Stüber D, Morelli G, Bujard H, Montenegro M A, Trautner T A
Mol Gen Genet. 1981;181(4):518-21. doi: 10.1007/BF00428745.
Transcriptional complexes formed in vitro using DNA of B. subtilis phage SPP1 as template and E. coli and B. subtilis RNA polymerases were analyzed by electron microscopy. Both enzymes recognize the same five strong promoters in the early region of the genome. Strand selection at these sites was identical with both enzymes. These results correlate well with data obtained from in vivo transcription studies. Transcriptional activity in the late region of the genome was very low, not permitting the identification of promoter sites.
以枯草芽孢杆菌噬菌体SPP1的DNA为模板,利用大肠杆菌和枯草芽孢杆菌的RNA聚合酶在体外形成转录复合物,并通过电子显微镜进行分析。两种酶在基因组早期区域识别相同的五个强启动子。在这些位点的链选择对两种酶来说是相同的。这些结果与体内转录研究获得的数据高度相关。基因组晚期区域的转录活性非常低,无法确定启动子位点。