Ream L W, Clark A J
Plasmid. 1983 Sep;10(2):101-10. doi: 10.1016/0147-619x(83)90062-8.
By cloning a 3.6-kb EcoRI fragment of the Escherichia coli chromosome with pBR322 we located more precisely recF relative to dnaN. By deletion mapping we localized functional recF to a 1.65-kb region of the cloned fragment and allowed rough mapping of the C terminus of dnaN. Cloned recF+, separated from functional flanking genes dnaN and gyrB, complemented chromosomal recF mutations presumably by coding for a cytodiffusible product. The protein encoded by dnaN was observed as a band on a polyacrylamide gel from minicells. Identification of a recF protein was not made.
通过用pBR322克隆大肠杆菌染色体的一个3.6 kb的EcoRI片段,我们相对于dnaN更精确地定位了recF。通过缺失作图,我们将功能性recF定位到克隆片段的一个1.65 kb区域,并对dnaN的C末端进行了粗略定位。与功能性侧翼基因dnaN和gyrB分离的克隆recF⁺,可能通过编码一种细胞可扩散产物来互补染色体recF突变。在来自小细胞的聚丙烯酰胺凝胶上观察到由dnaN编码的蛋白质条带。未鉴定出recF蛋白。