Copper toxicity towards Saccharomyces cerevisiae: dependence on plasma membrane fatty acid composition

One major mechanism of copper toxicity towards microorganisms is disruption of plasma membrane integrity. In this study, the influence of plasma membrane fatty acid composition on the susceptibility of Saccharomyces cerevisiae to Cu2+ toxicity was investigated. Microbial fatty acid composition is highly variable, depending on both intrinsic and environmental factors. Manipulation was achieved in this study by growth in fatty acid-supplemented medium. Whereas cells grown under standard conditions contained only saturated and monounsaturated fatty acids, considerable incorporation of the diunsaturated fatty acid linoleate (18:2) (to more than 65% of the total fatty acids) was observed in both whole-cell homogenates and plasma membrane-enriched fractions from cells grown in linoleate-supplemented medium. Linoleate enrichment had no discernible effect on the growth of S. cerevisiae. However, linoleate-enriched cells were markedly more susceptible to copper-induced plasma membrane permeabilization. Thus, after addition of Cu(NO3)2, rates of cellular K+ release (loss of membrane integrity) were at least twofold higher from linoleate-supplemented cells than from unsupplemented cells; this difference increased with reductions in the Cu2+ concentration supplied. Levels of cellular Cu accumulation were also higher in linoleate-supplemented cells. These results were correlated with a very marked dependence of whole-cell Cu2+ toxicity on cellular fatty acid unsaturation. For example, within 10 min of exposure to 5 microM Cu2+, only 3% of linoleate-enriched cells remained viable (capable of colony formation). In contrast, 100% viability was maintained in cells previously grown in the absence of a fatty acid supplement. Cells displaying intermediate levels of linoleate incorporation showed intermediate Cu2+ sensitivity, while cells enriched with the triunsaturated fatty acid linolenate (18:3) were most sensitive to Cu2+. These results demonstrate for the first time that changes in cellular and plasma membrane fatty acid compositions can dramatically alter microbial sensitivity to copper.

[1]  K. Sigler,et al.  Cd2+-induced damage to yeast plasma membrane and its alleviation by Zn2+: studies on Schizosaccharomyces pombe cells and reconstituted plasma membrane vesicles , 1996, Archives of Microbiology.

[2]  H. Joh,et al.  A Physiological Role for Saccharomyces cerevisiae Copper/Zinc Superoxide Dismutase in Copper Buffering (*) , 1995, The Journal of Biological Chemistry.

[3]  S. Avery,et al.  Temperature-dependent changes in plasma-membrane lipid order and the phagocytotic activity of the amoeba Acanthamoeba castellanii are closely correlated. , 1995, The Biochemical journal.

[4]  A. Rego,et al.  Dual effect of lipid peroxidation on the membrane order of retinal cells in culture. , 1995, Archives of biochemistry and biophysics.

[5]  A. Nakano,et al.  The plasma membrane of Saccharomyces cerevisiae: structure, function, and biogenesis. , 1995, Microbiological reviews.

[6]  M. V. van Dam-Mieras,et al.  Differential effects of endothelial cell fatty acid modification on the sensitivity of their membrane phospholipids to peroxidation. , 1995, Prostaglandins, leukotrienes, and essential fatty acids.

[7]  D. Bagchi,et al.  Oxidative mechanisms in the toxicity of metal ions. , 1995, Free radical biology & medicine.

[8]  A. Botha,et al.  The Distribution of the ω3- and ω6-Series of Cellular Long-chain Fatty Acids in Fungi , 1994 .

[9]  F. Gutiérrez-Corona,et al.  Copper resistance mechanisms in bacteria and fungi. , 1994, FEMS microbiology reviews.

[10]  C. Fanelli,et al.  Different Interactions of Fungi with Toxic Metals , 1994 .

[11]  A. Cossins Temperature adaptation of biological membranes , 1994 .

[12]  S. Avery,et al.  Mechanism of adsorption of hard and soft metal ions to Saccharomyces cerevisiae and influence of hard and soft anions , 1993, Applied and environmental microbiology.

[13]  D. White In situ measurement of microbial biomass, community structure and nutritional status , 1993, Philosophical Transactions of the Royal Society of London. Series A: Physical and Engineering Sciences.

[14]  D. Kosman,et al.  Distribution of 64Cu in Saccharomyces cerevisiae: kinetic analyses of partitioning. , 1993, Journal of general microbiology.

[15]  G. Gadd Interactions of fungip with toxic metals , 1993 .

[16]  M. Bailey,et al.  Subgrouping of bacterial populations by cellular fatty acid composition , 1993 .

[17]  S. Silver Bacterial plasmid resistances to copper, cadmium, and zinc , 1993 .

[18]  D. Stead,et al.  Evaluation of a commercial microbial identification system based on fatty acid profiles for rapid, accurate identification of plant pathogenic bacteria , 1992 .

[19]  C. Martín,et al.  Specificity of unsaturated fatty acid-regulated expression of the Saccharomyces cerevisiae OLE1 gene. , 1992, The Journal of biological chemistry.

[20]  D. Parke,et al.  Free radicals in biology and medicine (2nd Edition) : By Barry Halliwell and John M.C. Gutteridge; Clarendon Press; Oxford, 1989; xvi + 543 pages; £50.00 (cloth), £22.50 (paperback) , 1991 .

[21]  J. Harwood,et al.  The regulation of triacylglycerol biosynthesis in cocoa (Theobroma cacao) L. , 1991, Planta.

[22]  M. N. Hughes,et al.  Metal speciation and microbial growth-the hard (and soft) facts , 1991 .

[23]  G. Gadd,et al.  Ionic nutrition of yeast—physiological mechanisms involved and implications for biotechnology , 1990 .

[24]  D. Kosman,et al.  Cu,Zn superoxide dismutase and copper deprivation and toxicity in Saccharomyces cerevisiae , 1990, Journal of bacteriology.

[25]  C. Larsson,et al.  A Critical Evaluation of Markers Used in Plasma Membrane Purification , 1990 .

[26]  J. Hazel,et al.  The role of alterations in membrane lipid composition in enabling physiological adaptation of organisms to their physical environment. , 1990, Progress in lipid research.

[27]  M. Bossie,et al.  Nutritional regulation of yeast delta-9 fatty acid desaturase activity , 1989, Journal of bacteriology.

[28]  C. Martín,et al.  Isolation and characterization of OLE1, a gene affecting fatty acid desaturation from Saccharomyces cerevisiae. , 1989, The Journal of biological chemistry.

[29]  D C White,et al.  Lipid analysis in microbial ecology: quantitative approaches to the study of microbial communities. , 1989, Bioscience.

[30]  N. Murata Low-temperature effects on cyanobacterial membranes , 1989, Journal of bioenergetics and biomembranes.

[31]  Y. Anraku,et al.  Changes induced in the permeability barrier of the yeast plasma membrane by cupric ion , 1988, Journal of bacteriology.

[32]  R. Serrano H+-ATPase from plasma membranes of Saccharomyces cerevisiae and Avena sativa roots: purification and reconstitution. , 1988, Methods in enzymology.

[33]  G. Gadd,et al.  Measurement of copper uptake in Saccharomyces cerevisiae using a Cu2+-selective electrode , 1987 .

[34]  R. Mehlhorn The Interaction of Inorganic Species with Biomembranes , 1986 .

[35]  B. Halliwell,et al.  Free radicals in biology and medicine , 1985 .

[36]  H. Kappus 12 – Lipid Peroxidation: Mechanisms, Analysis, Enzymology and Biological Relevance , 1985 .

[37]  A. H. Rose,et al.  Effect of Plasma-membrane Phospholipid Unsaturation on Solute Transport into Saccharomyces cerevisiae NCYC 366 , 1982 .

[38]  K. Watson,et al.  Fatty-acyl Composition of the Lipids of Saccharomyces cerevisiae Grown Aerobically or Anaerobically in Media Containing Different Fatty Acids , 1980 .

[39]  P. Norris,et al.  Accumulation of Cadmium and Cobalt by Saccharomyces cerevisiae , 1977 .

[40]  M. M. Bradford A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. , 1976, Analytical biochemistry.

[41]  S. Ōmura,et al.  Substitution of cellular fatty acids in yeast cells by the antibiotic cerulenin and exogenous fatty acids. , 1975, Biochimica et biophysica acta.

[42]  H. Passow,et al.  The Binding of Mercury by the Yeast Cell in Relation to Changes in Permeability , 1960, The Journal of general physiology.

[43]  W. J. Dyer,et al.  A rapid method of total lipid extraction and purification. , 1959, Canadian journal of biochemistry and physiology.

[44]  K. Kellerman METALS AND MICRO-ORGANISMS. , 1910 .