JP2016511010A5 - - Google Patents
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- JP2016511010A5 JP2016511010A5 JP2016501949A JP2016501949A JP2016511010A5 JP 2016511010 A5 JP2016511010 A5 JP 2016511010A5 JP 2016501949 A JP2016501949 A JP 2016501949A JP 2016501949 A JP2016501949 A JP 2016501949A JP 2016511010 A5 JP2016511010 A5 JP 2016511010A5
- Authority
- JP
- Japan
- Prior art keywords
- gpd
- recombinant microorganism
- microorganism
- heterologous
- glycerol
- 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.)
- Pending
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- 244000005700 microbiome Species 0.000 claims description 160
- 108010041921 Glycerolphosphate Dehydrogenase Proteins 0.000 claims description 140
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 48
- 230000006696 biosynthetic metabolic pathway Effects 0.000 claims description 38
- 108090000623 proteins and genes Proteins 0.000 claims description 27
- 229930027945 nicotinamide-adenine dinucleotide Natural products 0.000 claims description 23
- 241000235648 Pichia Species 0.000 claims description 18
- 241000235070 Saccharomyces Species 0.000 claims description 17
- 230000037430 deletion Effects 0.000 claims description 17
- 238000012217 deletion Methods 0.000 claims description 17
- BOPGDPNILDQYTO-NNYOXOHSSA-N nicotinamide-adenine dinucleotide Chemical compound C1=CCC(C(=O)N)=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OC[C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC=NC(N)=C3N=C2)O)O1 BOPGDPNILDQYTO-NNYOXOHSSA-N 0.000 claims description 17
- 238000006467 substitution reaction Methods 0.000 claims description 16
- 241000588748 Klebsiella Species 0.000 claims description 12
- 102000004190 Enzymes Human genes 0.000 claims description 11
- 108090000790 Enzymes Proteins 0.000 claims description 11
- AWUCVROLDVIAJX-GSVOUGTGSA-N sn-glycerol 3-phosphate Chemical class OC[C@@H](O)COP(O)(O)=O AWUCVROLDVIAJX-GSVOUGTGSA-N 0.000 claims description 11
- 241000222120 Candida <Saccharomycetales> Species 0.000 claims description 7
- 241000193830 Bacillus <bacterium> Species 0.000 claims description 6
- 241000722885 Brettanomyces Species 0.000 claims description 6
- 241000186146 Brevibacterium Species 0.000 claims description 6
- 241000193403 Clostridium Species 0.000 claims description 6
- 241000186216 Corynebacterium Species 0.000 claims description 6
- 241000194033 Enterococcus Species 0.000 claims description 6
- 241000588698 Erwinia Species 0.000 claims description 6
- 241000588722 Escherichia Species 0.000 claims description 6
- 241000186660 Lactobacillus Species 0.000 claims description 6
- ACFIXJIJDZMPPO-NNYOXOHSSA-N NADPH Chemical compound C1=CCC(C(=O)N)=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OC[C@@H]2[C@H]([C@@H](OP(O)(O)=O)[C@@H](O2)N2C3=NC=NC(N)=C3N=C2)O)O1 ACFIXJIJDZMPPO-NNYOXOHSSA-N 0.000 claims description 6
- 241000235652 Pachysolen Species 0.000 claims description 6
- 241000589516 Pseudomonas Species 0.000 claims description 6
- 241000316848 Rhodococcus <scale insect> Species 0.000 claims description 6
- 241000607142 Salmonella Species 0.000 claims description 6
- 241000235346 Schizosaccharomyces Species 0.000 claims description 6
- 241000607720 Serratia Species 0.000 claims description 6
- 241000607768 Shigella Species 0.000 claims description 6
- 241000235013 Yarrowia Species 0.000 claims description 6
- 241000588901 Zymomonas Species 0.000 claims description 6
- 229940039696 lactobacillus Drugs 0.000 claims description 6
- 240000006439 Aspergillus oryzae Species 0.000 claims description 5
- 235000002247 Aspergillus oryzae Nutrition 0.000 claims description 5
- 241001123652 Candida versatilis Species 0.000 claims description 5
- 241000588724 Escherichia coli Species 0.000 claims description 5
- 102000000587 Glycerolphosphate Dehydrogenase Human genes 0.000 claims 30
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
- 102100036669 Glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic Human genes 0.000 description 104
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 76
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 33
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 25
- 229920001184 polypeptide Polymers 0.000 description 15
- 102000004196 processed proteins & peptides Human genes 0.000 description 15
- 108090000765 processed proteins & peptides Proteins 0.000 description 15
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 12
- 238000000034 method Methods 0.000 description 12
- ROWKJAVDOGWPAT-UHFFFAOYSA-N Acetoin Chemical compound CC(O)C(C)=O ROWKJAVDOGWPAT-UHFFFAOYSA-N 0.000 description 8
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 description 8
- 101710088194 Dehydrogenase Proteins 0.000 description 7
- 108010000200 Ketol-acid reductoisomerase Proteins 0.000 description 6
- 239000000758 substrate Substances 0.000 description 6
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 6
- 229920001791 ((R)-3-Hydroxybutanoyl)(n-2) Polymers 0.000 description 4
- JTEYKUFKXGDTEU-UHFFFAOYSA-N 2,3-dihydroxy-3-methylbutanoic acid Chemical compound CC(C)(O)C(O)C(O)=O JTEYKUFKXGDTEU-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 4
- WTLNOANVTIKPEE-UHFFFAOYSA-N 2-acetyloxypropanoic acid Chemical compound OC(=O)C(C)OC(C)=O WTLNOANVTIKPEE-UHFFFAOYSA-N 0.000 description 4
- QHHKKMYHDBRONY-RMNRSTNRSA-N 3-hydroxybutanoyl-CoA Chemical compound O[C@@H]1[C@H](OP(O)(O)=O)[C@@H](COP(O)(=O)OP(O)(=O)OCC(C)(C)[C@@H](O)C(=O)NCCC(=O)NCCSC(=O)CC(O)C)O[C@H]1N1C2=NC=NC(N)=C2N=C1 QHHKKMYHDBRONY-RMNRSTNRSA-N 0.000 description 4
- QHKABHOOEWYVLI-UHFFFAOYSA-N 3-methyl-2-oxobutanoic acid Chemical compound CC(C)C(=O)C(O)=O QHKABHOOEWYVLI-UHFFFAOYSA-N 0.000 description 4
- 108010000700 Acetolactate synthase Proteins 0.000 description 4
- LCTONWCANYUPML-UHFFFAOYSA-M Pyruvate Chemical compound CC(=O)C([O-])=O LCTONWCANYUPML-UHFFFAOYSA-M 0.000 description 4
- OJFDKHTZOUZBOS-CITAKDKDSA-N acetoacetyl-CoA Chemical compound O[C@@H]1[C@H](OP(O)(O)=O)[C@@H](COP(O)(=O)OP(O)(=O)OCC(C)(C)[C@@H](O)C(=O)NCCC(=O)NCCSC(=O)CC(=O)C)O[C@H]1N1C2=NC=NC(N)=C2N=C1 OJFDKHTZOUZBOS-CITAKDKDSA-N 0.000 description 4
- ZSLZBFCDCINBPY-ZSJPKINUSA-N acetyl-CoA Chemical compound O[C@@H]1[C@H](OP(O)(O)=O)[C@@H](COP(O)(=O)OP(O)(=O)OCC(C)(C)[C@@H](O)C(=O)NCCC(=O)NCCSC(=O)C)O[C@H]1N1C2=NC=NC(N)=C2N=C1 ZSLZBFCDCINBPY-ZSJPKINUSA-N 0.000 description 4
- OWBTYPJTUOEWEK-UHFFFAOYSA-N butane-2,3-diol Chemical compound CC(O)C(C)O OWBTYPJTUOEWEK-UHFFFAOYSA-N 0.000 description 4
- CRFNGMNYKDXRTN-CITAKDKDSA-N butyryl-CoA Chemical compound O[C@@H]1[C@H](OP(O)(O)=O)[C@@H](COP(O)(=O)OP(O)(=O)OCC(C)(C)[C@@H](O)C(=O)NCCC(=O)NCCSC(=O)CCC)O[C@H]1N1C2=NC=NC(N)=C2N=C1 CRFNGMNYKDXRTN-CITAKDKDSA-N 0.000 description 4
- KFWWCMJSYSSPSK-PAXLJYGASA-N crotonoyl-CoA Chemical compound O[C@@H]1[C@H](OP(O)(O)=O)[C@@H](COP(O)(=O)OP(O)(=O)OCC(C)(C)[C@@H](O)C(=O)NCCC(=O)NCCSC(=O)/C=C/C)O[C@H]1N1C2=NC=NC(N)=C2N=C1 KFWWCMJSYSSPSK-PAXLJYGASA-N 0.000 description 4
- GFAZHVHNLUBROE-UHFFFAOYSA-N hydroxymethyl propionaldehyde Natural products CCC(=O)CO GFAZHVHNLUBROE-UHFFFAOYSA-N 0.000 description 4
- 239000003575 carbonaceous material Substances 0.000 description 3
- 108010055682 3-hydroxybutyryl-CoA dehydrogenase Proteins 0.000 description 2
- 102000005345 Acetyl-CoA C-acetyltransferase Human genes 0.000 description 2
- 108010006229 Acetyl-CoA C-acetyltransferase Proteins 0.000 description 2
- 108010021809 Alcohol dehydrogenase Proteins 0.000 description 2
- 102000007698 Alcohol dehydrogenase Human genes 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- 108010068197 Butyryl-CoA Dehydrogenase Proteins 0.000 description 2
- 108090000489 Carboxy-Lyases Proteins 0.000 description 2
- 108700016168 Dihydroxy-acid dehydratases Proteins 0.000 description 2
- 108010023922 Enoyl-CoA hydratase Proteins 0.000 description 2
- 102000011426 Enoyl-CoA hydratase Human genes 0.000 description 2
- 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 description 2
- 102100039894 Hemoglobin subunit delta Human genes 0.000 description 2
- 101001072574 Homo sapiens Glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic Proteins 0.000 description 2
- 108090001042 Hydro-Lyases Proteins 0.000 description 2
- 102000004867 Hydro-Lyases Human genes 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 102100024639 Short-chain specific acyl-CoA dehydrogenase, mitochondrial Human genes 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 108010084631 acetolactate decarboxylase Proteins 0.000 description 2
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 2
- 108010036467 butanediol dehydrogenase Proteins 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000008103 glucose Substances 0.000 description 2
- 150000004715 keto acids Chemical class 0.000 description 2
- 239000013612 plasmid Substances 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 241000190909 Beggiatoa Species 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 206010013142 Disinhibition Diseases 0.000 description 1
- 101000904460 Encephalitozoon cuniculi (strain GB-M1) Probable glycerol-3-phosphate dehydrogenase Proteins 0.000 description 1
- 241000956293 Fulda Species 0.000 description 1
- 102000057621 Glycerol kinases Human genes 0.000 description 1
- 108700016170 Glycerol kinases Proteins 0.000 description 1
- 241000232920 Jaculus orientalis Species 0.000 description 1
- 241000222734 Leishmania mexicana Species 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- RNBGYGVWRKECFJ-ZXXMMSQZSA-N alpha-D-fructofuranose 1,6-bisphosphate Chemical compound O[C@H]1[C@H](O)[C@](O)(COP(O)(O)=O)O[C@@H]1COP(O)(O)=O RNBGYGVWRKECFJ-ZXXMMSQZSA-N 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- FPPNZSSZRUTDAP-UWFZAAFLSA-N carbenicillin Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)C(C(O)=O)C1=CC=CC=C1 FPPNZSSZRUTDAP-UWFZAAFLSA-N 0.000 description 1
- 229960003669 carbenicillin Drugs 0.000 description 1
- 210000000349 chromosome Anatomy 0.000 description 1
- PYLIXCKOHOHGKQ-UHFFFAOYSA-L disodium;hydrogen phosphate;heptahydrate Chemical compound O.O.O.O.O.O.O.[Na+].[Na+].OP([O-])([O-])=O PYLIXCKOHOHGKQ-UHFFFAOYSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229940025237 fructose 1,6-diphosphate Drugs 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- VYQNWZOUAUKGHI-UHFFFAOYSA-N monobenzone Chemical compound C1=CC(O)=CC=C1OCC1=CC=CC=C1 VYQNWZOUAUKGHI-UHFFFAOYSA-N 0.000 description 1
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
- 235000019796 monopotassium phosphate Nutrition 0.000 description 1
- 238000002703 mutagenesis Methods 0.000 description 1
- 231100000350 mutagenesis Toxicity 0.000 description 1
- 230000035772 mutation Effects 0.000 description 1
- 101150112552 plsB gene Proteins 0.000 description 1
- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 1
- 238000002708 random mutagenesis Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361782651P | 2013-03-14 | 2013-03-14 | |
| US61/782,651 | 2013-03-14 | ||
| US201461934096P | 2014-01-31 | 2014-01-31 | |
| US61/934,096 | 2014-01-31 | ||
| PCT/US2014/025714 WO2014160050A1 (en) | 2013-03-14 | 2014-03-13 | Glycerol 3- phosphate dehydrogenase for butanol production |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2016511010A JP2016511010A (ja) | 2016-04-14 |
| JP2016511010A5 true JP2016511010A5 (OSRAM) | 2017-04-13 |
Family
ID=50555264
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016501949A Pending JP2016511010A (ja) | 2013-03-14 | 2014-03-13 | ブタノール製造用のグリセロール３−ホスフェートデヒドロゲナーゼ |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US9441250B2 (OSRAM) |
| EP (1) | EP2970863B1 (OSRAM) |
| JP (1) | JP2016511010A (OSRAM) |
| CN (1) | CN105378057A (OSRAM) |
| AU (1) | AU2014244216A1 (OSRAM) |
| BR (1) | BR112015022612A2 (OSRAM) |
| CA (1) | CA2905912A1 (OSRAM) |
| ES (1) | ES2735024T3 (OSRAM) |
| HU (1) | HUE045200T2 (OSRAM) |
| WO (1) | WO2014160050A1 (OSRAM) |
| ZA (1) | ZA201507360B (OSRAM) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8945899B2 (en) | 2007-12-20 | 2015-02-03 | Butamax Advanced Biofuels Llc | Ketol-acid reductoisomerase using NADH |
| BRPI0808600A2 (pt) | 2007-04-18 | 2018-12-26 | Du Pont | "método para a conversão de acetolactato em dihidroxi-isovalerato, método para a produção de isobutanol, célula hospedeira recombinante e método para a identificação e isolameno de uma construção genética" |
| US8188250B2 (en) * | 2008-04-28 | 2012-05-29 | Butamax(Tm) Advanced Biofuels Llc | Butanol dehydrogenase enzyme from the bacterium Achromobacter xylosoxidans |
| BR112012016042A2 (pt) | 2009-12-29 | 2020-09-15 | Butamax Advanced Biofuels Llc | "celula hospedeira microbiana recombinante, metodo para a produção de isobutanol, método para a produção de 2-butanol e método para a produção de 14-butanol |
| MX357290B (es) | 2010-02-17 | 2018-07-04 | Butamax Tm Advanced Biofuels | Mejoramiento de la actividad de proteínas que requieren centros fe-s. |
| CN105950525A (zh) | 2010-09-07 | 2016-09-21 | 布特马斯先进生物燃料有限责任公司 | 整合编码催化丙酮酸至乙酰乳酸的转化的多肽的多核苷酸 |
| KR20140092759A (ko) | 2011-03-24 | 2014-07-24 | 부타맥스 어드밴스드 바이오퓨얼스 엘엘씨 | 숙주 세포 및 아이소부탄올의 제조 방법 |
| CN104321436A (zh) | 2011-12-30 | 2015-01-28 | 布特马斯先进生物燃料有限责任公司 | 醇类的发酵生产 |
| MX2014011355A (es) | 2012-03-23 | 2014-12-05 | Butamax Advanced Biofuels Llc | Complementacion con acetato de medio para butanologenos. |
| KR20150014953A (ko) | 2012-05-11 | 2015-02-09 | 부타맥스 어드밴스드 바이오퓨얼스 엘엘씨 | 케톨-산 리덕토아이소머라아제 효소 및 사용 방법 |
| AU2013305714A1 (en) | 2012-08-22 | 2015-02-05 | Butamax Advanced Biofuels Llc | Production of fermentation products |
| WO2014047421A1 (en) | 2012-09-21 | 2014-03-27 | Butamax(Tm) Advanced Biofuels Llc | Production of renewable hydrocarbon compositions |
| US9650624B2 (en) | 2012-12-28 | 2017-05-16 | Butamax Advanced Biofuels Llc | DHAD variants for butanol production |
| CA2905912A1 (en) | 2013-03-14 | 2014-10-02 | E. I. Du Pont De Nemours And Company | Glycerol 3- phosphate dehydrogenase for butanol production |
| WO2014151190A1 (en) | 2013-03-15 | 2014-09-25 | Butamax Advanced Biofuels Llc | Dhad variants and methods of screening |
| WO2014144210A2 (en) | 2013-03-15 | 2014-09-18 | Butamax Advanced Biofuels Llc | Competitive growth and/or production advantage for butanologen microorganism |
| WO2016025425A1 (en) | 2014-08-11 | 2016-02-18 | Butamax Advanced Biofuels Llc | Yeast preparations and methods of making the same |
| WO2018106656A1 (en) | 2016-12-06 | 2018-06-14 | Danisco Us Inc | Truncated lpmo enzymes and use thereof |
| WO2019074828A1 (en) | 2017-10-09 | 2019-04-18 | Danisco Us Inc | CELLOBIOSE DEHYDROGENASE VARIANTS AND METHODS OF USE |
| 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 |
| CN112430547B (zh) * | 2020-11-24 | 2022-04-29 | 华中农业大学 | 一种高产乙酰辅酶a的耐酸米曲霉菌株及其应用 |
| CN113247946B (zh) * | 2021-04-22 | 2022-07-05 | 哈尔滨工业大学 | 一种自组装纳米生物催化剂及其制备方法和在丁醇生产中的应用 |
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| US5686276A (en) | 1995-05-12 | 1997-11-11 | E. I. Du Pont De Nemours And Company | Bioconversion of a fermentable carbon source to 1,3-propanediol by a single microorganism |
| AU733534B2 (en) * | 1996-11-13 | 2001-05-17 | E.I. Du Pont De Nemours And Company | Method for the production of 1,3-propanediol by recombinant microorganisms |
| EP1020515A3 (en) | 1999-01-18 | 2002-08-07 | DAICEL CHEMICAL INDUSTRIES, Ltd. | Amino alcohol dehydrogenase, its production and use |
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| US9297028B2 (en) | 2005-09-29 | 2016-03-29 | Butamax Advanced Biofuels Llc | Fermentive production of four carbon alcohols |
| US9303225B2 (en) | 2005-10-26 | 2016-04-05 | Butamax Advanced Biofuels Llc | Method for the production of isobutanol by recombinant yeast |
| US8945899B2 (en) | 2007-12-20 | 2015-02-03 | Butamax Advanced Biofuels Llc | Ketol-acid reductoisomerase using NADH |
| US8273558B2 (en) | 2005-10-26 | 2012-09-25 | Butamax(Tm) Advanced Biofuels Llc | Fermentive production of four carbon alcohols |
| BRPI0619325B8 (pt) | 2005-10-26 | 2020-11-17 | Butamax Advanced Biofuels Llc | célula hospedeira microbiana recombinante e método para produção de isobutanol |
| US8828704B2 (en) | 2006-05-02 | 2014-09-09 | Butamax Advanced Biofuels Llc | Fermentive production of four carbon alcohols |
| US8962298B2 (en) | 2006-05-02 | 2015-02-24 | Butamax Advanced Biofuels Llc | Recombinant host cell comprising a diol dehydratase |
| US7659104B2 (en) | 2006-05-05 | 2010-02-09 | E.I. Du Pont De Nemours And Company | Solvent tolerant microorganisms and methods of isolation |
| US7541173B2 (en) | 2006-06-15 | 2009-06-02 | E.I. Du Pont De Nemours And Company | Solvent tolerant microorganisms and methods of isolation |
| US7741119B2 (en) | 2006-09-28 | 2010-06-22 | E. I. Du Pont De Nemours And Company | Xylitol synthesis mutant of xylose-utilizing zymomonas for ethanol production |
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-
2014
- 2014-03-13 CA CA2905912A patent/CA2905912A1/en not_active Abandoned
- 2014-03-13 JP JP2016501949A patent/JP2016511010A/ja active Pending
- 2014-03-13 WO PCT/US2014/025714 patent/WO2014160050A1/en not_active Ceased
- 2014-03-13 AU AU2014244216A patent/AU2014244216A1/en not_active Abandoned
- 2014-03-13 ES ES14719570T patent/ES2735024T3/es active Active
- 2014-03-13 US US14/208,474 patent/US9441250B2/en active Active
- 2014-03-13 HU HUE14719570A patent/HUE045200T2/hu unknown
- 2014-03-13 EP EP14719570.5A patent/EP2970863B1/en active Active
- 2014-03-13 BR BR112015022612A patent/BR112015022612A2/pt not_active IP Right Cessation
- 2014-03-13 CN CN201480027043.7A patent/CN105378057A/zh active Pending
-
2015
- 2015-10-05 ZA ZA2015/07360A patent/ZA201507360B/en unknown
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2016
- 2016-08-04 US US15/228,770 patent/US9944954B2/en active Active
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