Schmidt L S, Botta G, Park J T
J Bacteriol. 1981 Jan;145(1):632-7. doi: 10.1128/jb.145.1.632-637.1981.
Furazlocillin binds selectively to penicillin-binding protein 3 (PBP-3), prevents septation of Escherichia coli, and allows the cells to form long filaments without lysis. The effect of furazlocillin on the morphology, autolysis, and murein synthesis of E. coli mutants deficient in either PBP-1A, PBP-1Bs, or PBP-2 was studied. The results reveal that PBP-1A and PBP-1Bs functions are not equivalent since furazlocillin affects the morphology, autolysis, and murein synthesis of PBP1A- mutants quite differently from that of PBP-1Bs mutants. Different "PBP-2-" mutants were found to respond to furazlocillin in dramatically different ways: strain LS-1 cells formed elongated rods with a central bulge which eventually lysed, whereas SP6 cells formed stable "barbells" in which the two daughter cells were well separated but remained connected by a thick central region.
呋苄西林选择性地结合青霉素结合蛋白3(PBP-3),阻止大肠杆菌的隔膜形成,并使细胞形成长丝而不裂解。研究了呋苄西林对缺乏PBP-1A、PBP-1Bs或PBP-2的大肠杆菌突变体的形态、自溶和胞壁质合成的影响。结果表明,PBP-1A和PBP-1Bs的功能并不等同,因为呋苄西林对PBP1A-突变体的形态、自溶和胞壁质合成的影响与PBP-1Bs突变体有很大不同。发现不同的“PBP-2-”突变体对呋苄西林的反应截然不同:LS-1菌株细胞形成带有中央凸起的细长杆状,最终裂解,而SP6细胞形成稳定的“杠铃状”,其中两个子细胞分离良好,但通过一个厚的中央区域保持连接。