Manning P A, Morelli G, Fisseau C
Gene. 1984 Jan;27(1):121-3. doi: 10.1016/0378-1119(84)90245-2.
Chimeric plasmids containing the tra operon of the Escherichia coli K-12 F factor were used to map by electron microscopy the RNA polymerase binding sites within the contiguous F EcoRI restriction fragments f6, f16, f1, f17, f19 and f2. [These fragments have been previously cloned in the EcoRI site of pSC101 to give the chimeric plasmids pRS27 (f6, f15), pRS29 (f15, f1) and pRS31 (f17, f19 and f2)]. The results may reflect the presence of a number of previously unrecognized promoters within the traY----Z operon.
含有大肠杆菌K-12 F因子tra操纵子的嵌合质粒被用于通过电子显微镜对连续的F EcoRI限制性片段f6、f16、f1、f17、f19和f2内的RNA聚合酶结合位点进行定位。[这些片段先前已克隆到pSC101的EcoRI位点,以产生嵌合质粒pRS27(f6,f15)、pRS29(f15,f1)和pRS31(f17,f19和f2)]。结果可能反映了traY----Z操纵子内存在一些先前未被识别的启动子。