing appropriate supplements.
The medium used in the culturing may be a medium that satisfies particular conditions for growing a yeast cell. The medium may be one selected from the group consisting of a carbon source, a nitrogen source, a salt, trace elements, and a combination thereof.
The culturing condition for obtaining lactate from the genetically engineered yeast cell may be appropriately controlled. The culturing may be performed in an aerobic or anaerobic condition. For example, the yeast cell is cultured under an aerobic condition for its proliferation, and then, the yeast cell is cultured under an anaerobic condition to produce lactate. The anaerobic condition may include a dissolved oxygen (DO) concentration of 0% to 10%, for example, 0% to 8%, 0% to 6%, 0% to 4%, or 0% to 2%. A pH of a fermented solution may be controlled to be maintained in a range of about 2 to about 7.
The culturing of the yeast cell may be a continuous type, a semi-continuous type, a batch type, or a combination thereof.
The term “culture condition” indicates a condition for culturing a yeast cell. Such culture condition may be, for example, a carbon source, a nitrogen source, or an oxygen condition for the yeast cell to use. The carbon source used by the yeast cell includes monosaccharides, disaccharides, or polysaccharides. In particular, the carbon source may be glucose, fructose, mannose, or galactose. The nitrogen source used by the yeast cell may include an organic nitrogen compound or an inorganic nitrogen compound. In particular, the nitrogen source may be an amino acid, amide, amine, a nitrate, or an ammonium salt. The oxygen condition for culturing the yeast cell includes an aerobic condition of a normal oxygen partial pressure, a low-oxygen condition including 0.1% to 10% of oxygen in the atmosphere, or an anaerobic condition without oxygen. A metabolic pathway may be modified in accordance with the carbon source or the nitrogen source that may be practically used by the yeast cell.
Obtaining the lactate from the culture may be performed by separating the lactate from the culture by using a method commonly known in the art. The separation method may be centrifuge, filtration, ion-exchange chromatography, or crystallization. For example, the culture may be centrifuged at a low rate to remove a biomass, and the supernatant resulting therefrom may be separated through ion-exchange chromatography.
The present invention will be described in further detail with reference to the following examples. These examples are for illustrative purposes only and are not intended to limit the scope of the present invention.
In order to block a production pathway of ethanol and glycerol as main byproducts, a pyruvate decarboxylase (pdcl) gene, which is a main enzyme of alcohol fermentation, a NAD-dependent glycerol-3-phosphate dehydrogenase (GPD1) gene, which is a main enzyme of glycerol biosynthesis, and a L-lactate cytochrome-c oxidoreductase2 (cyb2) gene, which is a lactate lyase, were inactivated by homogenous recombination using Saccharomyces cerevisiae CEN.PK2-1D (MATa ura3-52; trp1-289; leu2-3,112; his3 Δ 1; MAL2-8C; SUC2, EUROSCARF accession number: 30000B) as a lactate production strain.
(1.1) Preparation of L-LDH Overexpression Vector and Inactivated Vectors of pdc1, GPD1, and cyb2 Genes
(1.1.1) Preparation of a L-LDH Overexpression Vector
A CCW12 promoter PCR fragment obtained by performing PCR with a genomic DNA of Saccharomyces cerevisiae CEN.PK2-1D as a template and using primers of SEQ ID NO: 26 and SEQ ID NO: 27 was digested with SacI and XbaI, and the resultant was inserted into p416-GPD vector (ATCC 87360™) digested with SacI and XbaI, producing p416-CCW12p vector.
Then, L-Idh gene (SEQ ID NO: 19) was amplified from Pelodiscus sinensis japonicus genomic DNA by PCR using primers of SEQ ID NO: 28 and SEQ ID NO: 29. The resulting L-Idh PCR fragment and p416-CCW12p obtained therefrom were digested with BamHI and SaII, and ligated, producing p416-CCW12p-LDH, which is an L-Idh expression vector.
The L-Idh expression vector has also a yeast autonomous replication sequence (ARS)/a yeast centrometric sequence (CEN) of SEQ ID NO: 20, a CYC promoter of SEQ ID NO: 21, a CCW12 promoter of SEQ ID NO: 73, and a CYC1 terminator of SEQ ID NO: 25. The L-Idh expression vector included a polynucleotide encoding L-Idh derived from Pelodiscus sinensis japonicus of SEQ ID NO: 19.
(1.1.2) Preparation of a Gene Exchange Vector
PDC1, CYB2, and GPD1 genes were deleted by using a homologous recombination method, and at the same time, a gene exchange vector for introducing an L-LDH gene was prepared in the same manner described below.
PCR was performed using the prepared p416-CCW12p-LDH as a template with primers of SEQ ID NOS: 30 and 31. The resulting PCR fragment and the prepared pUC57-ura3HA vector were digested with Sacl and ligated, producing pUC57-CCW12p-LDH-ura3HA.
PCR was performed using the produced pUC57-CCW12p-LDH-ura3HA as a template with primers of SEQ ID NOS: 32 and 33, producing a pdc1 gene deletion cassette.
PCR was performed using the produced pUC57-CCW12p-LDH-ura3HA as a template with primers of SEQ ID NOS: 34 and 35, producing a cyb2 gene deletion cassette.
PCR was performed using the produced pUC57-CCW12p-LDH-ura3HA as a template with primers of SEQ ID NOS: 36 and 37, producing a GPD1 gene deletion cassette.
(1.2) Inactivation of pdc1, GPD1, and cyb2 Genes
A mutant strain of Saccharomyces cerevisiae CEN.PK2-1D, in which pdc1 is deleted, was produced in the same manner as follows. Saccharomyces cerevisiae CEN.PK2-1D was plated onto a YPD agar plate (including 10 g of yeast extract, 20 g of peptone, and 20 g of glucose) and incubated for 24 hours at 30° C., and then, a colony obtained therefrom was inoculated in about 10 ml of a YPD liquid medium and cultured for about 18 hours at about 30° C. The sufficiently grown culture solution was inoculated in about 50 ml of a YPD liquid medium contained in a 250 ml-flask at a concentration of 1% (v/v) and cultured in an incubator at a rate of about 230 rpm and at 30° C. After about 4 to 5 hours, when the OD600 reached about 0.5, the culture was centrifuged at a rate of about 4,500 rpm for about 10 minutes to harvest cells, and the cells were resuspensed in a lithium acetate solution at a concentration of about 100 mM. Then, the cells were harvested by performing centrifugation at a rate of about 4,500 rpm for about 10 minutes, resuspensed in a lithium acetate solution at a concentration of about 1 M, and then divided into a volume of about 100 μl each.
In order to delete a pdc1 gene, the PDC1 deletion cassette produced in Example 1.1.2 was mixed with 50% of polyethyleneglycol and a single stranded carrier DNA and reacted in a water tub for about 1 hour at 42° C., and then, the culture solution was spread on a uracil-free minimal agar plate (including YSD, 6.7 g/L of yeast nitrogen base without amino acids, and 1.4 g/L of amino acid dropout mix (-ura)) and grown for about 24 hours or more at 30° C. Ten colonies (mutant strains) grown on the plate were selected, patched onto the fresh uracil-free minimal agar plate, and at the same time, inoculated into a liquid medium including the same components contained in the uracil-free minimal agar plate to isolate the genomic DNA from the above mutant strains by using a commonly used kit (Gentra Puregene Cell kit, Qiagen, USA). In order to confirm deletion of pdcl gene, PCR was performed using the isolated genomic DNA of the mutant strain as a template with primers of SEQ ID NOS: 38 and 39, and then, electrophoresis was performed on the obtained PCR product to confirm pdcl deletion. As a result, Saccharomyces cerevisiae CEN.PK2-1D (Δ pdc1::Idh+ura3) was obtained.
Also, for additional gene deletion using the gene exchange vector, a selection marker URA3 gene, which was introduced for the preparation of a CEN.PK2-1D (Δ pdc1::Idh+ura3) strain, was removed from those strain. Saccharomyces cerevisiae CEN.PK2-1D (Δ pdc1::Idh+ura3) was inoculated in about 10 ml of a YPD liquid medium, cultured for about 18 hours at 30° C., and spread on a 5-FOA plate (including YSD, 6.7 g/L of yeast nitrogen base without amino acids, 1.4 g/L of an amino acid dropout mix, and 1 μg/L of 5-fluoroorotic acid), and cultured for about 24 hours or more at 30° C. Ten colonies (a URA3 pop-out strain) grown on the 5-FOA plate were selected, patched onto the fresh 5-FOA plate, and, at the same time, cultured in a YPD liquid medium to isolate genomic DNA from the selected strain by using a commonly used kit (Gentra Puregene Cell kit, Qiagen, USA). In order to confirm deletion of URA3 gene by using the isolated genomic DNA of the URA3 pop-out strain as a template, PCR was performed using primers of SEQ ID NOS: 38 and 39, and then electrophoresis was performed on the obtained PCR product to confirm deletion of URA3 gene. As a result, Saccharomyces cerevisiae CEN.PK2-1D (Δ pdc1::Idh) was obtained.
A mutant strain of Saccharomyces cerevisiae CEN.PK2-1D (Δpdc1::Idh), in which cyb2 gene is deleted, was prepared in the same manner as used in the deletion of the pdc1 gene.
In order to delete a cyb2 gene, the cyb2 deletion cassette prepared in Example 1.1.2 was introduced to the Saccharomyces cerevisiae CEN.PK2-1D (Δ pdc1::Idh), which was resuspended in a lithium acetate solution, in the same manner as used in the deletion of the pdc1 gene, ten colonies grown on a plate were selected to isolate a genomic DNA. In order to confirm deletion of cyb2, PCR was performed by having the isolated genomic DNA as a template and primers of SEQ ID NOS: 40 and 41, and then electrophoresis was performed on the obtained PCR product to confirm deletion of cyb2 gene. As a result, Saccharomyces cerevisiae CEN.PK2-1D (Δ pdc1::Idh Δ cyb2::Idh+ura3) was obtained.
Also, for additional gene deletion using the gene deletion vector, a selection marker URA3 gene was removed from Saccharomyces cerevisiae CEN.PK2-1D (Δ pdc1::Idh Δ cyb2::Idh+ura3) in the same manner used in the URA3 pop-out method as described above. Ten colonies grown on a plate were selected to isolate a genomic DNA. In order to confirm deletion of URA3 gene by using the isolated genomic DNA of the URA3 pop-out strain as a template, PCR was performed using primers of SEQ ID NOS: 40 and 41, and then electrophoresis was performed on the obtained PCR product to confirm deletion of URA3 gene. As a result, Saccharomyces cerevisiae CEN.PK2-1D (Δ pdc1::Idh Δ cyb2::Idh) was obtained.
A mutant strain of Saccharomyces cerevisiae CEN.PK2-1D (Δ pdc1::Idh Δ cyb2::Idh), in which GPD1 gene is deleted, was prepared in the same manner as used in the deletion of the pdc1 gene.
In order to delete a GPD1 gene, the GPD1 deletion cassette prepared in Example 1.1.2 was introduced to the Saccharomyces cerevisiae CEN.PK2-1D (Δ pdc1::Idh Δ cyb2::Idh), which was resuspended in a lithium acetate solution, in the same manner as used in the deletion of the pdcl gene and the deletion of the cyb2 gene, ten colonies grown on a plate were selected to isolate a genomic DNA. In order to confirm deletion of GPD1, PCR was performed by having the isolated genomic DNA as a template and primers of SEQ ID NOS: 42 and 43, and then electrophoresis was performed on the obtained PCR product to confirm deletion of GPD1 gene. As a result, Saccharomyces cerevisiae CEN.PK2-1D (Δ pdc1::Idh Δ cyb2::Idh Δ GPD1::Idh+ura3) was obtained.
Also, for additional gene deletion using the gene deletion vector, a selection marker URA3 gene was removed from Saccharomyces cerevisiae CEN.PK2-1D (Δ pdc1::Idh Δ cyb2::Idh Δ gpd1::Idh+ura3) in the same manner used in the URA3 pop-out method as described above. Ten colonies grown on a plate were selected to isolate a genomic DNA. In order to confirm deletion of URA3 gene by using the isolated genomic DNA of the URA3 pop-out strain as a template, PCR was performed using primers of SEQ ID NOS: 42 and 43, and then electrophoresis was performed on the obtained PCR product to confirm deletion of URA3 gene. As a result, Saccharomyces cerevisiae CEN.PK2-1D (Δ pdc1::Idh Δ cyb2::Idh Δ gpd1::Idh) was obtained.
Saccharomyces cerevisiae CEN.PK2-1D (Δ pdc1::Idh Δ cyb2::Idh Δ gpd1::Idh) was deposited in Korean Collection for Type Cultures (KCTC) on May 30, 2013, and received an accession number KCTC 12415BP.
(1.3) LDH Enhancement
L-Idh may be additionally introduced to a genome to KCTC12415BP to additionally control and to enhance the lactate production pathway for increasing lactate production, such as redox balance enhancement or glycolysis pathway engineering, and the method is described below.
(1.3.1) Preparation of Vector with L-Idh Introduced into Genome
For additional introduction of L-Idh, a gene introduction vector was prepared as follows.
PCR was performed using the prepared p416-CCW12p-LDH as a template and primers of SEQ ID NO: 30 and SEQ ID NO: 31. The resulting PCR fragment and the pUC19-HIS3 vector obtained therefrom were digested with SacI, and ligated, producing pUC19-CCW12p-LDH-HIS3.
Also, for additional introduction of L-Idh into a genome of a KCTC12415BP strain, PCR was performed using the prepared pUC19-CCW12p-LDH-HIS3 as a template and primers of SEQ ID NO: 34 and SEQ ID NO: 45, thereby preparing a cassette to be inserted to a location of TRP1.
The cassette including L-Idh may be inserted to the locus of TRP1, and in this case, L-Idh may be inserted as the TRP1 gene is deleted. The L-Idh insertion mutant strain is prepared as follows.
The KCTC12415BP strain thus obtained was plated onto a YPD agar plate (including 10 g of yeast extract, 20 g of peptone, and 20 g of glucose) and incubated for 24 hours at 30° C., and then, a colony obtained therefrom was inoculated in about 10 ml of a YPD liquid medium and cultured for about 18 hours at about 30° C. The sufficiently grown culture solution was inoculated in about 50 ml of a YPD liquid medium contained in a 250 ml-flask at a concentration of 1% (v/v) and cultured in an incubator at a rate of about 230 rpm and at 30° C.
After about 4 to 5 hours, when the OD600 reached about 0.5, the culture was centrifuged at a rate of about 4,500 rpm for about 10 minutes to harvest cells, and the cells were resuspensed in a lithium acetate solution at a concentration of about 100 mM. Then, the cells were harvested by performing centrifugation at a rate of about 4,500 rpm for about 10 minutes, resuspensed in a lithium acetate solution at a concentration of about 1 M including 15% of glycerol, and then divided into a volume of about 100 μl each.
In order to express L-Idh, at the same time deleting TRP1, an L-Idh expression cassette including HIS3 prepared in Example 1.3.1 was mixed with 50% of polyethylene glycol and a single stranded carrier DNA and reacted in a water tub for about 1 hour at 42° C., and then, the culture solution was spread on a histidine-free minimal agar plate (including YSD, 6.7 g/L of yeast nitrogen base without amino acids, and 1.4 g/L of amino acid dropout mix (-his)) and grown for about 24 hours or more at 30° C. Ten colonies (mutant strains) grown on the plate were selected, patched onto the fresh histidin-free minimal agar plate, and at the same time, inoculated into a liquid medium including the same components contained in the histidin-free minimal agar plate to isolate the genomic DNA from the above mutant strains by using a commonly used kit (Gentra Puregene Cell kit, Qiagen, USA). PCR was performed using the isolated genomic DNA of the mutant stain as a template and primers of SEQ ID NOS: 46 and 47, and then, electrophoresis was performed on the obtained PCR product to confirm insertion of the L-Idh expression cassette. As a result, the strain thus obtained was named CEN.PK2-1D KCTC12415BP Δ trp1::Idh.
(2.1) Preparation of NDE1 gene deletion cassette
In order to delete NDE1 gene by using a homogenous recombination method, pUC57-CCW12p-LDH-ura3HA prepared in Example 1.1.2 was used as a vector for inactivating NDE1 gene. PCR was performed using the prepared pUC57-CCW12p-LDH-ura3HA as a template and primers of SEQ ID NOS: 48 and 49.
(2.2) Preparation of Saccharomyces cerevisiae Strain in Which NDE1 is Deleted
A mutant strain of Saccharomyces cerevisiae CEN.PK2-1D KCTC12415BP Δ trp1::Idh, in which ndel gene is deleted, was prepared in the same manner as follows. The Saccharomyces cerevisiae CEN.PK2-1D KCTC12415BP Δ trp1::Idh thus obtained was plated onto a YPD agar plate (including 10 g of yeast extract, 20 g of peptone, and 20 g of glucose) and incubated for 24 hours at 30° C., and then, a colony obtained therefrom was inoculated in about 10 ml of a YPD liquid medium and cultured for about 18 hours at about 30° C. The sufficiently grown culture solution was inoculated in about 50 ml of a YPD liquid medium contained in a 250 ml-flask at a concentration of 1% (v/v) and cultured in an incubator at a rate of about 230 rpm and at 30° C. After about 4 to 5 hours, when the OD600 reached about 0.5, the culture was centrifuged at a rate of about 4,500 rpm for about 10 minutes to harvest cells, and the cells were resuspensed in a lithium acetate solution at a concentration of about 100 mM. Then, the cells were harvested by performing centrifugation at a rate of about 4,500 rpm for about 10 minutes, resuspensed in a lithium acetate solution at a concentration of about 1 M including 15% of glycerol, and then divided into a volume of about 100 μl each.
In order to delete NDE1, the NDE1 deletion cassette prepared in Example 2.1 was introduced to the resuspended Saccharomyces cerevisiae CEN.PK2-1D KCTC12415BP Δ trp1::Idh in the same manner used in deletion of the pdc1, cyb2, and gpd1 genes. Ten colonies grown on the plate were selected to isolate the genomic DNA. PCR was performed using the isolated genomic DNA of the mutant stain as a template and primers of SEQ ID NOS: 50 and 51, and then, electrophoresis was performed on the obtained PCR product to confirm deletion of NDE1. As a result, Saccharomyces cerevisiae CEN.PK2-1D (KCTC12415BP Δ trp1::Idh Δ nde1+ura3) was obtained.
Also, for additional gene deletion using the gene deletion vector, a URA3 gene as a selection marker was removed from Saccharomyces cerevisiae CEN.PK2-1D (KCTC12415BP Δ trp1::Idh Δ nde1+ura3) by using the URA3 pop-out method as described above. Ten colonies grown on a plate were selected to isolate genomic DNA. In order to confirm deletion of URA3 gene by using the isolated genomic DNA of the URA3 pop-out strain as a template, PCR was performed using primers of SEQ ID NOS: 50 and 51, and then electrophoresis was performed on the obtained PCR product to confirm deletion of URA3 gene. As a result, Saccharomyces cerevisiae CEN.PK2-1D (KCTC12415BP Δ trp1::Idh Δ nde1) was obtained.
In order to prepare a strain with a depressed PYC1 and/or PYC2 activity, a PYC1 and/or PYC2 promoter (Ppyc1 and Ppyc2) were replaced with a promoter at a lower level of expression compared to the promoters as follows. The promoter at a lower level of expression compared to the promoter was a LEUM promoter (Pleum), a CYC1 promoter (Pcyc1), or a combination thereof. The LEUM promoter is a mutant of a LEU2 promoter, in which a LEU2 promoter is truncated.
(3.1) Preparation of Pleum and Pcyc1 and Preparation of Recombination Vector
In order to prepare a DNA fragment including a LEUM promoter (Pleum) (SEQ ID NO: 25), after extracting gDNA, which is a wild strain of Saccharomyces cerevisiae CEN.PK2-1D chromosome, by using a Genomic-tip system of Qiagen, PCR was performed using the gDNA as a template and a PCR HL premix kit (BIONEER).
As PCR for amplifying Pleum, 30 cycles of PCR was performed, each cycle including 30 seconds of denaturation at 94° C., 30 seconds of annealing at 52° C., and 30 seconds of elongation at 72° C. using primers of SEQ ID NO: 53 and SEC ID NO: 54. The PCR product was digested with EcoRI, and then the DNA fragment (hereinafter, referred to as “Rleum cassette 1”) was dissolved in 0.8% agarose gel by performing electrophoresis.
As PCR for amplifying Pleum, 30 cycles of PCR was performed, each cycle including 30 seconds of denaturation at 94° C., 30 seconds of annealing at 52° C., and 30 seconds of elongation at 72° C. using primers of SEQ ID NO: 58 and SEC ID NO: 59. The PCR product was digested with BamHI, and then the DNA fragment (hereinafter, referred to as “Pleum cassette 2”) was dissolved in 0.8% agarose gel by performing electrophoresis.
Also, in order to obtain a DNA fragment including a CYC1 promoter (Pcyc1) (SEQ ID NO: 55), after extracting gDNA, which is a wild strain of Saccharomyces cerevisiae CEN.PK2-1D chromosome, by using a Genomic-tip system of Qiagen, PCR was performed using the gDNA as a template and a PCR HL premix kit (BIONEER).
As PCR for amplifying Pcyc1, 30 cycles of PCR was performed, each cycle including 30 seconds of denaturation at 94° C., 30 seconds of annealing at 52° C., and 30 seconds of elongation at 72° C. using primers of SEQ ID NO: 56 and SEC ID NO: 57. The PCR product was digested with EcoRI, and then the DNA fragment (hereinafter, referred to as “Pcyc1 cassette 1”) was dissolved in 0.8% agarose gel by performing electrophoresis.
As PCR for amplifying Pcyc1, 30 cycles of PCR was performed, each cycle including 30 seconds of denaturation at 94° C., 30 seconds of annealing at 52° C., and 30 seconds of elongation at 72° C. using primers of SEQ ID NO: 60 and SEC ID NO: 61. The PCR product was digested with BamHI, and then the DNA fragment (hereinafter, referred to as “Pcyc1 cassette 2”) was dissolved in 0.8% agarose gel by performing electrophoresis.
The pUC19-Trp1 vector (Appl Environ Microbiol. 2002 May; 68(5):2095-100) and the prepared Pleum cassette 1 were treated with a restriction enzyme EcoRI and ligated to prepare a pUC19-Trp1-Pleum vector.
Also, the pUC19-Trp1 vector (Appl Environ Microbiol. 2002 May; 68(5):2095-100) and the prepared Pleum cassette 2 were treated with a restriction enzyme BamHI and ligated to prepare a pUC19-Leu2-Pleum vector.
In order to prepare a strain, in which Ppyc1 is replaced with Pleum and Ppyc2 is replaced with Pleum as described later, the pUC19-Trp1-Pleum vector and the pUC19-Leu2-Pleum vector having the same Pleum cassette and different markers were prepared.
The pUC19-Trp1 vector (Appl Environ Microbiol. 2002 May; 68(5):2095-100) plasmid and the prepared Pcyc1 cassette 1 were treated with a restriction enzyme EcoRI and ligated to prepare a pUC19-Trp1-Pcyc1 vector.
Also, the pUC19-Leu2 vector (Appl Environ Microbiol. 2002 May; 68(5):2095-100) plasmid and the prepared Pcyc1 cassette 2 were treated with a restriction enzyme BamHI and ligated to prepare a pUC19-Leu2-Pcyc1 vector.
(3.2) Preparation of Ppyc2 Deletion Cassette
In order to delete a Ppyc2 promoter (Ppyc2) by using a homogenous recombination method, the pUC57-ura3HA was used as a vector for inactivating a Ppyc2 promoter gene. To prepare a Ppyc2 promoter deletion cassette, PCR was performed using the prepared pUC57-ura3HA as a template and primers of SEQ ID NO: 62 and 63, and thus a Ppyc2 deletion cassette was prepared.
(3.3) Preparation of Strain with Pyc1 Promoter and/or Pyc2 Promoter Replaced with Pleum and Pcyc1 Fragment
(3.3.1) Preparation of Pyc1 Promoter and/or Pyc2 Promoter Eeplacement Cassette
In order to replace Ppyc1 with Pcyc1 or Pleum by using a homogenous recombination method, the pUC19-TRP1-Pcyc1 and pUC19-TRP1-Pleum were each respectively used. PCR was performed using the pUC19-TRP1-Pcyc1 as a template and primers of SEQ ID NOS: 68 and 69 to prepare a cassette for replacing Ppyc1 to Pcyc1, and PCR was performed using the pUC19-TRP1-Pleum as a template and primers of SEQ ID NOS: 68 and 70 to prepare a cassette for replacing Ppyc1 to Pleum.
In order to replace Ppyc2 with Pleum by using a homogenous recombination method, the pUC19-LEU2-Pleum was used. PCR was performed using the pUC19-LEU2-Pleum as a template and primers of SEQ ID NOS: 71 and 72 to prepare a cassette for replacing Ppyc2 to Pleum.
(3.3.2) Preparation of Strain in Which Ppyc1 is Replaced with Pleum
In order to replace Ppyc1 to Rleum, the replacement cassette prepared in Example 3.3.1 was mixed with 50% of polyethyleneglycol and a single stranded carrier DNA and reacted in a water tub for about 1 hour at 42° C., and then, the S. cerevisea CEN.PK2-1D (KCTC12415BP Δ trp1::Idh Δ nde1) culture solution was plated onto a uracil-free minimal agar plate (including YSD, 6.7 g/L of yeast nitrogen base without amino acids, and 1.4 g/L of amino acid dropout mix (-ura)) in a plate and cultured for 24 hours or more at 30° C.
Ten colonies (a mutant strain) formed in the plate were selected, transferred to another uracil-free minimal agar plate, and, at the same time, cultured in a liquid medium including the same components contained in the uracil-free minimal medium to separate genome DNA from the strain by using a commonly used kit (Gentra Puregene Cell kit, Qiagen, USA). In order to confirm replacement of Ppyc1 to Rleum by using the separated genome DNA of the mutant strain as a template, PCR was performed using primers of SEQ ID NOS: 64 and 65, and then, electrophoresis was performed on the obtained PCR product. As a result, Saccharomyces cerevisiae CEN.PK2-1D (KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pleum) was obtained.
(3.3.3) Preparation of Strain in Which Ppyc1 is Replaced with Pleum and Ppyc2 is Replaced with Pcyc1
In order to replace Ppyc1 to Rleum and Ppyc2 to Pcyc1, the replacement cassette prepared in Example 3.3.1 was mixed with 50% of polyethyleneglycol and a single stranded carrier DNA and reacted in a water tub for about 1 hour at 42° C., and then, the S. cerevisea CEN.PK2-1D (KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pleum) culture solution was plated onto a uracil-free minimal agar plate (including YSD, 6.7 g/L of yeast nitrogen base without amino acids, and 1.4 g/L of amino acid dropout mix (-ura)) in a plate and cultured for 24 hours or more at 30° C. Ten colonies (a mutant strain) formed in the plate were selected, transferred to another uracil-free minimal agar plate, and, at the same time, cultured in a liquid medium including the same components contained in the uracil-free minimal medium to separate genome DNA from the strain by using a commonly used kit (Gentra Puregene Cell kit, Qiagen, USA). In order to confirm replacement of Ppyc2 to Pcyc1 by using the separated genome DNA of the mutant strain as a template, PCR was performed using primers of SEQ ID NOS: 66 and 67, and then, electrophoresis was performed on the obtained PCR product. As a result, Saccharomyces cerevisiae CEN.PK2-1D (KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pleum Δ Ppyc2::Pcyc1) was obtained.
(3.3.4) Preparation of Strain in Which Ppyc1 is Replaced with Pleum and Ppyc2 is Replaced with Pleum
In order to replace Ppyc1 to Rleum and Ppyc2 to Pleum, the replacement cassette prepared in Example 3.3.1 was mixed with 50% of polyethyleneglycol and a single stranded carrier DNA and reacted in a water tub for about 1 hour at 42° C., and then, the S. cerevisea CEN.PK2-1D (KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::PLeum) culture solution was plated onto a uracil-free minimal agar plate (including YSD, 6.7 g/L of yeast nitrogen base without amino acids, and 1.4 g/L of amino acid dropout mix (-ura)) in a plate and cultured for 24 hours or more at 30° C. Ten colonies (a mutant strain) formed in the plate were selected, transferred to another uracil-free minimal agar plate, and, at the same time, cultured in a liquid medium including the same components contained in the uracil-free minimal medium to separate genome DNA from the strain by using a commonly used kit (Gentra Puregene Cell kit, Qiagen, USA). In order to confirm replacement of Ppyc2 to Pleum by using the separated genome DNA of the mutant strain as a template, PCR was performed using primers of SEQ ID NOS: 66 and 67, and then, electrophoresis was performed on the obtained PCR product. As a result, Saccharomyces cerevisiae CEN.PK2-1D (KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pleum Δ Ppyc2::Pleum) was obtained.
(3.3.5) Preparation of Strain in Which Ppyc1 is Replaced with Pcyc1
In order to replace Ppyc1 to Pcyc1 , the replacement cassette prepared in Example 3.3.1 was mixed with 50% of polyethyleneglycol and a single stranded carrier DNA and reacted in a water tub for about 1 hour at 42° C., and then, the S. cerevisea CEN.PK2-1D (KCTC12415BP Δ trp1::Idh Δ nde1) culture solution was plated onto a uracil-free minimal agar plate (including YSD, 6.7 g/L of yeast nitrogen base without amino acids, and 1.4 g/L of amino acid dropout mix (-ura)) in a plate and cultured for 24 hours or more at 30° C. Ten colonies (a mutant strain) formed in the plate were selected, transferred to another uracil-free minimal agar plate, and, at the same time, cultured in a liquid medium including the same components contained in the uracil-free minimal medium to separate genome DNA from the strain by using a commonly used kit (Gentra Puregene Cell kit, Qiagen, USA). In order to confirm replacement of Ppyc1 to Pcyc1 by using the separated genome DNA of the mutant strain as a template, PCR was performed using primers of SEQ ID NOS: 64 and 65, and then, electrophoresis was performed on the obtained PCR product. As a result, Saccharomyces cerevisiae CEN.PK2-1D (KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pcyc1) was obtained.
(3.3.6) Preparation of Strain in Which Ppyc1 is Replaced with Pcyc1 and Ppyc2 is Replaced with Pleum
In order to replace Ppyc1 to Pcyc1 and Ppyc2 to Pleum, the replacement cassette prepared in Example 3.3.1 was mixed with 50% of polyethyleneglycol and a single stranded carrier DNA and reacted in a water tub for about 1 hour at 42° C., and then, the S. cerevisea CEN.PK2-1D (KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pcyc1) culture solution was plated onto a uracil-free minimal agar plate (including YSD, 6.7 g/L of yeast nitrogen base without amino acids, and 1.4 g/L of amino acid dropout mix (-ura)) in a plate and cultured for 24 hours or more at 30° C. Ten colonies (a mutant strain) formed in the plate were selected, transferred to another uracil-free minimal agar plate, and, at the same time, cultured in a liquid medium including the same components contained in the uracil-free minimal medium to separate genome DNA from the strain by using a commonly used kit (Gentra Puregene Cell kit, Qiagen, USA). In order to confirm replacement of Ppyc1 to Pleum by using the separated genome DNA of the mutant strain as a template, PCR was performed using primers of SEQ ID NOS: 66 and 67, and then, electrophoresis was performed on the obtained PCR product to confirm replacement of Ppyc2 to Pcyc1. As a result, Saccharomyces cerevisiae CEN.PK2-1D (KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pcyc1 Δ Ppyc2::Pleum) was obtained.
(3.3.7) Preparation of Strain in Which Ppyc1 is Replaced with Pcyc1 and Ppyc2 is Deleted
In order to replace Ppyc1 to Pcyc1 and delete Ppyc2, the Ppyc2 deletion cassette prepared in Example 3.2 was mixed with 50% of polyethyleneglycol and a single stranded carrier DNA and reacted in a water tub for about 1 hour at 42° C., and then, the S. cerevisea CEN.PK2-1D (KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pcyc1) culture solution was plated onto a uracil-free minimal agar plate (including YSD, 6.7 g/L of yeast nitrogen base without amino acids, and 1.4 g/L of amino acid dropout mix (-ura)) in a plate and cultured for 24 hours or more at 30° C. Ten colonies (a mutant strain) formed in the plate were selected, transferred to another uracil-free minimal agar plate, and, at the same time, cultured in a liquid medium including the same components contained in the uracil-free minimal medium to separate genome DNA from the strain by using a commonly used kit (Gentra Puregene Cell kit, Qiagen, USA). In order to confirm deletion of Ppyc2 by using the separated genome DNA of the mutant strain as a template, PCR was performed using primers of SEQ ID NOS: 66 and 67, and then, electrophoresis was performed on the obtained PCR product to confirm replacement of Ppyc2 to Pcyc1. As a result, Saccharomyces cerevisiae CEN.PK2-1D (KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pcyc1 Δ Ppyc2) was obtained.
Each of the strains prepared in Examples 3.3.1 to 3.3.6 was spread on a YPD agar plate and incubated for 24 hours or more at 30° C., and then, a colony obtained therefrom was inoculated in about 50 ml of a YPD liquid medium including 40 g/L of glucose, and incubated in an aerobic condition for about 29.5 hours at 30° C. Fermentation was performed by measuring an amount of a cell concentration when an optical density at 600 nm (OD600) reached 5.0 by using a spectrophotometer, discarding the supernatant thereof after performing centrifuge, resuspending the cells, and inoculating again in 50 ml of a fresh YPD including 80 g/L of glucose.
The cells were fermented in a stirring incubator maintaining 90 rpm for 24 hours at 30° C. During the fermentation, a sample was periodically obtained from the flask, and the obtained sample was centrifuged at 13,000 rpm for 10 minutes, and concentrations of metabolic products including lactate and glucose in the supernatant were analyzed by using an HPLC. An initial amount of glucose was 82.6 g/L. A yield of lactate was calculated as a percent of an amount of produced lactate production divided by an amount of consumed glucose, and the results are shown in Table 1.
As shown in Table 1, a L-lactate production of KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pleum increased from 32.5 g/L to 35.1 g/L compared to that of KCTC12415BP Δ trp1::Idh Δ nde1, and a yield of KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pleum increased from 45.3% to 49.5% compared to that of KCTC12415BP Δ trp1::Idh Δ nde1.
The lactate production of KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::PLeum Δ Ppyc2::Pcyc1 increased from 32.5 g/L to 37.0 g/L compared to that of KCTC12415BP Δ trp1::Idh Δ nde1, and a yield of KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::PLeum Δ Ppyc2::Pcyc1 increased from 45.3% to 49.5% compared to that of KCTC12415BP Δ trp1::Idh Δ nde1.
The lactate production of L-lactate production of KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pleum Δ Ppyc2::Pleum increased from 32.5 g/L to 35.9 g/L compared to that of KCTC12415BP Δ trp1::Idh Δ nde1, and a yield of KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pleum Δ Ppyc2::Pleum increased from 45.3% to 49.9% compared to that of KCTC12415BP Δ trpl ::Idh Δ nde1.
The lactate production of L-lactate production of KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pcyc1 increased from 32.5 g/L to 35.3 g/L compared to that of KCTC12415BP Δ trp1::Idh Δ nde1, and a yield of KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pcyc1 increased from 45.3% to 48.9% compared to that of KCTC12415BP Δ trp1::Idh Δ nde1.
The lactate production of L-lactate production of KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pcyc1 Δ Ppyc2::Pleum increased from 32.5 g/L to 35.5 g/L compared to that of KCTC12415BP Δ trp1::Idh Δ nde1, and a yield of KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pcyc1 Δ Ppyc2::Pleum increased from 45.3% to 47.5% compared to that of KCTC12415BP Δ trpl ::Idh Δ nde1.
The lactate production of L-lactate production of KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pcyc1 Δ Ppyc2 increased from 32.5 g/L to 36.6 g/L compared to that of KCTC12415BP Δ trp1::Idh Δ nde1, and a yield of KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pcyc1 Δ Ppyc2 increased from 45.3% to 45.6% compared to that of KCTC12415BP Δ trp1::Idh Δ nde1.
KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pleum Δ Ppyc2::Pleum from the strains prepared in Examples 3.3.2 to 3.3.7 was spread on a YPD agar plate and incubated for 24 hours or more at 30° C., and then, a colony obtained therefrom was inoculated in about 100 ml of a YPD liquid medium including 80 g/L of glucose, and incubated in an aerobic condition for about 16 hours at 30° C.
Fermentation was performed by separately inoculating 100 ml of the strain culture solution in a bioreactor containing 1 L of a synthesis medium, and the fermentation condition included initially 60 g/L of glucose and 20 g/L of yeast extract at 30° C. During the fermentation, pH was maintained at pH 5 by using 5N Ca(OH)2 up to 16 hours, pH 4.5 up to 24 hours, and pH 3.0 up to 60 hours, and a concentration of glucose was maintained at 20 g/L. Additional synthesis medium components included 50 g/L of K2HPO4, 10 g/L of MgSO4, 0.1 g/L of tryptophan, and 0.1 g/L of histidine in addition to glucose.
A cell concentration in the culture was estimated by using a spectrophotometer, samples were periodically obtained from the bioreactor during the fermentation, the samples thus obtained were centrifuged at 13,000 rpm for 10 minutes, and then metabolic products and concentration s of lactate and glucose of the supernatants were analyzed by high pressure liquid chromatography (HPLC).
As shown in Table 2, an L-lactate production of KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pleum Δ Ppyc2::Pleum increased from 119.8 g/L to 122.8 g/L compared to that of KCTC12415BP Δ trp1::Idh Δ nde1, and a yield of KCTC12415BP Δ trp1::Idh Δ nde1 Δ Ppyc1::Pleum Δ Ppyc2::Pleum increased from 57.2% to 65.6% compared to that of KCTC12415BP Δ trp1::Idh Δ nde1.
[Accession Number]
Research Center Name: Korean Collection for Type Cultures (KTCT)
Accession Number: KCTC 12415BP
Accession Date: May 30, 2013
As described above, according to the one or more of the above embodiments of the present invention, a yeast cell may produce lactate at a high yield, and a method of producing lactate may produce lactate at a high yield.
It should be understood that the exemplary embodiments described therein should be considered in a descriptive sense only and not for purposes of limitation. Descriptions of features or aspects within each embodiment should typically be considered as available for other similar features or aspects in other embodiments.
While one or more embodiments of the present invention have been described with reference to the figures, it will be understood by those of ordinary skill in the art that various changes in form and details may be made therein without departing from the spirit and scope of the present invention as defined by the following claims.
All references, including publications, patent applications, and patents, cited herein are hereby incorporated by reference to the same extent as if each reference were individually and specifically indicated to be incorporated by reference and were set forth in its entirety herein.
The use of the terms “a” and “an” and “the” and “at least one” and similar referents in the context of describing the invention (especially in the context of the following claims) are to be construed to cover both the singular and the plural, unless otherwise indicated herein or clearly contradicted by context. The use of the term “at least one” followed by a list of one or more items (for example, “at least one of A and B”) is to be construed to mean one item selected from the listed items (A or B) or any combination of two or more of the listed items (A and B), unless otherwise indicated herein or clearly contradicted by context. The terms “comprising,” “having,” “including,” and “containing” are to be construed as open-ended terms (i.e., meaning “including, but not limited to,”) unless otherwise noted. Recitation of ranges of values herein are merely intended to serve as a shorthand method of referring individually to each separate value falling within the range, unless otherwise indicated herein, and each separate value is incorporated into the specification as if it were individually recited herein. All methods described herein can be performed in any suitable order unless otherwise indicated herein or otherwise clearly contradicted by context. The use of any and all examples, or exemplary language (e.g., “such as”) provided herein, is intended merely to better illuminate the invention and does not pose a limitation on the scope of the invention unless otherwise claimed. No language in the specification should be construed as indicating any non-claimed element as essential to the practice of the invention.
Preferred embodiments of this invention are described herein, including the best mode known to the inventors for carrying out the invention. Variations of those preferred embodiments may become apparent to those of ordinary skill in the art upon reading the foregoing description. The inventors expect skilled artisans to employ such variations as appropriate, and the inventors intend for the invention to be practiced otherwise than as specifically described herein. Accordingly, this invention includes all modifications and equivalents of the subject matter recited in the claims appended hereto as permitted by applicable law. Moreover, any combination of the above-described elements in all possible variations thereof is encompassed by the invention unless otherwise indicated herein or otherwise clearly contradicted by context.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2013-0151708 | Dec 2013 | KR | national |
