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首页> 外文期刊>Journal of Clinical Microbiology >Identification of 54 Mycobacterial Species by PCR-Restriction Fragment Length Polymorphism Analysis of the hsp65Gene
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Identification of 54 Mycobacterial Species by PCR-Restriction Fragment Length Polymorphism Analysis of the hsp65Gene

机译:hsp65基因PCR限制性片段长度多态性分析鉴定54种分枝杆菌

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A total of 121 reference and clinical strains of both slowly and rapidly growing mycobacteria belonging to 54 species were studied for restriction fragment length polymorphism of a PCR-amplified 439-bp segment of the gene encoding the 65-kDa heat shock protein. Restriction digests were separated by 10% polyacrylamide gel electrophoresis (PAGE). By including a size standard in each sample, the restriction fragment profile was calculated using a computer-aided comparison program. An algorithm describing these 54 species (including 22 species not previously described) is proposed. We found that this assay based on 10% PAGE provided a more precise estimate than that based on agarose gel electrophoresis of the real size of restriction fragments as deduced from the sequence analysis and allowed identification of mycobacteria whose PCR-restriction fragment length polymorphism analysis patterns were unequivocally identified by fragments shorter than 60 bp.
机译:对属于54个物种的缓慢和快速增长的分枝杆菌的121例参考和临床菌株进行了研究,研究了编码65 kDa热激蛋白的基因的PCR扩增439 bp片段的限制性片段长度多态性。通过10%聚丙烯酰胺凝胶电泳(PAGE)分离限制性消化物。通过在每个样品中加入大小标准品,使用计算机辅助比较程序计算限制性酶切片段谱。提出了描述这54种(包括先前未描述的22种)的算法。我们发现,基于序列分析推导的基于限制性酶切片段大小的琼脂糖凝胶电泳比基于琼脂糖凝胶电泳的分析方法提供了更精确的估计值,并允许鉴定PCR限制性片段长度多态性分析模式为分枝杆菌的分枝杆菌。短于60 bp的片段明确鉴定。

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