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Engineering of Escherichia coli for Krebs cycle-dependent production of malic acid.

Jean Marie FrançoisClément AuriolAudrey BaylacRomain IragueClémentine DressaireMarc Carnicer-HerasStéphanie HeuxJean Marie FrançoisThomas Walther
Published 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.
Keyphrases
  • escherichia coli
  • ms ms
  • high throughput
  • biofilm formation
  • cell wall
  • candida albicans