Blackwell K J, Tobin J M, Avery S V
School of Biological Sciences, Dublin City University, Ireland.
Appl Microbiol Biotechnol. 1997 Feb;47(2):180-4. doi: 10.1007/s002530050909.
The magnesium content of Saccharomyces cerevisiae was found to vary by up to fivefold at differing stages of batch growth and during growth in the presence of differing magnesium concentrations. Excess Mg was primarily sequestered in vacuoles. Mn(2+)-uptake experiments revealed that Mg-enriched cells had a markedly reduced capacity for Mn2+ accumulation. For example, after 6 h incubation in the presence of 50 microM Mn2+, Mn levels were approximately twofold higher in cells previously grown in unsupplemented medium than in those from Mg-supplemented medium. These differences were further accentuated at higher Mn2+ concentrations and were not attributable to altered cell-surface charge or altered cell-surface Mn2+ binding. Cellular Mg status also influenced Mn toxicity towards S. cerevisiae. During exposure to 5 mM Mn2+, 50% reductions in the viability of cells with initial Mg contents of approximately 1400 and 2700 nmol (10(9) cells)-1 occurred after approximately 1.6 h and 3.6 h respectively. In cells containing 3300 nmol Mg (10(9) cells)-1, more than 75% viability was still maintained after 7 h incubation with 5 mM Mn2+. It is concluded that Mn2+ uptake and toxicity in S. cerevisiae are strongly influenced by intracellular Mg, possibly through Mg-dependent regulation of divalent-cation transport activity.
研究发现,酿酒酵母的镁含量在分批培养的不同阶段以及在不同镁浓度存在下生长时,变化幅度可达五倍之多。过量的镁主要被隔离在液泡中。锰(Mn²⁺)摄取实验表明,富含镁的细胞积累Mn²⁺的能力明显降低。例如,在50微摩尔Mn²⁺存在下孵育6小时后,先前在未添加镁的培养基中生长的细胞中的锰含量比在添加镁的培养基中生长的细胞高出约两倍。在更高的Mn²⁺浓度下,这些差异进一步加剧,且这并非归因于细胞表面电荷的改变或细胞表面Mn²⁺结合的改变。细胞内的镁状态也影响锰对酿酒酵母的毒性。在暴露于5毫摩尔Mn²⁺的过程中,初始镁含量约为1400和2700纳摩尔(每10⁹个细胞)的细胞活力分别在约1.6小时和3.6小时后降低了50%。在含有3300纳摩尔镁(每10⁹个细胞)的细胞中,与5毫摩尔Mn²⁺孵育7小时后,仍有超过75%的细胞活力得以维持。得出的结论是,酿酒酵母中Mn²⁺的摄取和毒性受到细胞内镁的强烈影响,可能是通过镁依赖的二价阳离子转运活性调节来实现的。