JP6475620B2 - グルカンポリマー生成のためのグルコシルトランスフェラーゼ酵素 - Google Patents
グルカンポリマー生成のためのグルコシルトランスフェラーゼ酵素 Download PDFInfo
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- JP6475620B2 JP6475620B2 JP2015533292A JP2015533292A JP6475620B2 JP 6475620 B2 JP6475620 B2 JP 6475620B2 JP 2015533292 A JP2015533292 A JP 2015533292A JP 2015533292 A JP2015533292 A JP 2015533292A JP 6475620 B2 JP6475620 B2 JP 6475620B2
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Classifications
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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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
- C08B37/0006—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
- C08B37/0009—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid alpha-D-Glucans, e.g. polydextrose, alternan, glycogen; (alpha-1,4)(alpha-1,6)-D-Glucans; (alpha-1,3)(alpha-1,4)-D-Glucans, e.g. isolichenan or nigeran; (alpha-1,4)-D-Glucans; (alpha-1,3)-D-Glucans, e.g. pseudonigeran; Derivatives thereof
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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)
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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)
- C12N9/1051—Hexosyltransferases (2.4.1)
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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
- C12P19/04—Polysaccharides, i.e. compounds containing more than five saccharide radicals attached to each other by glycosidic bonds
-
- 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)
- C12Y204/01005—Dextransucrase (2.4.1.5)
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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)
- C12Y204/01267—Dolichyl-P-Glc:Man9GlcNAc2-PP-dolichol alpha-1,3-glucosyltransferase (2.4.1.267)
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
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| PCT/US2013/061579 WO2014052386A2 (en) | 2012-09-25 | 2013-09-25 | Glucosyltransferase enzymes for production of glucan polymers |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9034092B2 (en) * | 2012-05-24 | 2015-05-19 | E I Du Pont De Nemours And Company | Composition for preparing polysaccharide fibers |
| US9169506B2 (en) | 2013-09-05 | 2015-10-27 | E I Du Pont De Nemours And Company | Process for producing alpha-1,3-glucan polymer with reduced molecular weight |
| EP4163305B1 (en) | 2013-12-16 | 2024-07-10 | Nutrition & Biosciences USA 4, Inc. | Use of poly alpha-1,3-glucan ethers as viscosity modifiers |
| CN106029700B (zh) | 2013-12-18 | 2019-04-12 | 纳幕尔杜邦公司 | 阳离子聚α-1，3-葡聚糖醚 |
| WO2015103531A1 (en) | 2014-01-06 | 2015-07-09 | E. I. Du Pont De Nemours And Company | Production of poly alpha-1,3-glucan films |
| US10106626B2 (en) | 2014-01-17 | 2018-10-23 | Ei Du Pont De Nemours And Company | Production of poly alpha-1,3-glucan formate films |
| US9926541B2 (en) | 2014-02-14 | 2018-03-27 | E I Du Pont De Nemours And Company | Glucosyltransferase enzymes for production of glucan polymers |
| US9988657B2 (en) | 2014-02-27 | 2018-06-05 | E I Du Pont De Nemours And Company | Enzymatic hydrolysis of disaccharides and oligosaccharides using alpha-glucosidase enzymes |
| ES2734726T3 (es) | 2014-03-11 | 2019-12-11 | Du Pont | Poli alfa-1,2-glucano oxidado como reforzante de detergente |
| JP6708554B2 (ja) | 2014-03-25 | 2020-06-10 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニーＥ．Ｉ．Ｄｕ Ｐｏｎｔ Ｄｅ Ｎｅｍｏｕｒｓ Ａｎｄ Ｃｏｍｐａｎｙ | 代替のスクロース原料からのグルカンポリマーの生成 |
| US10907185B2 (en) | 2014-05-29 | 2021-02-02 | Dupont Industrial Biosciences Usa, Llc | Enzymatic synthesis of soluble glucan fiber |
| WO2015183714A1 (en) | 2014-05-29 | 2015-12-03 | E. I. Du Pont De Nemours And Company | Enzymatic synthesis of soluble glucan fiber |
| BR112016027867A2 (pt) * | 2014-05-29 | 2017-10-24 | Du Pont | composições de fibra e de carboidrato, produto alimentício, métodos para produzir uma composição de fibra, de carboidrato, para reduzir o índice glicêmico e para inibir a elevação do nível de açúcar, composição cosmética, uso da composição de fibra e composição |
| US20170198323A1 (en) * | 2014-05-29 | 2017-07-13 | E I Du Pont De Nemours And Company | Enzymatic synthesis of soluble glucan fiber |
| US9714403B2 (en) | 2014-06-19 | 2017-07-25 | E I Du Pont De Nemours And Company | Compositions containing one or more poly alpha-1,3-glucan ether compounds |
| WO2015195777A1 (en) | 2014-06-19 | 2015-12-23 | E. I. Du Pont De Nemours And Company | Compositions containing one or more poly alpha-1,3-glucan ether compounds |
| JP2017519507A (ja) * | 2014-06-26 | 2017-07-20 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニーＥ．Ｉ．Ｄｕ Ｐｏｎｔ Ｄｅ Ｎｅｍｏｕｒｓ Ａｎｄ Ｃｏｍｐａｎｙ | ポリα−１，３−グルカン食品ケーシングの製造 |
| JP6785242B2 (ja) | 2014-12-22 | 2020-11-18 | デュポン・インダストリアル・バイオサイエンシーズ・ユーエスエイ・エルエルシー | ポリアルファ−１，３−グルカンを含有するポリマーブレンド |
| EP3237455B1 (en) | 2014-12-22 | 2020-03-04 | DuPont Industrial Biosciences USA, LLC | Polysaccharide compositions for absorbing aqueous liquid |
| CN107205910A (zh) | 2015-02-06 | 2017-09-26 | 纳幕尔杜邦公司 | 基于聚α‑1,3‑葡聚糖的聚合物的胶体分散体 |
| WO2016196021A1 (en) * | 2015-06-01 | 2016-12-08 | E I Du Pont De Nemours And Company | Structured liquid compositions comprising colloidal dispersions of poly alpha-1,3-glucan |
| WO2016205391A1 (en) * | 2015-06-17 | 2016-12-22 | E I Du Pont De Nemours And Company | Modified glucosyltransferases for producing branched alpha-glucan polymers |
| ES2753181T3 (es) | 2015-08-28 | 2020-04-07 | Du Pont | Bencil-alfa-(1,3)-glucano y fibras del mismo |
| ES2937288T3 (es) | 2015-10-26 | 2023-03-27 | Nutrition & Biosciences Usa 4 Inc | Composición de alfa-(1,3->glucano) insoluble en agua |
| RU2729250C2 (ru) * | 2015-10-26 | 2020-08-05 | ДЮПОН ИНДАСТРИАЛ БАЙОСАЙЕНСИЗ ЮЭсЭй, ЭлЭлСи | Полисахаридные покрытия для бумаги |
| EP3371228B1 (en) * | 2015-11-05 | 2022-08-31 | Nutrition & Biosciences USA 4, Inc. | Dextran-poly alpha-1,3-glucan graft copolymers and synthesis methods thereof |
| CN108291344B (zh) * | 2015-11-10 | 2022-02-25 | 营养与生物科学美国4公司 | 非织造葡聚糖网 |
| WO2017083229A1 (en) * | 2015-11-13 | 2017-05-18 | E. I. Du Pont De Nemours And Company | Glucan fiber compositions for use in laundry care and fabric care |
| WO2017083226A1 (en) | 2015-11-13 | 2017-05-18 | E. I. Du Pont De Nemours And Company | Glucan fiber compositions for use in laundry care and fabric care |
| EP3374400B1 (en) | 2015-11-13 | 2022-04-13 | Nutrition & Biosciences USA 4, Inc. | Glucan fiber compositions for use in laundry care and fabric care |
| US10822383B2 (en) | 2015-11-26 | 2020-11-03 | E I Du Pont De Nemours And Company | Polypeptides capable of producing glucans having alpha-1,2 branches and use of the same |
| US10266861B2 (en) | 2015-12-14 | 2019-04-23 | E. I. Du Pont De Nemours And Company | Production and composition of fructose syrup |
| US10895028B2 (en) | 2015-12-14 | 2021-01-19 | Dupont Industrial Biosciences Usa, Llc | Nonwoven glucan webs |
| US10664466B2 (en) * | 2016-03-08 | 2020-05-26 | Microsoft Technology Licensing, Llc. | Specific content distribution across documents |
| CA3025953C (en) * | 2016-06-02 | 2024-01-16 | Nestec S.A. | Method of producing alpha glucans containing alpha 1-3 linked d-glucose units, and alpha glucans |
| US10301604B2 (en) | 2016-09-14 | 2019-05-28 | E I Du Pont De Nemours And Company | Engineered glucosyltransferases |
| US11505682B2 (en) | 2016-11-16 | 2022-11-22 | Nutrition & Biosciences USA 4, Inc. | Molded article comprising polysaccharide |
| CN110291113B (zh) * | 2017-02-16 | 2022-03-04 | 营养与生物科学美国4公司 | 交联的右旋糖酐和交联的右旋糖酐-聚α-1，3-葡聚糖接枝共聚物 |
| AU2018272823B2 (en) * | 2017-05-23 | 2024-05-09 | Nutrition & Biosciences USA 4, Inc. | Enzymatic production of alpha-1,3-glucan |
| AU2018334513B2 (en) * | 2017-09-13 | 2025-02-20 | Nutrition & Biosciences USA 4, Inc. | Engineered glucosyltransferases |
| EP3668970A1 (en) * | 2017-09-13 | 2020-06-24 | DuPont Industrial Biosciences USA, LLC | Engineered glucosyltransferases |
| WO2019055397A1 (en) | 2017-09-13 | 2019-03-21 | E. I. Du Pont De Nemours And Company | NONWOVEN LAYERS COMPRISING POLYSACCHARIDES |
| WO2019075301A1 (en) | 2017-10-13 | 2019-04-18 | E. I. Du Pont De Nemours And Company | Flowable bulk granular polysaccharide |
| CN111566128B (zh) * | 2017-11-10 | 2022-06-21 | 营养与生物科学美国4公司 | 独特形态的多糖 |
| JP2021507955A (ja) | 2017-12-14 | 2021-02-25 | デュポン・インダストリアル・バイオサイエンシーズ・ユーエスエイ・エルエルシー | α−１，３−グルカングラフトコポリマー |
| JP2021514681A (ja) * | 2018-03-09 | 2021-06-17 | ニュートリション・アンド・バイオサイエンシーズ・ユーエスエー・フォー，インコーポレイテッド | 遺伝子操作されたグルコシルトランスフェラーゼ |
| MX2021000109A (es) * | 2018-07-05 | 2021-03-09 | Dupont Nutrition Biosci Aps | Uso de glucosil transferasa para proporcionar una mejor textura a productos a base de leche fermentada. |
| CN113574074B (zh) | 2018-10-25 | 2023-03-21 | 营养与生物科学美国第四公司 | α-1,3-葡聚糖接枝共聚物 |
| WO2020131711A1 (en) | 2018-12-17 | 2020-06-25 | Dupont Industrial Biosciences Usa, Llc | Polysaccharide derivatives and compositions comprising same |
| AT522767B1 (de) | 2019-08-16 | 2021-01-15 | Mondi Ag | Transferpapier für Thermosublimationsdruck-Prozesse und Verfahren zur Herstellung von Transferpapier |
| EP4013241A1 (en) | 2019-08-16 | 2022-06-22 | Nutrition & Biosciences USA 4, Inc. | Flour- and meal-based food products comprising insoluble alpha-1,3-glucan |
| MX2022005441A (es) | 2019-11-06 | 2022-10-10 | Nutrition & Biosciences Usa 4 Inc | Alfa-1,3-glucano altamente cristalino. |
| EP4100446A1 (en) * | 2020-02-04 | 2022-12-14 | Nutrition & Biosciences USA 4, Inc. | Aqueous dispersions of insoluble alpha-glucan comprising alpha-1,3 glycosidic linkages |
| CN116134054A (zh) | 2020-06-04 | 2023-05-16 | 营养与生物科学美国4公司 | 右旋糖酐-α-葡聚糖接枝共聚物及其衍生物 |
| WO2021252569A1 (en) | 2020-06-10 | 2021-12-16 | Nutrition & Biosciences USA 4, Inc. | Poly alpha-1,6-glucan derivatives and compositions comprising same |
| WO2022178073A1 (en) | 2021-02-19 | 2022-08-25 | Nutrition & Biosciences USA 4, Inc. | Polysaccharide derivatives for detergent compositions |
| EP4334363A1 (en) | 2021-05-04 | 2024-03-13 | Nutrition & Biosciences USA 4, Inc. | Compositions comprising insoluble alpha-glucan |
| CN117337308A (zh) | 2021-05-04 | 2024-01-02 | 营养与生物科学美国4公司 | 包含氧化的不溶性α-葡聚糖的组合物 |
| EP4370560A1 (en) | 2021-07-13 | 2024-05-22 | Nutrition & Biosciences USA 4, Inc. | Cationic glucan ester derivatives |
| WO2023055902A1 (en) | 2021-09-30 | 2023-04-06 | Dupont Nutrition Biosciences Aps | Method for reducing sugar in food stuff |
| EP4426362A1 (en) | 2021-11-05 | 2024-09-11 | Nutrition & Biosciences USA 4, Inc. | Glucan derivatives for microbial control |
| EP4463519A1 (en) | 2022-01-12 | 2024-11-20 | Nutrition & Biosciences USA 4, Inc. | Coating compositions comprising rubber and insoluble alpha-glucan |
| EP4496834A1 (en) | 2022-03-21 | 2025-01-29 | Nutrition & Biosciences USA 4, Inc. | Compositions comprising insoluble alpha-glucan |
| CN114717213B (zh) * | 2022-05-05 | 2023-09-22 | 广西科学院 | 一种葡聚糖蔗糖酶的n端截短突变酶及其制备方法 |
| WO2024015769A1 (en) | 2022-07-11 | 2024-01-18 | Nutrition & Biosciences USA 4, Inc. | Amphiphilic glucan ester derivatives |
| EP4604740A1 (en) | 2022-10-17 | 2025-08-27 | International N&H Denmark ApS | Method for improving flavor in plant-based food stuff |
| EP4611720A1 (en) | 2022-11-02 | 2025-09-10 | Nutrition & Biosciences USA 4, Inc. | Compositions comprising xanthan gum and crystalline alpha-1,3-glucan |
| AU2024242918A1 (en) | 2023-03-29 | 2025-09-18 | Danisco Us Inc. | Methods for modifying texture in foodstuff via preferably in situ produced alpha-glucan |
| WO2025006691A2 (en) | 2023-06-30 | 2025-01-02 | Nutrition & Biosciences USA 4, Inc. | Porous alpha-1,3-glucan compositions |
| WO2025072416A1 (en) | 2023-09-29 | 2025-04-03 | Nutrition & Biosciences USA 4, Inc. | Polysaccharide derivatives |
| WO2025072417A1 (en) | 2023-09-29 | 2025-04-03 | Nutrition & Biosciences USA 4, Inc. | Polysaccharide derivatives |
| WO2025072419A1 (en) | 2023-09-29 | 2025-04-03 | Nutrition & Biosciences Usa 1, Llc | Crosslinked alpha-glucan derivatives |
| WO2025114053A1 (en) | 2023-11-30 | 2025-06-05 | Novozymes A/S | Biopolymers for use in detergent |
| WO2025198996A1 (en) | 2024-03-19 | 2025-09-25 | Danisco Us Inc. | Method for improving flavor in foodstuff |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1001736A1 (en) | 1996-10-11 | 2000-05-24 | Novo Nordisk A/S | STARCH BINDING DOMAINS (SBDs) FOR ORAL CARE PRODUCTS |
| US5952205A (en) | 1998-02-06 | 1999-09-14 | Neose Technologies, Inc. | Process for processing sucrose into glucose and fructose |
| KR20010101647A (ko) * | 1999-01-25 | 2001-11-14 | 메리 이. 보울러 | 폴리사카라이드 섬유 |
| US6867026B2 (en) | 2000-05-25 | 2005-03-15 | Nederlandse Organisatie Voor Toegepast Natuurwetenschappelijk Onderzoek Tno | Glucosyltransferases |
| US7524645B2 (en) | 2004-12-14 | 2009-04-28 | Centre National De La Recherche Scientifique (Cnrs) | Fully active alternansucrases partially deleted in its carboxy-terminal and amino-terminal domains and mutants thereof |
| EP1679374A1 (en) | 2005-01-10 | 2006-07-12 | Bayer CropScience GmbH | Transformed plant expressing a mutansucrase and synthesizing a modified starch |
| JP4595074B2 (ja) | 2006-08-22 | 2010-12-08 | 国立大学法人東北大学 | 新規グルカン及びその製造方法 |
| US8642757B2 (en) * | 2011-09-09 | 2014-02-04 | E I Du Pont De Nemours And Company | High titer production of highly linear poly (α 1,3 glucan) |
| US9080195B2 (en) | 2011-09-09 | 2015-07-14 | E I Du Pont De Nemours And Company | High titer production of poly (α 1,3 glucan) |
| US8962282B2 (en) * | 2011-12-19 | 2015-02-24 | E I Du Pont De Nemours And Company | Increased poly (alpha 1,3 glucan) yield using tetraborate |
| US8828689B2 (en) * | 2011-12-19 | 2014-09-09 | E I Du Pont De Nemours And Company | Increased poly (α 1, 3 glucan) yield using boric acid |
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