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Literature summary for 2.6.1.48 extracted from

  • Kim, H.T.; Khang, T.U.; Baritugo, K.A.; Hyun, S.M.; Kang, K.H.; Jung, S.H.; Song, B.K.; Park, K.; Oh, M.K.; Kim, G.B.; Kim, H.U.; Lee, S.Y.; Park, S.J.; Joo, J.C.
    Metabolic engineering of Corynebacterium glutamicum for the production of glutaric acid, a C5 dicarboxylic acid platform chemical (2019), Metab. Eng., 51, 99-109 .
    View publication on PubMed

Cloned(Commentary)

Cloned (Comment) Organism
gene davT, recombinant expression of N-terminal His6-tagged enzyme in Corynebacterium glutamicum strain KCTC 1857, coexpression with glutarate semialdehyde dehydrogenase (davD, EC 1.2.1.20) 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
gene dayB, recombinant expression in Corynebacterium glutamicum, co-expression with Pseudomonas putida dayA and dayB genes encoding encoding lysine 2-monooxygenase and delta-aminovaleramidase, respectively, and Corynebacterium glutamicum gabD gene encoding glutarate semialdehyde dehydrogenase Corynebacterium glutamicum
gene dayT, recombinant expression in Corynebacterium glutamicum, co-expression with Pseudomonas putida dayA, dayB, and dayD genes encoding lysine 2-monooxygenase, delta-aminovaleramidase, and glutarate semialdehyde dehydrogenase, respectively Pseudomonas putida

Protein Variants

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 with Pseudomonas putida dayA, dayB, and dayD genes encoding encoding lysine 2-monooxygenase, delta-aminovaleramidase, and glutarate semialdehyde dehydrogenase, respectively, in Corynebacterium glutamicum. Method optimization and evaluation Corynebacterium glutamicum
additional information metabolic engineering of Corynebacterium glutamicum for the production of glutaric acid, a C5 dicarboxylic acid platform chemical by co-expression with Pseudomonas putida dayA, dayB, and dayD genes encoding lysine 2-monooxygenase, delta-aminovaleramidase, and glutarate semialdehyde dehydrogenase, respectively, in Corynebacterium glutamicum. Method optimization and evaluation Pseudomonas putida
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. Method optimization and evaluation. 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 KCTC 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/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
5-aminopentanoate + 2-oxoglutarate Pseudomonas putida
-
5-oxopentanoate + L-glutamate
-
?
5-aminopentanoate + 2-oxoglutarate Pseudomonas putida DSM 6125
-
5-oxopentanoate + L-glutamate
-
?
5-aminopentanoate + 2-oxoglutarate Pseudomonas putida NCIMB 11950
-
5-oxopentanoate + L-glutamate
-
?
5-aminopentanoate + 2-oxoglutarate Pseudomonas putida ATCC 47054
-
5-oxopentanoate + L-glutamate
-
?

Organism

Organism UniProt Comment Textmining
Corynebacterium glutamicum A0A0U4XQS6
-
-
Pseudomonas putida
-
-
-
Pseudomonas putida Q88RB9
-
-
Pseudomonas putida ATCC 47054 Q88RB9
-
-
Pseudomonas putida DSM 6125 Q88RB9
-
-
Pseudomonas putida NCIMB 11950 Q88RB9
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
5-aminopentanoate + 2-oxoglutarate
-
Pseudomonas putida 5-oxopentanoate + L-glutamate
-
?
5-aminopentanoate + 2-oxoglutarate
-
Pseudomonas putida DSM 6125 5-oxopentanoate + L-glutamate
-
?
5-aminopentanoate + 2-oxoglutarate
-
Pseudomonas putida NCIMB 11950 5-oxopentanoate + L-glutamate
-
?
5-aminopentanoate + 2-oxoglutarate
-
Pseudomonas putida ATCC 47054 5-oxopentanoate + L-glutamate
-
?

Synonyms

Synonyms Comment Organism
5-aminovalerate transaminase
-
Pseudomonas putida
5-aminovalerate transaminase
-
Corynebacterium glutamicum
davT
-
Pseudomonas putida
dayT
-
Pseudomonas putida
GabT
-
Corynebacterium glutamicum

Cofactor

Cofactor Comment Organism Structure
pyridoxal 5'-phosphate
-
Pseudomonas putida

General Information

General Information Comment Organism
metabolism in the L-lysine catabolism pathway, 5-aminovaleric acid (5-AVA) is furter converted into glutarate semialdehyde by 5-aminovalerate transaminase encoded by davT Pseudomonas putida