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Enhancement of riboflavin production with Bacillus subtilis by expression and site-directed mutagenesis of zwf and gnd gene from Corynebacterium glutamicum
Authors:Wang Zhiwen  Chen Tao  Ma Xianghui  Shen Zhuo  Zhao Xueming
Institution:Key Laboratory of Systems Bioengineering, Ministry of Education, Tianjin University, Tianjin 300072, People’s Republic of China
Edinburg-Tianjin Joint Research Centre for Systems Biology and Synthetic Biology, Tianjin University, Tianjin 300072, People’s Republic of China
Department of Biochemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, People’s Republic of China
Abstract:Zwf (code for glucose-6-phosphate dehydrogenase) and gnd (code for 6-phosphogluconate dehydrogenase) genes from Corynebacterium glutamicum were firstly cloned, and then site-directed mutagenesis was successfully introduced to remove allosteric inhibition by intracellular metabolites. Expression of the mutant zwf and gnd in Bacillus subtilis RH33 resulted in significant enhancement of riboflavin productivity, while the specific growth rate decreased slightly and the specific glucose uptake rate was unchanged. Introduction of the mutant zwf and gnd led to approximately 18% and 22% increased riboflavin production, respectively. An improvement by 31% and 39% of the riboflavin production was obtained by co-expression of the mutated dehydrogenases in shaker flask and fed-batch cultivation. Intracellular metabolites analysis indicated that metabolites detected in pentose phosphate pathway or riboflavin synthesis pathway of engineered strains showed higher concentration, while TCA cycle and glycolysis metabolites detected were lower abundance than that of parent strain.
Keywords:FMN  flavin mononucleotide  FAD  flavin adenine dinucleotide  PPP  pentose phosphate pathway  G6PD  glucose-6-phosphate dehydrogenase  6GPD  6-phosphogluconate dehydrogenase  Ru5P  ribulose-5P  FBP  fructose 1  6-bisphosphate  Gra3P  d-glyceraldehyde 3-phosphate" target="_blank">d-glyceraldehyde 3-phosphate  MM  minimal medium  LB  Luria-Bertani  CDW  cell dry weight  LC-MS/MS  liquid chromatography-tandem quadrupole mass spectrometry  PEP  phosphoenolpyruvate  PRPP  phosphoribosyl pyrophosphate  l-Phe" target="_blank">l-Phe  l-phenylalanine" target="_blank">l-phenylalanine  CM-PDT  chorismate mutase-prephenate dehydratase  TCA  tricarboxylic acid  DPD  dihydropyrimidine dehydrogenase  iXylC  intracellular GH10 xylanase
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