Metabolic engineering of Escherichia coli for the production of 5-aminovalerate and glutarate as C5 platform chemicals

• Published in: Metabolic engineering 2013-03, Vol.16, p.42-47
• Main Authors: Park, Si Jae, Kim, Eun Young, Noh, Won, Park, Hye Min, Oh, Young Hoon, Lee, Seung Hwan, Song, Bong Keun, Jegal, Jonggeon, Lee, Sang Yup
• Format: Article
• Language: English
• Subjects: 5-aminovalerate; Amidohydrolases - biosynthesis; Amidohydrolases - genetics; Amino Acids, Neutral - biosynthesis; Amino Acids, Neutral - genetics; Bacterial Proteins - biosynthesis; Bacterial Proteins - genetics; Escherichia coli; Escherichia coli - genetics; Escherichia coli - metabolism; Gene Expression; Glutarate; Glutarates - metabolism; l-lysine; Metabolic engineering; Metabolic Engineering - methods; Mixed Function Oxygenases - biosynthesis; Mixed Function Oxygenases - genetics; Pseudomonas; Pseudomonas putida - enzymology; Pseudomonas putida - genetics; Recombinant Proteins - biosynthesis; Recombinant Proteins - genetics
• ISSN: 1096-7176; 1096-7184
• DOI: 10.1016/j.ymben.2012.11.011

5-Aminovalerate (5AVA) is the precursor of valerolactam, a potential building block for producing nylon 5, and is a C5 platform chemical for synthesizing 5-hydroxyvalerate, glutarate, and 1,5-pentanediol. Escherichia coli was metabolically engineered for the production of 5-aminovalerate (5AVA) and glutarate. When the recombinant E. coli WL3110 strain expressing the Pseudomonas putidadavAB genes encoding delta-aminovaleramidase and lysine 2-monooxygenase, respectively, were cultured in a medium containing 20g/L of glucose and 10g/L of l-lysine, 3.6g/L of 5AVA was produced by converting 7g/L of l-lysine. When the davAB genes were introduced into recombinant E. coli strainXQ56allowing enhanced l-lysine synthesis, 0.27 and 0.5g/L of 5AVA were produced directly from glucose by batch and fed-batch cultures, respectively. Further conversion of 5AVA into glutarate could be demonstrated by expression of the P. putida gabTD genes encoding 5AVA aminotransferase and glutarate semialdehyde dehydrogenase. When recombinant E. coli WL3110 strain expressing the davAB and gabTD genes was cultured in a medium containing 20g/L glucose, 10g/L l-lysine and 10g/L α-ketoglutarate, 1.7g/L of glutarate was produced. ► 5-aminovaleric acid and glutaric acid are important C5 platform chemicals. ► E. coli was metabolically engineered to produce 5-aminovaleric acid. ► E. coli was metabolically engineered to produce glutaric acid.