An electrogenic redox loop in sulfate reduction reveals a likely widespread mechanism of energy conservation

Américo G. Duarte, Teresa Catarino, Gaye F. White, Diana Lousa, Sinje Neukirchen, Cláudio M. Soares, Filipa L. Sousa, Thomas A. Clarke and Inês A. C. Pereira ()
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Américo G. Duarte: Universidade Nova de Lisboa
Teresa Catarino: Universidade Nova de Lisboa
Gaye F. White: University of East Anglia
Diana Lousa: Universidade Nova de Lisboa
Sinje Neukirchen: University of Vienna
Cláudio M. Soares: Universidade Nova de Lisboa
Filipa L. Sousa: University of Vienna
Thomas A. Clarke: University of East Anglia
Inês A. C. Pereira: Universidade Nova de Lisboa

Nature Communications, 2018, vol. 9, issue 1, 1-11

Abstract: Abstract The bioenergetics of anaerobic metabolism frequently relies on redox loops performed by membrane complexes with substrate- and quinone-binding sites on opposite sides of the membrane. However, in sulfate respiration (a key process in the biogeochemical sulfur cycle), the substrate- and quinone-binding sites of the QrcABCD complex are periplasmic, and their role in energy conservation has not been elucidated. Here we show that the QrcABCD complex of Desulfovibrio vulgaris is electrogenic, as protons and electrons required for quinone reduction are extracted from opposite sides of the membrane, with a H+/e− ratio of 1. Although the complex does not act as a H+-pump, QrcD may include a conserved proton channel leading from the N-side to the P-side menaquinone pocket. Our work provides evidence of how energy is conserved during dissimilatory sulfate reduction, and suggests mechanisms behind the functions of related bacterial respiratory complexes in other bioenergetic contexts.

Date: 2018
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DOI: 10.1038/s41467-018-07839-x

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