Reduction of Aerobic Acetate Production by Escherichia Coli
Overview
Microbiology
Authors
Affiliations
Acetate excretion by Escherichia coli during aerobic growth on glucose is a major obstacle to enhanced recombinant protein production. We report here that the fraction of carbon flux through the anaplerotic pathways is one of the factors influencing acetate excretion. Flux analysis of E. coli central metabolic pathways predicts that increasing the fraction of carbon flux through the phosphoenolpyruvate carboxylase (PPC) pathway and the glyoxylate bypass reduces acetate production. We tested this prediction by overexpressing PPC and deregulating the glyoxylate bypass by using a fadR strain. Results show that the acetate yield by the fadR strain with PPC overexpression is decreased more than fourfold compared to the control, while the biomass yield is relatively unaffected. Apparently, the fraction of carbon flux through the anaplerotic pathways is one of the factors that influence acetate excretion. These results confirm the prediction of our flux analysis and further suggest that E. coli is not fully optimized for efficient utilization of glucose.
A respiro-fermentative strategy to survive nanoxia in Acidobacterium capsulatum.
Trojan D, Garcia-Robledo E, Hausmann B, Revsbech N, Woebken D, Eichorst S FEMS Microbiol Ecol. 2024; 100(12).
PMID: 39557655 PMC: 11636273. DOI: 10.1093/femsec/fiae152.
Yang Y, Zou Y, Chen X, Sun H, Hua X, Johnston L Biotechnol Biofuels Bioprod. 2024; 17(1):82.
PMID: 38886801 PMC: 11184883. DOI: 10.1186/s13068-024-02530-4.
Gecse G, Labunskaite R, Pedersen M, Kilstrup M, Johanson T Front Bioeng Biotechnol. 2024; 12:1339054.
PMID: 38419731 PMC: 10899681. DOI: 10.3389/fbioe.2024.1339054.
Application of cofactors in the regulation of microbial metabolism: A state of the art review.
Sun Y, Zhang T, Lu B, Li X, Jiang L Front Microbiol. 2023; 14:1145784.
PMID: 37113222 PMC: 10126289. DOI: 10.3389/fmicb.2023.1145784.
Combined metabolic analyses for the biosynthesis pathway of l-threonine in .
Yang Q, Cai D, Chen W, Chen H, Luo W Front Bioeng Biotechnol. 2022; 10:1010931.
PMID: 36159692 PMC: 9500239. DOI: 10.3389/fbioe.2022.1010931.