Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary extracted from

  • Ishikawa, T.; Watabe, K.; Mukohara, Y.; Nakamura, H.
    Mechanism of stereospecific conversion of DL-5-substituted hydantoins to the corresponding L-amino acids by Pseudomonas sp. strain NS671 (1997), Biosci. Biotechnol. Biochem., 61, 185-187.
    View publication on PubMed

Application

EC Number Application Comment Organism
5.1.99.5 synthesis stereospecific production of L-amino acids from the corresponding DL-5-substituted hydantoins. DL-5-substituted hydantoins are converted exclusively to the L-forms of the corresponding N-carbamyl-amino acids by hydantoinase in combination with hydantoin racemase. The N-carbamyl-l-amino acids are then converted to L-amino acids by N-carbamyl-L-amino acid amidohydrolase Pseudomonas sp.

Organism

EC Number Organism UniProt Comment Textmining
3.5.1.87 Pseudomonas sp.
-
-
-
5.1.99.5 Pseudomonas sp.
-
-
-
5.1.99.5 Pseudomonas sp. NS671
-
-
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
3.5.1.87 N-carbamoyl-L-methionine + H2O
-
 Pseudomonas sp. L-methionine + CO2 + NH3
-
 ?
3.5.1.87 N-carbamoyl-L-methionine + H2O
-
 Pseudomonas sp. NS671 L-methionine + CO2 + NH3
-
 ?