Methods and compositions for amino acid production

A technology of aspartic acid and cystine methyl, applied in the field of microorganisms and molecular biology, can solve problems such as reducing the production efficiency of metabolites

Inactive Publication Date: 2008-06-25
米克罗比亚股份有限公司
View PDF7 Cites 11 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Accumulation of secondary mutations in mutant production strains and derivatives of these strains can

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Methods and compositions for amino acid production
  • Methods and compositions for amino acid production
  • Methods and compositions for amino acid production

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0418] Example 1. Construction of vectors for expression of genes that increase production of aspartic acid-derived amino acids

[0419] Plasmids were generated for the expression of genes involved in the production of aspartic acid-derived amino acids. A number of genes of interest are shown in Figures 1 and 2, which describe the majority of biosynthetic genes directly involved in the production of aspartate-derived amino acids. These plasmids, either autonomously replicating, or integrating into the host Corynebacterium glutamicum chromosome as described, are introduced into strains of Corynebacterium by electroporation as described (seeing Follettie, M.T., et al. J.Bacteriol.167:695-702, 1993). All plasmids contain the kanR gene, which confers kanamycin antibiotic resistance. Transformants were selected on media containing kanamycin (25 mg / L).

[0420] For the expression of episomal plasmids, vectors were constructed using derivatives of the cryptic C. glutamicum low-cop...

Embodiment 2

[0428] Example 2. Isolation of genes for increased production of aspartic acid-derived amino acids

[0429] Wild-type alleles of aspartokinase alpha (lysC-alpha) and beta (lysC-beta) and aspartate semialdehyde dehydrogenase (asd) from Mycobacterium smegmatis (Corynebacterium glutamicum homologues of lysC / asd in Streptomyces coelicolor); genes encoding aspartokinase-asd (lysC-asd), dapA and hom from Streptomyces coelicolor; metA and metYA from Thermobifida fusca and from Erwinia chrysanthemi dapA and ppc, obtained by PCR amplification using genomic DNA isolated from each organism. Furthermore, in some cases, the corresponding wild-type alleles of each gene can be isolated from C. glutamicum. Amplicons were subsequently cloned into pBluescript SK11 - For sequence verification; site-directed mutagenesis is also preferred in these vectors to generate activated alleles in specific instances. Genomic DNA was isolated from M. smegmatis grown in BHI medium at 37°C for 72 hours usin...

Embodiment 3

[0434] Example 3. Targeted Substitutions to Increase Gene Activity Involving Production of Aspartic Acid-Derivatized Amino Acids

[0435] Site-directed mutagenesis was carried out on several pBluescript SKII-plasmids containing the heterologous genes described in Example 2. Site-directed mutagenesis was performed using the QuikChange Site-Directed Mutagenesis Kit from Stratagene. For the heterologous aspartokinase (lysC / ask) gene, substitution mutations were constructed corresponding to the T311I, S301Y, A279P and G345D amino acid substitutions in the C. glutamicum protein. These substitutions reduce feedback inhibition by the combination of lysine and threonine. In all cases, the mutated lysC / ask allele was expressed in one operon together with the heterologous asd gene. The oligonucleotides used to construct the feedback-resistant lysC allele of Mycobacterium smegmatis are: 5'-GGCAAGACCGACATCATATTCACGTGTGCGCGTG-3' (SEQ ID NO: __) and 5'-CACGCGCACACGTGAATATGATGTCGGTCTTGCC-3...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

Methods and compositions for amino acid production using genetically modified bacteria are disclosed.

Description

[0001] Cross reference to related applications [0002] This application claims the benefit of the priority of U.S.S.N. 60 / 475,000 filed May 30, 2003 and U.S.S.N. 60 / 551,860 filed March 10, 2004. The entire contents of these applications are hereby incorporated by reference. technical field [0003] The present invention relates to microorganisms and molecular biology, and more particularly to methods and compositions for the preparation of amino acids. Background technique [0004] Industrial fermentation of bacteria is used commercially to produce useful metabolites such as amino acids, nucleotides, vitamins and antibodies. Many of the bacterial production strains used in these fermentations have been generated by random mutagenesis and selection of mutants (Demain, A.L. Trends Biotechnol. 18:26-31, 2000). Accumulation of secondary mutations in mutant production strains and derivatives of these strains can reduce the efficiency of metabolite production due to altered gro...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
IPC IPC(8): C12N9/00C12N9/12C12N1/20C12N15/00C07H21/04C12N9/02C12N9/14C07K1/00C07H21/02
Inventor 理查德・B・贝利保罗・布洛姆奎斯特里德・多滕爱德华・M・德里格斯凯文・T・马登杰西卡・奥利里乔治・A・奥图尔乔舒亚・特鲁哈特迈克尔・J・沃尔布里奇彼得・约吉
Owner 米克罗比亚股份有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap