Metabolic engineering of Corynebacterium glutamicum for the production of glutaric acid, a C5 dicarboxylic acid platform chemical

Abstract Corynebacterium glutamicum was metabolically engineered for the production of glutaric acid, a C5 dicarboxylic acid that can be used as platform building block chemical for nylons and plasticizers. C. glutamicum gabT and gabD genes and Pseudomonas putida davT and davD genes encoding 5-aminovalerate transaminase and glutarate semialdehyde dehydrogenase, respectively, were examined in C. glutamicum for the construction of a glutaric acid biosynthesis pathway along with P. putida davB and davA genes encoding lysine 2-monooxygenase and delta-aminovaleramidase, respectively. The glutaric acid biosynthesis pathway constructed in recombinant C. glutamicum was engineered by examining strong synthetic promoters P H30 and P H36 , C. glutamicum codon-optimized davTDBA genes, and modification of davB gene with an N-terminal His 6 -tag to improve the production of glutaric acid. It was found that use of N-terminal His 6 -tagged DavB was most suitable for the production of glutaric acid from glucose. Fed-batch fermentation using the final engineered C. glutamicum H30_GA His strain, expressing davTDA genes along with davB fused with His 6 -tag at N-terminus could produce 24.5 g/L of glutaric acid with low accumulation of l -lysine (1.7 g/L), wherein 5-AVA accumulation was not observed during fermentation.