拓扑异构酶 I 抑制剂吴茱萸碱可作为一种抗耐药肺炎克雷伯菌的抗菌药物。

Topoisomerase I inhibitor evodiamine acts as an antibacterial agent against drug-resistant Klebsiella pneumoniae.

机构信息

College of Medicine, Taipei Medical University, Taipei, Taiwan.

出版信息

Planta Med. 2013 Jan;79(1):27-9. doi: 10.1055/s-0032-1327925. Epub 2012 Nov 16.

Abstract

Topoisomerase inhibitors have been developed in a variety of clinical applications. We investigated the inhibitory effect of evodiamine on E. coli topoisomerase I, which may lead to an anti-bacterial effect. Evodiamine inhibits the supercoiled plasmid DNA relaxation that is catalyzed by E. coli topoisomerase I, and computer-aided docking has shown that the Arg161 and Asp551 residues of topoisomerase I interact with evodiamine. We investigated the bactericidal effect of evodiamine against multidrug-resistant Klebsiella pneumoniae. Evodiamine showed a significantly lower minimal inhibitory concentration value (MIC 128 µg/mL) compared with antibiotics (>512 µg/mL) against the clinical isolate of K. pneumoniae. The results suggested that evodiamine is a potential agent against drug-resistant bacteria.

摘要

拓扑异构酶抑制剂已在多种临床应用中得到开发。我们研究了吴茱萸碱对大肠杆菌拓扑异构酶 I 的抑制作用,这可能导致抗菌作用。吴茱萸碱抑制由大肠杆菌拓扑异构酶 I 催化的超螺旋质粒 DNA 的松弛,计算机辅助对接表明拓扑异构酶 I 的 Arg161 和 Asp551 残基与吴茱萸碱相互作用。我们研究了吴茱萸碱对多重耐药肺炎克雷伯菌的杀菌作用。与抗生素(>512µg/mL)相比,吴茱萸碱对肺炎克雷伯菌临床分离株的最小抑菌浓度值(MIC 128µg/mL)明显更低。结果表明,吴茱萸碱是一种有潜力的抗耐药菌药物。

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