KR20110118552A - Ethanol-resistant yeast strains and uses thereof - Google Patents

Abstract

The present invention relates to ethanol-resistant transformed yeast strains comprising the mutated SPT15 gene and uses thereof. Yeast strains of the present invention are yeast strains that can grow in high concentration ethanol, preferably 12.5-15% ethanol. Therefore, by inventing strains that exhibit high concentrations of ethanol, it will be useful for more efficient ethanol production, and will also have utility as a super strain of high efficiency ethanol production ability that is resistant to various stresses generated in the bioethanol production process.

Description

Ethanol-Resistant Yeast Strains and Uses Thereof

The present invention is directed to ethanol-resistant yeast strains and their use.

The production of bioethanol from plant or seaweed biomass has been of worldwide interest in terms of long-term availability and harmful environmental aspects of fossil fuels (Jeffries and Lindbladm, 2009; Ragauskas, et al. , 2006; Rubin, 2008). However, the relatively high production costs of bioethanol have hampered investment in related industries. Thus, much effort has been made to reduce the costs of biomass acquisition, pretreatment, fermentation and product recovery (Xu, et al. , 2009). During the bioethanol production process, ethanol-producing microorganisms face various stresses such as high concentrations of initial substrates, increased ethanol concentrations and accumulation of toxic byproducts. In addition to rapid growth and effective fermentation capacity, the ability to withstand the stresses described above is an important factor in selecting ethanol producers (Ding, et al. , 2009; Gibson, et al. , 2007; Yoshikawa, et al. , 2009). One way to improve ethanol production is to develop strains with increased stress resistance.

Yeast S. cerevisiae has been used in a variety of industries, including the production of bioethanol from biomass resources. Yeast cells are always exposed to various environmental stresses such as high concentrations of ethanol that occur during industrial ethanol fermentation, which in turn results in a decrease in cell growth, cell viability and ethanol production (Casey and Ingledew, 1986). Therefore, there has been a need for the development of yeast strains that can overcome the stress caused by high concentrations of ethanol. Furthermore, the use of genome-wide assays, such as microarrays and comprehensive expression pattern analysis, has been useful in identifying novel ethanol stress related genes (Hirasawa, et al. , 2007; Teixeira, et al. , 2009; Yoshikawa, et al. , 2009). Through this approach, many genes involved in ethanol resistance have been identified as non-essential genes. In addition, results related to ethanol resistance did not match, respectively, and reported that this discrepancy was due to strain and growth conditions (Teixeira, et al. , 2009). Thus, strains constructed from the genetic information described above do not always result in changes to ethanol stress conditions (Yoshikawa, et al. , 2009). In addition, a commercially available Saccharomyces cerevisiae deletion mutant library was used for genome-wide screening of genes involved in ethanol resistance (Fujita, et al. , 2006; Teixeira, et al. , 2009; Yoshikawa, et. al. , 2009). The above studies mainly selected mutants exhibiting ethanol sensitivity to identify the corresponding genes as genes required for growth under high ethanol conditions.

In general, many genes are known to affect important intracellular phenotypes (eg, overexpression of metabolites from pathological conditions). However, most cellular and metabolic engineering approaches have been carried out through deletion or overexpression of single genes due to experimental limitations of vector construction and transformation efficiency. This ruled out the investigation through modification of several genes.

To investigate the mechanism of ethanol stress resistance, there have been many studies. In particular, unsaturated fatty acids related to membrane fluidity have been reported and considered as important determinants of ethanol resistance in yeast (Kajiwara, et al. , 2000; You, et al , 2003). In addition, intracellular accumulation of trihalose (Kim, et al. , 1996) or proline (Takagi, et al. , 2005) improves yeast ethanol resistance and ergosterol to ethanol resistance to Saccharomyces cerevisiae. Has been reported to be an important factor associated with (Inoue, et al. , 2000).

To develop ethanol resistant strains, classical adaptations such as evolutionary adaptation (Stanley, et al., 2010), random chemical mutagenesis (Mobini-Dehkordi, et al. , 2008) and gene shuffling (Hou, 2010) In addition to strategies, three other strategies have recently been used: DNA microarray analysis across genomes (Hirasawa, et al. , 2007), transposon-mediated deletion mutation libraries (Takahashi, et al. , 2001), single genes Knock-out (SGKO) library (Auesukaree, et al. , 2009; Fujita, et al. , 2006; Kubota, et al. , 2004; Teixeira, et al. , 2009; van Voorst, et al. , 2006; Yoshikawa , et al. , 2009) screening and gTME (global transcriptional machinery engineering; Alper, et al. , 2006). In DNA microarray analysis, after up- or down-regulated genes induced by ethanol stress were first identified as target genes, the ability of the genes to confer ethanol resistance was overexpressed or down-regulated. Verified by deletion of regulated genes. For SGKO library screening, clones showing reduced or increased growth are preferentially separated by screening ethanol in the presence. Genes causing slowed growth in deletion are substantially associated with ethanol susceptibility and should be tested for association with ethanol resistance due to overexpression. In contrast, genes that result in increased growth of deletion can be used directly to prepare ethanol resistant strains. However, the problem with these two approaches is that a very large number of target genes must be identified. For example, the above methods can be used only when about 5-10% of genes encoded in the yeast genome are identified. The identification of ethanol sensitive genes can help to understand the molecular basis of ethanol resistance, but it does not guarantee the construction of ethanol resistance strains. Although it is easy and simple to verify whether overexpression of ethanol sensitive genes confer ethanol resistance, few successful cases have been reported (Gibson, et al. , 2007).

gTME reprograms the overall transcription profile through random mutagenesis of one or more common transcription factors. This approach was used for the first time to create strains with increased ethanol resistance by inducing mutations in the TATA-binding protein (TBP) encoded by the SPT15 gene previously reported to be able to grow at lethal ethanol concentrations. Alper, et al. , 2006). However, other authors have reported that this increased ethanol resistance is not regenerated in a rich medium that is not selected for industrial applications (Baerends, et al. , 2009). Nevertheless, SPT15 mutations alter transcription profiles through interaction with Spt3p, a subunit of the SAGA (Spt-Ada-Gcn5-acetyltransferase) complex that regulates many RNA polymerase II-dependent genes. In addition, SPT15 mutations have been identified as pleiotrophic (Eisenmann, et al. , 1989), and several mutations in the regulatory domain of SPT15 resulted in increased transcription (Cang, et al. , 1999). The above findings indicate that different mutations of SPT15 can induce the expression of different sets of genes.

In this study, gTME was performed as previously reported to develop strains in Saccharomyces cerevisiae with ethanol resistance (Alper, et al. , 2006). We obtained five ethanol resistant strains (ETSs) containing different SPT15 mutant alleles and investigated the effect of SPT15 mutations on ethanol resistance. Genome-wide microarrays were performed to identify genes involved in ethanol resistance and to further investigate their function using deletion mutants.

Numerous papers and patent documents are referenced and cited throughout this specification. The disclosures of cited papers and patent documents are incorporated herein by reference in their entirety, and the level of the technical field to which the present invention belongs and the contents of the present invention are more clearly explained.

We sought to develop ethanol-resistant yeast strains. As a result, the present inventors constructed a mutated SPT15 gene using PCR-mediated random mutagenesis and transformed it into yeast to isolate ethanol-resistant transformed yeast strains, which were highly concentrated ethanol (e.g., , 15% ethanol), thereby completing the present invention.

Accordingly, it is an object of the present invention to provide an ethanol-resistant transformed yeast strain.

Another object of the present invention is to provide a method for producing ethanol.

Other objects and advantages of the present invention will become apparent from the following detailed description, claims and drawings.

According to an aspect of the present invention, the present invention provides an ethanol-resistant transformed yeast strain comprising a mutated SPT15 gene.

We sought to develop ethanol-resistant yeast strains. As a result, the present inventors constructed a mutated SPT15 gene using PCR-mediated random mutagenesis and transformed it into yeast to isolate ethanol-resistant transformed yeast strains, which were highly concentrated ethanol (e.g., , 15% ethanol).

Ethanol, a flammable, volatile colorless liquid, is the most widely used solvent. Industrially, ethanol is used as a vehicle fuel and fuel additive and also as a perfume, flavorings, colorings and medicines. Ethanol is also the main psychoactive component in alcoholic beverages and has a calming effect on the central nervous system. Ethanol can be produced petrochemically through hydration of ethylene and biologically by fermenting sugars using yeast, which is produced by petrochemical processes that depend on the price of petroleum and grain feed products. Much more economical than Therefore, the development of yeast strains for the production of biological ethanol is very important.

According to the present invention, the present invention provides yeast strains that have transformed the SPT15 gene mutated by PCR in yeast.

According to a preferred embodiment of the invention, the mutation of the invention comprises a mutated amino acid sequence within the amino acid sequence of the wild type SPT15 gene, more preferably comprises three to five mutated amino acid sequences, most preferably The amino acid sequence consisting of SEQ ID NO: 6 to 10 sequences.

According to a preferred embodiment of the present invention, the mutated SPT15 gene of the present invention comprises an amino acid sequence of which the amino acid sequence of the K201, G216 and Q225 positions of the wild type SPT15 gene is mutated; Amino acid sequences of which the amino acid sequences of the L76 and L175 positions of the wild-type SPT15 gene are mutated; An amino acid sequence of which the amino acid sequences of the S42, C78, S163, and I212 positions of the wild-type SPT15 gene are mutated; An amino acid sequence of which the amino acid sequences of the F10 and M197 positions of the wild-type SPT15 gene are mutated; Or the mutated SPT15 gene comprising the mutated amino acid sequence of the amino acid sequence at positions K15, W26 and G192 of the wild-type SPT15 gene.

According to a more preferred embodiment of the present invention, the mutated SPT15 gene of the present invention comprises a mutant sequence (SEQ ID NO: 6) wherein the amino acid sequence of the K201, G216 and Q225 positions of the wild type SPT15 gene is mutated to K201Q, G216S and Q225Stop; Mutant sequences in which the amino acid sequences at the L76 and L175 positions of the wild-type SPT15 gene have been changed to L76V and L175S (SEQ ID NO: 7); Mutant sequences in which the amino acid sequences at positions S42, C78, S163 and I212 of the wild-type SPT15 gene have been changed to S42N, C78R, S163P and I212N (SEQ ID NO: 8); A mutant sequence in which the amino acid sequence of the F10 and M197 positions of the wild-type SPT15 gene is mutated to F10S and M197K (SEQ ID NO: 9); Or a mutated SPT15 gene comprising a mutated sequence (SEQ ID NO: 10) in which the amino acid sequences of the K15, W26, and G192 positions of the wild-type SPT15 gene are mutated to K15T, W26C, and G192D.

According to the present invention, the yeast strain transformed with the mutated SPT15 gene described above, preferably the mutated SPT15 gene consisting of SEQ ID NO: 6 to 10 sequence is a high concentration of ethanol, more preferably 5-15% ethanol, Even more preferably 10-15% ethanol, and most preferably 12.5-15% ethanol.

According to a preferred embodiment of the present invention, the mutated SPT15 gene described above may be introduced into yeast cells as a plasmid. In addition, according to a preferred embodiment of the present invention, the mutated SPT15 gene described above may be introduced into genomic DNA of yeast cells.

According to a preferred embodiment of the present invention, yeast strains that can be used for the transformation of the above-described mutated SPT15 gene are Saccharomyces spp., Schizosaccharomyces spp., Blood Pichia spp., Paffia spp., Kluyveromyces spp., Candida spp., Talaromyces spp., Bretanomyces sp . Brettanomyces spp.), Parkinson solren species (Pachysolen spp.), Deva Rio MRS species (Debaryomyces spp.) or including industrial diploid (polyploid) yeast strain, but are not limited to. More preferably, the yeast strain that can be used for the transformation of the mutated SPT15 gene described above is Saccharomyces species, even more preferably Saccharomyces cerevisiae, most preferably Saccharomyces The Seth Cervage is L3262.

According to another aspect of the present invention, the present invention provides an ethanol-resistant yeast strain comprising introducing the above-described mutated SPT15 gene copy into a yeast strain and / or mutating the endogenous SPT15 gene of the genome DNA of yeast cells. Provide a method.

According to another aspect of the present invention, the present invention provides a method for producing ethanol comprising culturing the yeast strain into which the above-described mutated SPT15 gene is inserted in a culture medium comprising at least one substrate capable of metabolizing with ethanol. do.

Since the method of the present invention includes the above-described yeast strain transformed with the mutated SPT15 gene of the present invention as an active ingredient, the overlapping content between the two is omitted in order to avoid excessive complexity of the present specification according to the overlapping description. Omit.

According to a preferred embodiment of the invention, the substrate which can be metabolized to ethanol comprises C6 sugars, and according to a more preferred embodiment of the invention, the C6 sugar comprises glucose, but is not limited thereto. no.

The present invention provides cells infected by recombinant vectors or transcripts thereof comprising the mutated SPT15 gene described above and transformed cells by gene introduction. The present invention also provides a recombinant vector comprising the mutated SPT15 gene described above or a transformant transformed with the mutated SPT15 protein described above.

The recombinant vector of the present invention comprises a nucleotide sequence encoding the amino acid sequence of SEQ ID NO: 6 to 10 or a complementary nucleotide sequence thereof. Vectors of the present invention can typically be constructed as vectors for cloning or vectors for expression. In addition, the vector of the present invention can be constructed using prokaryotic and eukaryotic cells as hosts. For example, prokaryotic cells include bacterial cells and archaea, and eukaryotic cells include yeast cells, mammalian cells, plant cells, insect cells, stem cells and fungi, most preferably yeast cells.

Preferably, the recombinant vector of the present invention comprises (i) a nucleotide sequence encoding the above-described expression target of the present invention; (Ii) a promoter that is operably linked to the nucleotide sequence of (iii) and acts on an animal cell to form an RNA molecule, and more preferably (iii) the above-mentioned SEQ ID NOs: 6 to 9 of the present invention A nucleotide sequence encoding an amino acid sequence of 10 sequences or a complementary nucleotide sequence thereof; (Ii) a promoter operably linked to the nucleotide sequence of (iii) and acting on animal cells to form RNA molecules; And (iii) a recombinant expression vector comprising a 3'-non-detoxification site that acts in an animal cell to cause 3'-end polyadenylation of the RNA molecule.

Preferably, the above-described expression target material includes, but is not limited to, mutated SPT15 protein, more preferably mutated SPT15 protein consisting of SEQ ID NO: 6 to 10 sequences.

As used herein, the term "promoter" refers to a DNA sequence that regulates the expression of a coding sequence or functional RNA. In the synthetic expression vector of the present invention, the expression-coding nucleotide sequence is operably linked to the promoter. As used herein, the term “operatively linked” refers to a functional binding between a nucleic acid expression control sequence (eg, a promoter sequence, a signal sequence, or an array of transcriptional regulator binding sites) and another nucleic acid sequence. Thus, the regulatory sequence will control the transcription and / or translation of the other nucleic acid sequence.

When the vector of the present invention is a prokaryotic cell as a host, powerful promoters capable of promoting transcription (e.g., tac promoter, lac promoter, lac UV5 promoter, lpp promoter, p _L ^λ promoter, p _R ^λ promoter, rac 5 Promoters, amp promoters, recA promoters, SP6 promoters, trp promoters, T7 promoters, etc.), ribosomal binding sites for initiation of translation and transcription / detox termination sequences. Even more preferably, the host cell used in the present invention is E. coli , most preferably E. coli DH5α. In addition, when E. coli is used as the host cell, the promoter and operator site of the E. coli tryptophan biosynthetic pathway (Yanofsky, C., J. Bacteriol. , 158: 1018-1024 (1984)) and the leftward promoter of phage λ (p _L ^λ promoter, Herskowitz, I. and Hagen, D., Ann. Rev. Genet. , 14: 399-445 (1980)) can be used as regulatory sites. On the other hand, vectors that can be used in the present invention are plasmids (eg, pRS316, pSC101, ColE1, pBR322, pUC8 / 9, pHC79, pUC19, pET, etc.), phages (eg, λgt4λB, λ-Charon) which are often used in the art. , λΔz1, M13, etc.) or viruses (eg, SV40, etc.).

In addition, when the recombinant vector of the present invention is applied to eukaryotic cells, preferably yeast cells, the promoters that can be used are those capable of regulating the transcription of the expression target material of the present invention, promoters derived from yeast cells, mammals Promoters derived from animal viruses and promoters derived from genomes of mammalian cells, including, for example, the yeast ( G. cerevisiae ) GAPDH (Glyceraldehyde 3-phosphate dehydrogenase) promoter, the yeast ( S. cerevisiae ) GAL1 to GAL10 promoters, yeast ( Pichia pastoris ) AOX1 or AOX2 promoter, CMV (cytomegalo virus) promoter, adenovirus late promoter, vaccinia virus 7.5K promoter, SV40 promoter, tk promoter of HSV, RSV promoter, EF1 alpha promoter, metallothionine promoter, beta Actin promoter, promoter of human IL-2 gene, promoter of human IFN gene, human IL-4 gene Promoter, one containing the promoter and the promoter of the human GM-CSF gene of the human lymphotoxin gene, and the like. Most preferably, it is a yeast GAPDH promoter.

Preferably, the expression constructs used in the present invention comprise a polyaninylation sequence (eg, a glial growth hormone terminator and a SV40 derived poly adenylation sequence).

The method of carrying the vector of the present invention into a host cell may use various methods known in the art, for example, when the host cell is a prokaryotic cell, the CaCl ₂ method (Cohen, et al., Proc. Natl. Acac Sci. USA , 9: 2110-2114 (1973)), one method (Cohen, et al., Proc. Natl. Acac. Sci. USA , 9: 2110-2114 (1973); and Hanahan, D., J. Mol. Biol. , 166: 557-580 (1983)) and electroporation methods (Dower, et al., Nucleic. Acids Res. , 16: 6127-6145 (1988)) and the like. For cells, electroporation, lipofection, microinjection, gene bombardment, yeast globular / cell fusion used in YAC, Agrobacterium-mediated trait used in plant cells It can carry out using a switching etc.

According to a preferred embodiment of the present invention, the expression-encoding nucleotide sequence used in the present invention has a structure of “promoter-expression encoding nucleotide sequence-poly adenylation sequence”.

The vector system of the present invention may be constructed through various methods known in the art, and specific methods thereof are disclosed in Sambrook et al., Molecular Cloning, A Laboratory Manual , Cold Spring Harbor Laboratory Press (2001), This document is incorporated herein by reference.

The production of transformed yeast cells using the recombinant expression vector of the present invention can be carried out by gene transfer methods commonly known in the art. For example, electroporation, lithium acetate / DMSO method (Hill, J., et al., (1991), DMSO-enhanced whole cell yeast transformation. Nucleic Acids Res. 19, 5791.), liposomes- Mediated Transfer Methods (Wong et al ., 1980), Retrovirus-Mediated Transfer Methods (Chen, et al., (1990), J. Reprod. Fert. 41: 173-182; Kopchick, et al., (1991) Methods for the introduction of recombinant DNA into chicken embryos.In Transgenic Animals, ed.NL First & FP Haseltine, pp. 275-293, Boston; Butterworth-Heinemann; Lee, M.-R. and Shuman, R. (1990) Proc. 4th World Congr. Genet. Appl. Livestock Prod. 16, 107-110).

On the other hand, in order to use the expression target protein of the present invention as an active ingredient to introduce the gene should be able to effectively penetrate into the cell. For example, when using the above-described mutated SPT15 protein as an active ingredient, it is preferable to attach a protein transduction domain (PTD) to the mutated SPT15 protein. That is, in order to introduce a mutated SPT15 protein of the present invention as an active ingredient into cells, a protein transduction domain (PTD) is fused with the protein to make a fusion protein. The protein transport domain (PTD) mainly contains basic amino acid residues such as lysine / arginine, and serves to permeate the proteins fused therewith into the cell through the cell membrane. The protein transport domain (PTD) is preferably in the HIV-1 Tat protein, the homeodomain of the drosophila antennafedia, the HSV VP22 transcriptional regulator protein, the MTS peptide derived from vFGF, the penetratin, the transpotane or the Pep-1 peptide. Including but not limited to sequences derived.

On the other hand, the yeast strain of the present invention can be used for the large-scale identification of ethanol resistance and / or sensitive yeast genes. More specifically, the identification may comprise the steps of: (i) performing transcriptome profiling from the transformed yeast strain and untransformed normal yeast of the present invention; And (ii) comparing / analyzing the transcript profiles, thereby allowing large amounts of ethanol resistant and / or sensitive yeast genes to be identified.

In the comparison / analysis of the transcript profile, when a hybridization signal is detected in a fold increase of 1.5 times or more in the transformed yeast strain than the normal yeast, it is determined that the gene up-regulates ethanol resistance. If the signal is detected by a fold decrease of more than 1.5-fold, it is considered a gene that down-regulates ethanol resistance.

Since the method of the present invention includes the above-described yeast strain transformed with the mutated SPT15 gene of the present invention as an active ingredient, the overlapping content between the two is omitted in order to avoid excessive complexity of the present specification according to the overlapping description. Omit.

According to a preferred embodiment of the present invention, the transcript profile of the present invention can be carried out by microarray.

In the microarray of the present invention, the probe is used as a hybridizable array element and is immobilized on a substrate. Preferred gases include, for example, membranes, filters, chips, slides, wafers, fibers, magnetic beads or non-magnetic beads, gels, tubing, plates, polymers, microparticles and capillaries, as suitable rigid or semi-rigid supports. The hybridization array elements are arranged and immobilized on the substrate. This immobilization is carried out by chemical bonding methods or by covalent binding methods such as UV. For example, the hybridization array element can be bonded to a glass surface modified to include an epoxy compound or an aldehyde group, and can also be bonded by UV at the polylysine coating surface. In addition, the hybridization array element may be coupled to the gas through a linker (e.g., ethylene glycol oligomer and diamine).

As used herein, the term “probe” refers to a linear oligomer of natural or modified monomers or linkages, includes deoxyribonucleotides and ribonucleotides, and can specifically hybridize to a target nucleotide sequence, naturally Present or artificially synthesized. Probes of the invention are preferably single chain and oligodioxyribonucleotides. Probes of the invention can include naturally occurring dNMPs (ie, dAMP, dGMP, dCMP and dTMP), nucleotide analogues or derivatives. In addition, the probes of the present invention may also comprise ribonucleotides. For example, the probes of the present invention may be selected from framework modified nucleotides such as peptide nucleic acids (PNA) (Egholm, et al. , Nature , 365: 566-568 (1993)), phosphorothioate DNA, phosphorodithioate DNA, Phosphoramidate DNA, amide-linked DNA, MMI-linked DNA, 2'-0-methyl RNA, alpha-DNA and methylphosphonate DNA, sugar modified nucleotides such as 2'-0-methyl RNA, 2 '-Fluoro RNA, 2'-amino RNA, 2'-0-alkyl DNA, 2'-0-allyl DNA, 2'-0-alkynyl DNA, hexose DNA, pyranosyl RNA and anhydrohexitol DNA, and nucleotides with base modifications such as C-5 substituted pyrimidines (substituents are fluoro-, bromo-, chloro-, iodo-, methyl-, ethyl-, vinyl-, formyl-, ethyl -, Propynyl-, alkynyl-, thiazolyl-, imidazoryl-, pyridyl-, 7-deazapurine with C-7 substituents (substituents are fluoro-, bromo-, chloro-, Iodo-, methyl-, Ethyl-, vinyl-, formyl-, alkynyl-, alkenyl-, thiazolyl-, imidazoryl-, pyridyl-), inosine and diaminopurine.

The sample DNA applied to the microarray of the present invention is labeled and hybridized with the array elements on the microarray. Hybridization conditions can vary. The detection and analysis of the hybridization degree can be variously carried out according to the labeling substance. According to a preferred embodiment of the present invention, the sample DNA of the present invention is synthesized by inserting aminoallyl-dUTP and labeled with NHS-ester Cy die, but is not limited thereto.

The nucleic acid sample to be analyzed can be prepared using mRNA obtained from various biosamples. The raw sample is preferably a yeast cell, most preferably the transformed yeast cell of the present invention described above. The hybridization reaction-based assay can be performed by labeling the cDNA to be analyzed instead of the probe.

If a probe is used, the probe is hybridized with the cDNA molecule. In the present invention, suitable hybridization conditions can be determined in a series of procedures by an optimization procedure. This procedure is carried out by a person skilled in the art in order to establish a protocol for use in the laboratory. For example, conditions such as temperature, concentration of components, hybridization and wash times, buffer components and their pH and ionic strength depend on various factors such as probe length and GC amount and target nucleotide sequence. Detailed conditions for hybridization are described in Sambrook, et al. , Molecular Cloning, A Laboratory Manual , Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY (2001); And MLM Anderson, Nucleic Acid Hybridization , Springer-Verlag New York Inc. NY (1999). For example, high stringency conditions were hybridized at 65 ° C in 0.5 M NaHPO ₄ , 7% SDS (sodium dodecyl sulfate) and 1 mM EDTA, followed by addition of 0.1 x SSC / 0.1% SDS Lt; RTI ID = 0.0 > 68 C < / RTI > Alternatively, high stringency conditions means washing at < RTI ID = 0.0 > 48 C < / RTI > in 6 x SSC / 0.05% sodium pyrophosphate. Low stringency conditions mean, for example, washing in 0.2 x SSC / 0.1% SDS at 42 ° C.

Labels of nucleic acid samples or probes can provide a signal to detect hybridization, which can be linked to oligonucleotides. Suitable labels include fluorophores (eg fluorescein, phycoerythrin, rhodamine, lissamine, and Cy3 and Cy5 (Pharmacia), chromophores, chemilumines, magnetic particles, radioisotopes Elements (P ³² and S ³⁵ ), mass labels, electron dense particles, enzymes (alkaline phosphatase or horseradish peroxidase), cofactors, substrates for enzymes, heavy metals (eg gold) and antibodies, streptavidin Hapten with specific binding partners, such as, but not limited to, biotin, digoxigenin and chelating groups. Labeling can be performed in a variety of ways conventionally practiced in the art, such as nick translation methods, random priming methods (Multiprime DNA labeling systems booklet, "Amersham" (1989)), and chination methods (Maxam & Gilbert, Methods). in Enzymology , 65: 499 (1986)). The label provides signals that can be detected by fluorescence, radioactivity, colorimetry, weighing, X-ray diffraction or absorption, magnetism, enzymatic activity, mass analysis, binding affinity, hybridization high frequency, and nanocrystals.

After the hybridization reaction, the hybridization signal coming out of the hybridization reaction is detected. The hybridization signal can be performed by various methods, for example, depending on the type of label bound to the nucleic acid sample or probe. For example, if labeled by an enzyme, the substrate of the enzyme can be reacted with the hybridization product to confirm hybridization. Combinations of enzymes / substrates that can be used include peroxidase (eg horseradish peroxidase) and chloronaphthol, aminoethylcarbazole, diaminobenzidine, D-luciferin, lucigenin (bis-N-methylacridinium). Nitrate), resorphin benzyl ether, luminol, amplex red reagent (10-acetyl-3,7-dihydroxyphenoxazine), p-phenylenediamine-HCl and pyrocatechol (HYR), tetramethylbenzidine (TMB), ABTS (2 , 2'-Azine-di [3-ethylbenzthiazoline sulfonate]), o -phenylenediamine (OPD) and naphthol / pyronine; Alkaline phosphatase with bromochloroindolyl phosphate (BCIP), nitro blue tetrazolium (NBT), naphthol-AS-B1-phosphate and ECF substrates; Glucose oxidase, t-NBT (nitroblue tetrazolium) and m-PMS (phenzaine methosulfate). When labeled with gold particles, it can be detected by silver dyeing using silver nitrate. Therefore, when large-scale identification of the ethanol resistant and / or susceptible yeast gene of the present invention is carried out on the basis of hybridization, specifically (i) a nucleic acid sample derived from the above-described yeast strain of the present invention and normal yeast is subjected to a microarray substrate. Hybridizing with a probe immobilized on the substrate; (ii) detecting whether the hybridization reaction occurs. By analyzing the intensity of the hybridization signal by the hybridization process, it is possible to determine whether the ethanol resistance and / or sensitive yeast gene. That is, if the hybridization signal in the sample is detected to be an increase fold of 1.5 times or more than the normal sample (normal cell), it is judged to be a gene that up-regulates ethanol resistance. It is judged to be a gene.

According to a preferred embodiment of the present invention, it can be reconfirmed by additionally measuring the expression level of ethanol resistant and / or sensitive yeast genes detected through the microarray of the present invention. The measurement of expression level can be carried out through various methods known in the art. For example, RT-PCR (Sambrook, et al. , Molecular Cloning. A Laboratory Manual , 3rd ed. Cold Spring Harbor Press (2001)), Northern blotting (Kaufma et al., Molecular and Cellular Methods in Biology and Medicine) , 102-108, CRC press) or in situ hybridization reaction (Sambrook, et al. , Molecular Cloning. A Laboratory Manual , 3rd ed. Cold Spring Harbor Press (2001)).

When performing according to the RT-PCR protocol, first, total RNA is isolated from the transformed yeast strain and untransformed normal yeast of the present invention, and then the first-chain cDNA is prepared using oligo dT primer and reverse transcriptase. do. Subsequently, the first chain cDNA is used as a template, and a PCR reaction is performed using a set of ethanol resistant and / or sensitive yeast gene-specific primers. The PCR amplification products are then electrophoresed and the formed bands are analyzed and compared to the microarray data described above to re-validate changes in expression levels of ethanol resistant and / or sensitive yeast genes.

The features and advantages of the present invention are summarized as follows:

(a) The present invention relates to an ethanol-resistant transformed yeast strain comprising a mutated SPT15 gene and use thereof.

(b) Yeast strains of the present invention are yeast strains that can grow in high concentration ethanol, preferably 12.5-15% ethanol.

(c) By inventing strains that are resistant to high concentrations of ethanol, they will be useful for the production of more efficient ethanol, and will also be useful as super strains of highly efficient ethanol-producing ability that are resistant to various stresses generated during bioethanol production. .

1 is a spot assay result showing increased ethanol resistance of five ETS1-5. Cells were grown up to OD ₆₀₀ value 1 in YSCD-Ura or YPD liquid medium and then serially diluted 10-fold. Aliquots (5 μl) of cultured cells were spotted in YSCD-Ura or YPD plate medium containing appropriate concentrations of ethanol and plates were incubated at 30 ° C. for 4-6 days. Control strains were prepared by transducing parental plasmids into L3262 (C-L3262) and BY4741 (C-BY4741). FIG. 1A shows the results of a spot assay of ETS1-5 on a YSCD-Ura plate. 1B shows that the plasmid recovered from ETS1-5 was transformed back into L3262 and BY4741 to prepare rL-ETS1-5 and rBY-ETS1-5, respectively, and spot assayed on YSCD-Ura plates. 1C shows the results of spot assays of ETS2 and ETS3 on YPD plates. 1D shows the integration of parent plasmids and plasmids recovered from ETS2 and ETS3 into the genome of L3262 to prepare iL3262, iETS2 and iETS3, respectively, and spot assays on YSCD-Ura (top panel) and YPD plate (bottom panel). Was carried out.
2 shows the ethanol sensitivity of ETS2 and ETS3. After ethanol shock at the indicated time, C-L3262, ETS2 and ETS3 were grown for 2 days in YSCD-Ura plates in the presence of 12.5% (A) and 15% (B) ethanol. Relative survival was expressed as% control after counting the number of colonies. Symbol: C-L3262, Δ; ETS2, ■; And ETS3, ●. The experiment was conducted three times.
3 shows microarray data analysis results of ETS2 and ETS3. Microarray analysis was performed using poly (A) ⁺ RNAs prepared from C-L3262 (control), ETS2 and ETS3 grown to mid-log phase without ethanol stress. Differently expressed genes with more than two-fold expression fold changes were profiled by clustering (A) and Venn diagram (B). 3C shows microarray data revalidated using semi-quantitative RT-PCR for Hsp30, Hsp42 and Hsp104. Numerals 1 and 2 represent two biologically independent runs.
4 is a spot assay result showing ethanol sensitivity of SGKO mutants. Individual clones corresponding to 30 genes that are commonly up-regulated in ETS2 and ETS3 were obtained from the BY4741 SGKO library. As in FIG. 1, a spot assay was performed. The parent strain BY4741 was used as a control. Cells were cultured in liquid YPD and spotted on solid YPD containing 0%, 6%, 8%, 10% and 12% ethanol and then incubated at 30 ° C. for 4-6 days.
5 shows the results of observing the fermentation capacity of ethanol resistant strains of iETS2 and iETS3. Exponentially growing control (iL3262, Δ) and two resistant strains, iETS2 (■) and iETS3 (●) cells were obtained and supplemented with 100 ml of YPD30E6 [30% glucose and 6% (v / v) ethanol. YP]. Starting cell density was adjusted to an OD ₆₀₀ value of 0.3. The cells were incubated at 30 ° C with shaking at 120 rpm. After samples were taken every 12 hours, cell growth (A) and ethanol concentration (B) were determined using cell density measurements and high-pressure liquid chromatography (HPLC), respectively. The experiment was conducted in triplicates.

Hereinafter, the present invention will be described in more detail with reference to Examples. These examples are only for illustrating the present invention in more detail, it will be apparent to those skilled in the art that the scope of the present invention is not limited by these examples in accordance with the gist of the present invention. .

Example

Materials and Experiments

Yeast Strains and Growth Conditions

S. cerevisiae L3262 ( MAT-α , ura3-52 leu2-3 ll2 his4-34 ; Biotechnology Research Institute, Daejeon) and BY4741 ( MATα his3Δ1 leu2Δ0 met15Δ0 ura3Δ0 ) are expressed as transformation recipients Used as. A nonnessential haploid Saccharomyces cerevisiae library was kindly provided by Dr. Won Weon-gi (Seoul National University, Seoul, Korea) and used to identify the identified genes. Unless otherwise noted, yeast cells additionally added YPD medium (1% Bacteria yeast extract, 2% Bactobacillus peptone and 2w / v% glucose, and 15% Bactobacillus-agar for solid plates) for non-selective propagation. Incubated at 30 ° C. in Difco, MI or yeast synthetic complete medium for selective propagation (YSCD medium; 0.67% yeast nitrogen base without amino acids, amino acid supplement mixture and 2% dextrose, and 1.5 for solid plates And additionally containing% bacto-agar; MP, OH). For plasmid construction, the pRS316 vector (Director of the Institute; CEN -based vector, Saccharomyces cerevisiae GAPDH promoter, URA3 selection marker) was used as the expression vector, E. Coli DH5α (Stratagene, Calif.) was used as a host and incubated at 37 ° C in Luria-Bertani medium (LB): Difco, MI supplemented with 100 mg / l Ampicillin (Sigma-Aldrich, Mo.).

Molecular Biological Methods

Plasmid preparation, cloning and sequencing were performed as previously described (Sambrook, 2001). E. coli DH5α (Stratagene, USA) was used as a host for plasmid preparation.

Reverse transcription-polymerase chain reaction (RT-PCR) and PCR

For RT, total RNA was extracted from exponentially growing cells. Primary strand cDNAs were synthesized by transcription of 2 μg total RNA using an optional hexamer and 200 U of M-MLV reverse transcriptase (Promega, Madison, WI, USA) as recommended by the manufacturer. Oligonucleotides used for PCR are listed in Table 1. Amplification conditions were as follows: 95 ° C., 1 minute; 55-60 ° C., 1 minute; And 72 ° C., an extension time appropriate for the length of DNA to be amplified. RT-PCR and general PCR performed 20 and 30 cycles, respectively. If necessary, PCR products were purified by gel extraction, cloned into pGEM-T easy vector (Promega) and sequenced (Bionics, Seoul).

STP15 Mutation Library Construction

Using the full open reading frame (ORF) of wild type SPT15 (SPT15wt) as genome DNA as a template, a sense primer (5'-gtag ggatcc tgagatggccgatgaggaacgtt-3 ', underlined sequence is BamH I position) and antisense primer (5'-gtag) gaTtc tcacatttttctaaattcacttag-3 ', the underlined sequence was PCR-amplified with EcoR I position) and cloned into pGEM-T easy vector to prepare pT-SPT15. The SPT15 mutation library was prepared using GeneTorph II random mutagenesis kit (Stratagene, La Jolla, CA, USA) as a template and primers described above. PCR products were cleaved with BamH I and EcoR I and cloned into pRS316-derived plasmid, pRS316-GCYH2gR, and cloned genes were glyceraldehyde-3-phosphate dehydrogenase promoter ( TDH3 _P ) and galactose-1. Located under the control of phosphate terminator (GAL7 _T ). The resulting plasmids were transformed into E. coli DH5α and incubated at 30 ° C. to prepare a primary library for SPT15 mutants with a total colony number of 4 × 10 ⁶ . Sequencing of 20 randomly selected colonies resulted in 70% molecular-based mutagenesis production. Mutations were found in at least one, mostly 3-5 positions, in the 14 colonies, with the remainder identical to the wild type. After amplification and large scale preparation, library plasmids (500 μg) were transformed into S326 cerevisiae with L3262 and incubated at 25 ° C. in solid YSCD-Ura. The total number of yeast colonies was about 5 × 10 ⁶ , indicating a transformation efficiency of about 4 × 10 ⁶ colony forming units (CFU) per 1 μg of DNA. All colonies were obtained by scraping a plate surface coated with 15 ml YSCD-Ura to prepare a yeast library for SPT15 mutants. After doubling the cell number at 25 ° C., aliquots of the cell suspension were stored at −80 ° C. in the presence of 20% glycerol until use.

Yeast transformation

All plasmids for yeast transformation were prepared manually without RNA cleavage. DNA concentration was determined by comparing the band intensities of known concentrations of control DNA. Mixtures of DNAs and RNAs were used for yeast transformation as previously described (Hirasawa, et al. , 2007).

Spot Assay

Aliquots (5 μl) of cells incubated with an OD ₆₀₀ value of 1 were serially diluted 10-fold and spotted on solid synthetic media or enriched media containing appropriate concentrations of ethanol. Plates were incubated at 30 ° C. for 4-6 days.

Ethanol Sensitization Assay

Cells cultured with an OD ₆₀₀ value of 1 were obtained and equally aliquoted in fresh YSCD-Ura medium containing 12.5% (v / v) and 15% (v / v) ethanol and incubated at 30 ° C. for 4-6 hours. . Aliquots were diluted at appropriate times and plated on solid YPD plates. Cell viability was measured over time and expressed in relative CFU numbers.

Genomic integration

The mutated SPT15 gene was cloned into the integration vector pRS406 and linearized with the unique Apa I position in URA3 and then transformed to Saccharomyces cerevisiae with L3262. In addition, a control strain, iL3262, was prepared by similarly treating the clone-free plasmid (inset-free plasmid). Genome integration was confirmed by PCR.

Transcriptome profiling and data analysis

For transcript profiles, Saccharomyces cerevisiae was used with 30K oligo microarrays (MYcroarray, Ann Arbor, MI, USA). As previously described, total RNA was extracted from exponentially growing cells and subjected to RNA quality control (QC) for microarray analysis (Park, et al ., 2007). CDNAs incorporating aminoallyl-dUTP were synthesized from 40-50 μg total RNA using the aminoallyl post DNA labeling kit (GeneChem, Daejeon, Korea) and Superscript reverse transcriptase (Invitrogen, Carlsbad, Calif., USA). The synthesized cDNA was labeled with NHS-ester Cy die and used for hybridization. Hybridized slides were washed with SSC buffer and then scanned with a ScanArray 5000 scanner (Hewlett-Packard, Palo Alto, Calif., USA). Raw microarray data was analyzed using ArrayNorm ( http://genome.tugraz.at/ ) and statistical analysis, a platform-independent Java means for standardization (Pieler, et al. , 2004). Clustering for genes that change more than twice as high on average was performed using Cluster 3.0 ( http://rana.lbl.gov/EisenSoftware.htm ). Enrichment of functional categories between differently expressed genes was analyzed using the MIPS Functional Catalog ( http://mips.gsf.de ). Specific gene function was based on Saccharomyces genome database ( http://www.yeastgenome.org ) and transcription factor binding sites were analyzed by YEATRACT ( http://www.yeastact.com/index.php ). To validate DNA microarray data, semi-quantitative reverse transcription PCR was performed as previously described with RNA samples used in microarray experiments (Oh, et al. , 2004).

Fermentation

Exponentially growing cells were obtained and transferred to 100 ml of YPD30E6 [YP supplemented with 30% glucose and 6% (v / v) ethanol]. Starting cell density was adjusted to an OD ₆₀₀ value of 0.3. The cells were incubated at 30 ° C with shaking at 120 rpm. After samples were taken every 12 hours, cell growth and ethanol concentration were determined using cell density measurements and high-pressure liquid chromatography (HPLC), respectively. Samples were loaded on an Aminex HPX-87H column (Bio-Rad, Hercules, CA, USA) set at 60 ° C. Glucose and ethanol were eluted with 0.5 mM H ₂ SO ₄ at a flow rate of 0.6 ml / min. Peaks were detected by refractory index and identified according to retention time and quantified according to a standard curve. Cell growth was monitored by measuring optical density at 600 nm.

Experiment result

Identification of Ethanol-Resistant Strains

In order to identify genes that confer ethanol-resistance through high-speed screening, it is generally useful to use strains with a low concentration of ethanol resistant background. Since the laboratory strains in the various Saccharomyces cerevisiae tested were most ethanol sensitive (not showing results), L3262 was chosen and used to build the yeast SPT15 mutant library. For the screening of ethanol resistant strains, aliquots of 5 × 10 ⁶ CFU yeast library stocks were plated on solid YSCD-Ura medium supplemented with 12.5% or 15% ethanol. Plates were sealed and incubated at 30 ° C. to inhibit ethanol evaporation. After 10 days, 9 and 6 colonies respectively appeared in the presence of 12.5% or 15% ethanol. The ethanol resistance of 15 colonies was examined by spot assay in solid YSCD-Ura medium containing up to 15% ethanol. As a result, five ethanol resistant strains (ETS; ETS1-5) were obtained. All five strains were resistant to 15% ethanol under synthetic medium, whereas the control group was not resistant to ethanol concentrations above 10% (FIG. 1A).

To confirm whether increased ethanol resistance is conferred by mutated SPT15, plasmids were converted to ETS15 (pSPT15-M1, -M2, -M3, -M4 and -M5, respectively, for the mutated alleles of SPT15). Recovered. The plasmids described above were individually reintroduced into L3262 and By4741 to produce rL-ETS1-5 and rBY-ETS1-5, respectively. To construct the control strain, pRS316-GCYH2gR comprising SPT15wt was reintroduced into L3262 and By4741 to produce C-L3262 and C-By4741, respectively. For the spot assays carried out on the synthetic medium, rL-ETS1-5 showed ethanol resistance even in the same manner as ETS1-5 (FIG. 1B, top panel). In contrast, rBY-ETS1-5 showed resistance in high ethanol such as 17.5% ethanol (FIG. 1B, bottom panel). This is not surprising because BY4741 is basically a strain that showed higher ethanol resistance than L3262 (no results shown). Thus, increased ethanol resistance of ETS1-5 could be regarded as the effect of mutated SPT15.

Next, each plasmid was sequenced to identify mutations. Table 1 lists the mutated amino acids in each SPT15 allele: K201Q, G216S and Q225Stop for SPT15-M1; L76V and L175S for SPT15-M2; For SPT15-M3, S42N, C78R, S163P and I212N; For SPT15-M4, F10S and M197K; For SPT15-M5, K15T, W26C and G192D.

Point mutations occurring in the SPT15 allele. Strain SPT15 allele Amino acid substitutions Of located point mutations
Structural domains ^a ETS1
ETS2
ETS3

ETS4
ETS5 SPT15-M1 ^b
SPT15-M2
SPT15-M3

SPT15-M4
SPT15-M5 K201Q, G216S, Q225Stop
L76V, L175S
S42N, C78R,
S163P, I212N
F10S, M197K
K15T, W26C, G192D S3'-S4 'Loop, S5', H2 '
S1-H1 loop, H1 '
N-terminus, S1-H1 loop,
S1 ', S5'
N-terminal, S3'-S4 'loop
N-terminal, N-terminal, S3 '

^a Chasman et al. Structural domain names as described in (1993): H, α-helix; S, β-sheet.

^b 16 amino acids deleted at the C-terminus due to N225Sto.

In particular, a silent mutation in SPT15-M1 produced a truncated version with 16 residues deleted at the C-terminus. As can be seen in Table 1, point mutations spread throughout the SPT15 ORF were not located in the structural domain associated with increased ethanol resistance. Only SPT15-M2 contained a mutation (L175S) in the domain that interacts with Spt3p, which is earlier included in gene transcriptional regulation. The above data is consistent with the suggestion that mutations in various subregions of Spt15p confer ethanol resistance, which is believed to be achieved through interaction with other components of the transcriptional mechanism in addition to Spt3p.

According to the data of FIG. 1B, ETS1 showed less resistance than ETS4 and ETS5, and ETS2 and ETS3 showed slightly more (or at least the same) resistance than ETS4 and ETS5. Therefore, ETS2 and ETS3 were selected for future experiments. S. cerevisiae laboratory strains used for the expression of specific genes always have mutations that are independent of each other in many genes encoding enzymes involved in amino acid biosynthesis, so they can supplement specific amino acids for growth when grown in a limited medium. There is a need. It was controversial that increased ethanol resistance could result from low leucine supplementation rather than mutated SPT15 (Baerends, et al. , 2009). More specifically, ethanol resistance was destroyed when cells were cultured in YPD complex rich media that were not suitable for industrial applications. In addition, because leucine and histidine supplementation are required for the growth of ETS2 and ETS3, the increased ethanol resistance of these strains may not be due to SPT15 mutations. Thus, ethanol resistance of ETS2 and ETS3 was tested with a spot assay on YPD. As can be seen in FIG. 1C, ETS2 was sensitive to 15% ethanol against the data of FIG. 1A, whereas ETS3 showed ethanol resistance similar to the results seen in synthetic media. However, C-L3262 Strainin, which was very sensitive to 15% ethanol in the synthetic medium, appeared to have some ethanol resistance on YPD, which means that the base level of ethanol resistance in the rich medium is higher than the synthetic medium. The overall data were in agreement with the conclusion that ETS3 is more resistant to ethanol on YPD than ETS2.

Cell-cell heterogeneity in expression is one of the problems that may be encountered when information obtained from episomal overexpression in laboratory strains extends to industrial applications. Heterogeneity is caused by the inability to control the copy number in spite of the constant presence of selective pressures that are not arbitrarily selectable for yeast culture in industrial applications. Thus, stable expression and maintenance of genes in the absence of selection pressure (ie integration into the chromosome) is highly desirable. In the present invention, we constructed strains in which SPT15-M2 and -M3 were integrated into the genome of L3262: the corresponding constructs were named iETS2 and iETS3, respectively. Control strain iL3262 was prepared from a plasmid containing SPT15wt. 1D shows the spot assay results of the three strains in YSCD (top panel) and YPD (bottom panel). The degree of ethanol resistance of iETS2 and iETS3 in YSCD was similar as in YPD (FIG. 1C). That is, in YPD iETS2 and iETS3 had higher ethanol resistance than in YSCD, the difference between the two was not observed even at 15% ethanol concentration.

To reconfirm spot assay results, the sensitivity to 12.5% and 15% was examined. Survival of both strains was significantly increased compared to the control in both 12.5% and 15% ethanol (FIG. 2). The time to show 50% survival (T ₅₀ ) in 12.5% ethanol was 4.5 hours for ETS2 and ETS3 and 3.5 hours for the control group. In 15% ethanol, a greater difference was observed in T ₅₀ with 100 minutes for ETS2 and ETS3 and 40 minutes for control. The data described above along with the spot assay data confirmed that ETS2 and ETS3 have increased ethanol resistance by SPT15 mutations.

Five strains with increased ethanol resistance were obtained through SPT15 mutant library screening. Plasmids were recovered from these strains and transformed back into the strains used for library construction (L3262) and other strains (BY4741). In addition, all newly constructed strains also showed increased ethanol resistance in limited media. Since the increased ethanol resistance of ETS2 and ETS3 was also maintained in complex rich media, increased ethanol resistance, as previously discussed (Baerends, et al. , 2009), has shown that leucine uptake and / or by certain SPT15 mutant alleles may increase . The possibility of being granted by activation of use is excluded. Increased ethanol resistance of ETS2 and ETS3 was confirmed by ethanol impact with ethanol sensitivity. Increased ethanol resistance was additionally observed in two integrated strains, with these SPT15 mutant alleles derived from ETS2 and ETS3 integrated on the L3262 genome.

Transcript Profile Analysis of Ethanol-Resistant Mutant Strains

We were interested in whether the expression levels of genes responsible for the increased ethanol resistance of ETS2 and ETS3 are regulated by SPT15 mutations. To this end, DNA microarrays for transcript profiles were performed using total RNAs extracted from control C-L3262, ETS2 and ETS3 cells grown in early-log phase in YSCD-Ura. After two microarray experiments, changes in expression fold were averaged. Primary data has been registered with Gene Expression Omnibus (GEO) under access number GSE23965. Clustering of genes with more than twofold changes in expression fold change compared to the control group resulted in different expression patterns between ETS2 and ETS3, reflecting the effects of different mutations of SPT15 on overall transcription (FIG. 3A). For ETS2, 49 and 11 genes were up- and down-regulated, respectively, while in ETS3 79 and 21 genes were up- and down-regulated, respectively (FIG. 3B). ETS2 and ETS3 shared 34 up-regulated genes and 8 down-regulated genes (FIG. 3C). To verify the microarray data, the actual expression levels of HSP30 and HSP42 above the cutoff value and HSP104 below the cutoff value were examined by RT-PCR. According to microarray data, HSP30, HSP42 and HSP104 were up-regulated 5.7, 4.5 and 1.7 times in ETS2 and 6.3, 4.1 and 1.8 times respectively in ETS3. Increasing folds of the genes described above were consistent with RT-PCR data (FIG. 3C).

Next, commonly up- and down-regulated genes were classified based on the indicated function. Functions of up-regulated genes include stress response and protein folding (11 genes); Pentose-phosphate pathway, cell wall and transport (two genes each); Metabolism of energy storage and energy generation (one gene); And unclassified proteins (15 genes) (Table 2).

List of genes commonly up-regulated in ethanol resistant strains ETS2 and ETS3 in the absence of ethanol stress. gene Increment multiple (Log ₂ ) Msn4p /
Msn2p Yap1p Hsf1p Hac1p ETS2 ETS3 Exp1 Exp2 Exp1 Exp2 Stress Response and Protein Folding APJ1
ALD3
CTT1
HSP12
HSP30
HSP31
HSP42
SDP1
SSA4
TSL1
YJL144W 1.4
2.5
1.7
1.1
2.7
1.5
2.3
2.0
1.0
1.2
3.7 1.1
1.8
1.7
1.5
2.3
1.6
1.9
1.3
1.7
1.2
2.3 1.3
1.6
1.4
1.0
3.0
4.5
1.8
1.8
1.4
1.1
3.4 1.3
2.1
1.9
1.5
2.3
1.5
2.3
1.6
2.0
1.9
2.7 3
2
4
7
0
One
3
3
3
7
One 0
One
2
0
2
One
0
0
One
0
One One
0
4
One
0
2
2
2
One
One
2 2
One
One
4
0
0
One
0
One
2
2 Pentose-phosphate pathway PGM2
SOL4 1.7
1.9 1.2
1.5 1.7
1.6 2.1
1.9 7
One One
0 0
6 One
0 Cell wall SPI1
OSW2 2.0
1.2 1.3
1.0 1.8
1.9 1.6
1.40 3
0 One
One 2
2 One
One carrying PIC2
BTN2 1.5
2.9 1.1
3.1 1.4
2.9 1.1
3.5 One
2 0
0 2
One 0
0 Metabolic process of energy storage GPH1 1.6 1.3 1.2 2.1 3 One 0 One Energy generation STF2 1.7 1.2 1.8 1.4 2 One One 2 Unclassified Proteins AIM17
FMP16
OM45
PHM8
RTC3
RTN2
USV1
RGI1
YBL029C-A
YBR285W
YER053C-A
YFR017C
YJR096W
YNR034W-A
YPR145C-A 2.4
1.2
1.4
1.5
2.4
3.4
2.4
3.3
1.3
1.7
1.3
3.1
1.4
3.4
1.3 1.0
1.3
1.0
1.6
2.1
1.7
1.0
1.1
1.0
1.2
1.1
1.1
1.3
2.5
1.0 1.8
1.0
1.0
1.6
2.1
1.6
1.8
3.1
1.3
1.6
1.3
2.6
1.7
3.3
1.6 1.9
1.6
1.5
1.0
1.6
2.4
1.7
2.2
1.1
1.3
1.0
1.6
1.6
3.1
1.0 3
One
3
4
4
One
6
4
4
2
2
2
One
5
0 0
One
One
0
One
0
One
One
One
One
0
0
One
One
0 2
0
4
2
0
2
0
4
0
2
0
0
2
0
0 2
0
3
0
0
0
4
3
0
One
0
One
One
0
0

Genes are described that exhibit an increase fold more than twofold. Genes that confer ethanol sensitivity to cells due to deletion are shown in bold type (see Figure 4A).

Stress response and protein folding genes include several heat shock genes (HSP42, HSP31, HSP30, HSP12) that function at many sub-cellular locations (e.g., nuclear, mitochondria, cytoplasm, cytoskeleton, membrane and cell wall). And oxidative stress response gene (CTT1) and endoplasmic reticulum and mitochondrial translocation gene (SSA4). Several genes reported to be induced by ethanol were also included: PGM2 involved in glycolysis, GPH1 involved in glyconogenesis, TSL1 involved in trihalose biosynthesis, and metabolic processes in energy storage. STF2 (Ma, M., and ZL Liu., 2010). Commonly functions of down-regulated genes include budding cell polarity and filament formation (one gene); Carbon compounds (C-compound) and carbohydrate metabolism (one gene); Mating (correction; one gene); Protein targeting sorting and migration (one gene); rRNA synthesis (one gene); And unclassified proteins (3 genes) (Table 3).

List of genes commonly down-regulated in ethanol resistant strains ETS2 and ETS3 in the absence of ethanol stress. gene Increment multiple (Log ₂ ) Msn4p /
Msn2p Yap1p Hsf1p Hac1p ETS2 ETS3 Exp1 Exp2 Exp1 Exp2 Budding cell polarity and filament formation RAX2 -1.3 -1.0 -1.0 -1.5 0 One 2 0 Carbon compound (C-compound) and carbohydrate metabolism BSC1 -2.1 -2.1 -1.5 -2.2 3 One One 0 Mating PRM7 -1.0 -1.0 -1.3 -1.2 0 0 0 2 Protein targeting classification and shift VTS1 -1.5 -1.1 -1.1 -1.1 2 0 2 0 rRNA synthesis RRN7 -1.7 -1.3 -4.0 -1.2 2 0 2 0 Unclassified Proteins VEL1
YGR035C
YOR387C -2.6
-1.8
-2.7 -1.0
-1.1
-1.0 -1.2
-1.1
-1.1 -5.1
-1.7
-4.5 0
0
0 0
0
0 2
2
2 0
One
One

Genes are described that exhibit an increase fold more than twofold. Genes that confer ethanol resistance to cells due to deletion are shown in bold type (see Figure 4B).

To obtain additional information on transcriptional regulation of commonly up- and down-regulated genes, we examined the presence of potential binding sites for transcription factors that are predicted to be involved in various stress responses. For example, the transcription factors include Msn2p / Msn4p (Watanabe, et al. , 2007), which are involved in general stress, Hac1p (Ogawa and Mori, 2004), which are involved in protein secretion stress, and Hsf1p (Yamamoto, which is involved in heat stress). et al. , 2008) and Yap1p (He and Fassler, 2005) involved in oxidative stress. Very interestingly, the binding sites for the aforementioned transcription factors were very abundantly upstream of the commonly up-regulated genes (Table 2). In particular, binding sites for Msn2p / Msn4p were commonly found in almost all up-regulated genes. On the other hand, Hac1p and Hsf1p have similar frequencies in up-regulated and down-regulated genes, while binding sites for Msn2p / Msn4p and Yap1p are rarely found in common in eight down-regulated genes. (Table 3). Comprehensive data suggest that Msn2p / Msn4p and Yap1p are responsible for the regulation of genes associated with ethanol resistance. Further research is needed to investigate whether the aforementioned transcription factors are directly or indirectly regulated by the mutated Spt15p, or whether they function in cooperation with the mutated Spt15p. This process will result in up- and down-regulation of a series of genes that confer increased ethanol resistance.

Effects of Commonly Regulated Genes on Ethanol-Resistance

The main concern was whether the common 34 up-regulated genes and 8 down-regulated genes had a cause or effect on ethanol resistance. If up-regulation of a gene increases ethanol resistance, deletion of the gene will most likely confer cells with sensitivity or resistance to ethanol. Conversely, the same would be true for down-regulated genes. Deletion mutants corresponding to 30 up-regulated genes and 6 down-regulated genes were obtained from the BY4741 SGKO library. Deletion mutants corresponding to four up-regulated genes (YER053C-A, YNR034W-A, YPR145C-A and YBL029C-A) and two down-regulated genes (RRN7 and YOR387C) were not useful, This is because of their lethality. As a control cultured to an OD ₆₀₀ value of 0.5, BY4741 and individual deletion mutants were serially diluted 10-fold and spotted in solid YPD medium containing different concentrations of ethanol.

The results for 30 deletion mutants corresponding to commonly up-regulated genes are shown in FIG. 4. Several deletion mutations were sensitive to low concentrations of ethanol, such as 6% ethanol, which were lower than those that had a toxic effect on BY4741. The total number of susceptible mutants increased in proportion to the increased ethanol concentration by 12%. Sensitivity to 6% ethanol was seen in deletion mutants of GPH1, SOL4 and SSA4. Seven additional mutants (ALD3, BTN2, SPI1, OM45, RTC3, USV1 and YFR017C) were sensitive to 8% ethanol. HSP12 deletion mutants were sensitive to 10% ethanol. Finally, deletion mutations in HSP30, CTT1, SDP1, STF2, AIM17, FMP16, RGI1 and PHM8 were sensitive to 12% ethanol. Thus, deletion of 19 of 30 genes commonly up-regulated in ETS2 and ETS3 conferred ethanol sensitivity. The contribution to ethanol sensitivity was greatest in GPH1, SOL4, or SSA4, followed by ALD3, BTN2, SPI1, OM45, RTC3, USV1, or YFR017C, followed by HSP12, followed by HSP30, CTT1, SDP1, Lowest in STF2, AIM17, FMP16, RGI1 and PHM8.

On the other hand, contrary to the expectations of the present inventors based on the hypotheses described above, none of the six deletion mutants corresponding to commonly down-regulated genes showed increased growth, Corresponding deletion mutants showed the same or higher degree of ethanol resistance as control. The reason for this is uncertain.

Effect of Mutated SPT15s on Ethanol Production

In addition to understanding the mechanisms for ethanol resistance, the purpose of producing ethanol resistant strains is to improve ethanol productivity and / or final yield. Compared to control strains, it is assumed that strains with increased ethanol resistance can better cope with the toxic effects of ethanol (Ding, et al. , 2009). After phenotypic characterization, the effect of increased ethanol resistance is usually determined by measuring the highest ethanol titers from batch cultures in complex rich media containing up to 30% glucose (Hong, et al. , 2009; Hou, 2009; Hou, et al. , 2009; Teixeira, et al. , 2009). However, the yields in the above studies did not significantly improve and only increased by 10% compared to the control strain. This may be because most of the laboratory parent strains used are able to produce essentially maximum levels of ethanol, making it difficult to observe the effect of increased ethanol resistance. Thus, it would be possible to observe such an effect only at ethanol concentrations that rarely exceed the basic ethanol-producing capacity of the parent strains. In the study of the present invention, YPD30E6 medium, YPD30 medium with 6% (v / v) ethanol added from the beginning, was used for fermentation.

When the fermentation was carried out as described in the test materials and test methods, the cell density of the control group (iL3262) and two ethanol resistant integrants (iETS2 and iETS3) decreased after reaching a maximum at 84 hours (FIG. 5A). The characteristic of this profile was that iL3262 required a longer lag period (24 hours) for adaptation to ethanol added from the start and no saturation plateau was observed. The growth rate of iETS3 over the next 24 hours was slightly higher than that of iL3262 and iETS2 growing at the same rate. In general, after 48 hours, the three strains grew at a similar growth rate up to 84 hours except at 60 hours (for iETS3). Thus, relatively short length inducers characterize ethanol resistant strains.

Fermentation capacity of iL3262, iETS2 and iETS3 was determined by measuring the ethanol titer from the YPD30E6 culture. 6% (v / v) of starting ethanol corresponded to 47.5 g / L on HPLC. As can be seen in FIG. 5B, the highest ethanol titers produced by iETS2 and iETS3 during the 120-hour fermentation were 95.0 g / L and 93.0 g / L, respectively, while the ethanol titers of the control group were 74.0 g / L. Interestingly, induction phase in ethanol production was not observed in the control strain as opposed to cell growth, for which reason is unclear. The net amount of ethanol produced during the fermentation process by subtracting ethanol (47.5 g / L) added from the start in the final titer yield is: control, 26.5 g / L; iETS2, 47.5 g / L; And iETS3, 45.5 g / L. Although the above yields were lower than expected, iETS2 and iETS3 showed about 80% higher fermentation capacity than the control at the experimental conditions used in the present invention.

Having described the specific part of the present invention in detail, it is apparent to those skilled in the art that such a specific technology is only a preferred embodiment, and the scope of the present invention is not limited thereto. Thus, the substantial scope of the present invention will be defined by the appended claims and equivalents thereof.

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<110> Ewha Womens University <120> Ethanol-Resistant Yeast Strains and Uses Thereof <130> PN100184D <150> KR 10-2010-0038818 <151> 2010-04-23 <160> 10 <170> KopatentIn 1.71 <210> 1 <211> 675 <212> DNA <213> Artificial Sequence <220> <223> SPT15_M1 <400> 1 atggccgatg aggaacgttt aaaggagttt aaagaggcaa acaagatagt gtttgatcca 60 aataccagac aagtatggga aaaccagaat cgagatggta caaaaccagc aactactttc 120 cagagtgaag aggacataaa aagagctgcc ccagaatctg aaaaagacac ctccgccaca 180 tcaggtattg ttccaacact acaaaacatt gtggcaactg tgactttggg gtgcaggtta 240 gatctgaaaa cagttgcgct acatgcccgt aatgcagaat ataaccccaa gcgttttgct 300 gctgtcatca tgcgtattag agagccaaaa actacagctt taatttttgc ctcagggaaa 360 atggttgtta ccggtgcaaa aagtgaggat gactcaaagc tggccagtag aaaatatgca 420 agaattatcc aaaaaatcgg gtttgctgct aaattcacag acttcaaaat acaaaatatt 480 gtcggttcgt gtgacgttaa attccctata cgtctagaag ggttagcatt cagtcatggt 540 actttctcct cctatgagcc agaattgttt cctggtttga tctatagaat ggtgaagccg 600 caaattgtgt tgttaatttt tgtttcagga aagattgttc ttactagtgc aaagcaaagg 660 gaagaaattt actaa 675 <210> 2 <211> 720 <212> DNA <213> Artificial Sequence <220> <223> SPT15_M2 <400> 2 atggccgatg aggaacgttt aaaggagttt aaagaggcaa acaagatagt gtttgatcca 60 aataccagac aagtatggga aaaccagaat cgagatggta caaaaccagc aactactttc 120 cagagtgaag aggacataaa aagagctgcc ccagaatctg aaaaagacac ctccgccaca 180 tcaggtattg ttccaacact acaaaacatt gtggcaactg taactgtggg gtgcaggtta 240 gatctgaaaa cagttgcgct acatgcccgt aatgcagaat ataaccccaa gcgttttgct 300 gctgtcatca tgcgtattag agagccaaaa actacagctt taatttttgc ctcagggaaa 360 atggttgtta ccggtgcaaa aagtgaggat gactcaaagc tggccagtag aaaatatgca 420 agaattatcc aaaaaatcgg gtttgctgct aaattcacag acttcaaaat acaaaatatt 480 gtcggttcgt gcgacgttaa attccctata cgtctagaag ggtcagcatt cagtcatggt 540 actttctcct cctatgagcc agaattgttt cctggtttga tctatagaat ggtgaagccg 600 aaaattgtgt tgttaatttt tgtttcagga aagattgttc ttactggtgc aaagcaaagg 660 gaagaaattt accaagcttt tgaagctata taccccgtgc taagtgaatt tagaaaaatg 720                                                                          720 <210> 3 <211> 720 <212> DNA <213> Artificial Sequence <220> <223> SPT15_M3 <400> 3 atggccgatg aggaacgttt aaaggagttt aaagaggcaa acaagatagt gtttgatcca 60 aataccagac aagtatggga aaaccagaat cgagatggta caaaaccagc aactactttc 120 cagaatgaag aggacataaa aagagctgcc ccagaatctg aaaaagacac ctccgccaca 180 tcaggtattg ttccaacact acaaaacatt gtggcaactg tgactttggg gcgcaggtta 240 gatctgaaaa cagttgcgct acatgcccgt aatgcagaat ataaccccaa gcgttttgct 300 gctgtcatca tgcgtattag agagccaaaa actacagctt taatttttgc ctcagggaaa 360 atggttgtta ccggtgcaaa aagtgaggat gactcaaagc tggccagtag aaaatatgca 420 agaattatcc aaaaaatcgg gtttgctgct aaattcacag acttcaaaat acaaaatatt 480 gtcggtccgt gtgacgttaa attccctata cgtctagaag ggttagcatt cagtcatggt 540 actttctcct cctatgagcc agaattgttt cctggtttga tctatagaat ggtgaagccg 600 aaaattgtgt tgttaatttt tgtttcagga aagaatgttc ttactggtgc aaagcaaagg 660 gaagaaattt accaagcttt tgaagctata taccctgtgc taagtgaatt tagaaaaatg 720                                                                          720 <210> 4 <211> 720 <212> DNA <213> Artificial Sequence <220> <223> SPT15_M4 <400> 4 atggccgatg aggaacgttt aaaggagtct aaagaggcaa acaagatagt gtttgatcca 60 aataccagac aagtatggga aaaccagaat cgagatggta caaaaccagc aactactttc 120 cagagtgaag aggacataaa aagagctgcc ccagaatctg aaaaagacac ctccgccaca 180 tcaggtattg ttccaacact acaaaacatt gtggcaactg tgactttggg gtgcaggtta 240 gatctgaaaa cagttgcgct acatgcccgt aatgcagaat ataaccccaa gcgttttgct 300 gctgtcatca tgcgtattag agagccaaaa actacagctt taatttttgc ctcagggaaa 360 atggttgtta ccggtgcaaa aagtgaggat gactcaaagc tggccagtag aaaatatgca 420 agaattatcc aaaaaatcgg gtttgctgct aaattcacag acttcaaaat acaaaatatt 480 gtcggttcgt gtgacgttaa attccctata cgtctggaag ggttagcatt cagtcatggt 540 actttctcct cctatgagcc agaattgttt cctggtttga tctatagaaa ggtgaagccg 600 aaaattgtgt tgttaatttt tgtttcagga aagattgttc ttactggtgc aaagcaaagg 660 gaagaaattt accaagcttt tgaagctata taccctgtgc taagtgaatt tagaaaaatg 720                                                                          720 <210> 5 <211> 720 <212> DNA <213> Artificial Sequence <220> <223> SPT15_M5 <400> 5 atggccgatg aggaacgttt aaaggagttt aaagaggcaa acacgatagt gtttgatcca 60 aataccagac aagtatgtga aaaccagaat cgagatggta caaaaccagc aactactttc 120 cagagtgaag aggacataaa aagagctgcc ccagaatctg aaaaagacac ctccgccaca 180 tcaggtattg ttccaacact acaaaacatt gtggcaactg tgactttggg gtgcaggtta 240 gatctgaaaa cagttgcgct acatgcccgt aatgcagaat ataaccccaa gcgttttgct 300 gctgtcatca tgcgtattag agagccaaaa actacagctt taatttttgc ctcagggaaa 360 atggttgtta ccggtgcaaa aagtgaggat gactcaaagc tggccagtag aaaatatgca 420 agaattatcc aaaaaatcgg gtttgctgct aaattcacag acttcaaaat acaaaatatt 480 gtcggttcgt gtgacgttaa attccctata cgtctagaag ggttagcatt cagtcatggt 540 actttctcct cctatgagcc agaattgttt cctgatttga tctatagaat ggtgaagccg 600 aaaattgtgt tgttaatttt tgtttcagga aagattgttc ttactggtgc aaagcaaagg 660 gaagaaattt accaagcttt tgaagctata taccctgtgc taagtgaatt tagaaaaatg 720                                                                          720 <210> 6 <211> 224 <212> PRT <213> Artificial Sequence <220> <223> SPT15_M1 <400> 6 Met Ala Asp Glu Glu Arg Leu Lys Glu Phe Lys Glu Ala Asn Lys Ile   1 5 10 15 Val Phe Asp Pro Asn Thr Arg Gln Val Trp Glu Asn Gln Asn Arg Asp              20 25 30 Gly Thr Lys Pro Ala Thr Thr Phe Gln Ser Glu Glu Asp Ile Lys Arg          35 40 45 Ala Ala Pro Glu Ser Glu Lys Asp Thr Ser Ala Thr Ser Gly Ile Val      50 55 60 Pro Thr Leu Gln Asn Ile Val Ala Thr Val Thr Leu Gly Cys Arg Leu  65 70 75 80 Asp Leu Lys Thr Val Ala Leu His Ala Arg Asn Ala Glu Tyr Asn Pro                  85 90 95 Lys Arg Phe Ala Ala Val Ile Met Arg Ile Arg Glu Pro Lys Thr Thr             100 105 110 Ala Leu Ile Phe Ala Ser Gly Lys Met Val Val Thr Gly Ala Lys Ser         115 120 125 Glu Asp Asp Ser Lys Leu Ala Ser Arg Lys Tyr Ala Arg Ile Ile Gln     130 135 140 Lys Ile Gly Phe Ala Ala Lys Phe Thr Asp Phe Lys Ile Gln Asn Ile 145 150 155 160 Val Gly Ser Cys Asp Val Lys Phe Pro Ile Arg Leu Glu Gly Leu Ala                 165 170 175 Phe Ser His Gly Thr Phe Ser Ser Tyr Glu Pro Glu Leu Phe Pro Gly             180 185 190 Leu Ile Tyr Arg Met Val Lys Pro Gln Ile Val Leu Leu Ile Phe Val         195 200 205 Ser Gly Lys Ile Val Leu Thr Ser Ala Lys Gln Arg Glu Glu Ile Tyr     210 215 220 <210> 7 <211> 240 <212> PRT <213> Artificial Sequence <220> <223> SPT15_M2 <400> 7 Met Ala Asp Glu Glu Arg Leu Lys Glu Phe Lys Glu Ala Asn Lys Ile   1 5 10 15 Val Phe Asp Pro Asn Thr Arg Gln Val Trp Glu Asn Gln Asn Arg Asp              20 25 30 Gly Thr Lys Pro Ala Thr Thr Phe Gln Ser Glu Glu Asp Ile Lys Arg          35 40 45 Ala Ala Pro Glu Ser Glu Lys Asp Thr Ser Ala Thr Ser Gly Ile Val      50 55 60 Pro Thr Leu Gln Asn Ile Val Ala Thr Val Thr Val Gly Cys Arg Leu  65 70 75 80 Asp Leu Lys Thr Val Ala Leu His Ala Arg Asn Ala Glu Tyr Asn Pro                  85 90 95 Lys Arg Phe Ala Ala Val Ile Met Arg Ile Arg Glu Pro Lys Thr Thr             100 105 110 Ala Leu Ile Phe Ala Ser Gly Lys Met Val Val Thr Gly Ala Lys Ser         115 120 125 Glu Asp Asp Ser Lys Leu Ala Ser Arg Lys Tyr Ala Arg Ile Ile Gln     130 135 140 Lys Ile Gly Phe Ala Ala Lys Phe Thr Asp Phe Lys Ile Gln Asn Ile 145 150 155 160 Val Gly Ser Cys Asp Val Lys Phe Pro Ile Arg Leu Glu Gly Ser Ala                 165 170 175 Phe Ser His Gly Thr Phe Ser Ser Tyr Glu Pro Glu Leu Phe Pro Gly             180 185 190 Leu Ile Tyr Arg Met Val Lys Pro Lys Ile Val Leu Leu Ile Phe Val         195 200 205 Ser Gly Lys Ile Val Leu Thr Gly Ala Lys Gln Arg Glu Glu Ile Tyr     210 215 220 Gln Ala Phe Glu Ala Ile Tyr Pro Val Leu Ser Glu Phe Arg Lys Met 225 230 235 240 <210> 8 <211> 240 <212> PRT <213> Artificial Sequence <220> <223> SPT15_M3 <400> 8 Met Ala Asp Glu Glu Arg Leu Lys Glu Phe Lys Glu Ala Asn Lys Ile   1 5 10 15 Val Phe Asp Pro Asn Thr Arg Gln Val Trp Glu Asn Gln Asn Arg Asp              20 25 30 Gly Thr Lys Pro Ala Thr Thr Phe Gln Asn Glu Glu Asp Ile Lys Arg          35 40 45 Ala Ala Pro Glu Ser Glu Lys Asp Thr Ser Ala Thr Ser Gly Ile Val      50 55 60 Pro Thr Leu Gln Asn Ile Val Ala Thr Val Thr Leu Gly Arg Arg Leu  65 70 75 80 Asp Leu Lys Thr Val Ala Leu His Ala Arg Asn Ala Glu Tyr Asn Pro                  85 90 95 Lys Arg Phe Ala Ala Val Ile Met Arg Ile Arg Glu Pro Lys Thr Thr             100 105 110 Ala Leu Ile Phe Ala Ser Gly Lys Met Val Val Thr Gly Ala Lys Ser         115 120 125 Glu Asp Asp Ser Lys Leu Ala Ser Arg Lys Tyr Ala Arg Ile Ile Gln     130 135 140 Lys Ile Gly Phe Ala Ala Lys Phe Thr Asp Phe Lys Ile Gln Asn Ile 145 150 155 160 Val Gly Pro Cys Asp Val Lys Phe Pro Ile Arg Leu Glu Gly Leu Ala                 165 170 175 Phe Ser His Gly Thr Phe Ser Ser Tyr Glu Pro Glu Leu Phe Pro Gly             180 185 190 Leu Ile Tyr Arg Met Val Lys Pro Lys Ile Val Leu Leu Ile Phe Val         195 200 205 Ser Gly Lys Asn Val Leu Thr Gly Ala Lys Gln Arg Glu Glu Ile Tyr     210 215 220 Gln Ala Phe Glu Ala Ile Tyr Pro Val Leu Ser Glu Phe Arg Lys Met 225 230 235 240 <210> 9 <211> 240 <212> PRT <213> Artificial Sequence <220> <223> SPT15_M4 <400> 9 Met Ala Asp Glu Glu Arg Leu Lys Glu Ser Lys Glu Ala Asn Lys Ile   1 5 10 15 Val Phe Asp Pro Asn Thr Arg Gln Val Trp Glu Asn Gln Asn Arg Asp              20 25 30 Gly Thr Lys Pro Ala Thr Thr Phe Gln Ser Glu Glu Asp Ile Lys Arg          35 40 45 Ala Ala Pro Glu Ser Glu Lys Asp Thr Ser Ala Thr Ser Gly Ile Val      50 55 60 Pro Thr Leu Gln Asn Ile Val Ala Thr Val Thr Leu Gly Cys Arg Leu  65 70 75 80 Asp Leu Lys Thr Val Ala Leu His Ala Arg Asn Ala Glu Tyr Asn Pro                  85 90 95 Lys Arg Phe Ala Ala Val Ile Met Arg Ile Arg Glu Pro Lys Thr Thr             100 105 110 Ala Leu Ile Phe Ala Ser Gly Lys Met Val Val Thr Gly Ala Lys Ser         115 120 125 Glu Asp Asp Ser Lys Leu Ala Ser Arg Lys Tyr Ala Arg Ile Ile Gln     130 135 140 Lys Ile Gly Phe Ala Ala Lys Phe Thr Asp Phe Lys Ile Gln Asn Ile 145 150 155 160 Val Gly Ser Cys Asp Val Lys Phe Pro Ile Arg Leu Glu Gly Leu Ala                 165 170 175 Phe Ser His Gly Thr Phe Ser Ser Tyr Glu Pro Glu Leu Phe Pro Gly             180 185 190 Leu Ile Tyr Arg Lys Val Lys Pro Lys Ile Val Leu Leu Ile Phe Val         195 200 205 Ser Gly Lys Ile Val Leu Thr Gly Ala Lys Gln Arg Glu Glu Ile Tyr     210 215 220 Gln Ala Phe Glu Ala Ile Tyr Pro Val Leu Ser Glu Phe Arg Lys Met 225 230 235 240 <210> 10 <211> 240 <212> PRT <213> Artificial Sequence <220> <223> SPT15_M5 <400> 10 Met Ala Asp Glu Glu Arg Leu Lys Glu Phe Lys Glu Ala Asn Thr Ile   1 5 10 15 Val Phe Asp Pro Asn Thr Arg Gln Val Cys Glu Asn Gln Asn Arg Asp              20 25 30 Gly Thr Lys Pro Ala Thr Thr Phe Gln Ser Glu Glu Asp Ile Lys Arg          35 40 45 Ala Ala Pro Glu Ser Glu Lys Asp Thr Ser Ala Thr Ser Gly Ile Val      50 55 60 Pro Thr Leu Gln Asn Ile Val Ala Thr Val Thr Leu Gly Cys Arg Leu  65 70 75 80 Asp Leu Lys Thr Val Ala Leu His Ala Arg Asn Ala Glu Tyr Asn Pro                  85 90 95 Lys Arg Phe Ala Ala Val Ile Met Arg Ile Arg Glu Pro Lys Thr Thr             100 105 110 Ala Leu Ile Phe Ala Ser Gly Lys Met Val Val Thr Gly Ala Lys Ser         115 120 125 Glu Asp Asp Ser Lys Leu Ala Ser Arg Lys Tyr Ala Arg Ile Ile Gln     130 135 140 Lys Ile Gly Phe Ala Ala Lys Phe Thr Asp Phe Lys Ile Gln Asn Ile 145 150 155 160 Val Gly Ser Cys Asp Val Lys Phe Pro Ile Arg Leu Glu Gly Leu Ala                 165 170 175 Phe Ser His Gly Thr Phe Ser Ser Tyr Glu Pro Glu Leu Phe Pro Asp             180 185 190 Leu Ile Tyr Arg Met Val Lys Pro Lys Ile Val Leu Leu Ile Phe Val         195 200 205 Ser Gly Lys Ile Val Leu Thr Gly Ala Lys Gln Arg Glu Glu Ile Tyr     210 215 220 Gln Ala Phe Glu Ala Ile Tyr Pro Val Leu Ser Glu Phe Arg Lys Met 225 230 235 240

Claims (13)

An ethanol-resistant transformed yeast strain comprising a mutated SPT15 gene.
The yeast strain of claim 1, wherein the mutation comprises three to five mutated amino acid sequences in the amino acid sequence of the wild type SPT15 gene.
The method of claim 1, wherein the mutated SPT15 gene comprises: an amino acid sequence of which the amino acid sequence of the K201, G216 and Q225 positions of the wild type SPT15 gene is mutated; Amino acid sequences of which the amino acid sequences of the L76 and L175 positions of the wild-type SPT15 gene are mutated; An amino acid sequence of which the amino acid sequences of the S42, C78, S163, and I212 positions of the wild-type SPT15 gene are mutated; An amino acid sequence of which the amino acid sequences of the F10 and M197 positions of the wild-type SPT15 gene are mutated; Or a mutated SPT15 gene comprising the mutated amino acid sequence of the amino acid sequence of the K15, W26 and G192 positions of the wild-type SPT15 gene.
The mutant SPT15 gene of claim 3, wherein the mutated SPT15 gene comprises a mutant sequence in which the amino acid sequence of the K201, G216 and Q225 positions of the wild-type SPT15 gene is mutated to K201Q, G216S and Q225Stop; Mutant sequences in which the amino acid sequences at the L76 and L175 positions of the wild-type SPT15 gene have been changed to L76V and L175S; Mutant sequences in which the amino acid sequences at positions S42, C78, S163 and I212 of the wild-type SPT15 gene have been changed to S42N, C78R, S163P and I212N; Mutant sequences in which the amino acid sequences of the F10 and M197 positions of the wild-type SPT15 gene have been changed to F10S and M197K; Or a mutated SPT15 gene comprising a mutant sequence mutated to K15T, W26C and G192D at the K15, W26 and G192 positions of the wild-type SPT15 gene.
The yeast strain according to claim 1, wherein the mutated SPT15 gene is introduced into yeast cells as a plasmid.
The yeast strain of claim 1, wherein the mutated SPT15 gene is introduced into genomic DNA of the yeast cell.
The yeast strain according to claim 1, wherein the yeast strain can grow under 5-15% ethanol culture conditions.
8. The yeast strain according to claim 7, wherein the yeast strain is capable of growing under 12.5-15% ethanol culture conditions.
According to claim 1, wherein the yeast strain Saccharomyces spp ( Saccharomyces spp.), Schizosaccharomyces spp., Pichia spp., Paffia spp. , Cluj Vero MRS species (Kluyveromyces spp.), Candida species (Candida spp.), Tallahassee in MRS species (Talaromyces spp.), Brescia Gaetano MRS species (Brettanomyces spp.), Parkinson solren species (Pachysolen spp.), Deva Rio Yeast strain, characterized in that it is a debaryomyces spp. Or industrial polyploid yeast strain.
10. The yeast strain according to claim 9, wherein said yeast strain is Saccharomyces species.
The ethanol production method comprising the step of culturing the yeast strain into which the mutated SPT15 gene of claim 1 is inserted in a culture medium comprising at least one substrate capable of being metabolized to ethanol.
12. The method of claim 11, wherein the substrate capable of metabolizing ethanol comprises C6 sugars.
13. The method of claim 12, wherein said C6 sugar is glucose.

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