Alonso M A, Vázquez D, Carrasco L
Antimicrob Agents Chemother. 1979 Dec;16(6):750-6. doi: 10.1128/AAC.16.6.750.
The regulation of translation has been investigated in yeast cells by means of ionophores and other compounds affecting the ionic concentration inside the cell. Treatment of a variety of cells with these compounds produces a drastic inhibition in the protein-synthesizing activity of the cell. Protein synthesis in yeast is strongly inhibited by amphotericin B and nystatin. Mammalian cells are blocked in their translation capacity by gramicidin D, nigericin, monensin, nystatin, A23187, and bromolasalocid. The effects of these compounds on protein synthesis in Escherichia coli and Staphylococcus aureus were also investigated. Amphotericin B is a powerful inhibitor of both protein and ribonucleic acid syntheses in yeast cells at concentrations that do not affect the transport of the labeled amino acid or nucleoside precursor. The analysis of the polysomal profiles in yeast spheroplasts could indicate that initiation is the target of amphotericin B action on translation. Studies on the reversion of the protein synthesis blockade by amphotericin B by increasing the potassium concentration in the medium suggest that changes in the potassium concentration in cellular cytoplasm might be responsible, at least in part, for the inhibition of protein synthesis.
通过离子载体和其他影响细胞内离子浓度的化合物,对酵母细胞中的翻译调控进行了研究。用这些化合物处理各种细胞会对细胞的蛋白质合成活性产生强烈抑制。两性霉素B和制霉菌素能强烈抑制酵母中的蛋白质合成。短杆菌肽D、尼日利亚菌素、莫能菌素、制霉菌素、A23187和溴化拉萨洛菌素会阻碍哺乳动物细胞的翻译能力。还研究了这些化合物对大肠杆菌和金黄色葡萄球菌蛋白质合成的影响。两性霉素B在不影响标记氨基酸或核苷前体转运的浓度下,是酵母细胞中蛋白质和核糖核酸合成的强力抑制剂。对酵母原生质体多核糖体图谱的分析表明,起始阶段是两性霉素B作用于翻译的靶点。通过增加培养基中的钾浓度来研究两性霉素B对蛋白质合成阻断的逆转,结果表明细胞质中钾浓度的变化可能至少部分地导致了蛋白质合成的抑制。