Peroxygenation mechanism for chloroperoxidase-catalyzed N-oxidation of arylamines.
Peroxygenation mechanism for chloroperoxidase-catalyzed N-oxidation of arylamines.
复制标题
氯过氧化物酶催化芳胺 N-氧化的过氧化机制。
DOI:
10.1021/tx00023a011
复制
发表时间:
1991
影响因子:
4.1
通讯作者:
Corbett,MD
中科院分区:
文献类型:
--
作者:
Doerge,DR;Corbett,MD
The metabolism of three arylamine substrates by H202 in the presence of each of the per-oxidative enzymes chloroperoxidase (CPX) and peaseed peroxygenase (PSM) was conducted with normal H202 and with 180-labeled H202. The resulting C-nitroso aromatic metabolites were examined byGC-MS methods to determine the extent of 180 incorporation. The arylamine substrates were p-toluidine, 4-chloroaniline, and 3, 4-dichloroaniline. For both enzymes, all three arylamines were found to give quantitative incorporation of 180 into their nitroso metabolites when [180] H202 was the oxidant substrate. The introduction of the oxygen atom into 4-chloronitrosobenzene was found to occur during the first step of this process, since it was found that when (4-chlorophenyl) hydroxylamine was employed as the substrate, no significant in-corporation of 180 occurred. These observations prove that CPX and PSM cause N-oxidation of primary arylamines via an oxygen transfer from the compound I activated forms of their heme functional groups. Therefore, these peroxidases are correctly called peroxygenases when acting in such a manner. A discussion of the reaction mechanisms for peroxidases and their relation to cytochrome P-450 oxidations is presented.