Ubiquinone Biosynthesis over the Entire O <sub>2</sub> Range: Characterization of a Conserved O <sub>2</sub> -Independent Pathway

Ludovic Pélosi(Institut polytechnique de Grenoble), Chau-Duy-Tam Vo(Centre National de la Recherche Scientifique), Sophie S. Abby(Institut polytechnique de Grenoble), Laurent Loiseau(Centre National de la Recherche Scientifique), Bérengère Rascalou(Institut polytechnique de Grenoble), Mahmoud Hajj Chehade(Institut polytechnique de Grenoble), Bruno Faivre(Centre National de la Recherche Scientifique), Mathieu Goussé(Institut polytechnique de Grenoble), Clothilde Chenal(Institut polytechnique de Grenoble), Nadia Touati(Centre National de la Recherche Scientifique), Laurent Binet(Centre National de la Recherche Scientifique), David Cornu(Institut de Biologie Intégrative de la Cellule), Cameron D. Fyfe(Centre National de la Recherche Scientifique), Marc Fontecave(Centre National de la Recherche Scientifique), Frédéric Barras(Centre National de la Recherche Scientifique), Murielle Lombard(Centre National de la Recherche Scientifique), Fabien Pierrel(Institut polytechnique de Grenoble)
mBio
July 8, 2019
Cited by 55Open Access
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Abstract

In order to colonize environments with large O 2 gradients or fluctuating O 2 levels, bacteria have developed metabolic responses that remain incompletely understood. Such adaptations have been recently linked to antibiotic resistance, virulence, and the capacity to develop in complex ecosystems like the microbiota. Here, we identify a novel pathway for the biosynthesis of ubiquinone, a molecule with a key role in cellular bioenergetics. We link three uncharacterized genes of Escherichia coli to this pathway and show that the pathway functions independently from O 2 . In contrast, the long-described pathway for ubiquinone biosynthesis requires O 2 as a substrate. In fact, we find that many proteobacteria are equipped with the O 2 -dependent and O 2 -independent pathways, supporting that they are able to synthesize ubiquinone over the entire O 2 range. Overall, we propose that the novel O 2 -independent pathway is part of the metabolic plasticity developed by proteobacteria to face various environmental O 2 levels.


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