RU2017111853A - Ферментативное трансфосфорилирование сахарных субстратов - Google Patents
Ферментативное трансфосфорилирование сахарных субстратов Download PDFInfo
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- RU2017111853A RU2017111853A RU2017111853A RU2017111853A RU2017111853A RU 2017111853 A RU2017111853 A RU 2017111853A RU 2017111853 A RU2017111853 A RU 2017111853A RU 2017111853 A RU2017111853 A RU 2017111853A RU 2017111853 A RU2017111853 A RU 2017111853A
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- Russia
- Prior art keywords
- glucose
- alpha
- phosphate
- phosphatase
- enzyme
- Prior art date
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- 239000000758 substrate Substances 0.000 title claims 9
- 229910019142 PO4 Inorganic materials 0.000 claims 9
- 238000000034 method Methods 0.000 claims 9
- 235000021317 phosphate Nutrition 0.000 claims 9
- 230000000694 effects Effects 0.000 claims 8
- 108090000790 Enzymes Proteins 0.000 claims 7
- 102000004190 Enzymes Human genes 0.000 claims 7
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 7
- 239000010452 phosphate Substances 0.000 claims 7
- 108020000005 Sucrose phosphorylase Proteins 0.000 claims 4
- HXXFSFRBOHSIMQ-VFUOTHLCSA-N alpha-D-glucose 1-phosphate Chemical compound OC[C@H]1O[C@H](OP(O)(O)=O)[C@H](O)[C@@H](O)[C@@H]1O HXXFSFRBOHSIMQ-VFUOTHLCSA-N 0.000 claims 3
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 claims 2
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 claims 2
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 claims 2
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 claims 2
- 229950010772 glucose-1-phosphate Drugs 0.000 claims 2
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 claims 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims 2
- MSWZFWKMSRAUBD-IVMDWMLBSA-N 2-amino-2-deoxy-D-glucopyranose Chemical compound N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O MSWZFWKMSRAUBD-IVMDWMLBSA-N 0.000 claims 1
- GSXOAOHZAIYLCY-UHFFFAOYSA-N D-F6P Natural products OCC(=O)C(O)C(O)C(O)COP(O)(O)=O GSXOAOHZAIYLCY-UHFFFAOYSA-N 0.000 claims 1
- RFSUNEUAIZKAJO-VRPWFDPXSA-N D-Fructose Natural products OC[C@H]1OC(O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-VRPWFDPXSA-N 0.000 claims 1
- NBSCHQHZLSJFNQ-GASJEMHNSA-N D-Glucose 6-phosphate Chemical compound OC1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H](O)[C@H]1O NBSCHQHZLSJFNQ-GASJEMHNSA-N 0.000 claims 1
- HEBKCHPVOIAQTA-QWWZWVQMSA-N D-arabinitol Chemical compound OC[C@@H](O)C(O)[C@H](O)CO HEBKCHPVOIAQTA-QWWZWVQMSA-N 0.000 claims 1
- SHZGCJCMOBCMKK-UHFFFAOYSA-N D-mannomethylose Natural products CC1OC(O)C(O)C(O)C1O SHZGCJCMOBCMKK-UHFFFAOYSA-N 0.000 claims 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 claims 1
- 229930091371 Fructose Natural products 0.000 claims 1
- 239000005715 Fructose Substances 0.000 claims 1
- PNNNRSAQSRJVSB-SLPGGIOYSA-N Fucose Natural products C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)C=O PNNNRSAQSRJVSB-SLPGGIOYSA-N 0.000 claims 1
- VFRROHXSMXFLSN-UHFFFAOYSA-N Glc6P Natural products OP(=O)(O)OCC(O)C(O)C(O)C(O)C=O VFRROHXSMXFLSN-UHFFFAOYSA-N 0.000 claims 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 claims 1
- 208000007976 Ketosis Diseases 0.000 claims 1
- LKDRXBCSQODPBY-AMVSKUEXSA-N L-(-)-Sorbose Chemical compound OCC1(O)OC[C@H](O)[C@@H](O)[C@@H]1O LKDRXBCSQODPBY-AMVSKUEXSA-N 0.000 claims 1
- SHZGCJCMOBCMKK-DHVFOXMCSA-N L-fucopyranose Chemical compound C[C@@H]1OC(O)[C@@H](O)[C@H](O)[C@@H]1O SHZGCJCMOBCMKK-DHVFOXMCSA-N 0.000 claims 1
- OVRNDRQMDRJTHS-UHFFFAOYSA-N N-acelyl-D-glucosamine Natural products CC(=O)NC1C(O)OC(CO)C(O)C1O OVRNDRQMDRJTHS-UHFFFAOYSA-N 0.000 claims 1
- OVRNDRQMDRJTHS-FMDGEEDCSA-N N-acetyl-beta-D-glucosamine Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O OVRNDRQMDRJTHS-FMDGEEDCSA-N 0.000 claims 1
- SQVRNKJHWKZAKO-PFQGKNLYSA-N N-acetyl-beta-neuraminic acid Chemical compound CC(=O)N[C@@H]1[C@@H](O)C[C@@](O)(C(O)=O)O[C@H]1[C@H](O)[C@H](O)CO SQVRNKJHWKZAKO-PFQGKNLYSA-N 0.000 claims 1
- MBLBDJOUHNCFQT-LXGUWJNJSA-N N-acetylglucosamine Natural products CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)[C@H](O)CO MBLBDJOUHNCFQT-LXGUWJNJSA-N 0.000 claims 1
- 102000007056 Recombinant Fusion Proteins Human genes 0.000 claims 1
- 108010008281 Recombinant Fusion Proteins Proteins 0.000 claims 1
- 229930006000 Sucrose Natural products 0.000 claims 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims 1
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 claims 1
- 150000001323 aldoses Chemical class 0.000 claims 1
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 claims 1
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 claims 1
- BGWGXPAPYGQALX-ARQDHWQXSA-N beta-D-fructofuranose 6-phosphate Chemical compound OC[C@@]1(O)O[C@H](COP(O)(O)=O)[C@@H](O)[C@@H]1O BGWGXPAPYGQALX-ARQDHWQXSA-N 0.000 claims 1
- MSWZFWKMSRAUBD-UHFFFAOYSA-N beta-D-galactosamine Natural products NC1C(O)OC(CO)C(O)C1O MSWZFWKMSRAUBD-UHFFFAOYSA-N 0.000 claims 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims 1
- SQVRNKJHWKZAKO-UHFFFAOYSA-N beta-N-Acetyl-D-neuraminic acid Natural products CC(=O)NC1C(O)CC(O)(C(O)=O)OC1C(O)C(O)CO SQVRNKJHWKZAKO-UHFFFAOYSA-N 0.000 claims 1
- 239000011942 biocatalyst Substances 0.000 claims 1
- 150000001720 carbohydrates Chemical class 0.000 claims 1
- 235000014633 carbohydrates Nutrition 0.000 claims 1
- 230000002255 enzymatic effect Effects 0.000 claims 1
- 229960002737 fructose Drugs 0.000 claims 1
- 229930182830 galactose Natural products 0.000 claims 1
- 229960003082 galactose Drugs 0.000 claims 1
- 229960002442 glucosamine Drugs 0.000 claims 1
- 239000008103 glucose Substances 0.000 claims 1
- 229960001031 glucose Drugs 0.000 claims 1
- 238000002955 isolation Methods 0.000 claims 1
- ZKLLSNQJRLJIGT-UYFOZJQFSA-N keto-D-fructose 1-phosphate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C(=O)COP(O)(O)=O ZKLLSNQJRLJIGT-UYFOZJQFSA-N 0.000 claims 1
- 150000002584 ketoses Chemical class 0.000 claims 1
- 229950006780 n-acetylglucosamine Drugs 0.000 claims 1
- 239000005720 sucrose Substances 0.000 claims 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 claims 1
- 229960002675 xylitol Drugs 0.000 claims 1
- 235000010447 xylitol Nutrition 0.000 claims 1
- 239000000811 xylitol Substances 0.000 claims 1
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
- C12P19/02—Monosaccharides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H1/00—Processes for the preparation of sugar derivatives
- C07H1/02—Phosphorylation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H11/00—Compounds containing saccharide radicals esterified by inorganic acids; Metal salts thereof
- C07H11/04—Phosphates; Phosphites; Polyphosphates
-
- 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
- C12N9/14—Hydrolases (3)
- C12N9/16—Hydrolases (3) acting on ester bonds (3.1)
-
- 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
- C12P19/26—Preparation of nitrogen-containing carbohydrates
-
- 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)
-
- 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)
- C12Y204/01007—Sucrose phosphorylase (2.4.1.7)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y301/00—Hydrolases acting on ester bonds (3.1)
- C12Y301/03—Phosphoric monoester hydrolases (3.1.3)
- C12Y301/0301—Glucose-1-phosphatase (3.1.3.10)
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Genetics & Genomics (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Molecular Biology (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Biomedical Technology (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Enzymes And Modification Thereof (AREA)
Claims (14)
1. Способ получения одного или более фосфатов сахаров посредством ферментативного трансфосфорилирования, включающий следующие стадии:
(i) обеспечение одного или более сахарных субстратов, выбранных из группы, состоящей из альдоз и кетоз.
(ii) обеспечение одного или более субстратов - доноров фосфата, выбранных из группы фосфорилированных углеводов
(iii) обеспечение альфа-глюкозо-1-фосфатазы или фермента, обладающего активностью альфа-глюкозо-1-фосфатазы,
(iv) инкубирование одного или более сахарных субстратов, обеспеченных на стадии (i), и одного или более субстратов - доноров фосфата, обеспеченных на стадии (ii), с альфа-глюкозо-1-фосфатазой или, соответственно, ферментом, обладающим активностью альфа-глюкозо-1-фосфатазы, обеспеченными на стадии (iii), в условиях, которые позволяют трансфосфорилирование,
(v) необязательно, очистку одного или более фосфатов сахаров, полученных на стадии (iv).
2. Способ по п. 1, в котором сахарный субстрат (субстраты) выбирают из группы, состоящей из глюкозы, глюкозамина, N-ацетилглюкозамина, фруктозы, галактозы, фукозы, маннозы, сорбозы, ксилозы, арабинозы, ксилита, арабитола, рамнозы и N-ацетилнейраминовой кислоты.
3. Способ по п. 1, в котором один или более субстратов - доноров фосфата выбирают из группы, состоящей из альфа-глюкозо-1-фосфата, глюкозо-6-фосфата, фруктозо-6-фосфата и фруктозо-1-фосфата.
4. Способ по п. 1, в котором субстрат - донор фосфата или один из субстратов - доноров фосфата, обеспеченных на стадии (ii), представляет собой альфа-глюкозо-1-фосфат.
5. Способ по п. 4, в котором стадия (ii) включает ферментативное превращение сахарозы в D-фруктозу и альфа-D-глюкозо-1-фосфат с помощью сахарозофосфорилазы или фермента, обладающего активностью сахарозофосфорилазы, в присутствии фосфата или одного или более источников фосфата.
6. Способ по п. 5, в котором стадию (ii) и стадию (iv) и необязательно стадию (iii) проводят одновременно.
7. Применение биокатализатора, обладающего сахарозофосфорилазной активностью и альфа-глюкозо-1-фосфатазной активностью и/или содержащего или состоящего из сахарозофосфорилазы и альфа-глюкозо-1-фосфатазы в способе по п. 5 или 6.
8. Способ по любому из пп. 1-6, в котором стадия (iii) включает экспрессию альфа-глюкозо-1-фосфатазы или фермента, обладающего активностью альфа-глюкозо-1-фосфатазы, клеткой-хозяином.
9. Способ по п. 8, в котором альфа-глюкозо-1-фосфатазу или фермент, обладающий активностью альфа-глюкозо-1-фосфатазы, соответственно, экспрессируется в виде рекомбинантного слитого белка, содержащего метку, подходящую для выделения альфа-глюкозо-1-фосфатазы или фермента, обладающего активностью альфа-глюкозо-1-фосфатазы.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14184303 | 2014-09-10 | ||
| EP14184303.7 | 2014-09-10 | ||
| PCT/EP2015/064785 WO2016037720A1 (en) | 2014-09-10 | 2015-06-30 | Enzymatic transphosphorylation of sugar substrates |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2017111853A true RU2017111853A (ru) | 2018-10-10 |
| RU2017111853A3 RU2017111853A3 (ru) | 2019-02-21 |
Family
ID=51518639
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2017111853A RU2017111853A (ru) | 2014-09-10 | 2015-06-30 | Ферментативное трансфосфорилирование сахарных субстратов |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US10533201B2 (ru) |
| EP (1) | EP3194606A1 (ru) |
| JP (1) | JP6738324B2 (ru) |
| KR (1) | KR20170051508A (ru) |
| CN (1) | CN106715705A (ru) |
| AU (1) | AU2015314601B2 (ru) |
| CA (1) | CA2960171A1 (ru) |
| IL (1) | IL250679A0 (ru) |
| RU (1) | RU2017111853A (ru) |
| WO (1) | WO2016037720A1 (ru) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US12215371B2 (en) | 2018-10-29 | 2025-02-04 | Bonumose, Inc. | Enzymatic production of hexoses |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK3274465T3 (da) | 2015-03-26 | 2022-10-24 | Basf Se | Biokatalytisk fremstilling af l-fucose |
| BR112018016789A2 (pt) | 2016-02-19 | 2018-12-26 | Basf Se | processo para preparação biocatalítica e preparação de um composto |
| US11180740B2 (en) * | 2018-04-23 | 2021-11-23 | Danisco Us Inc | Synthesis of glucan comprising beta-1,3 glycosidic linkages with beta-1,3-glucan phosphorylase enzymes |
| CN112877382B (zh) * | 2021-01-18 | 2023-02-21 | 江南大学 | 一种酶法制备磷酸酯淀粉的方法 |
| CN114088824B (zh) * | 2021-10-15 | 2023-08-08 | 陈炜瑶 | 一种检测氨基寡糖素农药中游离氨基葡萄糖的方法 |
| CN114805459A (zh) * | 2022-05-20 | 2022-07-29 | 江苏集萃工业生物技术研究所有限公司 | 一种ump钠盐的分离提取方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4227569C1 (de) * | 1992-08-20 | 1994-06-09 | Inst Chemo Biosensorik | Verfahren zum empfindlichen enzymatischen Nachweis von anorganischem Phosphat |
| JP3146361B1 (ja) * | 2000-01-27 | 2001-03-12 | 農林水産省食品総合研究所長 | ヘテロオリゴ糖の製造方法 |
| JPWO2005073399A1 (ja) * | 2004-01-28 | 2007-07-26 | 独立行政法人産業技術総合研究所 | リン酸イオンの定性・定量法およびリン酸イオンセンサ |
| EP1995323A1 (en) | 2007-05-24 | 2008-11-26 | Libragen | Method for preparing C-6 phosphorylated D-aldohexoses and C-6 phosphorylated D-aldohexose derivatives |
| ES2652559T3 (es) | 2007-07-04 | 2018-02-05 | Dpx Holdings B.V. | Preparación de una esterasa |
| FR2958157B1 (fr) | 2010-04-02 | 2012-06-29 | Libragen | Composition cosmetique et pharmaceutique comprenant du n-acetyl-glucosamine-6-phosphate |
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2015
- 2015-06-30 WO PCT/EP2015/064785 patent/WO2016037720A1/en not_active Ceased
- 2015-06-30 CA CA2960171A patent/CA2960171A1/en active Pending
- 2015-06-30 RU RU2017111853A patent/RU2017111853A/ru not_active Application Discontinuation
- 2015-06-30 JP JP2017513237A patent/JP6738324B2/ja active Active
- 2015-06-30 AU AU2015314601A patent/AU2015314601B2/en active Active
- 2015-06-30 US US15/509,993 patent/US10533201B2/en active Active
- 2015-06-30 CN CN201580048580.4A patent/CN106715705A/zh active Pending
- 2015-06-30 EP EP15738290.4A patent/EP3194606A1/en active Pending
- 2015-06-30 KR KR1020177009450A patent/KR20170051508A/ko not_active Withdrawn
-
2017
- 2017-02-20 IL IL250679A patent/IL250679A0/en unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US12215371B2 (en) | 2018-10-29 | 2025-02-04 | Bonumose, Inc. | Enzymatic production of hexoses |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2016037720A1 (en) | 2016-03-17 |
| JP6738324B2 (ja) | 2020-08-12 |
| CN106715705A (zh) | 2017-05-24 |
| EP3194606A1 (en) | 2017-07-26 |
| IL250679A0 (en) | 2017-04-30 |
| AU2015314601B2 (en) | 2019-07-04 |
| CA2960171A1 (en) | 2016-03-17 |
| US20180148753A1 (en) | 2018-05-31 |
| AU2015314601A1 (en) | 2017-03-16 |
| KR20170051508A (ko) | 2017-05-11 |
| US10533201B2 (en) | 2020-01-14 |
| JP2017526376A (ja) | 2017-09-14 |
| RU2017111853A3 (ru) | 2019-02-21 |
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