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应用任意引物聚合酶链反应(AP-PCR)进行牙龈卟啉单胞菌(拟杆菌属)的菌株鉴定。

Application of polymerase chain reaction with arbitrary primer (AP-PCR) to strain identification of Porphyromonas (Bacteroides) gingivalis.

作者信息

Ménard C, Brousseau R, Mouton C

机构信息

Groupe de Recherche en Ecologie Buccale, Ecole de Médecine dentaire, Université Laval, Québec, Canada.

出版信息

FEMS Microbiol Lett. 1992 Aug 15;74(2-3):163-8. doi: 10.1111/j.1574-6968.1992.tb05360.x.

Abstract

Several molecular methods are currently available for identification and discrimination of bacterial strains within the same species, which vary in efficiency and required labour. Here we applied a novel method for fingerprinting genomes, called arbitrarily primed PCR (AP-PCR), to the delineation of strains within the species Porphyromonas gingivalis. Using a single primer on a set of nine strains, nine simple distinct banding patterns, indicative of genetic polymorphism, were observed. Common amplicons and amplicons shared by only some strains were also observed, the latter suggesting that AP-PCR can be used to generate polymorphic markers. Genomic fingerprinting obtained by AP-PCR was independent of the quality of DNA. Assays performed directly using whole cells as a source of DNA template indicated that AP-PCR from colony is a quick, simple and accurate procedure.

摘要

目前有几种分子方法可用于鉴定和区分同一物种内的细菌菌株,这些方法在效率和所需工作量方面存在差异。在此,我们将一种名为任意引物PCR(AP-PCR)的新型基因组指纹图谱方法应用于牙龈卟啉单胞菌菌株的鉴定。在一组9个菌株上使用单一引物,观察到9种简单独特的条带模式,这表明存在遗传多态性。还观察到了共同的扩增子和仅为部分菌株所共有的扩增子,后者表明AP-PCR可用于生成多态性标记。通过AP-PCR获得的基因组指纹图谱与DNA质量无关。直接使用全细胞作为DNA模板进行的检测表明,来自菌落的AP-PCR是一种快速、简单且准确的方法。

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