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Enumeration of viable Escherichia coli by real-time PCR with propidium monoazide

机译:单叠氮化丙锭实时荧光定量PCR扩增活菌

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A photo-inducible DNA-binding dye, propidium monoazide(PMA), was used to distinguish viable and dead Escherichia coli cells. Microscopic observations using a combination of the dyes 4′, 6-diamidino-2-phenylindole and PMA indicated that PMA stained only dead cells, with membrane damage, red. Mixtures of viable and heat-treated E. coli cells were subjected to real-time polymerase chain reaction(PCR)with PMA treatment. Viable cell counts were linearly related to real-time PCR threshold cycle values for PMA-treated cells in the mixtures of viable and heat-treated cells, as long as the ratio of dead cells to viable cells was no greater than 10. In the wastewater treatment plants, total, viable and culturable E. coli were enumerated by real-time PCR, real-time PCR coupled with PMA treatment and the most probable number method using EC-MUG medium, respectively. The concentrations of viable E. coli in the wastewater treatment plants were much higher than those of culturable cells. In addition, viable cells were even more chlorine resistant than culturable ones.
机译:光诱导DNA结合染料,单叠氮化丙锭(PMA),用于区分活的和死亡的大肠杆菌细胞。使用染料4',6-二mid基-2-苯基吲哚和PMA的组合进行的显微镜观察表明,PMA仅将死细胞染色,膜受损,呈红色。对活的和热处理过的大肠杆菌细胞混合物进行PMA处理的实时聚合酶链反应(PCR)。只要死细胞与活细胞的比例不大于10,活细胞计数与经活细胞和热处理细胞混合物中经PMA处理的细胞的实时PCR阈值循环值线性相关。通过实时荧光定量PCR,实时荧光定量PCR结合PMA处理以及使用EC-MUG培养基的最可能数法分别对处理植物的总数,存活和可培养的大肠杆菌进行计数。废水处理厂中活的大肠杆菌浓度远高于可培养细胞。另外,活细胞比可培养细胞更具耐氯性。

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