Pouwels P H, de Groot G P
J Bacteriol. 1979 Aug;139(2):398-403. doi: 10.1128/jb.139.2.398-403.1979.
Ribonucleic acid (RNA) synthesis has been studied in vitro with a partially purified preparation of RNA polymerase from a mutant strain of Escherichia coli with a reduced rate of accumulation of tryptophan RNA (P.H. Pouwels and H.J. Scholten, J. Bacteriol. 139:393-397, 1979). The incorporation of radioactive label into RNA with polymerase from mutant bacteria is considerably lower than that with the enzyme from wild-type bacteria. These results are explained by the presence in mutant bacteria, but not in wild-type bacteria, of a factor which suppresses the accumulation of RNA. Mutant bacteria contain a factor which renders RNA synthesis with mutant and wild-type RNA polymerase resistant to various inhibitors of RNA synthesis, e.g. rifampin, streptolydigin, and heparin. We conclude that in mutant bacteria a factor is modified which suppresses the accumulation of some RNA species and lowers the sensitivity of RNA polymerase to some transcription inhibitors.
利用从一株色氨酸RNA积累速率降低的大肠杆菌突变株中部分纯化得到的RNA聚合酶制剂,对核糖核酸(RNA)合成进行了体外研究(P.H. 普韦尔斯和H.J. 斯科尔滕,《细菌学杂志》139:393 - 397, 1979)。与野生型细菌的酶相比,突变型细菌的聚合酶将放射性标记掺入RNA的量要低得多。这些结果可以解释为,突变型细菌中存在一种抑制RNA积累的因子,而野生型细菌中不存在。突变型细菌含有一种因子,它使突变型和野生型RNA聚合酶的RNA合成对各种RNA合成抑制剂(如利福平、链霉溶菌素和肝素)具有抗性。我们得出结论,在突变型细菌中,一种因子发生了修饰,它抑制了某些RNA种类的积累,并降低了RNA聚合酶对某些转录抑制剂的敏感性。