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Identification of a Ubiquinone-Ubiquinol Quinhydrone Complex in Bacterial Photosynthetic Membranes and Isolated Reaction Centers by Time-Resolved Infrared Spectroscopy.
Mezzetti, Alberto; Paul, Jean-François; Leibl, Winfried.
Afiliação
  • Mezzetti A; Laboratoire de Réactivité de Surface, LRS, Sorbonne Université, CNRS, 4 Place Jussieu, 75005 Paris, France.
  • Paul JF; Institute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Université Paris-Saclay, 91198 Gif sur Yvette, France.
  • Leibl W; Unité de Catalyse et Chimie du Solide, Centrale Lille Université d'Artois, Université de Lille, UMR CNRS 8181-UCCS, 59000 Lille, France.
Int J Mol Sci ; 24(6)2023 Mar 09.
Article em En | MEDLINE | ID: mdl-36982307
ABSTRACT
Ubiquinone redox chemistry is of fundamental importance in biochemistry, notably in bioenergetics. The bi-electronic reduction of ubiquinone to ubiquinol has been widely studied, including by Fourier transform infrared (FTIR) difference spectroscopy, in several systems. In this paper, we have recorded static and time-resolved FTIR difference spectra reflecting light-induced ubiquinone reduction to ubiquinol in bacterial photosynthetic membranes and in detergent-isolated photosynthetic bacterial reaction centers. We found compelling evidence that in both systems under strong light illumination-and also in detergent-isolated reaction centers after two saturating flashes-a ubiquinone-ubiquinol charge-transfer quinhydrone complex, characterized by a characteristic band at ~1565 cm-1, can be formed. Quantum chemistry calculations confirmed that such a band is due to formation of a quinhydrone complex. We propose that the formation of such a complex takes place when Q and QH2 are forced, by spatial constraints, to share a common limited space as, for instance, in detergent micelles, or when an incoming quinone from the pool meets, in the channel for quinone/quinol exchange at the QB site, a quinol coming out. This latter situation can take place both in isolated and membrane bound reaction centers Possible consequences of the formation of this charge-transfer complex under physiological conditions are discussed.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Rhodobacter sphaeroides / Complexo de Proteínas do Centro de Reação Fotossintética Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Rhodobacter sphaeroides / Complexo de Proteínas do Centro de Reação Fotossintética Idioma: En Ano de publicação: 2023 Tipo de documento: Article