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The fungicide cymoxanil impairs respiration in Saccharomyces cerevisiae via cytochrome c oxidase inhibition.
Mendes, Filipa; Santos-Pereira, Cátia; Vieira, Tatiana F; Martins Pinto, Mélanie; Castro, Bruno B; Sousa, Sérgio F; Sousa, Maria João; Devin, Anne; Chaves, Susana R.
Affiliation
  • Mendes F; CBMA - Centre of Molecular and Environmental Biology/ARNET - Aquatic Research Network, Department of Biology, School of Sciences, University of Minho, Braga, Portugal.
  • Santos-Pereira C; CEB - Centre of Biological Engineering, University of Minho, Braga, Portugal.
  • Vieira TF; LABBELS - Associate Laboratory, Braga, Portugal.
  • Martins Pinto M; UCIBIO/REQUIMTE, BioSIM - Departamento de Medicina, Faculdade de Medicina da Universidade Do Porto, Portugal.
  • Castro BB; Associate Laboratory i4HB - Institute for Health and Bioeconomy, Faculdade de Medicina, Universidade do Porto, Portugal.
  • Sousa SF; CNRS, UMR 5095, Institut de Biochimie et Génétique Cellulaires, Bordeaux, France.
  • Sousa MJ; CBMA - Centre of Molecular and Environmental Biology/ARNET - Aquatic Research Network, Department of Biology, School of Sciences, University of Minho, Braga, Portugal.
  • Devin A; IBS - Institute of Science and Innovation for Bio-Sustainability, School of Sciences, University of Minho, Braga, Portugal.
  • Chaves SR; UCIBIO/REQUIMTE, BioSIM - Departamento de Medicina, Faculdade de Medicina da Universidade Do Porto, Portugal.
FEBS Lett ; 598(13): 1655-1666, 2024 Jul.
Article de En | MEDLINE | ID: mdl-38750637
ABSTRACT
Cymoxanil (CYM) is a widely used synthetic acetamide fungicide, but its biochemical mode of action remains elusive. Since CYM inhibits cell growth, biomass production, and respiration in Saccharomyces cerevisiae, we used this model to characterize the effect of CYM on mitochondria. We found it inhibits oxygen consumption in both whole cells and isolated mitochondria, specifically inhibiting cytochrome c oxidase (CcO) activity during oxidative phosphorylation. Based on molecular docking, we propose that CYM blocks the interaction of cytochrome c with CcO, hampering electron transfer and inhibiting CcO catalytic activity. Although other targets cannot be excluded, our data offer valuable insights into the mode of action of CYM that will be instrumental in driving informed management of the use of this fungicide.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Saccharomyces cerevisiae / Complexe IV de la chaîne respiratoire / Simulation de docking moléculaire / Fongicides industriels / Mitochondries Langue: En Journal: FEBS Lett Année: 2024 Type de document: Article Pays d'affiliation: Portugal Pays de publication: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Saccharomyces cerevisiae / Complexe IV de la chaîne respiratoire / Simulation de docking moléculaire / Fongicides industriels / Mitochondries Langue: En Journal: FEBS Lett Année: 2024 Type de document: Article Pays d'affiliation: Portugal Pays de publication: Royaume-Uni