生产过剩
代谢工程
发酵
大肠杆菌
高丝氨酸
生物化学
化学
拉伤
细菌
新陈代谢
碳源
生物
群体感应
基因
解剖
毒力
遗传学
作者
Peng Liu,Ji-Song Liu,Wen-Yuan Zhu,Bo Zhang,Zhi‐Qiang Liu,Yu‐Guo Zheng
标识
DOI:10.1016/j.jbiotec.2020.11.002
摘要
O-Succinyl-l-homoserine (OSH) is an important platform chemical in production of C4 chemicals such as succinic acid, homoserine lactone, γ‑butyrolactone, and 1,4‑butanediol. The production of OSH through chemical method or the current engineering strain is difficult and not optimal, and thereby there remains a need to develop new engineering strategy. Here, we engineered an OSH overproducing Escherichia coli strain through deleting the degradation and competitive pathways, overexpressing thrA and metL to enhance the metabolic flux from l-asparate to l-homoserine. Additionally, increasing the precursor succinyl-CoA supply through simultaneously knocking out sucD and overexpressing sucA further increased the yield of OSH. The engineered strain OSH9/pTrc-metA11-yjeH with above strategies produced OSH at the concentration of 24.1 g/L (0.609 g/g glucose) in batch fermentation. To gain detailed insight into metabolism of the engineered strain, comparative metabolic profiling was performed between the engineered and wide-type strain. The metabolomics data deciphered that the carbon was directed toward the OSH biosynthesis resulting in less flexibility of the genetically modified strain than the wide-type strain.
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