Transport and metabolic engineering of the cell factory Corynebacterium glutamicum

被引:48
作者
Perez-Garcia, Fernando
Wendisch, Volker F. [1 ,2 ]
机构
[1] Bielefeld Univ, Fac Biol, Genet Prokaryotes, Univ Str 25, D-33615 Bielefeld, Germany
[2] Bielefeld Univ, Ctr Biotechnol CeBiTec, Univ Str 25, D-33615 Bielefeld, Germany
关键词
Corynebacterium glutamicum; metabolic engineering; transport engineering; amino acids; CRISPRi; synthetic consortia; E; coli; AMINO-ACID PRODUCTION; IMPROVED FERMENTATIVE PRODUCTION; GAMMA-AMINOBUTYRIC-ACID; L-CITRULLINE PRODUCTION; L-LYSINE; ESCHERICHIA-COLI; GENE-EXPRESSION; GLUCOSE-UTILIZATION; ANAEROBIC GROWTH; ALPHA-AMYLASE;
D O I
10.1093/femsle/fny166
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Corynebacterium glutamicum has a long and successful history in the biotechnological production of the amino acids l-glutamate and l-lysine. In the recent years, C. glutamicum has been engineered for the production of a broad catalog of value-added compounds including organic acids, vitamins, terpenoids and proteins. Moreover, this bacterium has been engineered to realize a flexible carbon source concept enabling product formation from various second generation feedstocks without competing uses in human and animal nutrition. In this review, we highlight transport engineering to improve product export and substrate uptake or to avoid loss of intermediates by excretion as well as the application of new metabolic engineering concepts for C. glutamicum strain development including the use of designed synthetic Escherichia coli-C. glutamicum consortia. As examples, pathway extension of l-lysine and l-glutamate biosynthesis to produce derived value-added chemicals is described. The described examples of C. glutamicum strain engineering reflect strategies to cope with the increasing complexity of biotechnological processes that are required for successful applications in the bioeconomy.
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页数:11
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