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An atypical PMR2 locus is responsible for hypersensitivity to sodium and lithium cations in the laboratory strain Saccharomyces cerevisiae CEN.PK113-7D

机译:非典型PMR2基因座负责实验室酿酒酵母CEN.PK113-7D对钠和锂阳离子的超敏反应

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摘要

Saccharomyces cerevisiae strains belonging to the CEN.PK family are widely used in fundamental and applied yeast research. These strains have been reported to be hypersensitive to sodium ions and a previous microarray-based genotyping study indicated an atypical organization of the PMR2 locus. In other S. cerevisiae strains, this locus harbours one to five ENA genes that encode plasma membrane sodium-pumping ATPases. Sequence analysis of the PMR2 locus in S. cerevisiae CEN.PK113-7D revealed the presence of a new ENA gene that showed substantial sequence differences, both at the nucleotide level and at the predicted amino acid sequence level, with previously described ENA genes. The presence of this single and atypical ENA gene correlated with hypersensitivity to sodium and, in particular, to lithium ions. The native ENA6 gene was transcriptionally induced by sodium and lithium ions, but, apparently, the capacity for sodium export upon full induction was insufficient to achieve the levels of sodium and lithium ion tolerance observed in other S. cerevisiae strains. The sodium and lithium hypersensitivity of CEN.PK strains, which is potentially detrimental during cultivation in sodium-rich media, could, however, be suppressed by overexpression of ENA6.
机译:属于CEN.PK家族的酿酒酵母菌株广泛用于基础酵母和应用酵母研究。据报道,这些菌株对钠离子过敏,以前的基于微阵列的基因分型研究表明,PMR2基因座是非典型的组织。在其他酿酒酵母菌株中,该基因座包含一到五个编码质膜钠泵ATPase的ENA基因。酿酒酵母CEN.PK113-7D中PMR2基因座的序列分析显示,存在一个新的ENA基因,该基因与先前描述的ENA基因在核苷酸水平和预测的氨基酸序列水平上均显示出明显的序列差异。该单一且非典型的ENA基因的存在与对钠,特别是对锂离子的超敏反应有关。天然的ENA6基因是由钠和锂离子转录诱导的,但是,显然,在完全诱导后钠输出的能力不足以达到在其他酿酒酵母菌株中观察到的钠和锂离子耐受性的水平。但是,ENA6的过表达可以抑制CEN.PK菌株的钠和锂超敏性,这在富含钠的培养基中培养期间可能有害。

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