SG11201906480QA - Engineered glycosyltransferases and steviol glycoside glucosylation methods - Google Patents
Engineered glycosyltransferases and steviol glycoside glucosylation methodsInfo
- Publication number
- SG11201906480QA SG11201906480QA SG11201906480QA SG11201906480QA SG11201906480QA SG 11201906480Q A SG11201906480Q A SG 11201906480QA SG 11201906480Q A SG11201906480Q A SG 11201906480QA SG 11201906480Q A SG11201906480Q A SG 11201906480QA SG 11201906480Q A SG11201906480Q A SG 11201906480QA
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- Singapore
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- enzymes
- california
- redwood city
- international
- penobscot
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- 108700023372 Glycosyltransferases Proteins 0.000 title abstract 10
- 239000004383 Steviol glycoside Substances 0.000 title abstract 2
- 102000045442 glycosyltransferase activity proteins Human genes 0.000 title abstract 2
- 108700014210 glycosyltransferase activity proteins Proteins 0.000 title abstract 2
- 229930182488 steviol glycoside Natural products 0.000 title abstract 2
- 235000019411 steviol glycoside Nutrition 0.000 title abstract 2
- 150000008144 steviol glycosides Chemical class 0.000 title abstract 2
- 235000019202 steviosides Nutrition 0.000 title abstract 2
- 102000051366 Glycosyltransferases Human genes 0.000 abstract 8
- 108010043934 Sucrose synthase Proteins 0.000 abstract 5
- 240000005020 Acaciella glauca Species 0.000 abstract 4
- 108090000790 Enzymes Proteins 0.000 abstract 4
- 102000004190 Enzymes Human genes 0.000 abstract 4
- 239000002157 polynucleotide Substances 0.000 abstract 4
- 102000040430 polynucleotide Human genes 0.000 abstract 4
- 108091033319 polynucleotide Proteins 0.000 abstract 4
- 229920001184 polypeptide Polymers 0.000 abstract 4
- 102000004196 processed proteins & peptides Human genes 0.000 abstract 4
- 108090000765 processed proteins & peptides Proteins 0.000 abstract 4
- 235000003499 redwood Nutrition 0.000 abstract 4
- 239000008103 glucose Substances 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 229930188195 rebaudioside Natural products 0.000 abstract 2
- RPYRMTHVSUWHSV-CUZJHZIBSA-N rebaudioside D Chemical compound O([C@H]1[C@H](O)[C@@H](CO)O[C@H]([C@@H]1O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)O[C@]12C(=C)C[C@@]3(C1)CC[C@@H]1[C@@](C)(CCC[C@]1([C@@H]3CC2)C)C(=O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O RPYRMTHVSUWHSV-CUZJHZIBSA-N 0.000 abstract 2
- 239000013598 vector Substances 0.000 abstract 2
- 239000001512 FEMA 4601 Substances 0.000 abstract 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 abstract 1
- HELXLJCILKEWJH-SEAGSNCFSA-N Rebaudioside A Natural products O=C(O[C@H]1[C@@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1)[C@@]1(C)[C@@H]2[C@](C)([C@H]3[C@@]4(CC(=C)[C@@](O[C@H]5[C@H](O[C@H]6[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O6)[C@@H](O[C@H]6[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O6)[C@H](O)[C@@H](CO)O5)(C4)CC3)CC2)CCC1 HELXLJCILKEWJH-SEAGSNCFSA-N 0.000 abstract 1
- 239000006227 byproduct Substances 0.000 abstract 1
- HELXLJCILKEWJH-UHFFFAOYSA-N entered according to Sigma 01432 Natural products C1CC2C3(C)CCCC(C)(C(=O)OC4C(C(O)C(O)C(CO)O4)O)C3CCC2(C2)CC(=C)C21OC(C1OC2C(C(O)C(O)C(CO)O2)O)OC(CO)C(O)C1OC1OC(CO)C(O)C(O)C1O HELXLJCILKEWJH-UHFFFAOYSA-N 0.000 abstract 1
- 239000002773 nucleotide Substances 0.000 abstract 1
- 230000008520 organization Effects 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- HELXLJCILKEWJH-NCGAPWICSA-N rebaudioside A Chemical compound O([C@H]1[C@H](O)[C@@H](CO)O[C@H]([C@@H]1O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)O[C@]12C(=C)C[C@@]3(C1)CC[C@@H]1[C@@](C)(CCC[C@]1([C@@H]3CC2)C)C(=O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O HELXLJCILKEWJH-NCGAPWICSA-N 0.000 abstract 1
- 235000019203 rebaudioside A Nutrition 0.000 abstract 1
- GSGVXNMGMKBGQU-PHESRWQRSA-N rebaudioside M Chemical compound C[C@@]12CCC[C@](C)([C@H]1CC[C@@]13CC(=C)[C@@](C1)(CC[C@@H]23)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H]1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C(=O)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H]1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O GSGVXNMGMKBGQU-PHESRWQRSA-N 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/10—Transferases (2.)
- C12N9/1048—Glycosyltransferases (2.4)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/10—Transferases (2.)
- C12N9/1048—Glycosyltransferases (2.4)
- C12N9/1051—Hexosyltransferases (2.4.1)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/10—Transferases (2.)
- C12N9/1048—Glycosyltransferases (2.4)
- C12N9/1051—Hexosyltransferases (2.4.1)
- C12N9/1062—Sucrose synthase (2.4.1.13)
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/88—Lyases (4.)
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P19/00—Preparation of compounds containing saccharide radicals
- C12P19/18—Preparation of compounds containing saccharide radicals produced by the action of a glycosyl transferase, e.g. alpha-, beta- or gamma-cyclodextrins
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P19/00—Preparation of compounds containing saccharide radicals
- C12P19/44—Preparation of O-glycosides, e.g. glucosides
- C12P19/56—Preparation of O-glycosides, e.g. glucosides having an oxygen atom of the saccharide radical directly bound to a condensed ring system having three or more carbocyclic rings, e.g. daunomycin, adriamycin
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y204/00—Glycosyltransferases (2.4)
- C12Y204/01—Hexosyltransferases (2.4.1)
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y204/00—Glycosyltransferases (2.4)
- C12Y204/01—Hexosyltransferases (2.4.1)
- C12Y204/01013—Sucrose synthase (2.4.1.13)
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
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- Bioinformatics & Cheminformatics (AREA)
- Genetics & Genomics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Medicinal Chemistry (AREA)
- Biomedical Technology (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Enzymes And Modification Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
- Saccharide Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Abstract
OHNDP-glucose Acceptor Accept2113-giucoside GT R—OH HO OR 0 OH P OH —Nucleotide R'—OH Syathase Byproduct HO O HO HO OH OH —0 O OH OH (12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (43) International Publication Date 09 August 2018 (09.08.2018) WIP0 I PCT omit °nolo olo Ho ioo (10) International Publication Number WO 2018/144679 A3 (51) International Patent Classification: C12P 19/56 (2006.01) Cl 2N 9/10 (2006.01) (21) International Application Number: PCT/US2018/016359 (22) International Filing Date: 01 February 2018 (01.02.2018) (25) Filing Language: English (26) Publication Language: English (30) Priority Data: 62/454,417 03 February 2017 (03.02.2017) US 62/479,262 30 March 2017 (30.03.2017) US (71) Applicant: CODEXIS, INC. [US/US]; 200 Penobscot Dri- ve, Redwood City, California 94063 (US). (72) Inventors: VROOM, Jonathan; 200 Penobscot Dri- ve, Redwood City, California 94063 (US). GALANIE, Stephanie, Sue; 200 Penobscot Drive, Redwood City, Cali- fornia 94063 (US). DELLAS, Nikki; 200 Penobscot Drive, Redwood City, California 94063 (US). LIANG, Jack; 200 Penobscot Drive, Redwood City, California 94063 (US). LIU, Joyce; 200 Penobscot Drive, Redwood City, Cali- fornia 94063 (US). ENTWISTLE, David; 200 Penobscot Drive, Redwood City, California 94063 (US). MOFFETT, Courtney, Dianne; 555 4th Street, Unit 615, San Francisco, California 94107 (US). (74) Agent: MACKNIGHT, Kamrin, T.; Codexis, Inc., 200 Penobscot Drive, Redwood City, California 94063 (US). (81) Designated States (unless otherwise indicated, for every kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DJ, DK, DM, DO, (54) Title: ENGINEERED GLYCOSYLTRANSFERASES AND STEVIOL GLYCOSIDE GLUCOSYLATION METHODS OH OH Glucose donor FIG. 1 (57) : The present invention provides engineered glycosyltransferase (GT) enzymes, polypeptides having GT activity, and polynucleotides encoding these enzymes, as well as vectors and host cells comprising these polynucleotides and polypeptides. The present invention provides engineered sucrose synthase (SuS) enzymes, polypeptides having SuS activity, and polynucleotides encod- ing these enzymes, as well as vectors and host cells comprising these polynucleotides and polypeptides. The present invention also provides compositions comprising the GT enzymes and methods of using the engineered GT enzymes to make products with 0-glucose linkages. The present invention further provides compositions and methods for the production of rebaudiosides (e.g., rebaudioside M, rebaudioside A, rebaudioside I, and rebaudioside D). The present invention also provides compositions comprising the SuS enzymes and methods of using them. Methods for producing GT and SuS enzymes are also provided. [Continued on next page] WO 2018/144679 A3 IMEDIMOM0101011MENOMMHOIEINEHOMEEN DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, HN, HR, HU, ID, IL, IN, IR, IS, JO, JP, KE, KG, KH, KN, KP, KR, KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (84) Designated States (unless otherwise indicated, for every kind of regional protection available): ARIPO (BW, GH, GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, SM, TR), OAPI (BF, BJ, CF, CG, CI, CM, GA, GN, GQ, GW, KM, ML, MR, NE, SN, TD, TG). Published: with international search report (Art. 21(3)) before the expiration of the time limit for amending the claims and to be republished in the event of receipt of amendments (Rule 48.2(h)) with sequence listing part of description (Rule 5.2(a)) (88) Date of publication of the international search report: 13 December 2018 (13.12.2018)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US201762454417P | 2017-02-03 | 2017-02-03 | |
US201762479262P | 2017-03-30 | 2017-03-30 | |
PCT/US2018/016359 WO2018144679A2 (en) | 2017-02-03 | 2018-02-01 | Engineered glycosyltransferases and steviol glycoside glucosylation methods |
Publications (1)
Publication Number | Publication Date |
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SG11201906480QA true SG11201906480QA (en) | 2019-08-27 |
Family
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Family Applications (1)
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SG11201906480QA SG11201906480QA (en) | 2017-02-03 | 2018-02-01 | Engineered glycosyltransferases and steviol glycoside glucosylation methods |
Country Status (14)
Country | Link |
---|---|
US (4) | US20180223264A1 (en) |
EP (3) | EP3577229A4 (en) |
JP (4) | JP7248302B2 (en) |
KR (2) | KR102606350B1 (en) |
CN (1) | CN110914445A (en) |
AU (4) | AU2018215335B2 (en) |
BR (1) | BR112019015992A2 (en) |
CA (3) | CA3175070A1 (en) |
IL (2) | IL268121B2 (en) |
MX (4) | MX2019009233A (en) |
PH (1) | PH12019501698A1 (en) |
SG (1) | SG11201906480QA (en) |
TW (3) | TW202237834A (en) |
WO (2) | WO2018144679A2 (en) |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2018144679A2 (en) | 2017-02-03 | 2018-08-09 | Codexis, Inc. | Engineered glycosyltransferases and steviol glycoside glucosylation methods |
AU2019304965A1 (en) * | 2018-07-16 | 2021-02-11 | Manus Bio, Inc. | Production of steviol glycosides through whole cell biotransformation |
EP3830106A4 (en) * | 2018-07-30 | 2022-07-06 | Codexis, Inc. | Engineered glycosyltransferases and steviol glycoside glucosylation methods |
CN111500566B (en) * | 2019-01-28 | 2022-02-15 | 江南大学 | Trehalose synthetase mutant and preparation method and application thereof |
WO2020237226A1 (en) * | 2019-05-23 | 2020-11-26 | Arzeda Corp. | Compositions and methods for producing steviol glycosides |
BR112021026306A2 (en) | 2019-06-25 | 2022-09-06 | Manus Bio Inc | URIDINE DIPHOSPHATE GLYCOSYLTRANSFERASE ENZYME |
JP2023506242A (en) * | 2019-12-16 | 2023-02-15 | マナス バイオ インコーポレイテッド | Microbial production of mogrol and mogrosides |
CN111662942A (en) * | 2020-05-25 | 2020-09-15 | 安徽金禾实业股份有限公司 | Method for producing rebaudioside-A through double-enzyme fermentation catalysis |
US20230304055A1 (en) | 2020-07-03 | 2023-09-28 | C-Lecta Gmbh | One-pot cell-free glycosylation process |
WO2022084482A1 (en) | 2020-10-22 | 2022-04-28 | Dsm Ip Assets B.V. | Microorganisms for diterpene production |
KR102546737B1 (en) * | 2020-11-25 | 2023-06-22 | 씨제이제일제당 주식회사 | Composition comprising transglycosylated steviol glycoside |
CN114958791B (en) * | 2021-01-08 | 2023-07-28 | 中国科学院华南植物园 | Spermidine derivative glycosyltransferase LbUGT62 and encoding gene and application thereof |
CN112704731B (en) * | 2021-01-13 | 2023-08-25 | 中国农业科学院哈尔滨兽医研究所(中国动物卫生与流行病学中心哈尔滨分中心) | Application and method of protease S273R for inhibiting cell apoptosis |
JP2024505906A (en) * | 2021-01-27 | 2024-02-08 | コリア アドバンスト インスティテュート オブ サイエンス アンド テクノロジー | C-glycosyltransferase variants and their uses |
JP2024520118A (en) | 2021-06-01 | 2024-05-21 | エーバイオケム バイオテクノロジー(グループ)カンパニー,リミティド | Glycosyltransferases and uses thereof |
CN115449514B (en) * | 2021-06-08 | 2023-09-29 | 弈柯莱生物科技(上海)股份有限公司 | Beta-1, 2-glycosyltransferase and application thereof |
CN113462670B (en) * | 2021-08-23 | 2023-03-24 | 兴化格林生物制品有限公司 | Glycosyltransferase mutant and method for catalytically synthesizing rebaudioside M by using same |
WO2023044368A1 (en) * | 2021-09-17 | 2023-03-23 | Doublerainbow Biosciences Inc. | Method for producing glycosylated therapeutics by using an immobilized enzyme preparation |
KR20230057275A (en) * | 2021-10-19 | 2023-04-28 | 씨제이제일제당 (주) | A method for preparation of rebaudioside D and rebaudioside M |
KR20230098493A (en) * | 2021-12-24 | 2023-07-04 | 주식회사 삼양사 | Rebaudioside production |
WO2024050533A2 (en) * | 2022-09-02 | 2024-03-07 | Arzeda Corp. | Compositions and methods for producing rebaudioside m |
WO2024121721A1 (en) | 2022-12-05 | 2024-06-13 | Tate & Lyle Solutions Usa Llc | Methods for obtaining steviol glycosides |
CN116426506B (en) * | 2023-03-10 | 2024-01-30 | 云南师范大学 | Beta-xylosidase mutant D259G with improved low-temperature activity and application thereof |
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2021
- 2021-02-24 JP JP2021027088A patent/JP7176786B2/en active Active
-
2022
- 2022-08-19 JP JP2022131026A patent/JP2022163224A/en not_active Withdrawn
- 2022-11-11 AU AU2022268390A patent/AU2022268390A1/en active Pending
-
2023
- 2023-07-30 IL IL304833A patent/IL304833A/en unknown
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