Sitailo L A, Zagariya A M, Arnold P J, Vedantam G, Hecht D W
Department of Medicine, VA Hospital, Hines, Illinois 60141, USA.
J Bacteriol. 1998 Sep;180(18):4922-8. doi: 10.1128/JB.180.18.4922-4928.1998.
The Bacteroides fragilis conjugal plasmid pBFTM10 contains two genes, btgA and btgB, and a putative oriT region necessary for transfer in Bacteroides fragilis and Escherichia coli. The BtgA protein was predicted to contain a helix-turn-helix motif, indicating possible DNA binding activity. DNA sequence analysis of the region immediately upstream of btgA revealed three sets of inverted repeats, potentially locating the oriT region. A 304-bp DNA fragment comprising this putative oriT region was cloned and confirmed to be the functional pBFTM10 oriT by bacterial conjugation experiments using E. coli and B. fragilis. btgA was cloned and overexpressed in E. coli, and the purified protein was used in electrophoretic mobility shift assays, demonstrating specific binding of BtgA protein to its cognate oriT. DNase I footprint analysis demonstrated that BtgA binds apparently in a single-stranded fashion to the oriT-containing fragment, overlapping inverted repeats I, II, and III and the putative nick site.
脆弱拟杆菌接合质粒pBFTM10包含两个基因btgA和btgB,以及一个在脆弱拟杆菌和大肠杆菌中进行转移所必需的假定oriT区域。预测BtgA蛋白含有一个螺旋-转角-螺旋基序,表明可能具有DNA结合活性。对btgA上游紧邻区域的DNA序列分析揭示了三组反向重复序列,可能定位了oriT区域。通过使用大肠杆菌和脆弱拟杆菌的细菌接合实验,克隆了包含该假定oriT区域的304 bp DNA片段,并证实其为功能性pBFTM10 oriT。克隆btgA并在大肠杆菌中过表达,将纯化的蛋白用于电泳迁移率变动分析,证明BtgA蛋白与其同源oriT特异性结合。DNase I足迹分析表明,BtgA以单链方式明显结合到含oriT的片段上,与反向重复序列I、II和III以及假定的切口位点重叠。