Paradkar A S, Aidoo K A, Wong A, Jensen S E
Department of Biological Sciences, University of Alberta, Edmonton, Canada.
J Bacteriol. 1996 Nov;178(21):6266-74. doi: 10.1128/jb.178.21.6266-6274.1996.
A Streptomyces clavuligerus gene (designated pcbR) which is located immediately downstream from the gene encoding isopenicillin N synthase in the cephamycin gene cluster was characterized. Nucleotide sequence analysis and database searching of PcbR identified a significant similarity between PcbR and proteins belonging to the family of high-molecular-weight group B penicillin-binding proteins (PBPs). Eight of nine boxes (motifs) conserved within this family of proteins are present in the PcbR protein sequence in the same order and with approximately the same spacing between them. When a mutant disrupted in pcbR was constructed by gene replacement, the resulting pcbR mutant exhibited a significant decrease in its resistance to benzylpenicillin and cephalosporins, indicating that pcbR is involved in beta-lactam resistance in this organism. Western blot (immunoblot) analysis of S. clavuligerus cell membranes using PcbR-specific antibodies suggested that PcbR is a membrane protein. PcbR was also present in cell membranes when expressed in Escherichia coli and was able to bind radioactive penicillin in a PBP assay, suggesting that PcbR is a PBP. When genomic DNAs from several actinomycetes were probed with pcbR, hybridization was observed to some but not all beta-lactam-producing actinomycetes.
对链霉菌属产棒酸链霉菌中一个基因(命名为pcbR)进行了表征,该基因位于头孢霉素基因簇中编码异青霉素N合酶的基因紧邻下游。对PcbR进行核苷酸序列分析和数据库搜索发现,PcbR与高分子量B组青霉素结合蛋白(PBPs)家族的蛋白质具有显著相似性。该蛋白质家族中保守的九个框(基序)中的八个以相同顺序且它们之间具有大致相同的间距存在于PcbR蛋白序列中。当通过基因置换构建pcbR中断的突变体时,所得的pcbR突变体对苄青霉素和头孢菌素的抗性显著降低,这表明pcbR参与了该生物体中的β-内酰胺抗性。使用PcbR特异性抗体对产棒酸链霉菌细胞膜进行的蛋白质免疫印迹(免疫印迹)分析表明PcbR是一种膜蛋白。当在大肠杆菌中表达时,PcbR也存在于细胞膜中,并且在PBP测定中能够结合放射性青霉素,这表明PcbR是一种PBP。当用pcbR探测几种放线菌的基因组DNA时,观察到一些但不是所有产β-内酰胺的放线菌发生了杂交。