McCorquodale D J, Chen C W, Joseph M K, Woychik R
J Virol. 1981 Dec;40(3):958-62. doi: 10.1128/JVI.40.3.958-962.1981.
RNA polymerase from cells of Escherichia coli infected with T5 were recovered as a complex with two pre-early phage-coded polypeptides, the 60,000-dalton product of gene A1 and a previously reported 11,000-dalton polypeptide. This RNA polymerase complex had altered transcriptional specificity, in that it transcribed pre-early genes less efficiently than it did early genes.
从感染了T5噬菌体的大肠杆菌细胞中回收的RNA聚合酶,是与两种前早期噬菌体编码的多肽形成的复合物,即基因A1的60000道尔顿产物和先前报道的11000道尔顿多肽。这种RNA聚合酶复合物具有改变的转录特异性,即它转录前早期基因的效率低于转录早期基因的效率。