Kotera Y, Inoue M, Mitsuhashi S
Episome Institute, Gunma, Japan.
Antimicrob Agents Chemother. 1990 Jul;34(7):1323-5. doi: 10.1128/AAC.34.7.1323.
The inhibitory activity of KB-5246 against Escherichia coli DNA gyrase and the antibacterial activity and apparent uptake in E. coli and Salmonella typhimurium outer membrane mutants of KB-5246 were measured. The 50% inhibitory concentrations of KB-5246, ciprofloxacin, oflaxacin, and norfloxacin for E. coli KL-16 DNA gyrase were 0.72, 0.62, 0.84, and 1.16 micrograms/ml, respectively. The activity of KB-5246 was twofold lower against an OmpF-deficient mutant and twofold higher against a mutant which produced OmpF constitutively than against the parent with osmoregulated OmpF production. KB-5246 had twofold-higher activity against a deep rough mutant of S. typhimurium than against the parent. The apparent uptake of KB-5246 in the OmpF-deficient mutant was decreased and its uptake in the deep rough mutant was increased when compared with those in the parents. These results suggest that KB-5246 is taken up by porin and nonporin pathways and has strong inhibitory activity against DNA gyrase, resulting in potent antibacterial activity.
测定了KB - 5246对大肠杆菌DNA促旋酶的抑制活性以及KB - 5246在大肠杆菌和鼠伤寒沙门氏菌外膜突变体中的抗菌活性和表观摄取量。KB - 5246、环丙沙星、氧氟沙星和诺氟沙星对大肠杆菌KL - 16 DNA促旋酶的50%抑制浓度分别为0.72、0.62、0.84和1.16微克/毫升。与渗透压调节OmpF产生的亲本相比,KB - 5246对OmpF缺陷突变体的活性低两倍,对组成型产生OmpF的突变体的活性高两倍。KB - 5246对鼠伤寒沙门氏菌的深粗糙突变体的活性比对亲本高两倍。与亲本相比,KB - 5246在OmpF缺陷突变体中的表观摄取量降低,而在深粗糙突变体中的摄取量增加。这些结果表明,KB - 5246通过孔蛋白和非孔蛋白途径摄取,对DNA促旋酶具有很强的抑制活性,从而产生强大的抗菌活性。