The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: 2-Amino-4,5-dihydrothiazole-4-carboxylic acid(SMILESS: O=C(C1N=C(N)SC1)O,cas:2150-55-2) is researched.Recommanded Product: 591-54-8. The article 《Enzymatic characteristics in the bioconversion of D,L-ATC to L-cysteine》 in relation to this compound, is published in Sanop Misaengmul Hakhoechi. Let’s take a look at the latest research on this compound (cas:2150-55-2).
The bioconversion of DL-2-aminothiazoline-4-carboxylic acid (I) to L-cysteine (II) was investigated. After the intracellular enzyme of a Pseudomonas species was inducibly formed by addition of I in the middle of culture, the cells were isolated and treated with sonication to prepare the crude enzyme solution I was the only isomeric form of the amino acid produced from I and its production could be enhanced several 10-fold by addition of Mn2+ which was required as a cofactor in the enzymic reaction. In addition, this reaction suffered from feedback inhibition of II. On the other hand, since a II-decomposing enzyme coexisted in the crude enzyme solution, most of the II formed disappeared in the absence of its inhibitor. However, hydroxylamine was a potent inhibitor which could successfully prevent the decomposition of II.
Here is a brief introduction to this compound(2150-55-2)COA of Formula: C4H6N2O2S, if you want to know about other compounds related to this compound(2150-55-2), you can read my other articles.