Sorokin V M, Goncharov E K, Mishan'kin B N
Mol Gen Mikrobiol Virusol. 1989 Jun(6):39-42.
Molecules of the plasmids pBR322 and pRD17 have been compared by electron microscopy technique of R-loops visualization. Comparative location of R-loops on the plasmids has been computerized on minicomputer HP9825A due to the program making possible to define the coordinates of the transcription start and direction. The 5.1 kb fragment coding for pesticin I and immunity protein to pesticin I and cloned in pBR322 vector plasmid is flanked by Bam HI-EcoRI sites. Five promoter regions and direction of transcription were localized on the fragment.
已通过R环可视化电子显微镜技术对质粒pBR322和pRD17的分子进行了比较。由于该程序能够确定转录起始坐标和方向,因此已在小型计算机HP9825A上对质粒上R环的相对位置进行了计算机处理。编码杀稻瘟菌素I和杀稻瘟菌素I免疫蛋白并克隆于pBR322载体质粒中的5.1kb片段,其两侧为Bam HI - EcoRI位点。在该片段上定位了五个启动子区域和转录方向。