Literature DB >> 24430197

Multicopper oxidases: intramolecular electron transfer and O2 reduction.

Scot Wherland1, Ole Farver, Israel Pecht.   

Abstract

The multicopper oxidases are an intriguing, widespread family of enzymes that catalyze the reduction of O2 to water by a variety of single-electron and multiple-electron reducing agents. The structure and properties of the copper binding sites responsible for the latter chemical transformations have been studied for over 40 years and a detailed picture is emerging. This review focuses particularly on the kinetics of internal electron transfer between the type 1 (blue) copper site and the trinuclear center, as well as on the nature of the intermediates formed in the oxygen reduction process.

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Year:  2014        PMID: 24430197     DOI: 10.1007/s00775-013-1080-7

Source DB:  PubMed          Journal:  J Biol Inorg Chem        ISSN: 0949-8257            Impact factor:   3.358


  63 in total

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Journal:  FEBS Lett       Date:  1979-12-15       Impact factor: 4.124

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Journal:  FEBS Lett       Date:  1978-05-01       Impact factor: 4.124

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Journal:  J Mol Evol       Date:  1993-01       Impact factor: 2.395

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Authors:  Armand W J W Tepper; Thijs J Aartsma; Gerard W Canters
Journal:  Faraday Discuss       Date:  2011       Impact factor: 4.008

6.  Low activation barriers characterize intramolecular electron transfer in ascorbate oxidase.

Authors:  O Farver; I Pecht
Journal:  Proc Natl Acad Sci U S A       Date:  1992-09-01       Impact factor: 11.205

Review 7.  Steering electrons on moving pathways.

Authors:  David N Beratan; Spiros S Skourtis; Ilya A Balabin; Alexander Balaeff; Shahar Keinan; Ravindra Venkatramani; Dequan Xiao
Journal:  Acc Chem Res       Date:  2009-10-20       Impact factor: 22.384

8.  Identification of a radical intermediate in the enzymatic reduction of oxygen by a small laccase.

Authors:  Armand W J W Tepper; Sergey Milikisyants; Silvia Sottini; Erik Vijgenboom; Edgar J J Groenen; Gerard W Canters
Journal:  J Am Chem Soc       Date:  2009-08-26       Impact factor: 15.419

Review 9.  Multicopper oxidases: a workshop on copper coordination chemistry, electron transfer, and metallophysiology.

Authors:  Daniel J Kosman
Journal:  J Biol Inorg Chem       Date:  2009-10-09       Impact factor: 3.358

10.  Crystal structure of a blue laccase from Lentinus tigrinus: evidences for intermediates in the molecular oxygen reductive splitting by multicopper oxidases.

Authors:  Marta Ferraroni; Nina M Myasoedova; Vadim Schmatchenko; Alexey A Leontievsky; Ludmila A Golovleva; Andrea Scozzafava; Fabrizio Briganti
Journal:  BMC Struct Biol       Date:  2007-09-26
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  4 in total

Review 1.  Electron transfer and reaction mechanism of laccases.

Authors:  Stephen M Jones; Edward I Solomon
Journal:  Cell Mol Life Sci       Date:  2015-01-09       Impact factor: 9.261

Review 2.  Lignin engineering through laccase modification: a promising field for energy plant improvement.

Authors:  Jinhui Wang; Juanjuan Feng; Weitao Jia; Sandra Chang; Shizhong Li; Yinxin Li
Journal:  Biotechnol Biofuels       Date:  2015-09-15       Impact factor: 6.040

3.  Functional Inactivation of Putative Photosynthetic Electron Acceptor Ferredoxin C2 (FdC2) Induces Delayed Heading Date and Decreased Photosynthetic Rate in Rice.

Authors:  Juan Zhao; Zhennan Qiu; Banpu Ruan; Shujing Kang; Lei He; Sen Zhang; Guojun Dong; Jiang Hu; Dali Zeng; Guangheng Zhang; Zhenyu Gao; Deyong Ren; Xingming Hu; Guang Chen; Longbiao Guo; Qian Qian; Li Zhu
Journal:  PLoS One       Date:  2015-11-24       Impact factor: 3.240

Review 4.  The nature of the rate-limiting step of blue multicopper oxidases: Homogeneous studies versus heterogeneous.

Authors:  Claire Stines-Chaumeil; Elodie Roussarie; Nicolas Mano
Journal:  Biochim Open       Date:  2017-02-03
  4 in total

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