Yoneyama H, Yamano Y, Nakae T
Department of Molecular Life Science, Tokai University School of Medicine, Isehara, Japan.
Biochem Biophys Res Commun. 1995 Aug 4;213(1):88-95. doi: 10.1006/bbrc.1995.2102.
We inserted deletions in the chromosomal genes of Pseudomonas aeruginosa coded for the outer membrane porins, proteins C, D2, or E1, and all possible combinations of these proteins by the gene replacement technique and selecting for imipenem-resistance. Determination of the minimum inhibitory concentrations of beta-lactams, fluoroquinolones, chloramphenicol and gentamicin in these mutants revealed that most mutants showed equal susceptibility to the porin-sufficient strain. The only exception was that imipenem and meropenem showed increased minimum inhibitory concentrations in all of the mutants lacking protein D2. These results firmly established that the P. aeruginosa porins identified so far form the pores do not accommodate the passage of most antipseudomonal antibiotics, with the exception of carbapenems.
我们通过基因置换技术在编码铜绿假单胞菌外膜孔蛋白、蛋白C、D2或E1的染色体基因中引入缺失,并选择对亚胺培南耐药的菌株。对这些突变体中β-内酰胺类、氟喹诺酮类、氯霉素和庆大霉素的最低抑菌浓度进行测定,结果显示大多数突变体对孔蛋白充足的菌株具有相同的敏感性。唯一的例外是,在所有缺乏蛋白D2的突变体中,亚胺培南和美罗培南的最低抑菌浓度有所增加。这些结果确凿地表明,迄今为止鉴定出的铜绿假单胞菌孔蛋白所形成的孔道,除碳青霉烯类抗生素外,不能容纳大多数抗铜绿假单胞菌抗生素通过。