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用于检测污水中大肠杆菌的uid基因聚合酶链反应扩增效率

Efficiency of the polymerase chain reaction amplification of the uid gene for detection of Escherichia coli in contaminated water.

作者信息

Iqbal S, Robinson J, Deere D, Saunders J R, Edwards C, Porter J

机构信息

Department of Genetics and Microbiology, University of Liverpool, UK.

出版信息

Lett Appl Microbiol. 1997 Jun;24(6):498-502. doi: 10.1046/j.1472-765x.1997.00160.x.

Abstract

Direct detection of Escherichia coli from polluted river water was achieved using polymerase chain reaction (PCR) amplification of the uid gene. Amplification using DNA from environmental samples resulted in non-specific DNA fragments. Specific amplification was achieved through use of the touch-down PCR procedure. Targeting the uidA structural region of the gene gave reproducibly better amplification than targeting the uidR regulatory region. The data demonstrate conditions for optimal specific detection.

摘要

通过对uid基因进行聚合酶链反应(PCR)扩增,实现了对污染河水中大肠杆菌的直接检测。使用环境样品的DNA进行扩增产生了非特异性DNA片段。通过使用降落PCR程序实现了特异性扩增。靶向该基因的uidA结构区域比靶向uidR调控区域能产生更可重复的良好扩增效果。这些数据证明了最佳特异性检测的条件。

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