Evidence for endogenous hydrogen peroxide production by E. coli fatty acyl-CoA dehydrogenase.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2024
Historique:
received: 28 06 2024
accepted: 21 08 2024
medline: 22 10 2024
pubmed: 22 10 2024
entrez: 22 10 2024
Statut: epublish

Résumé

Aerobic organisms continuously generate internal superoxide and hydrogen peroxide, which can damage enzymes and impair growth. To avoid this problem cells maintain high levels of superoxide dismutases, catalases, and peroxidases. Surprisingly, we do not know the primary sources of these reactive oxygen species (ROS) in living cells. However, in vitro studies have shown that flavoenzymes can inadvertently transfer electrons to oxygen. Therefore, it seems plausible that substantial ROS may be generated when large metabolic fluxes flow through flavoproteins. Such a situation may arise during the catabolism of fatty acids. Acyl-CoA dehydrogenase (FadE) is a flavoprotein involved in each turn of the beta-oxidation cycle. In the present study the catabolism of dodecanoic acid specifically impaired the growth of strains that lack enzymes to scavenge hydrogen peroxide. The defect was absent from fadE mutants. Direct measurements confirmed that the beta-oxidation pathway amplified the rate of intracellular hydrogen peroxide formation. Scavenging-proficient cells did not display the FadE-dependent growth defect. Those cells also did not induce the peroxide stress response during dodecanoate catabolism, indicating that the basal defenses are sufficient to cope with moderately elevated peroxide formation. In vitro work still is needed to test whether the ROS evolve specifically from the FadE flavin site and to determine whether superoxide as well as peroxide is released. At present such experiments are challenging because the natural redox partner of FadE has not been identified. This study supports the hypothesis that the degree of internal ROS production can depend upon the type of active metabolism inside cells.

Identifiants

pubmed: 39436877
doi: 10.1371/journal.pone.0309988
pii: PONE-D-24-26458
doi:

Substances chimiques

Hydrogen Peroxide BBX060AN9V
lauric acid 1160N9NU9U
Lauric Acids 0
Acyl-CoA Dehydrogenase EC 1.3.8.7
Reactive Oxygen Species 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0309988

Informations de copyright

Copyright: © 2024 Sirithanakorn, Imlay. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Chaiyos Sirithanakorn (C)

Division of Molecular and Cellular Medicine, King Mongkut's Institute of Technology Ladkrabang, Faculty of Medicine, Bangkok, Thailand.
Department of Microbiology, University of Illinois, Urbana, Illinois, United States of America.

James A Imlay (JA)

Department of Microbiology, University of Illinois, Urbana, Illinois, United States of America.

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Classifications MeSH