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头孢美唑:一种对耐甲氧西林和耐头孢菌素的金黄色葡萄球菌有效的广谱头孢菌素类抗生素。

Cefmetazole: a broad spectrum cephem antibiotic effective on methicillin- and cephem-resistant Staphylococcus aureus.

作者信息

Yokota T, Yoshida R, Utsui Y, Tajima M

出版信息

Drugs Exp Clin Res. 1985;11(1):29-38.

PMID:3915273
Abstract

Antibacterial activity of cefmetazole (CMZ) was investigated by the plate dilution method. Since CMZ is stable to any type of bacterial beta-lactamases, it inhibited growth of Escherichia coli carrying R plasmids, Klebsiella spp., Proteus vulgaris, and Bacteroides fragilis at the concentration of less than 0.78 to 25.0 micrograms/ml. The distinct characteristic of CMZ is its anti-MRSA (methicillin- and cephem-resistant Staphylococcus aureus) activity. Exclusively in MRSA, a new fraction of penicillin binding proteins (PBP) with a relative molecular mass of 78 kd apears, and the 78 kd/PBP possesses low binding affinity to beta-lactam antibiotics. By the competitive binding experiment of beta-lactam drugs to the PBPs of MRSA, it was revealed that CMZ and cephaloridine retain binding affinities to the new 78kd/PBP fraction of MRSA.

摘要

采用平板稀释法研究了头孢美唑(CMZ)的抗菌活性。由于CMZ对任何类型的细菌β-内酰胺酶都稳定,它在浓度低于0.78至25.0微克/毫升时能抑制携带R质粒的大肠杆菌、克雷伯菌属、普通变形杆菌和脆弱拟杆菌的生长。CMZ的显著特点是其抗MRSA(耐甲氧西林和头孢菌素的金黄色葡萄球菌)活性。仅在MRSA中,出现了一种相对分子质量为78 kd的新型青霉素结合蛋白(PBP),且该78 kd/PBP对β-内酰胺抗生素的结合亲和力较低。通过β-内酰胺类药物与MRSA的PBPs的竞争性结合实验,发现CMZ和头孢立定对MRSA新的78 kd/PBP组分仍保持结合亲和力。

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