Pinho M G, de Lencastre H, Tomasz A
Laboratory of Microbiology, The Rockefeller University, New York, New York 10021, USA.
J Bacteriol. 1998 Dec;180(23):6077-81. doi: 10.1128/JB.180.23.6077-6081.1998.
Sequencing of the vicinity of the staphylococcal pbp2 gene and transcriptional analysis by primer extension and promoter fusions were used to show that pbp2 is part of an operon that also includes a gene with high homology to prfA of Bacillus subtilis. Two distinct promoters were identified directing transcription of pbp2 either alone or together with prfA. It was recently reported that transposon inactivation of pbp2 causes a reduction in methicillin resistance, but complementation experiments were not fully successful. We now show that introduction of the intact pbp2 gene with its two newly identified promoters into the chromosome of the transposon mutant resulted in the full recovery of high-level methicillin resistance.
对葡萄球菌pbp2基因附近区域进行测序,并通过引物延伸和启动子融合进行转录分析,结果表明pbp2是一个操纵子的一部分,该操纵子还包括一个与枯草芽孢杆菌prfA具有高度同源性的基因。鉴定出了两个不同的启动子,分别单独指导pbp2的转录或与prfA一起指导转录。最近有报道称,pbp2的转座子失活会导致耐甲氧西林能力降低,但互补实验并不完全成功。我们现在表明,将完整的pbp2基因及其两个新鉴定的启动子导入转座子突变体的染色体中,可使高水平耐甲氧西林能力完全恢复。