Cloned (Comment) | Organism |
---|---|
gene davD, recombinant expression in Corynebacterium glutamicum strain KCTC 1857, coexpression with 5-aminovalerate transaminase (davT, EC 2.6.1.48) from Pseudomonas putida, 4-aminobutyrate-2-oxoglutarate transaminase (gabT, EC 2.6.1.19) from Corynebacterium glutamicum, and NADP-dependent succinic semialdehyde dehydrogenase (gabD, EC 1.2.1.79) from Corynebacterium glutamicum, as well as N-terminal His6-tagged lysine 2-monooxygenase (davB, EC 1.13.12.2) from Pseudomonas putida | Pseudomonas putida |
Protein Variants | Comment | Organism |
---|---|---|
additional information | metabolic engineering of Corynebacterium glutamicum for the production of glutaric acid, a C5 dicarboxylic acid platform chemical, by co-expression of Pseudomonas putida davT, davB, and davD genes encoding lysine 2-monooxygenase, delta-aminovaleramidase, and glutarate semialdehyde dehydrogenase, respectively, in Corynebacterium glutamicum. The glutaric acid biosynthesis pathway constructed in recombinant Corynebacterium glutamicum is engineered by examining strong synthetic promoters H30 and H36, Corynebacterium glutamicum codon-optimized davTDBA genes, and modification of davB gene with an N-terminal His6-tag to improve the production of glutaric acid. The use of N-terminal His6-tagged DavB is most suitable for the production of glutaric acid from glucose. Fed-batch fermentation on of the final engineered Corynebacterium glutamicum H30_GAHis strain, expressing davTDA genes along with davB fused with His6-tag at N-terminus can produce 24.5 g/l of glutaric acid with low accumulation of L-lysine (1.7 g/l), wherein 5-aminovaleric acid (5-AVA) ccumulation is not observed during fermentation. Metabolically engineered Corynebacterium glutamicum strain H30_GA-2 (engineered strain KCTC 1857) is able for catalysis of the biosynthesis of glutaric acid from glucose. Method optimization and evaluation, overview | Pseudomonas putida |
Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|
5-oxopentanoate + NADP+ + H2O | Pseudomonas putida | - |
glutarate + NADPH + H+ | - |
? | |
5-oxopentanoate + NADP+ + H2O | Pseudomonas putida DSM 6125 | - |
glutarate + NADPH + H+ | - |
? | |
5-oxopentanoate + NADP+ + H2O | Pseudomonas putida NCIMB 11950 | - |
glutarate + NADPH + H+ | - |
? | |
5-oxopentanoate + NADP+ + H2O | Pseudomonas putida ATCC 47054 | - |
glutarate + NADPH + H+ | - |
? |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Pseudomonas putida | Q88RC0 | - |
- |
Pseudomonas putida ATCC 47054 | Q88RC0 | - |
- |
Pseudomonas putida DSM 6125 | Q88RC0 | - |
- |
Pseudomonas putida NCIMB 11950 | Q88RC0 | - |
- |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
5-oxopentanoate + NADP+ + H2O | - |
Pseudomonas putida | glutarate + NADPH + H+ | - |
? | |
5-oxopentanoate + NADP+ + H2O | - |
Pseudomonas putida DSM 6125 | glutarate + NADPH + H+ | - |
? | |
5-oxopentanoate + NADP+ + H2O | - |
Pseudomonas putida NCIMB 11950 | glutarate + NADPH + H+ | - |
? | |
5-oxopentanoate + NADP+ + H2O | - |
Pseudomonas putida ATCC 47054 | glutarate + NADPH + H+ | - |
? |
Synonyms | Comment | Organism |
---|---|---|
davD | - |
Pseudomonas putida |
glutarate semialdehyde dehydrogenase | - |
Pseudomonas putida |
Cofactor | Comment | Organism | Structure |
---|---|---|---|
NADP+ | - |
Pseudomonas putida |
General Information | Comment | Organism |
---|---|---|
metabolism | glutarate semialdehyde dehydrogenase encoded by davD converts glutarate semialdehyde into glutaric acid. In the natural L-lysine catabolic pathway of Pseudomonas strains, glutaric acid is then further converted to acetyl-CoA, a main intermediate of Krebs cycle | Pseudomonas putida |