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Controlling the transcription levels of argGH redistributed L-arginine metabolic flux in N-acetylglutamate kinase and ArgR-deregulated Corynebacterium crenatum.
Zhao, Qinqin; Luo, Yuchang; Dou, Wenfang; Zhang, Xian; Zhang, Xiaomei; Zhang, Weiwei; Xu, Meijuan; Geng, Yan; Rao, Zhiming; Xu, Zhenghong.
Afiliación
  • Zhao Q; School of Pharmaceutical Science, Jiangnan University, Wuxi, 214122, People's Republic of China.
  • Luo Y; School of Pharmaceutical Science, Jiangnan University, Wuxi, 214122, People's Republic of China.
  • Dou W; School of Pharmaceutical Science, Jiangnan University, Wuxi, 214122, People's Republic of China.
  • Zhang X; Key Laboratory of Industrial Biotechnology of Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi, 214122, People's Republic of China.
  • Zhang X; School of Pharmaceutical Science, Jiangnan University, Wuxi, 214122, People's Republic of China.
  • Zhang W; School of Pharmaceutical Science, Jiangnan University, Wuxi, 214122, People's Republic of China.
  • Xu M; Key Laboratory of Industrial Biotechnology of Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi, 214122, People's Republic of China.
  • Geng Y; School of Pharmaceutical Science, Jiangnan University, Wuxi, 214122, People's Republic of China.
  • Rao Z; Key Laboratory of Industrial Biotechnology of Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi, 214122, People's Republic of China. raozhm@jiangnan.edu.cn.
  • Xu Z; School of Pharmaceutical Science, Jiangnan University, Wuxi, 214122, People's Republic of China. zhenghxu@jiangnan.edu.cn.
J Ind Microbiol Biotechnol ; 43(1): 55-66, 2016 Jan.
Article en En | MEDLINE | ID: mdl-26521658
ABSTRACT
Corynebacterium crenatum SYPA5-5, an L-arginine high-producer obtained through multiple mutation-screening steps, had been deregulated by the repression of ArgR that inhibits L-arginine biosynthesis at genetic level. Further study indicated that feedback inhibition of SYPA5-5 N-acetylglutamate kinase (CcNAGK) by L-arginine, as another rate-limiting step, could be deregulated by introducing point mutations. Here, we introduced two of the positive mutations (H268N or R209A) of CcNAGK into the chromosome of SYPA5-5, however, resulting in accumulation of large amounts of the intermediates (L-citrulline and L-ornithine) and decreased production of L-arginine. Genetic and enzymatic levels analysis involved in L-arginine biosynthetic pathway of recombinants SYPA5-5-NAGKH268N (H-7) and SYPA5-5-NAGKR209A (R-8) showed that the transcription levels of argGH decreased accompanied with the reduction of argininosuccinate synthase and argininosuccinase activities, respectively, which led to the metabolic obstacle from L-citrulline to L-arginine. Co-expression of argGH with exogenous plasmid in H-7 and R-8 removed this bottleneck and increased L-arginine productivity remarkably. Compared with SYPA5-5, fermentation period of H-7/pDXW-10-argGH (H-7-GH) reduced to 16 h; meanwhile, the L-arginine productivity improved about 63.6%. Fed-batch fermentation of H-7-GH in 10 L bioreactor produced 389.9 mM L-arginine with the productivity of 5.42 mM h(-1). These results indicated that controlling the transcription of argGH was a key factor for regulating the metabolic flux toward L-arginine biosynthesis after deregulating the repression of ArgR and feedback inhibition of CcNAGK, and therefore functioned as another regulatory mode for L-arginine production. Thus, deregulating all these three regulatory modes was a powerful strategy to construct L-arginine high-producing C. crenatum.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Arginina / Proteínas Bacterianas / Transcripción Genética / Fosfotransferasas (aceptor de Grupo Carboxilo) / Corynebacterium / Análisis de Flujos Metabólicos Idioma: En Revista: J Ind Microbiol Biotechnol Asunto de la revista: BIOTECNOLOGIA / MICROBIOLOGIA Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Arginina / Proteínas Bacterianas / Transcripción Genética / Fosfotransferasas (aceptor de Grupo Carboxilo) / Corynebacterium / Análisis de Flujos Metabólicos Idioma: En Revista: J Ind Microbiol Biotechnol Asunto de la revista: BIOTECNOLOGIA / MICROBIOLOGIA Año: 2016 Tipo del documento: Article