Literature DB >> 19213324

Efficient electrocatalytic oxygen reduction by the 'blue' copper oxidase, laccase, directly attached to chemically modified carbons.

Christopher F Blanford1, Carina E Foster, Rachel S Heath, Fraser A Armstrong.   

Abstract

This discussion describes efforts to produce a stable, efficient electrocatalyst for four-electron O2 reduction through the direct attachment of fungal laccase, a 'blue' copper oxidase, to functionalised carbon electrode materials. Commercially available carbons, including fibrous and porous materials, offer important opportunities for achieving high conductivity over high surface areas that can be chemically functionalised. A promising approach for attaching laccase to a carbon surface is to use the diazonium coupling reaction to generate protrusive aromatic functionalities that can bind to hydrophobic residues close to the 'blue' Cu site: this site provides a fast, intramolecular electron relay into the buried trinuclear Cu active site that converts O2 rapidly and cleanly to H2O. This enhancement procedure makes possible the stable, direct electrocatalytic reduction of O2 at high potential with high efficiency in terms of turnover frequency per enzyme active site engaged with the electrode. The absence of electron-transfer mediators and simplicity of electrode system reveals the more inherent characteristics of the electrocatalytic mechanism that are masked in the waveform when a mediator is used. The study includes experiments to assess the effects of methanol and chloride ions on laccase electrocatalysis, complementing studies carried out by other groups, particularly those in which laccase is embedded in an electron-mediating gel.

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Year:  2008        PMID: 19213324     DOI: 10.1039/b808939f

Source DB:  PubMed          Journal:  Faraday Discuss        ISSN: 1359-6640            Impact factor:   4.008


  13 in total

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Review 3.  Direct enzymatic bioelectrocatalysis: differentiating between myth and reality.

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4.  Catalysis of dioxygen reduction by Thermus thermophilus strain HB27 laccase on ketjen black electrodes.

Authors:  Peter Agbo; James R Heath; Harry B Gray
Journal:  J Phys Chem B       Date:  2012-11-28       Impact factor: 2.991

5.  Direct, Electrocatalytic Oxygen Reduction by Laccase on Anthracene-2-methanethiol Modified Gold.

Authors:  Matthew S Thorum; Cyrus A Anderson; Jeremy J Hatch; Andrew S Campbell; Nicholas M Marshall; Steven C Zimmerman; Yi Lu; Andrew A Gewirth
Journal:  J Phys Chem Lett       Date:  2010-08       Impact factor: 6.475

6.  Type-zero copper proteins.

Authors:  Kyle M Lancaster; Serena DeBeer George; Keiko Yokoyama; John H Richards; Harry B Gray
Journal:  Nat Chem       Date:  2009-12       Impact factor: 24.427

7.  Inhibition of electrocatalytic O(2) reduction of functional CcO models by competitive, non-competitive, and mixed inhibitors.

Authors:  James P Collman; Abhishek Dey; Christopher J Barile; Somdatta Ghosh; Richard A Decréau
Journal:  Inorg Chem       Date:  2009-11-16       Impact factor: 5.165

8.  Bilirubin Oxidase from Myrothecium verrucaria Physically Absorbed on Graphite Electrodes. Insights into the Alternative Resting Form and the Sources of Activity Loss.

Authors:  Federico Tasca; Diego Farias; Carmen Castro; Cristina Acuna-Rougier; Riccarda Antiochia
Journal:  PLoS One       Date:  2015-07-21       Impact factor: 3.240

9.  Site directed confinement of laccases in a porous scaffold towards robustness and selectivity.

Authors:  Fangfang Yang; Rénal Backov; Jean-Luc Blin; Bernadett Fáklya; Thierry Tron; Yasmina Mekmouche
Journal:  Biotechnol Rep (Amst)       Date:  2021-06-09

10.  A biosynthetic model of cytochrome c oxidase as an electrocatalyst for oxygen reduction.

Authors:  Sohini Mukherjee; Arnab Mukherjee; Ambika Bhagi-Damodaran; Manjistha Mukherjee; Yi Lu; Abhishek Dey
Journal:  Nat Commun       Date:  2015-10-12       Impact factor: 14.919

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