Doran K S, Helinski D R, Konieczny I
Department of Biology, Center for Molecular Genetics, University of California, San Diego, La Jolla, CA 92093-0634, USA.
Mol Microbiol. 1999 Aug;33(3):490-8. doi: 10.1046/j.1365-2958.1999.01491.x.
The replication origin of the broad-host-range plasmid RK2, oriV, contains four DnaA boxes, which bind the DnaA protein isolated from Escherichia coli. Using a transformation assay, mutational analysis of these boxes showed a differential requirement for replication in different Gram-negative bacteria. DnaA boxes 3 and 4 were required in E. coli and Pseudomonas putidabut not as strictly in Azotobacter vinelandii and not at all in P. aeruginosa. In vitro replication results using an extract prepared from E. coli demonstrated that the activity of origin derivatives containing mutations in boxes 3 or 4 or a deletion of all four DnaA boxes could be restored by the addition of increasing amounts of purified DnaA protein. High levels of DnaA protein in the presence of the TrfA protein also resulted in the stimulation of open complex formation and DnaB helicase loading on oriV, even in the absence of the four DnaA boxes. These observations at least raise the possibility that an alternative mechanism of initiation of oriV is being used in the absence of the four DnaA boxes and that this mechanism may be similar to that used in P. aeruginosa, which does not require these four DnaA boxes for replication.
广宿主质粒RK2的复制起点oriV含有四个DnaA框,它们能结合从大肠杆菌中分离出的DnaA蛋白。通过转化分析对这些框进行突变分析,结果表明在不同的革兰氏阴性细菌中,复制对它们的需求存在差异。在大肠杆菌和恶臭假单胞菌中,DnaA框3和4是必需的,但在维氏固氮菌中要求没那么严格,而在铜绿假单胞菌中则完全不需要。使用从大肠杆菌制备的提取物进行的体外复制结果表明,通过添加越来越多的纯化DnaA蛋白,可以恢复在框3或框4中含有突变或四个DnaA框全部缺失的起点衍生物的活性。即使在没有四个DnaA框的情况下,在TrfA蛋白存在时高水平的DnaA蛋白也会导致开放复合物形成以及DnaB解旋酶在oriV上的装载受到刺激。这些观察结果至少提出了一种可能性,即在没有四个DnaA框的情况下,正在使用oriV起始的替代机制,并且这种机制可能与铜绿假单胞菌中使用的机制类似,后者复制不需要这四个DnaA框。