Patent Application
20190055614
This disclosure relates to a fungus belonging to the genus Trichoderma having a mutant BXL1 gene lacking β-xylosidase (BXL1) activity and a method of producing xylo-oligosaccharides and glucose from a cellulose-based biomass using the same.
Xylo-oligosaccharide is a general term of oligosaccharides formed by 3-glycosidic linkages of a plurality of xylose units. Xylo-oligosaccharides are also used as a material for functional foods because of, for example, its excellent intestine-regulating function (Aachary A. A. et al., Compre. Rev. Food. Sci. Food Saf. 10, 2-16 (2011)).
Xylo-oligosaccharides can be obtained through hydrolysis of xylan contained in cellulose-based biomass. Known hydrolysis methods include hydrothermal treatment method (Moniz P. et al., Ind. Crops. Prod. 62, 460-465 (2014)), acid hydrolysis method (Akpinar O. et al., Carbohydr. Res. 344, 660-666 (2009)), and enzyme treatment method (JP 4675139 B).
When biomass is to be hydrolyzed with enzymes, filamentous fungi are suitably applied because of their excellent capacity of producing cellulase which is an enzyme that degrades cellulose and xylan. However, it is known that cellulase produced by filamentous fungi degrades xylo-oligosaccharides into monosaccharide xylose in the reaction with biomass. β-xylosidase is known as an enzyme that degrades xylo-oligosaccharides into xylose, and β-xylosidase 1 derived from Trichoderma reesei has been reported to react with xylo-oligosaccharides from disaccharide (xylobiose) to heptasaccharide (xyloheptose) to generate xylose (Herrmann M. C. et al., Biochem. J. 321, 375-381 (1997)).
β-xylosidase 1 belongs to glycoside hydrolase family 3 (GH3) (Carbohydrate-Active EnZYmes Database). Enzymes belonging to GH3 comprise a plurality of highly conserved regions (domains), and β-xylosidase 1 of Trichoderma reesei comprises N- and C-terminal domains of GH3. In β-xylosidase of Trichoderma reesei, amino acid residues at positions 264, 311, and 464 are considered essential for its activity (Rasmussen L. E. et al., Biotech. Bioeng. 94, 5, 869-876 (2006) and Margolles-Clark E. et al., Appl. Environ. Microbiol. 62, 10, 3840-3846 (1996)). Other than these domains, β-xylosidase 1 comprises Fn3-like domain, but the function of Fn3-like domain is not known.
Thus, there is a problem with the use of cellulase of a fungus belonging to the genus Trichoderma in that it degrades xylan into xylose.
The Applicant hereby incorporates by reference the sequence listing contained in the ASCII text file titled SequenceListing.txt, created Sep. 26, 2018 and having 35.9 KB of data.
We found that the use of a fungus belonging to the genus Trichoderma in which the amino acid sequence of β-xylosidase 1 comprises the N- and C-terminal domains of GH3 and lacks the Fn3-like domain results in deletion of β-xylosidase activity and increase in β-glucosidase activity.
We thus provide:
(1) A fungus belonging to the genus Trichoderma comprising a mutant BXL1 gene encoding mutant β-xylosidase 1 which has N- and C-terminal domains of glycoside hydrolase family 3 (GH3) and lacks Fn3-like domain in β-xylosidase 1 consisting of the amino acid sequence of SEQ ID NO: 2 or in a polypeptide consisting of an amino acid sequence having a sequence identity of 80% or more to the amino acid sequence of SEQ ID NO: 2 and having β-xylosidase activity, the mutant β-xylosidase 1 lacking β-xylosidase activity.
(2) The fungus belonging to the genus Trichoderma according to (1), wherein the sequence identity is 95% or more.
(3) The fungus belonging to the genus Trichoderma according to (1) or (2), wherein the mutant BXL1 gene encodes a mutant polypeptide having N- and C-terminal domains of GH3, and lacks the Fn3-like domain in the amino acid sequence of SEQ ID NO: 2.
(4) The fungus belonging to the genus Trichoderma according to any one of (1) to (3), wherein deletion of the Fn3-like domain is caused by a frame shift by base deletion or insertion, or a stop codon mutation by base substitution, within a gene region encoding a region downstream of the C-terminal domain and upstream of the Fn3-like domain.
(5) The fungus belonging to the genus Trichoderma according to any one of (1) to (4), wherein the fungus belonging to the genus Trichoderma is a non-recombinant.
(6) The fungus belonging to the genus Trichoderma according to any one of (1) to (5), wherein the fungus belonging to the genus Trichoderma is Trichoderma reesei.
(7) The fungus belonging to the genus Trichoderma according to (5), wherein the fungus belonging to the genus Trichoderma is a strain in which carbon catabolite repression is removed.
(8) A method of producing a cellulase composition, the method comprising the step of culturing the fungus belonging to the genus Trichoderma according to any one of (1) to (7).
(9) A method of producing glucose and xylo-oligosaccharides, the method comprising the steps of: recovering a cellulase composition produced by the method according to (8); and hydrolyzing a biomass containing xylan and cellulose with the obtained cellulase composition.
By using a fungus belonging to the genus Trichoderma having a gene encoding mutant β-xylosidase 1 which has N- and C-terminal domains of glycoside hydrolase family 3 (GH3) and lacks Fn3-like domain in β-xylosidase 1, the β-xylosidase activity can be deleted and β-glucosidase activity can be increased. Further, the cellulase composition derived from the fungus belonging to the genus Trichoderma can be used for efficient production of glucose and xylo-oligosaccharides.
Our Trichoderma fungus and methods are based on the new finding that the β-xylosidase activity can be deleted by using a fungus belonging to the genus Trichoderma having a gene encoding mutant BXL1 lacking Fn3-like domain, which is a domain in β-xylosidase of fungus belonging to the genus Trichoderma with unknown function.
The fungus belonging to the genus Trichoderma is not restricted as long as it has a capacity to produce proteins. Specific examples of the fungi belonging to the genus Trichoderma include Trichoderma vixens, Trichoderma harzianum, Trichoderma atroviride, Trichoderma gamsii, and Trichoderma reesei. Among them, preferred is Trichoderma reesei. Mutant strains derived from the genus Trichoderma and having been subjected to mutagenesis with a mutagen or ultraviolet irradiation to obtain improved protein productivity may also be used. Preferred examples of the mutant strains include known mutant strains derived from Trichoderma reesei such as QM6a strain (NBRC 31326), QM9414 strain (NBRC31329), PC-3-7 strain (ATCC66589), QM9123 strain (NBRC31327), RutC-30 strain (ATCC56765), CL-847 strain (Enzyme. Microbiol. Technol. 10, 341-346 (1988)), MCG77 strain (Biotechnol. Bioeng. Symp. 8, 89(1978)) and MCG80 strain (Biotechnol. Bioeng. 12, 451-459 (1982)), and derivative strains thereof.
Preferred fungi belonging to the genus Trichoderma are those in which carbon catabolite repression is removed. The strains in which carbon catabolite repression is removed can produce more proteins because the production of proteins such as cellulase is elevated. More preferred strains are those in which carbon catabolite repression mediated by carbon catabolite repressor I is removed. The carbon catabolite repression mediated by carbon catabolite repressor I is removed, for example, by a mutation in the carbon catabolite repressor I gene (crel). It is known that CRE1 protein encoded by crel gene suppresses the expression of cellulase gene through catabolite repression by glucose (FEBS Lett., 376, 103-107, 1995). Therefore, when the crel gene is mutated, suppression of the expression of the cellulase gene is canceled and the production of cellulase is increased. Therefore, strains with a mutation in crel gene are more suitable for producing proteins and cellulase compositions. Specific examples of mutation in the carbon.cre1 gene includes a mutation in the crel gene of PC-3-7 strain (ATCC66589), in which A at position 232 is substituted with C, resulting in substitution of threonine at position 78 of the amino acid sequence with proline. It is known that this mutation elevates the production of cellulase (Biosci. Biotechnol. Biochem., 77 (3), 534-543, 2013). It is known that in the RutC-30 strain (ATCC 56765) the crel gene is partly cleaved so that the carbon catabolite repression is removed (BMC Genomics., 9, 327, 2008). Strains having a mutation in the crel gene include strains having a frame shift by deletion or insertion of a base, a stop codon mutation by base substitution, or a base cleavage within the crel gene region, generated by a gene mutating agent, ultraviolet irradiation or the like. Also included are strains in which all or part of the crel gene is removed or replaced with another gene by recombination or the like. Specifically, PC-3-7 strain (ATCC66589) and RutC-30 strain (ATCC56765), as well as strains that have inherited the characteristics of PC-3-7 strain (ATCC66589) or RutC-30 strain (ATCC56765) are preferably used, and more preferably PC-3-7 strain (ATCC66589), and strains that have inherited the characteristics of PC-3-7 strain (ATCC66589). The strains that have inherited the characteristics of PC-3-7 (ATCC66589) or RutC-30 strain (ATCC56765) also include those that have inherited the characteristics of PC-3-7 strain (ATCC66589) or RutC-30 strain (ATCC56765) and are newly mutated, and those that have a function improved by recombination.
The amino acid sequence of BXL1 of Trichoderma reesei is shown in SEQ ID NO: 2, and the base sequence encoding this amino acid sequence is shown in SEQ ID NO: 1. A gene encoding the amino acid sequence of SEQ ID NO: 2 can be preferably used as an original gene before deletion of Fn3-like domain. A gene encoding a polypeptide consisting of an amino acid sequence having a sequence identity of 80% or more, preferably 85% or more, more preferably 90% or more, still more preferably 93% or more, still more preferably 95% or more, still more preferably 97% or more, still more preferably 99% or more to the amino acid sequence of SEQ ID NO: 2 and having β-xylosidase activity can also be used as the original gene (hereinafter, the amino acid sequence of a polypeptide consisting of an amino acid sequence having a sequence identity of 80% or more to the amino acid sequence of SEQ ID NO: 2 and having β-xylosidase activity is conveniently referred to as “amino acid sequence similar to SEQ ID NO: 2”). The sequence identity between two amino acid sequences represents a percentage determined by aligning the sequences such that the number of matching amino acids is maximized and dividing the number of matching amino acids by the total number of amino acids (by the number of longer amino acids when the total numbers of amino acids are different), and can be easily calculated by using a well-known software such as BLAST. Similarly, the sequence identity between two base sequences represents a percentage determined by aligning the sequences such that the number of matching bases is maximized and dividing the number of matching bases by the total number of bases (by the number of longer bases when the total numbers of bases are different), and can be easily calculated by using a well-known software such as BLAST.
The fungus belonging to the genus Trichoderma lacks β-xylosidase activity. β-xylosidase is an enzyme that degrades xylobiose formed by β-1,4-linkage of xylose units to produce xylose. The enzyme activity (U: unit) of β-xylosidase can be measured, for example, by using p-nitrophenyl-β-xylopyranoside (pNP-Xyl) as a substrate. “Lacking the β-xylosidase activity” means that the β-xylosidase activity is reduced to 1/10 or less, more preferably 1/20 or less, still more preferably 1/50 or less, still more preferably 1/80 or less, most preferably 1/100 or less, compared to that of parent strain before deleting the FN3-like domain in the BXL1 gene. The activity is calculated as U per mg of protein contained in the enzyme solution.
The lack of β-xylosidase activity is carried out by deletion of the Fn3-like domain in BXL1. In BXL1 consisting of the amino acid sequence of SEQ ID NO: 2, the Fn3-like domain represents the region from 695th to 759th residue in SEQ ID NO: 2. In amino acid sequence similar to SEQ ID NO: 2, the Fn3-like domain represents a region corresponding to the region from 695th to 759th residue in SEQ ID NO: 2. “Corresponding region” refers to the region aligning to the region from 695th to 759th residue in SEQ ID NO: 2 when the amino acid sequence of SEQ ID NO: 2 and the amino acid sequence similar to SEQ ID NO: 2 are aligned such that the number of matching amino acids is maximized. Similarly, in the base sequence of SEQ ID NO: 1, “corresponding region” refers to the region aligning to the region in the base sequence of SEQ ID NO: 1 when the base sequence of SEQ ID NO: 1 and the other base sequence are aligned such that the number of matching bases is maximized. Although the following descriptions are made with respect to the amino acid sequence of SEQ ID NO: 2 representing the amino acid sequence of BXL1 of Trichoderma reesei and the base sequence of the gene coding therefor (SEQ ID NO: 1), these descriptions are also applicable to the amino acid sequence similar to SEQ ID NO: 2 and the base sequence of the gene coding therefor. In this case, a specific region within SEQ ID NO: 2 or SEQ ID NO: 1 refers to a corresponding region in the amino acid sequence similar to SEQ ID NO: 2 or in the base sequence coding therefor.
“Deletion of Fn3-like domain” refers to loss of the entire or a part of the domain, change of the entire or a part of the domain into different amino acid(s), or a combination thereof. More specifically, the term means that the sequence identity to the original amino acid sequence of the Fn3-like domain before mutation (SEQ ID NO: 2 or amino acid sequence similar to SEQ ID NO: 2) decreases to 80% or less, preferably to 50% or less, more preferably to 20% or less, still more preferably to 10% or less, still more preferably to 5% or less, still more preferably to 3% or less, still more preferably to 1% or less, most preferably to 0%.
Deletion of the Fn3-like domain is carried out by a mutating treatment with a mutagen, ultraviolet irradiation or the like, or gene recombination. Specifically, the deletion of the Fn3-like domain is caused by a frame shift by base deletion or insertion, or a stop codon mutation by base substitution within a gene region encoding a region upstream of the Fn3-like domain (the region of 1929-2082th bases in the base sequence of BXL1 gene of Trichoderma reesei shown in SEQ ID NO: 1) at downstream of the C-terminal domain (described later). Alternatively, the deletion is caused by a frame shift by base deletion or insertion, or a stop codon mutation by base substitution within the base sequence of the Fn3-like domain. On the other hand, the deletion of the Fn3-like domain by gene recombination is achieved such that a part or the entire of amino acids of the Fn3-like domain is lost or changed.
The mutant BXL1 gene has lost the genetic sequence encoding the Fn3-like domain, but has the genetic sequences encoding N- and C-terminal domains of glycoside hydrolase family 3 (GH3). The N-terminal domain of GH3 refers to 84th to 375th residues of BXL1 (SEQ ID NO: 2), and the C-terminal domain of GH3 refers to 414th to 642nd residues of BXL1 (SEQ ID NO: 2). The N- and C-terminal domains of GH3 are considered to be involved in the β-xylosidase activity. The N- and C-terminal regions of GH3 family also comprise the above-described 264th, 311th, and 464th amino acid residues which are considered to be involved in the β-xylosidase activity. “Having a domain” means that the amino acid sequence of the domain does not change at all from SEQ ID NO: 2. Conservation of the Fn3-like domain or N- and C-terminal sequences of GH3 family in the amino acid sequence of β-glucosidase can be confirmed by using an amino acid sequence analysis software “Conserved Domains” provided online by NCBI (The National Center for Biotechnology Information).
A fungus belonging to the genus Trichoderma having the mutant BXL1 gene can be obtained by using a gene recombination technique or a non-recombination technique using mutagenesis or the like. Specifically, the fungus belonging to the genus Trichoderma having the mutant BXL1 gene can be obtained by: conducting a mutagenesis with NTG treatment or the like; culturing the selected colonies; determining the activity for degrading p-nitrophenyl-β-xylopyranoside; and obtaining the strain having a reduced activity. Non-recombinants can be used for the manufacture more advantageously than recombinants because the containment measures are not necessary, which measures are necessary in case of using a recombinant.
A cellulase composition can be obtained by culturing the fungus belonging to the genus Trichoderma. Glucose and xylo-oligosaccharides can be produced by hydrolyzing a biomass containing xylan and cellulose with the obtained cellulase composition.
The cellulase composition is a mixture of various hydrolases that hydrolyze glycosidic linkages within β-1,4-glucans. Examples of hydrolases contained in the cellulase composition include cellobiohydrolase, xylanase, endoglucanase, β-glucosidase, β-xylosidase, arabinofuranosidase, xylanesterase, ferulic acid esterase, α-glucuronidase, chitosanase, chitinase, mannanase, mannosidase, α-galactosidase, and β-galactosidase.
In the cellulase composition obtained, among the above-described hydrolases, the β-xylosidase activity is deleted while the β-glucosidase activity is increased.
β-glucosidase is an enzyme that degrades cellobiose formed by β-1,4-linkage of glucose units to produce glucose. The enzyme activity (U: unit) of β-glucosidase can be measured, for example, by using p-nitrophenyl-β-glucopyranoside (pNP-Glu) as a substrate. “The β-glucosidase activity is increased” means that the β-glucosidase activity is increased by 0.2% or more, more preferably by 0.5% or more, still more preferably by 1% or more, still more preferably by 2% or more compared to that of parent strain before deleting the Fn3-like domain in the BXL1 gene.
The method of culturing the fungus belonging to the genus Trichoderma is not restricted as long as the cellulase composition can be produced, including well-known methods of culturing the fungi belonging to the genus Trichoderma. A biomass is preferably used as the carbon source contained in the culture medium to be used and as an inducer. As the nitrogen source to be used, for example, polypeptone, bouillon, CSL, soybean cake or the like is used. In addition to these, components required for producing the desired cellulase can be added to the culture medium. For the culture, various culturing methods such as shaking culture, stirring culture, stirring and shaking culture, standing culture, and continuous culture can be employed, and among them, shaking culture and stirring culture are preferred. The culture temperature is usually 20° C. to 35° C., preferably 25° C. to 31° C. The culture time is usually 3 to 10 days, preferably 4 to 9 days.
An inducer may be added to increase the amount of the cellulase composition during culture. The inducer is not restricted and a biomass is preferably used. Biomass is an organic resource derived from a renewable organism. Among various biomass, those containing cellulose and xylan are preferably used. Specific examples of the biomass includes grass biomass such as pulp, bagasse, switchgrass, napier grass, Erianthus, corn stover, corn hull, rice straw, and wheat straw; and woody biomass such as trees, and waste building materials.
These inducers may be treated to be suitable for addition to the culture media. As specific treatment methods, known methods such as acid treatment, sulfuric acid treatment, dilute sulfuric acid treatment, alkali treatment, hydrothermal treatment, subcritical treatment, fine grinding, and steaming can be used.
The xylan content in the biomass as an inducer is not particularly limited, and is preferably at least 5% by weight, more preferably at least 10% by weight, still more preferably at least 20% by weight, based on the solid weight of the biomass. The method of measuring cellulose content and the xylan content in the biomass is not restricted, and specifically the following method can be employed. First, the biomass sample to be measured is air-dried and pulverized with a Wiley mill or the like. After taking an appropriate amount of the sample and drying it at 105° C., the water content (wt %) is calculated from the weight loss. Thereafter, an appropriate amount (about 0.3 g) of the sample is weighed, 3 mL of 72% sulfuric acid is added, and the mixture is allowed to stand at 30° C. for 1 hour with intermittent stirring. The reaction liquid is mixed with 84 mL of purified water and then decomposed by heating in an autoclave at 120° C. for 1 hour. After the thermal decomposition, residues are filtered off from the decomposed liquid. The filtrate and the residue washings are combined to the volume of 100 mL. The monosaccharides (such as glucose and xylose) are quantified by high performance liquid chromatography. The content (cellulose, xylan) in the sample is calculated from the concentration of the obtained monosaccharide (glucose, xylose) and the amount of decomposed sample (dry basis weight calculated from the water content).
The amount of biomass used as an inducer is not particularly limited, and is preferably 5 to 20% by weight, more preferably 8 to 15% by weight, still more preferably 8 to 12% by weight.
The method of using the cellulase composition produced is not restricted, and the cellulase composition may preferably be used in the production of sugars, more preferably in the production of xylo-oligosaccharides, still more preferably in the production of xylo-oligosaccharides and glucose.
“Xylo-oligosaccharides” refer to those formed by β-glycosidic linkage of at least two xylose units. The degree of polymerization of xylo-oligosaccharides is not particularly limited, and preferred are from disaccharide (xylobiose) to hexasaccharide (xylohexaose) having high water solubility. Most preferred xylo-oligosaccharides include xylobiose, xylotriose, and xylotetraose which are easily utilized as carbon sources by enteric bacteria.
The cellulase composition is obtained by culturing the fungus belonging to the genus Trichoderma, and used in saccharification reaction of a biomass. The method of preparing the cellulase composition is not restricted, and preferably the cells of the fungus belonging to the genus Trichoderma contained in the culture medium are removed, or preferably the fungus belonging to the genus Trichoderma does not grow to prevent consumption by the fungal cells of glucose and xylo-oligosaccharides generated by saccharification reaction of cellulase composition and biomass. Examples of the method of removing the fungal cells include centrifugation and membrane separation. The treatment methods of preventing the bacterial cells from growing include heat treatment, chemical treatment, acid/alkali treatment, and UV treatment.
Next, the hydrolysis reaction will be described. The biomass subjected to the hydrolysis reaction is not restricted as long as it is a biomass containing cellulose and xylan, and examples of the biomass include plants such as seed plants, pteridophytes, bryophytes, algae, and water plants, as well as pulp and waste building materials. Seed plants are divided into gymnosperms and angiosperms, both of which can be used preferably. Specific examples of gymnosperms include cycad, ginkgo, pine, fir, spruce, and cryptomeria. Angiosperms are further divided into monocotyledons and dicotyledons. Specific examples of monocotyledons include bagasse, switchgrass, napier grass, Erianthus, corn stover, corncob, rice straw, and wheat straw. Specific examples of dicotyledons used preferably include beet pulp, eucalyptus, oak, and white birch.
The biomass containing cellulose and xylan may be pretreated so that the hydrolysis reaction proceeds easily. The pretreatment method is not restricted and specifically, known methods such as acid treatment, sulfuric acid treatment, dilute sulfuric acid treatment, alkali treatment, hydrothermal treatment, subcritical treatment, fine grinding treatment, and steaming treatment can be used. The reaction pH is not restricted and is preferably about 3 to 7, more preferably 4 to 6, still more preferably about 5. The reaction temperature is not restricted and is preferably 40° C. to 70° C. The amount of the cellulase composition used in the reaction is also not restricted. The reaction time is also not restricted.
The post-reaction liquid produced from the saccharification reaction may contain, in addition to xylo-oligosaccharides and glucose, for example, monosaccharides such as mannose, arabinose, and galactose; and oligosaccharides such as cellobiose, cellotetraose, mannobiose, and galactobiose, which are generated by hydrolases contained in the cellulase composition.
The post-reaction liquid produced from the saccharification reaction may contain, for example, inorganic salts, amino acids, proteins, and lignin as impurities. Purification may be carried out to remove these impurities. As the purification, known techniques such as ion exchange, membrane separation, crystallization, and demineralization can be employed.
A fraction containing monosaccharides (such as glucose, and xylose) and a fraction containing xylo-oligosaccharides and so on produced are preferably separated in a post-process. Glucose is preferably used as a fermentation raw material in the production of chemical products, while xylo-oligosaccharides are preferably used for feeds, foods and cosmetic applications. Specific examples of the chemical products include alcohols such as ethanol, 1,3-propanediol, 1,4-butanediol, and glycerol; organic acids such as acetic acid, lactic acid, pyruvic acid, succinic acid, malic acid, itaconic acid, and citric acid; nucleosides such as inosine and guanosine; nucleotides such as inosinic acid and guanylic acid; and amine compounds such as cadaverine.
Our fungus and methods will now be described in detail with reference to the Examples. However, this disclosure is not limited to them.
A commercially available reagent for measuring protein concentration (Quick Start Bradford protein assay, Bio-Rad) was used. Five microliters of a diluted filamentous fungus-derived cellulase solution was added to 250 μL of the protein concentration measurement reagent which was previously returned to room temperature. After leaving the mixture to stand at room temperature for 5 minutes, the absorbance at 595 nm was measured using a microplate reader. Using BSA as a standard, the protein concentration was calculated based on the calibration curve. Reference Example 2 Method of measuring β-xylosidase activity
The specific method of measuring β-xylosidase activity was as follows. To 90 μL of 50 mM acetate buffer containing 1 mM p-nitrophenyl-β-xylopyranoside (Sigma-Aldrich Japan), was added 10 μL of enzyme dilution, and the mixture was allowed to react at 30° C. for 30 minutes. Then, 10 μL of 2 M sodium carbonate was added and mixed well to stop the reaction, and the increase in absorbance at 405 nm was determined. Release of 1 μmol of p-nitrophenol per minute was defined as 1 U of activity. For blanks, to 90 μL of 50 mM acetate buffer containing 1 mM p-nitrophenyl-β-xylopyranoside, was added 10 μL of 2 M sodium carbonate and mixed well. Then, 10 μL of enzyme dilution was added to the mixture and allowed to react at 30° C. for 30 minutes. Then, the increase in absorbance at 405 nm was determined.
The specific method of determining β-glucosidase activity was as follows. To 90 μL of 50 mM acetate buffer containing 1 mM p-nitrophenyl-β-glucopyranoside (Sigma-Aldrich Japan), was added 10 μL of enzyme dilution, and the mixture was allowed to react at 30° C. for 10 minutes. Then, 10 μL of 2 M sodium carbonate was added and mixed well to stop the reaction, and the increase in absorbance at 405 nm was determined. Release of 1 μmol of p-nitrophenol per minute was defined as 1 U of activity. For blanks, to 90 μL of 50 mM acetate buffer containing 1 mM p-nitrophenyl-β-glucopyranoside, was added 10 μL of 2 M sodium carbonate and mixed well. Then, 10 μL of enzyme dilution was added to the mixture and allowed to react at 30° C. for 30 minutes. Then, the increase in absorbance at 405 nm was determined.
The specific method of measuring cellobiohydrolase activity was as follows. To 90 μL of 50 mM acetate buffer containing 1 mM p-nitrophenyl-β-lactopyranoside (Sigma-Aldrich Japan), was added 10 μL of enzyme dilution, and the mixture was allowed to react at 30° C. for 60 minutes. Then, 10 μL of 2 M sodium carbonate was added and mixed well to stop the reaction, and the increase in absorbance at 405 nm was determined. Release of 1 μmol of p-nitrophenol per minute was defined as 1 U of activity. For blanks, to 90 μL of 50 mM acetate buffer containing 1 mM p-nitrophenyl-β-lactopyranoside, was added 10 μL of 2 M sodium carbonate and mixed well. Then, 10 μL of enzyme dilution was added to the mixture and allowed to react at 30° C. for 30 minutes. Then, the increase in absorbance at 405 nm was determined.
Quantitative analysis of xylo-oligosaccharide, glucose, and xylose was carried out using LaChrom Eite high performance liquid chromatography (HITACHI) under the following conditions.
The quantitative analyses were based on calibration curves prepared with standards of xylobiose, xylotriose, xylotetraose, xylopentaose, and xylohexaose which are xylo-oligosaccharides, and with glucose and xylose standards. The xylo-oligosaccharides described in this example refer to xylo-oligosaccharides in which 2 to 6 xylose units are bound by β-glycosidic bonds.
Mobile phase: water
Detection method: RI
Flow rate: 0.5 mL/min
A non-limiting method of disrupting a gene of interest by homologous recombination comprises: carrying out PCR using primers designed to add portions homologous to the introduction target site, to upstream and downstream of the DNA containing a marker gene; and transforming a filamentous fungus with the obtained PCR fragments.
The transformation was carried out by a standard method (PEG-mediated protoplast transformation). The host used was PC-3-7 strain, and the marker used was acetamidase (AmdS) gene.
Introduction of AmdS gene into the obtained transformant was confirmed by culturing the transformant in PDA medium; extracting genomic DNA from the transformant; and carrying out PCR using the extract as the template. PDA medium contained 24 g/L Difco Potato Dextrose Broth (BD) as an ingredient. From the result, substitution of BXL1 gene with AmdS gene cassette in the transformant was confirmed. The PC-3-7 strain in which AmdS gene cassette was introduced into BXL1 locus, obtained from the above step, is hereinafter referred to as PC-3-7/ΔBXL1 strain. The strain had lost all three domains in the ORF of the BXL1 gene.
The base sequence of SEQ ID NO: 3 was used as the mutant BXL1 gene. The mutant BXL1 gene had lost the base sequence of 1940th and 1941th bases in the BXL1 gene of Trichoderma reesei (SEQ ID NO: 1), thus having a frameshift in the subsequent amino acid sequence. The homology between the amino acid sequence encoded by the mutant BXL1 gene and the amino acid sequence of Fn3-like domain of SEQ ID NO: 2 was 0%. The mutant BXL1 gene was prepared by artificial synthesis.
A non-limiting method of inserting a DNA containing the mutant BXL1 gene into downstream of the promoter of BXL1 in a chromosome by homologous recombination comprises: carrying out PCR using primers designed to add portions homologous to the introduction target site, to upstream and downstream of the DNA containing mutant BXL1 gene; and transforming a filamentous fungus with the obtained PCR fragments.
The transformation was carried out by a standard method (PEG-mediated protoplast transformation). The host used was PC-3-7 strain, and the marker used was acetamidase (AmdS) gene.
Introduction of the gene of interest into the obtained transformant was confirmed by culturing the transformant in PDA medium; extracting genomic DNA from the transformant; and carrying out PCR using the extract as the template. Specifically, designed primers (SEQ ID NOS: 7 and 8) were used for the confirmation. From the result, introduction of the mutant BXL1 gene cassette from the start codon of the BXL1 gene was confirmed in the transformant. The obtained PC-3-7 strain is hereinafter referred to as PC-3-7/mutant BXL1 strain.
Spores of Trichoderma reesei strain PC-3-7 were suspended in physiological saline to 1.0×107/mL, and 2.5 mL of the spore suspension was inoculated into 250 mL of a preculture medium having the composition described in Table 1 and placed in a 1 L baffled flask. The inoculated preculture medium was incubated at 28° C. and 160 rpm for 3 days.
The preculture of Trichoderma reesei strain PC-3-7 in an amount of 250 mL were each inoculated into 2.5 L of the main culture medium (further containing 250 g of biomass) shown in Table 2 and placed in a 5 L mini jar. The inoculum was cultured at 28° C., 700 rpm, 1 vvm, pH5, for 5 days. Neutralization was performed with 10% ammonia and 1 N sulfuric acid. ARBOCEL (registered trademark) (J. Rettenmaier & Sohne) was used as the biomass.
Every three days from the start of culture, 500 μL of the culture was collected. The culture was centrifuged at 15,000×g, 4° C. for 10 minutes to obtain a supernatant. The supernatant was filtered through a 0.22 μm filter, and the filtrate was used as a culture supernatant. For enzyme activity measurement and saccharification reaction, the culture supernatant on day 5 of culture was used (Table 3).
Preparation was carried out in the same manner as in Comparative Example 2 except that Trichoderma reesei PC-3-7/ΔBXL1 strain was used. For enzyme activity measurement and saccharification reaction, the culture supernatant on day 5 of culture was used (Table 3). The results show that the β-xylosidase activity was markedly decreased compared to that with parent PC-3-7 strain.
Preparation was carried out in the same manner as in Comparative Example 2 except that Trichoderma reesei PC-3-7/mutant BXL1 strain was used. For enzyme activity measurement and saccharification reaction, the culture supernatant on day 5 of culture was used (Table 3). The results show that the β-xylosidase activity was decreased to the same level as Trichoderma reesei PC-3-7/ΔBXL1 strain. Further, we found that the β-glucosidase activity was increased compared to that with Trichoderma reesei PC-3-7/ΔBXL1 strain.
The filtrate obtained in Comparative Example 2 was used for saccharification. The bagasse used in saccharification reaction had been subjected to alkali treatment (pretreatment). The saccharification reaction was carried out as follows. After 50 mg by dry weight of the alkali-treated bagasse was placed in a 2 mL tube, pure water was added so that the solid content concentration of the bagasse at the start of reaction was 5% by weight, while pH was adjusted to 5.0 with diluted hydrochloric acid. To the pretreatment product with the adjusted pH, was added a cellulase composition to 8 mg/g-biomass, and then the reaction was initiated under reaction conditions of pH 5.0 and at 50° C. using a heat block rotator. During the reaction, the pH was appropriately adjusted to 5. After 8 hours, the reaction mixture was immersed in a water bath at 99° C. for 5 minutes to stop the reaction. The reaction liquid was centrifuged at 8,000×g for 5 minutes to obtain a supernatant. The supernatant was filtered through a 0.22 μm filter, and the filtrate was used for analyses of xylo-oligosaccharides and glucose according to Reference Example 5 (Table 4).
The filtrate obtained in Comparative Example 3 was used for saccharification. The saccharification reaction was carried out in the same manner as in Comparative Example 4 (Table 4). The results show that the yield of xylo-oligosaccharides was markedly increased compared to the parent PC-3-7 strain.
The saccharification reaction was carried out using the filtrate obtained in Example 2 in the same manner as in Comparative Example 4 (Table 4). The results show that xylo-oligosaccharides yield comparable to that of the filtrate obtained with Trichoderma reesei PC-3-7/ΔBXL1 strain was achieved, and also the glucose yield was increased.
The β-xylosidase activity can be lost via deletion of Fn3-like domain from the BXL1 gene. Furthermore, the β-glucosidase activity is increased compared to that with a strain in which all three domains in the BXL1 gene are disrupted, thus enabling efficient production of xylo-oligosaccharides and glucose.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2016-070690 | Mar 2016 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2017/013379 | 3/30/2017 | WO | 00 |
