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喹诺酮类药物对原核和真核DNA拓扑异构酶I和II的抑制作用。

Inhibitory effects of quinolones on pro- and eucaryotic DNA topoisomerases I and II.

作者信息

Moreau N J, Robaux H, Baron L, Tabary X

机构信息

Centre d'Etudes et de Recherche en Chimie Organique Appliquée, Centre National de la Recherche Scientifique, Thiais, France.

出版信息

Antimicrob Agents Chemother. 1990 Oct;34(10):1955-60. doi: 10.1128/AAC.34.10.1955.

Abstract

As a means of gaining information on the selectivity of quinolone antibacterial agents, we examined their effect on four topoisomerases, topoisomerases I and II purified from Escherichia coli and calf thymus. The inhibition of supercoiling and relaxation activities was monitored by using the classical gel electrophoresis assay. Eight quinolones were assayed by using the four enzymes. Gyrase was much more sensitive to quinolones than the other topoisomerases which can therefore be inhibited by moderate concentrations of certain quinolones. No good correlation was observed between the activity on gyrase and on the other enzymes, since the ratio varied from 15 to more than 8,500. On the contrary, there was a good correlation between early inhibition of DNA synthesis, inhibition of gyrase, and MICs.

摘要

作为获取喹诺酮类抗菌剂选择性信息的一种方法,我们研究了它们对四种拓扑异构酶的作用,即从大肠杆菌和小牛胸腺中纯化得到的拓扑异构酶I和II。通过经典的凝胶电泳分析监测超螺旋和松弛活性的抑制情况。使用这四种酶对八种喹诺酮类药物进行了检测。与其他拓扑异构酶相比,gyrase对喹诺酮类药物更为敏感,因此某些喹诺酮类药物的中等浓度即可抑制其他拓扑异构酶。在gyrase和其他酶上的活性之间未观察到良好的相关性,因为该比值在15到超过8500之间变化。相反,DNA合成的早期抑制、gyrase的抑制与最低抑菌浓度之间存在良好的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a092/171971/ac66758a8657/aac00066-0128-a.jpg

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