Direct electron transfer reactions of laccases from different origins on carbon electrodes

被引:203
作者
Shleev, S
Jarosz-Wilkolazka, A
Khalunina, A
Morozova, O
Yaropolov, A
Ruzgas, T
Gorton, L
机构
[1] Lund Univ, Dept Analyt Chem, SE-22100 Lund, Sweden
[2] Marie Curie Sklodowska Univ, Dept Biochem, PL-20031 Lublin, Poland
[3] Russian Acad Sci, AN Bach Inst Biochem, Moscow 119071, Russia
[4] Malmo Univ, Biomed Lab Sci Hlth & Soc, SE-20506 Malmo, Sweden
基金
俄罗斯基础研究基金会;
关键词
laccase; redox potential; T1; site; carbon electrode;
D O I
10.1016/j.bioelechem.2005.02.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Electrochemical studies of laccases from basidiomycetes, i.e., Trametes hirsuta, Trametes ochracea, Coriolopsis fulvocinerea, Cerrena maxima, and Cerrena unicolor, have been performed. Direct (mediatorless) electrochemistry of laccases on graphite electrodes has been investigated with cyclic voltammetry, square wave voltammetry as well as potentiometry. For all mentioned high potential laccases direct electron transfer (DET) has been registered at spectrographic graphite and highly ordered pyrolytic graphite electrodes. The characteristics of DET reactions of the enzymes were analysed under aerobic and anaerobic conditions. It is shown that the T I site of the laccase is the primary electron acceptor, both in solution (homogenous case) and at surface of the graphite electrode (heterogeneous case). A mechanism of ET for the process of the electroreduction of oxygen at the laccase-modified graphite electrodes is proposed and the similarity of this heterogeneous process to the laccase catalysed oxygen reduction homogeneous reaction is concluded. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:115 / 124
页数:10
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