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Penicillin-Binding Protein 2 Is Essential for Expression of High-Level Vancomycin Resistance and Cell Wall Synthesis in Vancomycin- Resistant Staphylococcus aureus Carrying the Enterococcal vanA Gene Complex

机译:青霉素结合蛋白2是表达高水平万古霉素耐药和携带肠球菌vanA基因复合体的耐万古霉素金黄色葡萄球菌细胞壁合成所必需的

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摘要

A combination of biochemical and genetic experiments were performed in order to better understand the mechanism of expression of high-level vancomycin resistance in Staphylococcus aureus. The transcription of pbp2 of the highly vancomycin- and oxacillin-resistant strain COLVA200 and its mutant derivative with inactivated mecA were put under the control of an inducible promoter, and the dependence of oxacillin and vancomycin resistance and cell wall composition on the concentration of the isopropyl-β-d-thiogalactopyranoside inducer was determined. The results indicate that mecA—the genetic determinant of oxacillin resistance—while essential for oxacillin resistance, is not involved with the expression of vancomycin resistance. Penicillin binding protein 2A, the protein product of mecA, appears to be unable to utilize the depsipeptide cell wall precursor produced in the vancomycin-resistant cells for transpeptidation. The key penicillin binding protein essential for vancomycin resistance and for the synthesis of the abnormally structured cell walls characteristic of vancomycin-resistant S. aureus (A. Severin, K. Tabei, F. Tenover, M. Chung, N. Clarke, and A. Tomasz, J. Biol. Chem. 279:3398-3407, 2004) is penicillin binding protein 2.
机译:为了更好地了解金黄色葡萄球菌中高水平万古霉素耐药性的表达机制,进行了生化和遗传实验相结合的研究。将高度耐万古霉素和奥沙西林的菌株COLVA200的pbp2的转录及其具有灭活的mecA的突变衍生物置于诱导型启动子的控制下,并且奥沙西林和万古霉素的耐药性以及细胞壁组成对异丙基浓度的依赖性确定了-β-d-硫代半乳糖吡喃糖苷诱导剂。结果表明,mecA(奥沙西林抗性的遗传决定因素)虽然对奥沙西林具有抗性,但与万古霉素抗性的表达无关。青霉素结合蛋白2A(mecA的蛋白质产物)似乎无法利用在耐万古霉素的细胞中产生的二肽细胞壁前体进行转肽作用。关键的青霉素结合蛋白是万古霉素耐药性和耐万古霉素金黄色葡萄球菌特征的异常结构化细胞壁合成所必需的(A. Severin,K。Tabei,F。Tenover,M。Chung,N。Clarke和A Tomasz,J.Biol.Chem.279:3398-3407,2004)是青霉素结合蛋白2。

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