大肠杆菌
代谢工程
合成生物学
生产(经济)
生物技术
生化工程
计算生物学
生物
工程类
生物化学
经济
基因
宏观经济学
作者
Chenghu Chen,Cong Gao,Guipeng Hu,Wanqing Wei,Xiaoge Wang,Jian Wen,Xiulai Chen,Li Liu,Wei Song,Jing Wu
标识
DOI:10.1021/acssynbio.4c00366
摘要
Salicylate plays a pivotal role as a pharmaceutical intermediate in drugs, such as aspirin and lamivudine. The low catalytic efficiency of key enzymes and the inherent toxicity of salicylates to cells pose significant challenges to large-scale microbial production. In this study, we introduced the salicylate synthase Irp9 into an l-phenylalanine-producing Escherichia coli, constructing the shortest salicylate biosynthetic pathway. Subsequent protein engineering increased the catalytic efficiency of Irp9 by 33.5%. Furthermore, by integrating adaptive evolution with transcriptome analysis, we elucidated the crucial mechanism of efflux proteins in salicylate tolerance. The elucidation of this mechanism guided us in the targeted modification of these transport proteins, achieving a reported maximum level of 3.72 g/L of salicylate in a shake flask. This study highlights the importance of efflux proteins for enhancing the productivity of microbial cell factories in salicylate production, which also holds potential for application in the green synthesis of other phenolic acids.
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