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

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(2) reduction. MCOs have been characterized in details in solution or immobilized on electrode surfaces. The nature of the...

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Autores principales: Stines-Chaumeil, Claire, Roussarie, Elodie, Mano, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801829/
https://www.ncbi.nlm.nih.gov/pubmed/29450139
http://dx.doi.org/10.1016/j.biopen.2017.01.001
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author Stines-Chaumeil, Claire
Roussarie, Elodie
Mano, Nicolas
author_facet Stines-Chaumeil, Claire
Roussarie, Elodie
Mano, Nicolas
author_sort Stines-Chaumeil, Claire
collection PubMed
description 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(2) 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(2) to water.
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spelling pubmed-58018292018-02-15 The nature of the rate-limiting step of blue multicopper oxidases: Homogeneous studies versus heterogeneous Stines-Chaumeil, Claire Roussarie, Elodie Mano, Nicolas Biochim Open Invited review article 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(2) 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(2) to water. Elsevier 2017-02-03 /pmc/articles/PMC5801829/ /pubmed/29450139 http://dx.doi.org/10.1016/j.biopen.2017.01.001 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Invited review article
Stines-Chaumeil, Claire
Roussarie, Elodie
Mano, Nicolas
The nature of the rate-limiting step of blue multicopper oxidases: Homogeneous studies versus heterogeneous
title The nature of the rate-limiting step of blue multicopper oxidases: Homogeneous studies versus heterogeneous
title_full The nature of the rate-limiting step of blue multicopper oxidases: Homogeneous studies versus heterogeneous
title_fullStr The nature of the rate-limiting step of blue multicopper oxidases: Homogeneous studies versus heterogeneous
title_full_unstemmed The nature of the rate-limiting step of blue multicopper oxidases: Homogeneous studies versus heterogeneous
title_short The nature of the rate-limiting step of blue multicopper oxidases: Homogeneous studies versus heterogeneous
title_sort nature of the rate-limiting step of blue multicopper oxidases: homogeneous studies versus heterogeneous
topic Invited review article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801829/
https://www.ncbi.nlm.nih.gov/pubmed/29450139
http://dx.doi.org/10.1016/j.biopen.2017.01.001
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