A 4-aminofurazan derivative-A189-inhibits assembly of bacterial cell division protein FtsZ in vitro and in vivo

被引:39
作者
Ito, Hideaki
Ura, Atsushi
Oyamada, Yoshihiro
Tanitame, Akihiko
Yoshida, Hiroaki
Yamada, Sakuo
Wachi, Masaaki
Yamagishi, Jun-ichi
机构
[1] Dainippon Sumitomo Pharma Co Ltd, Pharmacol Res Labs, Osaka 5640053, Japan
[2] Dainippon Sumitomo Pharma Co Ltd, Drug Dev Div, Osaka 5640053, Japan
[3] Dainippon Sumitomo Pharma Co Ltd, Chem Res Labs, Osaka 5640053, Japan
[4] Kawasaki Med Sch, Dept Microbiol, Okayama 7010192, Japan
[5] Tokyo Inst Technol, Dept Bioengn, Kanagawa 2268501, Japan
[6] Dainippon Sumitomo Pharma Co Ltd, Technol Res & Dev Ctr, Osaka 5410045, Japan
关键词
cell division; FtsZ; A inhibitor(s); anucleate cell;
D O I
10.1111/j.1348-0421.2006.tb03851.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Out of 95,000 commercially available chemical compounds screened by the anucleate cell blue assay, 138 selected hit compounds were further screened. As a result, A189, a 4-aminofurazan derivative was found to inhibit FtsZ GTPase with an IC50 of 80 mu g/ml and to exhibit antibacterial activity against Staphylococcus aureus and Escherichia coli. Light scattering demonstrated that A189 inhibited FtsZ assembly in vitro, and microscopic observation of A189-treated E. coli indicated that A189 perturbed FtsZ ring formation and made bacterial cells filamentous. However, nucleoids staining with DAPI revealed that A189 did not affect DNA replication and chromosome segregation in bacterial filamentous cells. Furthermore, A189 made sulA-deleted E. coli cells filamentous. Taken together, these findings suggest that A189 inhibits FtsZ GTPase activity, resulting in perturbation of FtsZ ring formation, which leads to bacterial cell death.
引用
收藏
页码:759 / 764
页数:6
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