Copper-dioxygen complex mediated C-H bond oxygenation: relevance for particulate methane monooxygenase (pMMO)

被引:181
作者
Himes, Richard A. [1 ]
Karlin, Kenneth D. [1 ]
机构
[1] Johns Hopkins Univ, Dept Chem, Baltimore, MD 21218 USA
基金
美国国家卫生研究院;
关键词
METHYLOCOCCUS-CAPSULATUS BATH; ACTIVE-SITE; BIS(MU-OXO)DICOPPER(III) COMPLEX; ELECTRONIC-STRUCTURES; OLEFIN EPOXIDATION; ATOM INSERTION; METAL CENTERS; HYDROXYLATION; REACTIVITY; OXIDATION;
D O I
10.1016/j.cbpa.2009.02.025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Particulate methane monooxygenase (pMMO), an integral membrane protein found in methanotrophic bacteria, catalyzes the oxidation of methane to methanol. Expression and greater activity of the enzyme in the presence of copper ion suggest that pMMO is a cuprous metalloenzyme. Recent advances especially the first crystal structures of pMMO - have energized the field, but the nature of the active site(s) and the mechanism of methane oxidation remain poorly understood-yet hotly contested. Herein the authors briefly review the current understanding of the pMMO metal sites and discuss advances in small molecule CU-O(2) chemistry that may contribute to an understanding of copper-ion mediated hydrocarbon oxidation chemistry.
引用
收藏
页码:119 / 131
页数:13
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