AU2013246405B2 - Microbial production of alkanolamides and amidoamines and uses thereof - Google Patents
Microbial production of alkanolamides and amidoamines and uses thereof Download PDFInfo
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- AU2013246405B2 AU2013246405B2 AU2013246405A AU2013246405A AU2013246405B2 AU 2013246405 B2 AU2013246405 B2 AU 2013246405B2 AU 2013246405 A AU2013246405 A AU 2013246405A AU 2013246405 A AU2013246405 A AU 2013246405A AU 2013246405 B2 AU2013246405 B2 AU 2013246405B2
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- 238000004519 manufacturing process Methods 0.000 title claims description 30
- 230000000813 microbial effect Effects 0.000 title claims description 4
- 150000002193 fatty amides Chemical class 0.000 claims abstract description 192
- 244000005700 microbiome Species 0.000 claims abstract description 138
- 238000000034 method Methods 0.000 claims abstract description 83
- -1 acyl thioester Chemical class 0.000 claims abstract description 59
- 238000006243 chemical reaction Methods 0.000 claims abstract description 28
- 238000012258 culturing Methods 0.000 claims abstract description 9
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 140
- 102000004196 processed proteins & peptides Human genes 0.000 claims description 140
- 229920001184 polypeptide Polymers 0.000 claims description 139
- 150000007523 nucleic acids Chemical group 0.000 claims description 77
- 108090000623 proteins and genes Proteins 0.000 claims description 72
- 108091028043 Nucleic acid sequence Proteins 0.000 claims description 65
- 239000000194 fatty acid Substances 0.000 claims description 62
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 61
- 229930195729 fatty acid Natural products 0.000 claims description 61
- 150000004665 fatty acids Chemical class 0.000 claims description 58
- 150000003141 primary amines Chemical class 0.000 claims description 46
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 39
- 241000588724 Escherichia coli Species 0.000 claims description 33
- 108020004414 DNA Proteins 0.000 claims description 30
- VWGZHNDNCJLJRW-UHFFFAOYSA-N n-(4-aminobutyl)hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(=O)NCCCCN VWGZHNDNCJLJRW-UHFFFAOYSA-N 0.000 claims description 24
- 239000000758 substrate Substances 0.000 claims description 21
- 108020002982 thioesterase Proteins 0.000 claims description 21
- 102000005488 Thioesterase Human genes 0.000 claims description 20
- 102000040430 polynucleotide Human genes 0.000 claims description 20
- 108091033319 polynucleotide Proteins 0.000 claims description 20
- 239000002157 polynucleotide Substances 0.000 claims description 20
- 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 description 17
- 239000008103 glucose Substances 0.000 claims description 17
- 101150071111 FADD gene Proteins 0.000 claims description 15
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 claims description 15
- 150000001413 amino acids Chemical group 0.000 claims description 14
- 230000001851 biosynthetic effect Effects 0.000 claims description 14
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- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 claims description 11
- 230000015572 biosynthetic process Effects 0.000 claims description 10
- 241000233866 Fungi Species 0.000 claims description 9
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims description 9
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 claims description 9
- IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical compound CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 claims description 9
- 150000002185 fatty acyl-CoAs Chemical group 0.000 claims description 9
- 241000193830 Bacillus <bacterium> Species 0.000 claims description 8
- 239000005700 Putrescine Substances 0.000 claims description 8
- 101710198056 Serine decarboxylase Proteins 0.000 claims description 8
- 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 claims description 8
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 claims description 8
- 230000002018 overexpression Effects 0.000 claims description 8
- FWMNVWWHGCHHJJ-SKKKGAJSSA-N 4-amino-1-[(2r)-6-amino-2-[[(2r)-2-[[(2r)-2-[[(2r)-2-amino-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoyl]amino]hexanoyl]piperidine-4-carboxylic acid Chemical compound C([C@H](C(=O)N[C@H](CC(C)C)C(=O)N[C@H](CCCCN)C(=O)N1CCC(N)(CC1)C(O)=O)NC(=O)[C@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 FWMNVWWHGCHHJJ-SKKKGAJSSA-N 0.000 claims description 6
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- 239000001963 growth medium Substances 0.000 claims description 6
- 108091032973 (ribonucleotides)n+m Proteins 0.000 claims description 5
- FAXDZWQIWUSWJH-UHFFFAOYSA-N 3-methoxypropan-1-amine Chemical compound COCCCN FAXDZWQIWUSWJH-UHFFFAOYSA-N 0.000 claims description 5
- 235000014469 Bacillus subtilis Nutrition 0.000 claims description 5
- 241000195493 Cryptophyta Species 0.000 claims description 5
- 102100037611 Lysophospholipase Human genes 0.000 claims description 5
- IWBKAHRYLFPHRI-UHFFFAOYSA-N N-(4-amino-2-hydroxybutyl)tetradecanamide Chemical compound CCCCCCCCCCCCCC(=O)NCC(O)CCN IWBKAHRYLFPHRI-UHFFFAOYSA-N 0.000 claims description 5
- 241000235015 Yarrowia lipolytica Species 0.000 claims description 5
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 claims description 4
- ASUDFOJKTJLAIK-UHFFFAOYSA-N 2-methoxyethanamine Chemical compound COCCN ASUDFOJKTJLAIK-UHFFFAOYSA-N 0.000 claims description 4
- 244000063299 Bacillus subtilis Species 0.000 claims description 4
- WUGQZFFCHPXWKQ-UHFFFAOYSA-N Propanolamine Chemical compound NCCCO WUGQZFFCHPXWKQ-UHFFFAOYSA-N 0.000 claims description 4
- 241000196250 Prototheca Species 0.000 claims description 4
- 241000588625 Acinetobacter sp. Species 0.000 claims description 3
- 241000192700 Cyanobacteria Species 0.000 claims description 3
- 241000644323 Escherichia coli C Species 0.000 claims description 3
- 241000901842 Escherichia coli W Species 0.000 claims description 3
- LTYOQGRJFJAKNA-KKIMTKSISA-N Malonyl CoA Natural products S(C(=O)CC(=O)O)CCNC(=O)CCNC(=O)[C@@H](O)C(CO[P@](=O)(O[P@](=O)(OC[C@H]1[C@@H](OP(=O)(O)O)[C@@H](O)[C@@H](n2c3ncnc(N)c3nc2)O1)O)O)(C)C LTYOQGRJFJAKNA-KKIMTKSISA-N 0.000 claims description 3
- 241000192041 Micrococcus Species 0.000 claims description 3
- 241001074118 Prototheca moriformis Species 0.000 claims description 3
- 241001597169 Prototheca stagnorum Species 0.000 claims description 3
- 241000223252 Rhodotorula Species 0.000 claims description 3
- 241000122973 Stenotrophomonas maltophilia Species 0.000 claims description 3
- 241000187432 Streptomyces coelicolor Species 0.000 claims description 3
- 241000192560 Synechococcus sp. Species 0.000 claims description 3
- LTYOQGRJFJAKNA-DVVLENMVSA-N malonyl-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)=O)O[C@H]1N1C2=NC=NC(N)=C2N=C1 LTYOQGRJFJAKNA-DVVLENMVSA-N 0.000 claims description 3
- 241000928234 uncultured bacterium RM44 Species 0.000 claims description 3
- OSJPPGNTCRNQQC-UWTATZPHSA-N 3-phospho-D-glyceric acid Chemical compound OC(=O)[C@H](O)COP(O)(O)=O OSJPPGNTCRNQQC-UWTATZPHSA-N 0.000 claims description 2
- 241000589291 Acinetobacter Species 0.000 claims description 2
- 102100022089 Acyl-[acyl-carrier-protein] hydrolase Human genes 0.000 claims description 2
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 claims description 2
- 241001148070 Vibrio furnissii Species 0.000 claims description 2
- LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 claims description 2
- 235000021588 free fatty acids Nutrition 0.000 claims description 2
- 230000034659 glycolysis Effects 0.000 claims description 2
- 108010047495 alanylglycine Proteins 0.000 claims 4
- XOLLWQIBBLBAHQ-WDSOQIARSA-N Trp-Pro-Leu Chemical compound [H]N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(O)=O XOLLWQIBBLBAHQ-WDSOQIARSA-N 0.000 claims 3
- ZVFVBBGVOILKPO-WHFBIAKZSA-N Ala-Gly-Ala Chemical compound C[C@H](N)C(=O)NCC(=O)N[C@@H](C)C(O)=O ZVFVBBGVOILKPO-WHFBIAKZSA-N 0.000 claims 2
- KHGPWGKPYHPOIK-QWRGUYRKSA-N Asp-Gly-Phe Chemical compound [H]N[C@@H](CC(O)=O)C(=O)NCC(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O KHGPWGKPYHPOIK-QWRGUYRKSA-N 0.000 claims 2
- AAKRWBIIGKPOKQ-ONGXEEELSA-N Leu-Val-Gly Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)NCC(O)=O AAKRWBIIGKPOKQ-ONGXEEELSA-N 0.000 claims 2
- AJHCSUXXECOXOY-UHFFFAOYSA-N N-glycyl-L-tryptophan Natural products C1=CC=C2C(CC(NC(=O)CN)C(O)=O)=CNC2=C1 AJHCSUXXECOXOY-UHFFFAOYSA-N 0.000 claims 2
- BRGQQXQKPUCUJQ-KBIXCLLPSA-N Ser-Glu-Ile Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O BRGQQXQKPUCUJQ-KBIXCLLPSA-N 0.000 claims 2
- AYHNXCJKBLYVOA-KSZLIROESA-N Val-Trp-Pro Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC1=CNC2=CC=CC=C21)C(=O)N3CCC[C@@H]3C(=O)O)N AYHNXCJKBLYVOA-KSZLIROESA-N 0.000 claims 2
- KOSRFJWDECSPRO-UHFFFAOYSA-N alpha-L-glutamyl-L-glutamic acid Natural products OC(=O)CCC(N)C(=O)NC(CCC(O)=O)C(O)=O KOSRFJWDECSPRO-UHFFFAOYSA-N 0.000 claims 2
- 108010060035 arginylproline Proteins 0.000 claims 2
- 108010055341 glutamyl-glutamic acid Proteins 0.000 claims 2
- 108010049041 glutamylalanine Proteins 0.000 claims 2
- 108010005942 methionylglycine Proteins 0.000 claims 2
- 108010070643 prolylglutamic acid Proteins 0.000 claims 2
- 108010026333 seryl-proline Proteins 0.000 claims 2
- 241001300301 uncultured bacterium Species 0.000 claims 2
- QPUQFUKWLQUBQJ-ZQIUZPCESA-N (2s)-2-[[2-[[(2s)-2-[[(2s)-1-(2-aminoacetyl)pyrrolidine-2-carbonyl]amino]-4-methylpentanoyl]amino]acetyl]amino]-3-methylbutanoic acid Chemical compound CC(C)[C@@H](C(O)=O)NC(=O)CNC(=O)[C@H](CC(C)C)NC(=O)[C@@H]1CCCN1C(=O)CN QPUQFUKWLQUBQJ-ZQIUZPCESA-N 0.000 claims 1
- KJJPLEZQSCZCKE-UHFFFAOYSA-N 2-aminopropane-1,3-diol Chemical compound OCC(N)CO KJJPLEZQSCZCKE-UHFFFAOYSA-N 0.000 claims 1
- GXIURPTVHJPJLF-UWTATZPHSA-N 2-phospho-D-glyceric acid Chemical compound OC[C@H](C(O)=O)OP(O)(O)=O GXIURPTVHJPJLF-UWTATZPHSA-N 0.000 claims 1
- LFLUCDOSQPJJBE-UHFFFAOYSA-N 3-phosphonooxypyruvic acid Chemical compound OC(=O)C(=O)COP(O)(O)=O LFLUCDOSQPJJBE-UHFFFAOYSA-N 0.000 claims 1
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Natural products CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 claims 1
- LGQPPBQRUBVTIF-JBDRJPRFSA-N Ala-Ala-Ile Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O LGQPPBQRUBVTIF-JBDRJPRFSA-N 0.000 claims 1
- ODWSTKXGQGYHSH-FXQIFTODSA-N Ala-Arg-Ala Chemical compound C[C@H](N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(O)=O ODWSTKXGQGYHSH-FXQIFTODSA-N 0.000 claims 1
- FSBCNCKIQZZASN-GUBZILKMSA-N Ala-Arg-Met Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCSC)C(O)=O FSBCNCKIQZZASN-GUBZILKMSA-N 0.000 claims 1
- YWWATNIVMOCSAV-UBHSHLNASA-N Ala-Arg-Phe Chemical compound NC(=N)NCCC[C@H](NC(=O)[C@@H](N)C)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 YWWATNIVMOCSAV-UBHSHLNASA-N 0.000 claims 1
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- CCDFBRZVTDDJNM-GUBZILKMSA-N Ala-Leu-Glu Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(O)=O CCDFBRZVTDDJNM-GUBZILKMSA-N 0.000 claims 1
- DCVYRWFAMZFSDA-ZLUOBGJFSA-N Ala-Ser-Ala Chemical compound [H]N[C@@H](C)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(O)=O DCVYRWFAMZFSDA-ZLUOBGJFSA-N 0.000 claims 1
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- YYOVLDPHIJAOSY-DCAQKATOSA-N Arg-Ala-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCCN=C(N)N YYOVLDPHIJAOSY-DCAQKATOSA-N 0.000 claims 1
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
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| US201261623711P | 2012-04-13 | 2012-04-13 | |
| US61/623,711 | 2012-04-13 | ||
| PCT/US2013/030502 WO2013154721A1 (en) | 2012-04-13 | 2013-03-12 | Microbial production of alkanolamides and amidoamines and uses thereof |
Publications (2)
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| AU2013246405A1 AU2013246405A1 (en) | 2014-10-30 |
| AU2013246405B2 true AU2013246405B2 (en) | 2018-08-02 |
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| AU2013246405B2 (en) | 2012-04-13 | 2018-08-02 | Genomatica, Inc. | Microbial production of alkanolamides and amidoamines and uses thereof |
| WO2015085271A1 (en) | 2013-12-05 | 2015-06-11 | REG Life Sciences, LLC | Microbial production of fatty amines |
| CN105884643B (zh) * | 2016-05-12 | 2018-03-27 | 浙江海正药业股份有限公司 | 一种不饱和脂肪酸酰胺类化合物及其制备方法和用途 |
| CN107022513A (zh) * | 2017-03-17 | 2017-08-08 | 河北美邦工程科技股份有限公司 | 一种重组大肠杆菌菌株生产长链二元酸的方法 |
| CN109082387B (zh) * | 2018-03-14 | 2022-03-18 | 重庆理工大学 | 一种可低温去除高氨氮的异养硝化-好氧反硝化复合菌剂及其应用 |
| EP3844269A4 (en) | 2018-08-31 | 2022-07-27 | Genomatica, Inc. | PRODUCTION OF NON-NATIVE MONO-UNSATURATED FATTY ACIDS IN BACTERIA |
| WO2020176547A1 (en) | 2019-02-25 | 2020-09-03 | Ginkgo Bioworks, Inc. | Biosynthesis of cannabinoids and cannabinoid precursors |
| WO2020185627A1 (en) * | 2019-03-08 | 2020-09-17 | Massachusetts Institute Of Technology | Human gut microbiome-derived biosynthetic enzymes for production of fatty acid amides |
| CN110272839B (zh) * | 2019-05-08 | 2020-10-30 | 江南大学 | 一株不动杆菌及其在生产手性3-环己烯-1-甲酸中的应用 |
| GB202019175D0 (en) * | 2020-12-04 | 2021-01-20 | Univ Tartu | Biosynthesis method |
| US11286467B1 (en) | 2020-12-14 | 2022-03-29 | United Arab Emirates University | System and method for production of fatty acid ethanolamides |
| EP4493675A1 (en) | 2022-03-16 | 2025-01-22 | Genomatica, Inc. | Microorganisms and methods for production of fatty acid derivatives with reduced levels of byproducts |
| WO2023178193A1 (en) | 2022-03-16 | 2023-09-21 | Genomatica, Inc. | Acyl-acp thioesterase variants and uses thereof |
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| US5000000A (en) | 1988-08-31 | 1991-03-19 | University Of Florida | Ethanol production by Escherichia coli strains co-expressing Zymomonas PDC and ADH genes |
| US5028539A (en) | 1988-08-31 | 1991-07-02 | The University Of Florida | Ethanol production using engineered mutant E. coli |
| US5424202A (en) | 1988-08-31 | 1995-06-13 | The University Of Florida | Ethanol production by recombinant hosts |
| US5482846A (en) | 1988-08-31 | 1996-01-09 | University Of Florida | Ethanol production in Gram-positive microbes |
| US5602030A (en) | 1994-03-28 | 1997-02-11 | University Of Florida Research Foundation | Recombinant glucose uptake system |
| US6428767B1 (en) | 1995-05-12 | 2002-08-06 | E. I. Du Pont De Nemours And Company | Method for identifying the source of carbon in 1,3-propanediol |
| US5576282A (en) | 1995-09-11 | 1996-11-19 | The Procter & Gamble Company | Color-safe bleach boosters, compositions and laundry methods employing same |
| MA24136A1 (fr) | 1996-04-16 | 1997-12-31 | Procter & Gamble | Fabrication d'agents de surface . |
| ES2201441T3 (es) | 1997-03-07 | 2004-03-16 | THE PROCTER & GAMBLE COMPANY | Composiciones de blanqueantes que contienen un catalizador metalico del blanqueante, y activadores de blanqueantes y/o acidos percarboxilicos organicos. |
| DE19731881C1 (de) | 1997-07-24 | 1998-10-22 | Henkel Kgaa | Verwendung von Elektrolytgemischen als Sequestriermittel |
| JP4817495B2 (ja) | 1998-05-29 | 2011-11-16 | ニューロサイエンシーズ・リサーチ・ファウンデーション・インコーポレーテッド | 外因性カンナビノイドでの痛みの制御 |
| WO2008100251A1 (en) | 2007-02-13 | 2008-08-21 | Ls9, Inc. | Modified microorganism uses therefor |
| CN101490241A (zh) * | 2006-05-19 | 2009-07-22 | Ls9公司 | 脂肪酸及其衍生物的制备 |
| US20100242345A1 (en) | 2006-05-19 | 2010-09-30 | LS9, Inc | Production of fatty acids & derivatives thereof |
| MX344588B (es) | 2006-05-19 | 2016-12-20 | Reg Life Sciences Llc | Produccion de acidos grasos y derivados de los mismos. |
| BRPI0809345A2 (pt) * | 2007-03-28 | 2014-10-07 | Ls9 Inc | Células recombinantes, composições produzidas por estas, métodos para produzir derivados de ácidos graxos em uma célula recombinante, para aumentar a produção de derivados de ácidos graxos em uma célula recombinante, construto recombinante, vetores, métodos para aumentar a produção de derivados de ácidos graxos em uma célula hospedeira de produção, para produzir derivados de ácidos graxos, derivados de ácidos graxos, composições de biocombustível. |
| US8048654B2 (en) * | 2010-06-09 | 2011-11-01 | Joule Unlimited Technologies, Inc. | Methods and compositions for the recombinant biosynthesis of fatty acids and esters |
| EP2975122B1 (en) | 2008-10-07 | 2018-06-06 | REG Life Sciences, LLC | Method and compositions for producing fatty aldehydes |
| CA2740037C (en) | 2008-10-28 | 2019-06-18 | Ls9, Inc. | Methods for producing a fatty alcohol in a host cell |
| ES2730713T3 (es) | 2008-12-23 | 2019-11-12 | Reg Life Sciences Llc | Métodos y composiciones relacionados con enzimas tioesterasas |
| BRPI1014952A2 (pt) | 2009-04-10 | 2019-09-24 | Ls9 Inc | "composição produzida por um microrganismo e composição de biocombustível." |
| US9133406B2 (en) | 2009-09-25 | 2015-09-15 | REG Life Sciences, LLC | Production of fatty acid derivatives |
| WO2011100667A1 (en) | 2010-02-14 | 2011-08-18 | Ls9, Inc. | Surfactant and cleaning compositions comprising microbially produced branched fatty alcohols |
| AU2013246405B2 (en) | 2012-04-13 | 2018-08-02 | Genomatica, Inc. | Microbial production of alkanolamides and amidoamines and uses thereof |
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