Yokota T, Yoshida R, Utsui Y, Tajima M
Drugs Exp Clin Res. 1985;11(1):29-38.
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.
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。