Toward Genome-Based Metabolic Engineering in Bacteria

被引:6
|
作者
Oesterle, Sabine [1 ]
Wuethrich, Irene [1 ]
Panke, Sven [1 ]
机构
[1] Swiss Fed Inst Technol, Basel, Switzerland
关键词
ESCHERICHIA-COLI; CORYNEBACTERIUM-GLUTAMICUM; BACILLUS-SUBTILIS; HOMOLOGOUS RECOMBINATION; RECOMBINEERING SYSTEM; ENHANCED PRODUCTION; LACTOCOCCUS-LACTIS; PROTEIN EXPRESSION; ETHANOL-PRODUCTION; SYNTHETIC BIOLOGY;
D O I
10.1016/bs.aambs.2017.07.001
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Prokaryotes modified stably on the genome are of great importance for production of fine and commodity chemicals. Traditional methods for genome engineering have long suffered from imprecision and low efficiencies, making construction of suitable high-producer strains laborious. Here, we review the recent advances in discovery and refinement of molecular precision engineering tools for genome-based metabolic engineering in bacteria for chemical production, with focus on the lambda-Red recombineering and the clustered regularly interspaced short palindromic repeats/Cas9 nuclease systems. In conjunction, they enable the integration of in vitro-synthesized DNA segments into specified locations on the chromosome and allow for enrichment of rare mutants by elimination of unmodified wild-type cells. Combination with concurrently developing improvements in important accessory technologies such as DNA synthesis, high-throughput screening methods, regulatory element design, and metabolic pathway optimization tools has resulted in novel efficient microbial producer strains and given access to new metabolic products. These new tools have made and will likely continue to make a big impact on the bioengineering strategies that transform the chemical industry.
引用
收藏
页码:49 / 82
页数:34
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