N-carbamoyl-L-cysteine as an intermediate in the bioconversion from D,L-2-amino-Delta(2)-thiazoline-4-carboxylic acid to L-cysteine by Pseudomonas sp. ON-4a
Y. Tamura et al., N-carbamoyl-L-cysteine as an intermediate in the bioconversion from D,L-2-amino-Delta(2)-thiazoline-4-carboxylic acid to L-cysteine by Pseudomonas sp. ON-4a, BIOS BIOT B, 62(11), 1998, pp. 2226-2229
We investigated the conversion of D,L-2-amino-Delta(2)-thiazoline-4-carboxy
lic acid (D,L-ATC) to L-cysteine with Pseudomonas sp. ON-4a, an ATC-assimil
ating bacterium. Cysteine and N-carbamoylcysteine (NCC), but not S-carbamoy
lcysteine (SCC), were produced from D,L-ATC by a cell-free extract from the
strain. These products were isolated from the reaction mixture and then id
entified as the L-form. Similar results were obtained with P. putida AJ3865
and unidentified strain TG-3, an ATC-assimilating bacteria. It became clea
r that L-NCC is an intermediate in the conversion of D,L-ATC to L-cysteine
in these Pseudomonas strains. Furthermore, it was suggested that these bact
eria have L-ATC hydrolase and L-NCC amidohydrolase.