Iqbal S, Robinson J, Deere D, Saunders J R, Edwards C, Porter J
Department of Genetics and Microbiology, University of Liverpool, UK.
Lett Appl Microbiol. 1997 Jun;24(6):498-502. doi: 10.1046/j.1472-765x.1997.00160.x.
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.
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。