Multidimensional engineering of Escherichia coli for efficient synthesis of L-tryptophan

被引:9
|
作者
Tang, Mi [1 ,2 ]
Pan, Xuewei [1 ,2 ]
Yang, Tianjin [1 ,2 ]
You, Jiajia [1 ,2 ]
Zhu, Rongshuai [1 ,2 ]
Yang, Taowei [1 ,2 ]
Zhang, Xian [1 ,2 ]
Xu, Meijuan [1 ,2 ]
Rao, Zhiming [1 ,2 ]
机构
[1] Jiangnan Univ, Sch Biotechnol, Lab Appl Microorganisms & Metab Engn, Key Lab Ind Biotechnol,Minist Educ, Wuxi 214122, Peoples R China
[2] Yixing Inst Food & Biotechnol Co Ltd, Yixing 214200, Peoples R China
基金
中国国家自然科学基金;
关键词
Escherichia coli; L-tryptophan; Riboswitch; High-throughput screening; Multidimensional engineering; GENE-EXPRESSION; DESIGN; BIOSENSOR; BIOSYNTHESIS; IMPROVEMENT; RIBOSWITCH; SEQUENCE; PLATFORM;
D O I
10.1016/j.biortech.2023.129475
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
Development of microbial cell factory for L-tryptophan (L-trp) production has received widespread attention but still requires extensive efforts due to weak metabolic flux distribution and low yield. Here, the riboswitch-based high-throughput screening (HTS) platform was established to construct a powerful L-trp-producing chassis cell. To facilitate L-trp biosynthesis, gene expression was regulated by promoter and N-terminal coding sequences (NCS) engineering. Modules of degradation, transport and by-product synthesis related to L-trp production were also fine-tuned. Next, a novel transcription factor YihL was excavated to negatively regulate L-trp biosynthesis. Self-regulated promoter-mediated dynamic regulation of branch pathways was performed and cofactor supply was improved for further L-trp biosynthesis. Finally, without extra addition, the yield of strain Trp30 reached 42.5 g/L and 0.178 g/g glucose after 48 h of cultivation in 5-L bioreactor. Overall, strategies described here worked up a promising method combining HTS and multidimensional regulation for developing cell factories for products in interest.
引用
收藏
页数:10
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