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甲烷氧化的生物化学

The biochemistry of methane oxidation.

作者信息

Hakemian Amanda S, Rosenzweig Amy C

机构信息

Department of Biochemistry, Northwestern University, Evanston, Illinois 60208, USA.

出版信息

Annu Rev Biochem. 2007;76:223-41. doi: 10.1146/annurev.biochem.76.061505.175355.

Abstract

Methanotrophic bacteria oxidize methane to methanol in the first step of their metabolic pathway. Two forms of methane monooxygenase (MMO) enzymes catalyze this reaction: soluble MMO (sMMO) and membrane-bound or particulate MMO (pMMO). pMMO is expressed when copper is available, and its active site is believed to contain copper. Whereas sMMO is well characterized, most aspects of pMMO biochemistry remain unknown and somewhat controversial. This review emphasizes advances in the past two to three years related to pMMO and to copper uptake and copper-dependent regulation in methanotrophs. The pMMO metal centers have been characterized spectroscopically, and the first pMMO crystal structure has been determined. Significant effort has been devoted to improving in vitro pMMO activity. Proteins involved in sMMO regulation and additional copper-regulated proteins have been identified, and the Methylococcus capsulatus (Bath) genome has been sequenced. Finally, methanobactin (mb), a small copper chelator proposed to facilitate copper uptake, has been characterized.

摘要

在其代谢途径的第一步中,甲烷营养菌将甲烷氧化为甲醇。两种形式的甲烷单加氧酶(MMO)催化此反应:可溶性MMO(sMMO)和膜结合或颗粒状MMO(pMMO)。当有铜存在时,pMMO会表达,并且其活性位点被认为含有铜。虽然sMMO已得到充分表征,但pMMO生物化学的大多数方面仍然未知且存在一定争议。本综述着重介绍了过去两到三年中与pMMO以及甲烷营养菌中铜摄取和铜依赖性调控相关的进展。已通过光谱法对pMMO金属中心进行了表征,并确定了首个pMMO晶体结构。人们已投入大量精力来提高体外pMMO活性。已鉴定出参与sMMO调控的蛋白质以及其他铜调控蛋白,并且已对荚膜甲基球菌(巴斯德菌株)的基因组进行了测序。最后,已对甲烷菌素(mb)进行了表征,甲烷菌素是一种小型铜螯合剂,被认为有助于铜的摄取。

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