Engineering of Escherichia coli for Krebs cycle-dependent production of malic acid.
Jean Marie FrançoisClément AuriolAudrey BaylacRomain IragueClémentine DressaireMarc Carnicer-HerasStéphanie HeuxJean Marie FrançoisThomas WaltherPublished in: Microbial cell factories (2018)
Since more NAD(P)H and ATP cofactors are generated in the Krebs cycle-dependent malate production when compared to pathways which depend on the function of anaplerotic PEP carboxylase or PEP carboxykinase enzymes, the engineered strain developed in this study can serve as a platform to increase biosynthesis of malate-derived metabolites such as 2,4-dihydroxybutyric acid.