首页> 外文期刊>Journal of Inorganic Biochemistry: An Interdisciplinary Journal >Cobaltocene-mediated catalytic monooxygenation using holo and heme domain cytochrome P450BM3
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Cobaltocene-mediated catalytic monooxygenation using holo and heme domain cytochrome P450BM3

机译:钴和介导的整体和血红素域细胞色素P450BM3催化单氧合

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摘要

The feasibility of replacing NADPH with 1,1'-dicarboxycobaltocene in the catalytic cycle of cytochrome P450 BM3 has been explored. Using the holoprotein, the surrogate mediator was observed to reduce both the FAD and FMN in the reductase domain, as well as the iron in the heme domain. In an electrochemical system, the mediator was able to support lauric acid hydroxylation at a rate of 16.5 nmol productmol enzyme/minute. Similar electron transfer and catalysis were observed for the heme domain alone in the presence of the metallocene; the turnover rate in this case was 1.8 nmol productmol enzyme/minute. Parallel studies under the same conditions using a previously reported cobalt sepulchrate mediator showed that the two systems give similar results for both the holoenzyme and the heme domain. (C) 2004 Elsevier Inc. All rights reserved.
机译:研究了在细胞色素P450 BM3的催化循环中用1,1'-二羧基钴茂取代NADPH的可行性。使用全蛋白,可以观察到替代介体在还原酶结构域中还原FAD和FMN,以及在血红素结构域中还原铁。在电化学系统中,介体能够以16.5 nmol产物/ nmol酶/分钟的速率支持月桂酸羟基化。在茂金属存在下,仅对血红素结构域观察到类似的电子转移和催化。在这种情况下,周转率为1.8nmol产物/ nmol酶/分钟。使用先前报道的钴硫化钴介体在相同条件下进行的并行研究表明,两种系统对于全酶和血红素结构域均提供相似的结果。 (C)2004 Elsevier Inc.保留所有权利。

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