Norfloxacin-induced DNA cleavage occurs at the dif resolvase locus in Escherichia coli and is the result of Interaction with topoisomerase IV

被引:39
作者
Hojgaard, A
Szerlong, H
Tabor, C
Kuempel, P [1 ]
机构
[1] Univ Colorado, Dept Mol Cellular & Dev Biol, Boulder, CO 80309 USA
[2] Univ Utah, Dept Pathol, Salt Lake City, UT 84112 USA
[3] Univ Utah, Dept Mol Biol, Salt Lake City, UT 84112 USA
关键词
D O I
10.1046/j.1365-2958.1999.01545.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The dif locus is a site-specific recombination site located within the terminus region of the chromosome of Escherichia coli. Recombination at dif resolves circular dimer chromosomes to monomers, and this recombination requires the XerC, XerD and FtsK proteins, as well as cell division. In order to characterize other enzymes that interact at dif,we tested whether quinolone-induced cleavage occurs at this site. Quinolone drugs, such as norfloxacin, inhibit the type 2 topoisomerases, DNA gyrase and topoisomerase IV, and can cleave DNA at sites where these enzymes interact with the chromosome. Using strains in which either DNA gyrase or topoisomerase IV, or both, were resistant to norfloxacin, we determined that specific interactions between dif and topoisomerase IV caused cleavage at that site. This interaction required XerC and XerD, but did not require the C-terminal region of FtsK or cell division.
引用
收藏
页码:1027 / 1036
页数:10
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