Quinone extraction drives atmospheric carbon monoxide oxidation in bacteria
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2025-07-01
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Nature Chemical Biology
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Springer Science and Business Media LLC
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Biochemistry and Pharmacology
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Journal Article
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Kropp, A., Gillett, D. L., Venugopal, H., Gonzálvez, M. A., Lingford, J. P., Jain, S., Barlow, C. K., Zhang, J., Greening, C. & Grinter, R. (2025). Quinone extraction drives atmospheric carbon monoxide oxidation in bacteria. Nature Chemical Biology, 21 (7), pp.1058-1068. https://doi.org/10.1038/s41589-025-01836-0.
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Abstract
Diverse bacteria and archaea use atmospheric CO as an energy source for long-term survival. Bacteria use [MoCu]-CO dehydrogenases (Mo-CODH) to convert atmospheric CO to carbon dioxide, transferring the obtained electrons to the aerobic respiratory chain. However, it is unknown how these enzymes oxidize CO at low concentrations and interact with the respiratory chain. Here, we use cryo-electron microscopy and structural modeling to show how Mo-CODHMs (CoxSML) from Mycobacterium smegmatis interacts with its partner, the membrane-bound menaquinone-binding protein CoxG. We provide electrochemical, biochemical and genetic evidence that Mo-CODH transfers CO-derived electrons to the aerobic respiratory chain through CoxG. Lastly, we show that Mo-CODH and CoxG genetically and structurally associate in diverse bacteria and archaea. These findings reveal the basis of the biogeochemically and ecologically important process of atmospheric CO oxidation, while demonstrating that long-range quinone transport is a general mechanism of energy conservation, which convergently evolved on multiple occasions.