Nnalue N A
Department of Microbiology and Immunology, Stanford University School of Medicine, California 94305.
Mol Microbiol. 1990 Jan;4(1):107-17. doi: 10.1111/j.1365-2958.1990.tb02019.x.
Pasteurella multocida transconjugants isolated after mating with Escherichia coli strains that carry one or the other of two Tn7-containing suicide plasmids, pRKTV5 and pUW964 (pRKTV5::Tn5), were analysed. These plasmids have the ColE1 replication origin and were thus expected to deliver transposons but not be maintained as free replicons in Pasteurella. Five out of six transconjugants selected for acquisition of Tn7 from E. coli (pRKTV5) had simple insertions of the transposon, in either orientation, at a single chromosomal location, while the sixth had pRKTV5 integrated at the same location. By contrast, all of 27 transconjugants selected for acquisition of either Tn7 or Tn5 from E. coli (pUW964) maintained pUW964. Of seven subsequently examined at the molecular level, all had pUW964 (in one case, a deletion derivative) integrated at the same location as the Tn7 insertions obtained with pRKTV5. A copy of Tn7 was present at each boundary between the integrated plasmids (pRKTV5 or pUW964) and the chromosome in each strain. The two copies of Tn7 at either end of an integrated plasmid were either in the same (six cases) or in opposite (two cases) orientations with respect to each other. These seem to be products of replicative transposition by Tn7 but can also derive from conservative mechanisms.
分析了多杀性巴氏杆菌与携带两种含Tn7自杀质粒(pRKTV5和pUW964(pRKTV5::Tn5))之一的大肠杆菌菌株交配后分离得到的接合子。这些质粒具有ColE1复制起点,因此预计会传递转座子,但不会在巴氏杆菌中作为游离复制子维持。从大肠杆菌(pRKTV5)获得Tn7的六个接合子中有五个在单个染色体位置以任一方向简单插入了转座子,而第六个则在同一位置整合了pRKTV5。相比之下,从大肠杆菌(pUW964)获得Tn7或Tn5的27个接合子都维持了pUW964。在随后进行分子水平检测的七个接合子中,所有接合子的pUW964(在一个案例中为缺失衍生物)都整合在与用pRKTV5获得的Tn7插入相同的位置。在每个菌株中,整合质粒(pRKTV5或pUW964)与染色体之间的每个边界处都存在一份Tn7。整合质粒两端的两份Tn7彼此之间要么方向相同(六个案例),要么方向相反(两个案例)。这些似乎是Tn7复制转座的产物,但也可能源自保守机制。