Effect of key notes of TCA cycle on L-glutamate production.
- Author:
Zhina QIAO
1
;
Meijuan XU
1
;
Mengfei LONG
1
;
Taowei YANG
1
;
Xian ZHANG
1
;
Nakanishi HIDEKI
1
;
Zhiming RAO
1
Author Information
- Publication Type:Journal Article
- Keywords: CRISPR/dCas9; Corynebacterium glutamicum; glutamic acid; oxaloacetate node; ribosome binding site optimization; α-ketoglutarate node
- MeSH: Citric Acid Cycle; Corynebacterium glutamicum/metabolism*; Glutamic Acid/metabolism*; Metabolic Engineering; Metabolic Networks and Pathways/genetics*
- From: Chinese Journal of Biotechnology 2020;36(10):2113-2125
- CountryChina
- Language:Chinese
- Abstract: Glutamic acid is an important amino acid with wide range of applications and huge market demand. Therefore, by performing transcriptome sequencing and re-sequencing analysis on Corynebacterium glutamicum E01 and high glutamate-producing strain C. glutamicum G01, we identified and selected genes with significant differences in transcription and gene levels in the central metabolic pathway that may have greatly influenced glutamate synthesis and further increased glutamic acid yield. The oxaloacetate node and α-ketoglutarate node play an important role in glutamate synthesis. The oxaloacetate node and α-ketoglutarate node were studied to explore effect on glutamate production. Based on the integrated strain constructed from the above experimental results, the growth rate in a 5-L fermenter was slightly lower than that of the original strain, but the glutamic acid yield after 48 h reached (136.1±5.53) g/L, higher than the original strain (93.53±4.52) g/L, an increase by 45.5%; sugar-acid conversion rate reached 58.9%, an increase of 13.7% compared to 45.2% of the original strain. The application of the above experimental strategy improved the glutamic acid yield and the sugar-acid conversion rate, and provided a theoretical basis for the metabolic engineering of Corynebacterium glutamicum.
