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PMID: 9457848 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Toxicity of linoleic acid hydroperoxide to Saccharomyces cerevisiae: involvement of a respiration-related process for maximal sensitivity and adaptive response.

Journal of bacteriology ·Vol. 180 ·No. 3 ·1998-02-00 ·Pages 483-90

Evans MV, Turton HE, Grant CM, Dawes IW

Abstract

Linoleic acid hydroperoxide (LoaOOH) formed during free radical attack on long-chain unsaturated fatty acids is an important source of biomembrane damage and is implicated in the onset of atherosclerosis, hepatic diseases, and food rancidity. LoaOOH is toxic to wild-type Saccharomyces cerevisiae at a very low concentration (0.2 mM) relative to other peroxides. By using isogenic mutant strains, the possible roles of glutathione (gsh1 and gsh2), glutathione reductase (glr1), respiratory competence ([rho0] petite), and yAP-1p-mediated expression (yap1) in conferring LoaOOH resistance have been examined. Respiration-related processes were essential for maximal toxicity and adaptation, as evidenced by the fact that the [rho0] petite mutant was most resistant to LoaOOH but could not adapt. Furthermore, when respiration was blocked by using inhibitors of respiration and mutants defective in respiratory-chain components, cells became more resistant. An important role for reduced glutathione and yAP-1 in the cellular response to LoaOOH was shown, since the yap1 and glr1 mutants were more sensitive than the wild type. In addition, total glutathione peroxidase activity increased following treatment with LoaOOH, indicating a possible detoxification role for this enzyme. Yeast also showed an adaptive response when pretreated with a nonlethal dose of LoaOOH (0.05 mM) and subsequently treated with a lethal dose (0.2 mM), and de novo protein synthesis was required, since adaptation was abolished upon treatment of cells with cycloheximide (25 microg ml-1). The wild-type adaptive response to LoaOOH was independent of those for the superoxide-generating agents paraquat and menadione and also of those for the organic hydroperoxides cumene hydroperoxide and tert-butyl hydroperoxide. Pretreatment with LoaOOH induced resistance to hydrogen peroxide, while pretreatment of cells with malondialdehyde (a lipid peroxidation product) and heat shock (37 degrees C) gave cross-adaptation to LoaOOH, indicating that yeast has effective overlapping defense systems that can detoxify fatty acid hydroperoxides directly or indirectly.

MeSH Terms
Adaptation, Physiological Drug Resistance, Microbial Electron Transport Fungal Proteins/biosynthesis Glutathione/metabolism Heat-Shock Response Hydrogen Peroxide/pharmacology Linoleic Acids/pharmacology Lipid Peroxides/pharmacology Malondialdehyde/pharmacology Oxygen/pharmacology Oxygen Consumption Saccharomyces cerevisiae/drug effects,metabolism Superoxides/pharmacology Transcription Factor AP-1/metabolism
Chemicals
Fungal Proteins Linoleic Acids Lipid Peroxides Transcription Factor AP-1 Superoxides linoleic acid hydroperoxide Malondialdehyde Hydrogen Peroxide Glutathione Oxygen
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Evans M V
School of Biochemistry and Molecular Genetics and Cooperative Research Centre for Food Industry Innovation, University of New South Wales, Sydney, Australia.
Turton H E
Grant C M
Dawes I W
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1998-02-00
Pages
483-90
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC106912
Subset
IM
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