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Amino acid production

An amino acid and lysine technology, applied in the direction of microorganism-based methods, microorganisms, acyltransferase, etc., can solve problems such as rising

Inactive Publication Date: 2020-03-03
EVONIK DEGUSSA GMBH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Also, since the cost of these starting materials will be correlated to oil prices (which are expected to rise in future oil prices), the price of methionine will also increase relative to the increase in oil prices

Method used

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  • Amino acid production
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  • Amino acid production

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0180] Formation of o-acetyl-L-homoserine from ethane using Escherichia coli.

[0181] 对于乙烷至o-乙酰基-L-高丝氨酸的生物转化,使用遗传修饰的菌株大肠杆菌CGSC 12149 lysCfbr_Ec thrAfbr_Ec pACYC184{PalkS}[alkS_PpGPo1]{PalkB}[bmoXYBZ_Tb PROKKA_02001_Tb PROKKA_02000_Tb bmoC_1_Tb PROKKA_01998_Tb bmoG_Tb]pBR322{PalkS} [alkS_PpGPo1]{PalkB}[adhA_Cg aldH_Cg]{Placuv5}[metX_Cg]{Ptac}[thrA_fbr_Ec]. This strain has the following characteristics:

[0182] i. Modification of the E. coli CGSC 12149 lysC gene (SEQ ID NO: 33) encoding a feedback-resistant variant of aspartokinase 3.

[0183] ii. Modification of the E. coli CGSC 12149 thrA gene (SEQ ID NO: 34) encoding a feedback-resistant variant of the bifunctional aspartokinase 1 / homoserine dehydrogenase 1 (using the native promoter).

[0184] iii. Thauera butanivorans DSM 2080 butane monooxygenase operon (SEQ ID NO: 35) expression, said operon comprises bmoX_Tb (butane monooxygenase hydroxylase BMOH α subunit), bmoY_Tb (butane monooxygenase BMOH α subunit), bmoY_Tb (but...

Embodiment 2

[0329] Formation of lysine from ethane using Escherichia coli.

[0330] 对于乙烷至L-赖氨酸的生物转化,使用遗传修饰的菌株大肠杆菌CGSC 12149lysCfbr_Ec thrAfbr_Ec pACYC184{PalkS}[alkS_PpGPo1]{PalkB}[bmoXYBZ_Tb PROKKA_02001_Tb PROKKA_02000_Tb bmoC_1_Tb PROKKA_01998_Tb bmoG_Tb]pBR322{PalkS}[alkS_PpGPo1]{PalkB }[adhA_Cg aldH_Cg]{Placuv5}[metX_Cg]{Ptac}[thrA_fbr_Ec]. This strain has the following characteristics:

[0331] i) Modification of the E. coli CGSC 12149 lysC gene (SEQ ID NO: 33) encoding a feedback-resistant variant of aspartokinase 3.

[0332] ii) Expression of Thauera butanivorans DSM 2080 butane monooxygenase operon (SEQ ID NO: 35) comprising bmoX_Tb (butane monooxygenase hydroxylase BMOH alpha subunit), bmoY_Tb (butane monooxygenase bmoZ_Tb (butane monooxygenase gamma subunit), bmoB_Tb (butane monooxygenase regulatory protein), bmoC_1_Tb (butane monooxygenase reductase), bmoG_Tb (similar to groEL of Escherichia coli) and three putative ORFs PROKKA_02001_Tb, PROKKA_02000_Tb and PROKKA_01998_Tb. ...

Embodiment 3

[0353] As listed in Table 1, different amino acids were produced by various bacteria in which the expression of specific enzymes was increased as referenced in the table. An alkane mixture comprising ethane, propane and butane in a weight ratio of 1:1:1 was used as alkane. All enzyme entries are NCBI accession numbers. For enzymes E6 of types E6a, E6c, E6e, E6k, E61 and E6s, feedback insensitive variants of the indicated sequences can also be used.

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Abstract

The present invention relates to amino acid production. The invention relates to a microbial cell for producing at least one L-amino acid from at least one C1-C4 alkane, wherein the cell comprises: (i) an increased expression relative to the wild type cell of Enzyme E1 capable of converting the alkane to a corresponding 1-alkanol; (ii) an increased expression relative to the wild type cell of Enzyme E2 capable of converting the 1-alkanol of (i) to a corresponding aldehyde; and either (iii) (A) an increased expression relative to the wild type cell of Enzyme E3 capable of converting the aldehyde of (ii) to a corresponding alkanoic acid; and a wild-type level expression of Enzyme E4 or an increased expression relative to the wild type cell of Enzyme E4 capable of converting the alkanoic acidof (iii) to a corresponding fatty acyl thioester; or (B) an increased expression relative to the wild type cell of Enzyme E5 capable of converting the aldehyde of (ii) to a corresponding fatty acyl thioester; and(iv) an increased expression relative to the wild type cell of Enzyme E6 capable of converting the fatty acyl thioester of (iii) to a corresponding amino acid.

Description

technical field [0001] The present invention relates to a biotechnological process for the production of amino acids. In particular, the method makes it possible to use alkanes as starting materials for the production of L-amino acids. Background technique [0002] Amino acids are particularly useful as additives in animal feed and as nutritional supplements for humans. They can also be used in infusion solutions and can function as synthetic intermediates used in the manufacture of pharmaceuticals and agricultural chemicals. Compounds such as methionine, lysine, tryptophan and threonine are generally produced industrially for use as food or feed additives and in pharmaceuticals. Specifically, the essential amino acid methionine, which cannot be synthesized by animals, plays an important role in many bodily functions. L-methionine is currently produced by chemical synthesis from hydrogen cyanide, acrolein and methyl mercaptan. These petroleum-based starting materials suc...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N1/21C12N1/19C12N1/13C12P13/08C12P13/06C12R1/01C12R1/07C12R1/13C12R1/89C12R1/145C12R1/15C12R1/185C12R1/22C12R1/38C12R1/42C12R1/41C12R1/865C12R1/84C12R1/125C12R1/39C12R1/40
CPCC12N9/0006C12N9/0008C12N9/0016C12N9/0036C12N9/0071C12N9/0073C12N9/0077C12N9/0083C12N9/0093C12N9/1029C12N9/1217C12N9/88C12N9/93C12P13/06C12P13/08C12Y101/01001C12Y101/01002C12Y101/0302C12Y101/99C12Y102/01003C12Y102/01004C12Y102/01005C12Y102/0101C12Y102/01011C12Y104/01016C12Y114/13025C12Y114/15003C12Y114/18003C12Y114/99039C12Y203/01008C12Y203/01019C12Y203/01038C12Y203/01039C12Y207/02001C12Y207/02004C12Y207/02007C12Y207/02012C12Y207/02015C12Y401/0102C12Y401/01031C12Y602/01001C12Y602/01002C12Y602/01003C12Y602/0102C12Y604/01001C12N15/52C12P13/04C12N1/20
Inventor P·恩格尔S·沙菲尔O·图姆H·安德烈C·格林B·格伦德
Owner EVONIK DEGUSSA GMBH