Systematic Metabolic Engineering for Enhanced Cytidine 5′-Monophosphate Production in Escherichia coli

被引:1
作者
Dong, Tiantian [1 ,2 ]
Shen, Wei [1 ,3 ]
Xia, Yuanyuan [1 ,3 ]
Chen, Xianzhong [1 ,3 ]
Yang, Haiquan [1 ,2 ]
机构
[1] Jiangnan Univ, Minist Educ, Sch Biotechnol, Wuxi 214122, Peoples R China
[2] Jiangnan Univ, Minist Educ, Key Lab Carbohydrate Chem & Biotechnol, Wuxi 214122, Peoples R China
[3] Jiangnan Univ, Minist Educ, Key Lab Ind Biotechnol, Wuxi 214122, Peoples R China
关键词
5 '-CMP; green production; Escherichiacoli; systematic metabolic engineering; SUBSTRATE SPECIFICITIES; UMP-KINASE; IDENTIFICATION; EXPRESSION; PHOSPHATASE; DEAMINASE; MUTANTS; URIDINE; ENZYME; GENES;
D O I
10.1021/acs.jafc.4c09127
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Cytidine 5 '-monophosphate (5 '-CMP) is a key intermediate in various nucleotide derivatives and is widely used in the food and pharmaceutical industries. In this study, the titer of 5 '-CMP in engineered Escherichia coli CM006, which blocks the degradation pathway of 5 '-CMP, increased 134.7-fold compared to E. coli MG1655. Integrated expression of the 5 '-CMP diphosphate hydrolase gene nudG significantly enhanced the 5 '-CMP titer, reduced orotic acid accumulation, and alleviated feedback inhibition in the 5 '-CMP synthesis pathway. By blocking cytidine degradation and increasing carbon flux from cytidine to 5 '-CMP, the 5 '-CMP titer in E. coli CM011 was increased to 338.2 mg/L. Furthermore, by enhancing the supply of the precursor 5-phospho-alpha-D-ribose 1-diphosphate (PRPP), the 5 '-CMP titer in E. coli CM012 reached 417.9 mg/L, the highest value reported to date. The results and methods presented in this study are of great significance for the sustainable industrial production of 5 '-CMP.
引用
收藏
页码:27346 / 27354
页数:9
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