McDowell T D, Buchanan C E, Coyette J, Swavely T S, Shockman G D
Antimicrob Agents Chemother. 1983 May;23(5):750-6. doi: 10.1128/AAC.23.5.750.
Although some strains of streptococci seem to be virtually inert to mecillinam, the growth of other strains, notably certain viridans streptococci (Streptococcus mutans and Streptococcus sanguis) was inhibited by relatively low concentrations of the drug. Inhibition of the synthesis of peptidoglycan, RNA, protein, and DNA in two tolerant strains, S. mutans FA-1 and GS-5, was studied over a wide range of concentrations of mecillinam, benzylpenicillin, and cefoxitin. The responses of both strains to all three beta-lactams were very similar; that is, synthesis of insoluble peptidoglycan was most susceptible. Inhibition of peptidoglycan synthesis was followed rapidly and sequentially by substantial but less severe inhibitions of RNA and protein synthesis. Significant inhibition of DNA synthesis was not observed. Binding studies with [14C]benzylpenicillin alone or after preexposure of membrane preparations to benzylpenicillin, mecillinam, or cefoxitin suggest that reasonably selective binding of a beta-lactam antibiotic to one or two of the major penicillin-binding proteins (PBP 1 or PBP 4) of S. mutans GS-5 and FA-1 may be the initial step in the series of events that results in the inhibition of growth and in the inhibition of insoluble peptidoglycan assembly and of RNA and protein synthesis.
虽然某些链球菌菌株似乎对美西林几乎没有反应,但其他菌株的生长,尤其是某些草绿色链球菌(变形链球菌和血链球菌),会被相对低浓度的该药物抑制。在美西林、苄青霉素和头孢西丁的广泛浓度范围内,研究了两种耐受菌株——变形链球菌FA-1和GS-5中肽聚糖、RNA、蛋白质和DNA合成的抑制情况。两种菌株对所有三种β-内酰胺类药物的反应非常相似;也就是说,不溶性肽聚糖的合成最敏感。肽聚糖合成的抑制之后,紧接着是对RNA和蛋白质合成的显著但不太严重的抑制。未观察到对DNA合成的显著抑制。单独使用[14C]苄青霉素或在膜制剂预先暴露于苄青霉素、美西林或头孢西丁后进行的结合研究表明,β-内酰胺类抗生素与变形链球菌GS-5和FA-1的一种或两种主要青霉素结合蛋白(PBP 1或PBP 4)的合理选择性结合,可能是导致生长抑制以及不溶性肽聚糖组装、RNA和蛋白质合成抑制这一系列事件的初始步骤。