BR112021016818A2 - Método para síntese in vivo de 4-hidroximetilfurfural e derivados do mesmo - Google Patents
Método para síntese in vivo de 4-hidroximetilfurfural e derivados do mesmoInfo
- Publication number
- BR112021016818A2 BR112021016818A2 BR112021016818A BR112021016818A BR112021016818A2 BR 112021016818 A2 BR112021016818 A2 BR 112021016818A2 BR 112021016818 A BR112021016818 A BR 112021016818A BR 112021016818 A BR112021016818 A BR 112021016818A BR 112021016818 A2 BR112021016818 A2 BR 112021016818A2
- Authority
- BR
- Brazil
- Prior art keywords
- formylfuran
- carboxylate
- furandimethanol
- dicarbaldehyde
- fdca
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 5
- GYQBROOJXNICMZ-UHFFFAOYSA-N 4-(hydroxymethyl)furan-2-carbaldehyde Chemical compound OCC1=COC(C=O)=C1 GYQBROOJXNICMZ-UHFFFAOYSA-N 0.000 title abstract 2
- 230000015572 biosynthetic process Effects 0.000 title abstract 2
- 238000001727 in vivo Methods 0.000 title abstract 2
- 238000003786 synthesis reaction Methods 0.000 title abstract 2
- VGJYVADXDZIDMK-UHFFFAOYSA-N 4-formylfuran-2-carboxylic acid Chemical compound OC(=O)C1=CC(C=O)=CO1 VGJYVADXDZIDMK-UHFFFAOYSA-N 0.000 abstract 3
- IRYKMSRWDXXLJL-UHFFFAOYSA-N 5-formylfuran-3-carboxylic acid Chemical compound OC(=O)C1=COC(C=O)=C1 IRYKMSRWDXXLJL-UHFFFAOYSA-N 0.000 abstract 3
- HKGMKJJFLRJMEN-UHFFFAOYSA-N [4-(hydroxymethyl)furan-2-yl]methanol Chemical compound OCC1=COC(CO)=C1 HKGMKJJFLRJMEN-UHFFFAOYSA-N 0.000 abstract 3
- VZFHZYTUWACMRI-UHFFFAOYSA-N furan-2,4-dicarbaldehyde Chemical compound O=CC1=COC(C=O)=C1 VZFHZYTUWACMRI-UHFFFAOYSA-N 0.000 abstract 3
- UCIWCPXQZAENQS-UHFFFAOYSA-N 4-(hydroxymethyl)furan-2-carboxylic acid Chemical compound OCC1=COC(C(O)=O)=C1 UCIWCPXQZAENQS-UHFFFAOYSA-N 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 244000005700 microbiome Species 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 150000007523 nucleic acids Chemical class 0.000 abstract 1
- 102000039446 nucleic acids Human genes 0.000 abstract 1
- 108020004707 nucleic acids Proteins 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 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
- 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
- C12P17/04—Oxygen as only ring hetero atoms containing a five-membered hetero ring, e.g. griseofulvin, vitamin C
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/70—Vectors or expression systems specially adapted for E. coli
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- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
- C12N15/80—Vectors or expression systems specially adapted for eukaryotic hosts for fungi
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- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/0004—Oxidoreductases (1.)
- C12N9/0006—Oxidoreductases (1.) acting on CH-OH groups as donors (1.1)
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- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/0004—Oxidoreductases (1.)
- C12N9/0008—Oxidoreductases (1.) acting on the aldehyde or oxo group of donors (1.2)
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- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/0004—Oxidoreductases (1.)
- C12N9/0065—Oxidoreductases (1.) acting on hydrogen peroxide as acceptor (1.11)
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- 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)
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- C12Y301/03—Phosphoric monoester hydrolases (3.1.3)
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- C12Y402/00—Carbon-oxygen lyases (4.2)
- C12Y402/03—Carbon-oxygen lyases (4.2) acting on phosphates (4.2.3)
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- C12Y101/00—Oxidoreductases acting on the CH-OH group of donors (1.1)
- C12Y101/01—Oxidoreductases acting on the CH-OH group of donors (1.1) with NAD+ or NADP+ as acceptor (1.1.1)
- C12Y101/01001—Alcohol dehydrogenase (1.1.1.1)
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- C12Y102/00—Oxidoreductases acting on the aldehyde or oxo group of donors (1.2)
- C12Y102/01—Oxidoreductases acting on the aldehyde or oxo group of donors (1.2) with NAD+ or NADP+ as acceptor (1.2.1)
- C12Y102/01003—Aldehyde dehydrogenase (NAD+) (1.2.1.3)
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- C12Y102/00—Oxidoreductases acting on the aldehyde or oxo group of donors (1.2)
- C12Y102/01—Oxidoreductases acting on the aldehyde or oxo group of donors (1.2) with NAD+ or NADP+ as acceptor (1.2.1)
- C12Y102/01004—Aldehyde dehydrogenase (NADP+) (1.2.1.4)
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- C12Y102/00—Oxidoreductases acting on the aldehyde or oxo group of donors (1.2)
- C12Y102/01—Oxidoreductases acting on the aldehyde or oxo group of donors (1.2) with NAD+ or NADP+ as acceptor (1.2.1)
- C12Y102/01005—Aldehyde dehydrogenase [NAD(P)+] (1.2.1.5)
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- C12Y207/00—Transferases transferring phosphorus-containing groups (2.7)
- C12Y207/01—Phosphotransferases with an alcohol group as acceptor (2.7.1)
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Genetics & Genomics (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Biomedical Technology (AREA)
- Molecular Biology (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Biophysics (AREA)
- Physics & Mathematics (AREA)
- Mycology (AREA)
- Plant Pathology (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Furan Compounds (AREA)
- Polyesters Or Polycarbonates (AREA)
- Enzymes And Modification Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
método para síntese in vivo de 4-hidroximetilfurfural e derivados do mesmo. a presente divulgação fornece micro-organismos recombinantes e métodos para a produção de 4-hmf, 2,4-furandimetanol, furan-2,4-dicarbaldeído, ácido 4-(hidroximetil)furoico, 2-formilfuran-4-carboxilato, 4-formilfuran-2-carboxilato e/ou 2,4-fdca a partir de uma fonte de carbono. o método prevê micro-organismos manipulados que expressam moléculas de ácido nucleico endógenas e/ou exógenas que catalisam a conversão de uma fonte de carbono em 4-hmf, 2,4-furandimetanol, furan-2,4-dicarbaldeído, ácido 4-(hidroximetil)furoico, 2-formilfuran-4-carboxilato, 4-formilfuran-2-carboxilato e/ou 2,4-fdca. a divulgação fornece ainda métodos de produção de polímeros derivados de 4-hmf, 2,4-furandimetanol, furan-2,4-dicarbaldeído, ácido 4-(hidroximetil)furoico, 2-formilfuran-4-carboxilato, 4-formilfuran-2-carboxilato e/ou 2,4-fdca.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201962812904P | 2019-03-01 | 2019-03-01 | |
PCT/BR2020/050064 WO2020176958A1 (en) | 2019-03-01 | 2020-03-02 | Method for the in vivo synthesis of 4-hydroxymethylfurfural and derivatives thereof |
Publications (1)
Publication Number | Publication Date |
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BR112021016818A2 true BR112021016818A2 (pt) | 2021-11-16 |
Family
ID=70189623
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR112021016818A BR112021016818A2 (pt) | 2019-03-01 | 2020-03-02 | Método para síntese in vivo de 4-hidroximetilfurfural e derivados do mesmo |
Country Status (9)
Country | Link |
---|---|
US (5) | US11339414B2 (pt) |
EP (1) | EP3921435A1 (pt) |
JP (1) | JP2022523540A (pt) |
KR (1) | KR20210136044A (pt) |
CN (1) | CN113748211A (pt) |
BR (1) | BR112021016818A2 (pt) |
CA (1) | CA3132051A1 (pt) |
MX (1) | MX2021010457A (pt) |
WO (1) | WO2020176958A1 (pt) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11541105B2 (en) | 2018-06-01 | 2023-01-03 | The Research Foundation For The State University Of New York | Compositions and methods for disrupting biofilm formation and maintenance |
JP2023527820A (ja) * | 2020-05-29 | 2023-06-30 | ブラスケン・エス.エー. | フランジカルボキシル酸ジエステルの2,4-異性体に基づく可塑剤の生産及び使用 |
US11692210B2 (en) | 2020-09-01 | 2023-07-04 | Braskem S.A. | Anaerobic fermentative production of furandicarboxylic acid |
WO2022047559A1 (en) | 2020-09-01 | 2022-03-10 | Braskem S.A. | Anaerobic fermentative production of furandimethanol and enzymatic production of furandicarboxylic acid |
CN117043225A (zh) | 2021-01-29 | 2023-11-10 | 布拉斯科公司 | 具有提高的结晶控制的2,4-fdca的共聚酯 |
US20230002363A1 (en) | 2021-06-16 | 2023-01-05 | Braskem S.A. | Furanic diglycidyl ethers and esters and use thereof |
CN113913448B (zh) * | 2021-07-23 | 2023-10-20 | 中国人民解放军军事科学院军事医学研究院 | 一种提高甲基营养菌吡咯喹啉醌产量的方法及应用 |
GB202217116D0 (en) * | 2022-11-16 | 2022-12-28 | Univ Nottingham | biosynthesis of plastics precursors |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
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US6740506B2 (en) | 1995-12-07 | 2004-05-25 | Diversa Corporation | End selection in directed evolution |
US6033861A (en) | 1997-11-19 | 2000-03-07 | Incyte Genetics, Inc. | Methods for obtaining nucleic acid containing a mutation |
JP5285617B2 (ja) | 2006-12-18 | 2013-09-11 | アドバンスド バイオニュートリション コーポレーション | 生きたプロバイオティクスを含む乾燥食物製品 |
WO2011003300A1 (zh) | 2009-07-09 | 2011-01-13 | 中国科学技术大学 | 羟甲基糠醛的制备方法 |
CN102834386B (zh) | 2009-09-02 | 2016-12-07 | 普拉克生物化学有限公司 | 具有氧化还原酶活性的多肽及其用途 |
NL2006359C2 (en) * | 2011-03-08 | 2012-04-24 | Bird Engineering B V | Genetically modified cell and process for use of said cell. |
CN105658796B (zh) | 2012-12-12 | 2021-10-26 | 布罗德研究所有限公司 | 用于序列操纵的crispr-cas组分系统、方法以及组合物 |
US9937207B2 (en) | 2013-03-21 | 2018-04-10 | Sangamo Therapeutics, Inc. | Targeted disruption of T cell receptor genes using talens |
NL2011027C2 (en) * | 2013-06-24 | 2014-12-29 | Univ Delft Tech | Process for the preparation of 2,5-furandicarboxylic acid. |
AU2016220612B2 (en) * | 2015-02-17 | 2021-09-30 | Purac Biochem B.V. | Dehydrogenase-catalysed production of FDCA |
EP3378931A1 (en) * | 2017-03-21 | 2018-09-26 | Purac Biochem B.V. | Fdca-decarboxylating monooxygenase-deficient host cells for producing fdca |
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2020
- 2020-03-02 CN CN202080032050.1A patent/CN113748211A/zh active Pending
- 2020-03-02 WO PCT/BR2020/050064 patent/WO2020176958A1/en unknown
- 2020-03-02 JP JP2021551764A patent/JP2022523540A/ja active Pending
- 2020-03-02 EP EP20717077.0A patent/EP3921435A1/en active Pending
- 2020-03-02 KR KR1020217030955A patent/KR20210136044A/ko unknown
- 2020-03-02 CA CA3132051A patent/CA3132051A1/en active Pending
- 2020-03-02 MX MX2021010457A patent/MX2021010457A/es unknown
- 2020-03-02 BR BR112021016818A patent/BR112021016818A2/pt unknown
- 2020-03-02 US US16/806,728 patent/US11339414B2/en active Active
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2021
- 2021-02-01 US US17/163,838 patent/US11566269B2/en active Active
- 2021-03-31 US US17/219,792 patent/US11566270B2/en active Active
- 2021-12-08 US US17/545,616 patent/US12006523B2/en active Active
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2022
- 2022-05-20 US US17/750,293 patent/US20220298535A1/en active Pending
Also Published As
Publication number | Publication date |
---|---|
JP2022523540A (ja) | 2022-04-25 |
CN113748211A (zh) | 2021-12-03 |
CA3132051A1 (en) | 2020-09-10 |
US12006523B2 (en) | 2024-06-11 |
KR20210136044A (ko) | 2021-11-16 |
US11566270B2 (en) | 2023-01-31 |
US20220298535A1 (en) | 2022-09-22 |
EP3921435A1 (en) | 2021-12-15 |
US20210238639A1 (en) | 2021-08-05 |
WO2020176958A1 (en) | 2020-09-10 |
US20200277639A1 (en) | 2020-09-03 |
US20220090153A1 (en) | 2022-03-24 |
MX2021010457A (es) | 2021-12-10 |
US11339414B2 (en) | 2022-05-24 |
US11566269B2 (en) | 2023-01-31 |
US20210222217A1 (en) | 2021-07-22 |
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