谷氨酸棒杆菌
代谢工程
生物化学
精氨酸
转录组
生产(经济)
生物
计算生物学
基因组学
生物技术
合成生物学
氨基酸
生化工程
工程类
细菌
基因组
基因表达
经济
宏观经济学
基因
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.
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