| Literature DB >> 29289340 |
Yan Zhang1, Feifei Luo1, Yating Zhang1, Luqi Zhu1, Yi Li1, Shuangli Zhao1, Pingang He1, Qingjiang Wang2.
Abstract
The detection of Salmonella enterica serovar Typhimurium (S. Typhimurium) is very important for the prevention of food poisoning and other infectious diseases. Here we reported a simple and sensitive strategy to test S. Typhimurium by microchip capillary electrophoresis couple with laser-induced fluorescence (MCE-LIF) based on the specific reaction between the bacterium and corresponding aptamers. Based on the differences in charge to mass ratio between bacteria-aptamer complexes and free aptamers, a separation of the complexes and free aptamers could be obtained by MCE. The optimal parameters of the specific reaction including fluorescent dye concentration, Mg2+ concentration, incubation time, and pH of incubation solution were carefully investigated. Meanwhile, a non-specific DNA was exploited as a contrast for the detection of S. Typhimurium. Under the optimal conditions, a rapid separation of the bacteria-aptamer complex and free aptamers was achieved within 135 s with a limit of detection (S/N = 3) of 3.37 × 102 CFU mL-1. This method was applied for the detection of S. Typhimurium in fresh milk samples and a recovery rate of 95.8% was obtained. The experimental results indicated that the specific aptamers are of enough biostability and the established method could be used to analyze S. Typhimurium in foods.Entities:
Keywords: Aptamer; Bacteria; Fluorescent dye; Microchip capillary electrophoresis; Milk sample; Salmonella enterica serovar; Typhimurium
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Year: 2017 PMID: 29289340 DOI: 10.1016/j.chroma.2017.12.054
Source DB: PubMed Journal: J Chromatogr A ISSN: 0021-9673 Impact factor: 4.759