Literature DB >> 17602558

Electrochemical study of a reconstituted photosynthetic electron-transfer chain.

Vincent Fourmond1, Bernard Lagoutte, Pierre Sétif, Winfried Leibl, Christophe Demaille.   

Abstract

A multi-enzyme electron-transfer chain involving solubilized photosystem I (PSI) as photocatalytic unit, cytochrome c6 and ferredoxin as electron carriers and ferredoxin/NADPH oxidoreductase (FNR) as electron acceptor was reconstituted in an electrochemical cell and studied by cyclic voltammetry. The working gold electrodes were modified to react selectively with cytochrome c6. Quantitative analysis of the photocatalytic current under continuous illumination allowed the determination of the values kon and koff for the ferredoxin/PSI interaction. An efficient recycling system for NADPH was established, and the dissociation constant of the oxidized ferredoxin/semiquinone FNR complex was extracted by modeling the catalytic efficiency of the chain as a function of ferredoxin concentration. The value determined hereby is consistent with a shift of -50 to -100 mV of the reduction potential of ferredoxin when complexed with FNR.

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Year:  2007        PMID: 17602558     DOI: 10.1021/ja0714787

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  2 in total

1.  Photosynthetic electron partitioning between [FeFe]-hydrogenase and ferredoxin:NADP+-oxidoreductase (FNR) enzymes in vitro.

Authors:  Iftach Yacoby; Sergii Pochekailov; Hila Toporik; Maria L Ghirardi; Paul W King; Shuguang Zhang
Journal:  Proc Natl Acad Sci U S A       Date:  2011-05-23       Impact factor: 11.205

2.  Sustainability of in vitro light-dependent NADPH generation by the thylakoid membrane of Synechocystis sp. PCC6803.

Authors:  Xiaomeng Tong; Eui-Jin Kim; Jeong K Lee
Journal:  Microb Cell Fact       Date:  2022-05-28       Impact factor: 6.352

  2 in total

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