Effect of a single-gene knockout on the metabolic regulation in Escherichia coli for D-lactate production under microaerobic condition

• Published in: Metabolic engineering 2005-03, Vol.7 (2), p.104-115
• Main Authors: Zhu, Jiangfeng, Shimizu, Kazuyuki
• Format: Article
• Language: English
• Subjects: Aerobiosis - genetics; Aerobiosis - physiology; Enzyme activity; Escherichia coli; Escherichia coli - genetics; Escherichia coli - metabolism; Escherichia coli Proteins - genetics; Escherichia coli Proteins - metabolism; Gene Deletion; Gene Expression Regulation, Bacterial; Gene Expression Regulation, Enzymologic; Lactate production; Lactic Acid - biosynthesis; Metabolic flux analysis; Metabolite concentration; Pyruvate metabolism
• ISSN: 1096-7176; 1096-7184
• DOI: 10.1016/j.ymben.2004.10.004

The effects of several single-gene knockout mutants ( pykF, ppc, pflA, pta, and adhE mutants) on the metabolic flux distribution in Escherichia coli were investigated under microaerobic condition. The intracellular metabolite concentrations and enzyme activities were measured, and the metabolic flux distribution was computed to study the metabolic regulation in the cell. The pflA, pta and ppc mutants produced large amount of lactate when using glucose as a carbon source under microaerobic condition. Comparing the flux distribution and the enzyme activities in the mutants, it was shown that the lactate production was promoted by the inactivation of pyruvate formate lyase and the resulting overexpression of lactate dehydrogenase. The flux through Pta–Ack pathways and the ethanol production were limited by the available acetyl coenzyme A. It was shown that the glycolysis was activated in pykF mutant in microaerobic culture. The glycolytic flux was related with Pyk activity except for pykF mutant. The cell growth rate was shown to be affected by the flux through phosphoenolpyruvate carboxylase. The quantitative regulation analysis was made based on the deviation indexes.