Noguchi N, Katayama J, Sasatsu M
Department of Microbiology, School of Pharmacy, Tokyo University of Pharmacy and Life Science, 1432-1 Horinouchi, Hachioji, 192-0392, Tokyo, Japan.
FEMS Microbiol Lett. 2000 Nov 15;192(2):175-8. doi: 10.1111/j.1574-6968.2000.tb09378.x.
The mphB gene for macrolide 2'-phosphotransferase II is located on two plasmids, pTZ3721 and pTZ3723, in Escherichia coli BM2506. We examined translocation of mphB that originated from pTZ3721. The transposable element carrying mphB is 39 kb long and has a Tn21-like transposition module at one end and a Tn1721-like transposition module at other. The structure of the transposition modules of this element resembles that of Tn2610. However, the gene arrangement of the internal region on the transposon carrying mphB was reverse to that of Tn2610. The nucleotide sequences of both terminal regions suggested that the inversion of the DNA fragment occurred between the res sites by resolvase-mediated recombination.
在大肠杆菌BM2506中,编码大环内酯2'-磷酸转移酶II的mphB基因位于两个质粒pTZ3721和pTZ3723上。我们研究了源自pTZ3721的mphB的易位情况。携带mphB的转座元件长39 kb,一端有一个Tn21样转座模块,另一端有一个Tn1721样转座模块。该元件转座模块的结构与Tn2610的相似。然而,携带mphB的转座子内部区域的基因排列与Tn2610的相反。两个末端区域的核苷酸序列表明,DNA片段的倒位是由解离酶介导的重组在res位点之间发生的。