谷氨酸棒杆菌
代谢工程
生物化学
精氨酸
精氨琥珀酸合成酶
生物
操纵子
精氨酸脱氨酶
钩虫贪铜菌
发酵
胍丁胺
氨基酸
突变体
酶
精氨酸酶
细菌
基因
羟基烷酸
遗传学
作者
Zhenqiang Zhao,Mengmeng Cai,Yunran Liu,Mengkai Hu,Fengyu Yang,Rongshuai Zhu,Meijuan Xu,Zhiming Rao
标识
DOI:10.1016/j.biortech.2022.128054
摘要
l-arginine is a semi-essential amino acid that is broadly used as food additives and pharmaceutical intermediates. The synthesis of l-arginine is restricted by complex metabolic mechanisms and suboptimal fermentation conditions. Initially, a mutant strain that accumulated 19.4 g/L l-arginine was generated by random mutagenesis. Subsequently, a mutation of the repressor protein (argRG159D) in the l-arginine operon and glutamate synthase (gltD) with 532-fold upregulation were identified to be vital for l-arginine production by multi-omic analysis. Systematic metabolic engineering was used to modify the strain, which included interfering with α-ketoglutarate dehydrogenase complex (ODHC) activity by knocking out serine/threonine-protein kinase (pknG), enhancing the expression of multiple key enzymes in the l-arginine synthesis pathway, and increasing the availability of intracellular cofactor (NADPH) and energy (ATP). Finally, C. glutamicum ARG12 produced 71.3 g/L l-arginine, with a yield of 0.43 g/g glucose by fermentation optimization. This study provides new ideas to boost l-arginine production.
科研通智能强力驱动
Strongly Powered by AbleSci AI