Dharmgrongartama B, Mahadik S P, Srinivasan P R
Proc Natl Acad Sci U S A. 1973 Oct;70(10):2845-9. doi: 10.1073/pnas.70.10.2845.
E. coli B cells infected with T3 phage contain a modified host RNA polymerase in addition to the normal RNA polymerase found in uninfected cells. The modified RNA polymerase behaves differently in its elution properties from the normal enzyme on DEAE-cellulose, phosphocellulose, and DNA-cellulose column chromatography. The modified enzyme also differs from the normal polymerase in some of its enzymatic parameters. The specific activity of the modified RNA polymerase is markedly lower (i.e., (1/4)) than that of the normal enzyme. The decrease in activity is probably due to an alteration in the beta' subunit of the polymerase. A similar modification is also observed in nonpermissive cells infected with a gene-l amber mutant incapable of producing active T3 specific polymerase. An analogous modification in host RNA polymerase does not seem to occur in E. coli cells infected with T7 phage.
被T3噬菌体感染的大肠杆菌B细胞,除了含有未感染细胞中正常的RNA聚合酶外,还含有一种经过修饰的宿主RNA聚合酶。在DEAE - 纤维素、磷酸纤维素和DNA - 纤维素柱层析中,这种经过修饰的RNA聚合酶的洗脱特性与正常酶不同。修饰后的酶在一些酶学参数上也与正常聚合酶不同。修饰后的RNA聚合酶的比活性明显低于正常酶(即(1/4))。活性降低可能是由于聚合酶的β'亚基发生了改变。在被无法产生活性T3特异性聚合酶的基因1琥珀突变体感染的非允许细胞中也观察到类似的修饰。在被T7噬菌体感染的大肠杆菌细胞中,宿主RNA聚合酶似乎不会发生类似的修饰。