CA2943348A1 - Compositions and methods for producing chemicals and derivatives thereof - Google Patents
Compositions and methods for producing chemicals and derivatives thereof Download PDFInfo
- Publication number
- CA2943348A1 CA2943348A1 CA2943348A CA2943348A CA2943348A1 CA 2943348 A1 CA2943348 A1 CA 2943348A1 CA 2943348 A CA2943348 A CA 2943348A CA 2943348 A CA2943348 A CA 2943348A CA 2943348 A1 CA2943348 A1 CA 2943348A1
- Authority
- CA
- Canada
- Prior art keywords
- conversion
- acid
- ddg
- fdca
- glucose
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 238000000034 method Methods 0.000 title claims abstract description 162
- 239000000126 substance Substances 0.000 title claims abstract description 30
- 239000000203 mixture Substances 0.000 title description 13
- 238000006243 chemical reaction Methods 0.000 claims abstract description 346
- CHTHALBTIRVDBM-UHFFFAOYSA-N furan-2,5-dicarboxylic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)O1 CHTHALBTIRVDBM-UHFFFAOYSA-N 0.000 claims abstract description 229
- 230000002255 enzymatic effect Effects 0.000 claims abstract description 122
- IZSRJDGCGRAUAR-MROZADKFSA-M 5-dehydro-D-gluconate Chemical compound OCC(=O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O IZSRJDGCGRAUAR-MROZADKFSA-M 0.000 claims abstract description 101
- 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 abstract description 91
- 239000000758 substrate Substances 0.000 claims abstract description 72
- 230000037361 pathway Effects 0.000 claims abstract description 66
- 239000008103 glucose Substances 0.000 claims abstract description 62
- AEMOLEFTQBMNLQ-UHFFFAOYSA-N beta-D-galactopyranuronic acid Natural products OC1OC(C(O)=O)C(O)C(O)C1O AEMOLEFTQBMNLQ-UHFFFAOYSA-N 0.000 claims abstract description 59
- AEMOLEFTQBMNLQ-BZINKQHNSA-N D-Guluronic Acid Chemical compound OC1O[C@H](C(O)=O)[C@H](O)[C@@H](O)[C@H]1O AEMOLEFTQBMNLQ-BZINKQHNSA-N 0.000 claims abstract description 58
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- AEMOLEFTQBMNLQ-CLQWQSTFSA-N l-iduronic acid Chemical compound O[C@H]1O[C@H](C(O)=O)[C@H](O)[C@@H](O)[C@@H]1O AEMOLEFTQBMNLQ-CLQWQSTFSA-N 0.000 claims abstract description 42
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- QUURPCHWPQNNGL-ZAFYKAAXSA-N 5-dehydro-4-deoxy-D-glucaric acid Chemical group OC(=O)[C@H](O)[C@@H](O)CC(=O)C(O)=O QUURPCHWPQNNGL-ZAFYKAAXSA-N 0.000 claims description 11
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- 238000012360 testing method Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical compound CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- 238000012795 verification Methods 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
Classifications
-
- 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
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
- C12P7/58—Aldonic, ketoaldonic or saccharic acids
-
- 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
- C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
- C12P17/02—Oxygen as only ring hetero atoms
- C12P17/06—Oxygen as only ring hetero atoms containing a six-membered hetero ring, e.g. fluorescein
-
- 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
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
- C12P7/44—Polycarboxylic acids
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US14/222,453 US9528133B2 (en) | 2012-09-21 | 2014-03-21 | Compositions and methods for producing chemicals and derivatives thereof |
| US14/222,453 | 2014-03-21 | ||
| PCT/US2015/021848 WO2015143381A2 (en) | 2014-03-21 | 2015-03-20 | Compositions and methods for producing chemicals and derivatives thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2943348A1 true CA2943348A1 (en) | 2015-09-24 |
Family
ID=54145486
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2943348A Abandoned CA2943348A1 (en) | 2014-03-21 | 2015-03-20 | Compositions and methods for producing chemicals and derivatives thereof |
Country Status (7)
| Country | Link |
|---|---|
| EP (1) | EP3119899A4 (de) |
| CN (1) | CN106414753A (de) |
| AU (1) | AU2015231000B2 (de) |
| BR (1) | BR112016021298A2 (de) |
| CA (1) | CA2943348A1 (de) |
| SG (1) | SG11201607745WA (de) |
| WO (1) | WO2015143381A2 (de) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10927363B2 (en) | 2016-04-04 | 2021-02-23 | Mie University | DNA sequence and expression vector for alginate lyase |
| CN107954959A (zh) * | 2017-11-22 | 2018-04-24 | 南京工业大学 | 一种制备2,5-呋喃二甲酸及其前体物质的方法 |
| CN109824630B (zh) * | 2019-03-13 | 2020-08-04 | 浙江大学 | 一种甲酸供氢下木糖一锅法制备糠醇的方法 |
| US20230272364A1 (en) * | 2019-07-11 | 2023-08-31 | Bp Corporation North America Inc. | Gluconate dehydratase enzymes and recombinant cells |
| CN113527374B (zh) * | 2020-04-22 | 2025-12-02 | 中国科学院上海有机化学研究所 | 一种甘露糖醛酸寡糖的制备方法及其中间体 |
| JP2024513175A (ja) * | 2021-03-26 | 2024-03-22 | アーチャー-ダニエルズ-ミッドランド カンパニー | 酒石酸塩による阻害に耐性のある熱安定性d-グルカル酸デヒドラターゼ |
| US12295919B2 (en) | 2022-03-16 | 2025-05-13 | Mie University | Methods of treatment and prevention using 4-deoxy-L-erythro-5-hexoseulose uronic acid |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3184479A (en) * | 1965-05-18 | Process for the preparation of | ||
| JP2850515B2 (ja) * | 1990-09-25 | 1999-01-27 | 東洋紡績株式会社 | グルコースデヒドロゲナーゼおよびその製造法 |
| AU2008249370B2 (en) * | 2007-05-08 | 2013-09-05 | Ensuiko Sugar Refining Co., Ltd. | Method for producing glucuronic acid by glucuronic acid fermentation |
| US8835147B2 (en) * | 2008-04-04 | 2014-09-16 | Massachusetts Institute Of Technology | Cellular production of glucaric acid through recombinant expression of uronate dehydrogenase and myo-inositol oxygenase |
| EP2281034B1 (de) * | 2008-04-30 | 2015-10-21 | DuPont Nutrition Biosciences ApS | Verfahren zur Verwendung von Pseudoglucanobacter saccharoketogenes Alcohol Dehydrogenase |
| FI20086236A0 (fi) * | 2008-12-23 | 2008-12-23 | Valtion Teknillinen | Heksuronihapon konversio heksarihapoksi |
| US8363666B2 (en) * | 2010-02-22 | 2013-01-29 | Cisco Technology, Inc. | Multiple network architecture providing for migration of devices |
| US9079844B2 (en) * | 2012-04-04 | 2015-07-14 | Stichting Dienst Landbouwkundig Onderzoek | Catalytic oxidation of uronic acids to aldaric acids |
| CN105026548B (zh) * | 2012-06-04 | 2019-06-18 | 盐水港精糖株式会社 | D-葡萄糖二酸生产菌及d-葡萄糖二酸的制造方法 |
| BR112015006255A2 (pt) * | 2012-09-21 | 2017-08-22 | Synthetic Genomics Inc | Métodos para a produção de produtos químicos e derivados dos mesmos |
-
2015
- 2015-03-20 CN CN201580021486.XA patent/CN106414753A/zh active Pending
- 2015-03-20 BR BR112016021298A patent/BR112016021298A2/pt not_active Application Discontinuation
- 2015-03-20 WO PCT/US2015/021848 patent/WO2015143381A2/en not_active Ceased
- 2015-03-20 EP EP15764217.4A patent/EP3119899A4/de not_active Withdrawn
- 2015-03-20 SG SG11201607745WA patent/SG11201607745WA/en unknown
- 2015-03-20 CA CA2943348A patent/CA2943348A1/en not_active Abandoned
- 2015-03-20 AU AU2015231000A patent/AU2015231000B2/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| EP3119899A4 (de) | 2017-11-29 |
| WO2015143381A3 (en) | 2015-11-12 |
| AU2015231000A1 (en) | 2016-10-13 |
| AU2015231000B2 (en) | 2017-10-26 |
| EP3119899A2 (de) | 2017-01-25 |
| WO2015143381A2 (en) | 2015-09-24 |
| BR112016021298A2 (pt) | 2017-10-03 |
| SG11201607745WA (en) | 2016-11-29 |
| CN106414753A (zh) | 2017-02-15 |
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| Date | Code | Title | Description |
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Effective date: 20200831 |