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蓝色多铜氧化酶限速步骤的本质:均相研究与非均相研究

The nature of the rate-limiting step of blue multicopper oxidases: Homogeneous studies heterogeneous.

作者信息

Stines-Chaumeil Claire, Roussarie Elodie, Mano Nicolas

机构信息

CNRS, CRPP, UPR 8641, F-33600 Pessac, France.

Univ. Bordeaux, CRPP, UPR 8641, F-33600 Pessac, France.

出版信息

Biochim Open. 2017 Feb 3;4:36-40. doi: 10.1016/j.biopen.2017.01.001. eCollection 2017 Jun.

Abstract

Multicopper oxidases (MCOs) catalyzed two half reactions (linked by an intramolecular electron transfer) through a Ping-Pong mechanism: the substrate oxidation followed by the O reduction. MCOs have been characterized in details in solution or immobilized on electrode surfaces. The nature of the rate-limiting steps, which is controversial in the literature, is discussed in this mini review for both cases. Deciphering such rate-limiting steps is of particular importance to efficiently use MCOs in any applications requiring the reduction of O to water.

摘要

多铜氧化酶(MCOs)通过乒乓机制催化两个半反应(通过分子内电子转移相连):底物氧化,然后是氧还原。MCOs已在溶液中或固定在电极表面进行了详细表征。本文的小型综述讨论了这两种情况下限速步骤的性质,这在文献中存在争议。在任何需要将氧还原为水的应用中,解读此类限速步骤对于有效利用MCOs尤为重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b688/5801829/4d4f5dfdd72e/sc1.jpg

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