Tsuda M, Iino T
Department of Biology, Faculty of Science, University of Tokyo, Japan.
Mol Gen Genet. 1988 Jul;213(1):72-7. doi: 10.1007/BF00333400.
A Pseudomonas TOL plasmid pWW0 possesses toluene degradative pathway (xyl) genes. Unstable maintenance of a pWW0 derivative in Escherichia coli allowed us to identify two transposable elements each carrying all the xyl genes. One element corresponded to a 56 kb transposon, Tn4651, which we had previously characterized. The other element newly identified in this study was 70 kb long, and this element, designated Tn4653, completely included Tn4651. Genetic analysis of Tn4653 demonstrated that its transposition involves two steps, i.e. cointegrate formation and its subsequent resolution. The former step required a trans-acting factor, transposase, which was encoded in a 3.0 kb fragment at one end of Tn4653, and the latter step was inferred to be mediated by the factors necessary for resolution of the Tn4651-mediated cointegrate. The transposase functions were not interchangeable between the two transposons.
假单胞菌TOL质粒pWW0含有甲苯降解途径(xyl)基因。pWW0衍生物在大肠杆菌中稳定性较差,这使我们能够鉴定出两个各自携带所有xyl基因的转座元件。其中一个元件对应于一个56 kb的转座子Tn4651,我们之前已对其进行了表征。本研究中新鉴定出的另一个元件长度为70 kb,该元件被命名为Tn4653,它完全包含Tn4651。对Tn4653的遗传分析表明,其转座涉及两个步骤,即共整合体的形成及其随后的拆分。前一步骤需要一种反式作用因子——转座酶,它由Tn4653一端的一个3.0 kb片段编码,而后一步骤据推测是由Tn4651介导的共整合体拆分所需的因子介导的。这两个转座子之间的转座酶功能不可互换。