Avery S V, Howlett N G, Radice S
School of Biological and Molecular Sciences, Oxford Brookes University, Headington, United Kingdom.
Appl Environ Microbiol. 1996 Nov;62(11):3960-6. doi: 10.1128/aem.62.11.3960-3966.1996.
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.
铜对微生物产生毒性的一个主要机制是破坏细胞膜的完整性。在本研究中,研究了细胞膜脂肪酸组成对酿酒酵母对Cu2+毒性敏感性的影响。微生物的脂肪酸组成高度可变,这取决于内在因素和环境因素。本研究通过在补充脂肪酸的培养基中培养来实现调控。在标准条件下生长的细胞仅含有饱和脂肪酸和单不饱和脂肪酸,而在补充亚油酸的培养基中生长的细胞的全细胞匀浆和富含细胞膜的组分中,均观察到大量二不饱和脂肪酸亚油酸(18:2)的掺入(占总脂肪酸的65%以上)。亚油酸富集对酿酒酵母的生长没有明显影响。然而,富含亚油酸的细胞对铜诱导的细胞膜通透性明显更敏感。因此,添加Cu(NO3)2后,补充亚油酸的细胞中细胞钾离子释放率(膜完整性丧失)比未补充的细胞至少高两倍;随着所提供的Cu2+浓度降低,这种差异增大。补充亚油酸的细胞中细胞铜积累水平也更高。这些结果与全细胞Cu2+毒性对细胞脂肪酸不饱和度的非常明显的依赖性相关。例如,在暴露于5 microM Cu2+的10分钟内,只有3%的富含亚油酸的细胞仍具有活力(能够形成菌落)。相比之下,在先前未添加脂肪酸的培养基中生长的细胞保持100%的活力。显示亚油酸掺入中间水平的细胞表现出中间的Cu2+敏感性,而富含三不饱和脂肪酸亚麻酸(18:3)的细胞对Cu2+最敏感。这些结果首次证明细胞和细胞膜脂肪酸组成的变化可显著改变微生物对铜的敏感性。