Synthetic Route of C4H6N2O2S. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: 2-Amino-4,5-dihydrothiazole-4-carboxylic acid, is researched, Molecular C4H6N2O2S, CAS is 2150-55-2, about Progress on enzymatic synthesis of L-cysteine from DL-ATC by Pseudomonas sp.. Author is Wu, Min; Chen, Wei-qing; Wang, Pu; He, Jun-yao.
A review. The microbial transformation method for L-cysteine production shows evident advantages, because of its short cycle time, low cost, high region and stereoselectivity, easy control of reaction condition, and environment-friendly. Recently, studies on the bioconversion of DL-2-amino-Δ2-thiazoline-4-carboxylic acid (DL-ATC) to L-cysteine by intracellular enzymes were reported. The research progresses on L-cysteine production by microbial bioconversion, especially Pseudomonas sp., or its crude enzyme extract are summarized. The applications of immobilization technol. in the biotransformation of DL-ATC to L-cysteine are introduced. The genetically engineered bacteria and the study progresses of L-cysteine desulfhydrase were also discussed.
There is still a lot of research devoted to this compound(SMILES：O=C(C1N=C(N)SC1)O)Synthetic Route of C4H6N2O2S, and with the development of science, more effects of this compound(2150-55-2) can be discovered.