Burkardt H J, Riess G, Pühler A
J Gen Microbiol. 1979 Oct;114(2):341-8. doi: 10.1099/00221287-114-2-341.
The molecular relationships of the IncP1 plasmids RP1, RP4, R68 and RK2 were tested by electron microscopic examination of heteroduplexes. In several hybridization experiments molecules were detected which had a 7.8% portion of incomplete reannealing. This 'heterologous region' could be explained by the typical renaturation behaviour of the transposon Tn1. The identity of the Tn1 transposon present in RP1 and RP4 was proved by heteroduplex experiments with lambda phage DNA containing this transposon. These results indicated that the plasmids RP1 and RP4 are identical. Additional heteroduplex experiments between plasmids R68.45 and RP8 and between R68.45 and RK2 were performed. R68.45, a derivative of R68, has a small DNA insertion and RP8 can be regarded as a large insertion mutant of RP4; both insertions were used as single-stranded hybridization markers. From the hybrid molecules formed, it was deduced that R68 and RK2 are identical with RP1 and RP4 as far as molecular structure is revealed by the technique used.
通过对异源双链体进行电子显微镜检查,测试了IncP1质粒RP1、RP4、R68和RK2之间的分子关系。在几个杂交实验中,检测到分子中有7.8%的部分未完全复性。这个“异源区域”可以用转座子Tn1的典型复性行为来解释。通过与含有该转座子的λ噬菌体DNA进行异源双链实验,证实了RP1和RP4中存在的Tn1转座子的同一性。这些结果表明质粒RP1和RP4是相同的。还进行了质粒R68.45与RP8以及R68.45与RK2之间的额外异源双链实验。R68.45是R68的衍生物,有一个小的DNA插入片段,而RP8可被视为RP4的一个大插入突变体;这两个插入片段都用作单链杂交标记。从形成的杂交分子推断,就所用技术揭示的分子结构而言,R68和RK2与RP1和RP4相同。