利用含有热诱导启动子- lacZ转录融合的金黄色葡萄球菌报告菌株开发的生物检测系统检测抗葡萄球菌和有毒化合物。

Palas Kumar Chanda, Tridib Ganguly, Malabika Das, Chia Yen Lee, Thanh T Luong, Subrata Sau
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引用次数: 9

摘要

此前有报道称,多种细胞壁活性抗生素可诱导金黄色葡萄球菌groES-groEL操纵子的启动子。为了利用上述启动子鉴定新型抗葡萄球菌药物,我们克隆了金黄色葡萄球菌(S. aureus Newman) groES-groEL操纵子的启动子含区(P(g)),发现上述启动子可被包括细胞壁活性抗生素在内的多种抗生素亚致死浓度诱导。将P(g)-lacZ转录融合片段插入到金黄色葡萄球菌RN4220染色体中,构建了金黄色葡萄球菌RN4220报告菌株SAU006。用SAU006建立的琼脂糖实验表明,不同种类的抗生素对单拷贝的P(g)也有明显的诱导作用。数据表明,环丙沙星、利福平、氨苄西林和头孢菌素是强诱导剂,而四环素、链霉素和万古霉素对上述启动子的诱导作用较弱。亚致死浓度的环丙沙星和氨苄西林甚至在培养的SAU006中有效诱导P(g)。进一步的研究首次表明上述启动子也被砷酸盐和过氧化氢弱诱导。综上所述,我们的SAU006检测系统不仅可以用于新型抗葡萄球菌化合物的筛选和检测,还可以用于不同毒性化学物质的筛选和检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Detection of antistaphylococcal and toxic compounds by biological assay systems developed with a reporter Staphylococcus aureus strain harboring a heat inducible promoter - lacZ transcriptional fusion.

Previously it was reported that promoter of groES-groEL operon of Staphylococcus aureus is induced by various cell-wall active antibiotics. In order to exploit the above promoter for identifying novel antistaphylococcal drugs, we have cloned the promoter containing region (P(g)) of groES-groEL operon of S. aureus Newman and found that the above promoter is induced by sublethal concentrations of many antibiotics including cell-wall active antibiotics. A reporter S. aureus RN4220 strain (designated SAU006) was constructed by inserting the P(g)-lacZ transcriptional fusion into its chromosome. Agarose-based assay developed with SAU006 shows that P(g) in single-copy is also induced distinctly by different classes of antibiotics. Data indicate that ciprofloxacin, rifampicin, ampicillin, and cephalothin are strong inducers, whereas, tetracycline, streptomycin and vancomycin induce the above promoter weakly. Sublethal concentrations of ciprofloxacin and ampicilin even have induced P(g) efficiently in microtiter plate grown SAU006. Additional studies show for the first time that above promoter is also induced weakly by arsenate salt and hydrogen peroxide. Taken together, we suggest that our simple and sensitive assay systems with SAU006 could be utilized for screening and detecting not only novel antistaphylococcal compounds but also different toxic chemicals.

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