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Isolation, Amplification and Characterization of Foodborne Pathogen Disease Bacteria Gene for Rapid Kit Test Development

机译:食品源病原体疾病菌类基因的分离,扩增与表征快速试剂盒试验发育

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There is a lot of public concern over food safety. Food-safety cases recently, including many food poisoning cases in both the developed and developing countries, considered to be the national security threats which involved police investigation. Quick and accurate detection methods are needed to handle the food poisoning cases with a big number of sufferers at the same time. Therefore, the research is aimed to develop a specific, sensitive, and rapid result molecular detection tool for foodborne pathogen bacteria. We, thus, propose genomic level approach with Polymerase Chain Reaction. The research has successfully produced a specific primer to perform amplification to fim-C S. typhi, E. coli, and pef Salmonella typhimurium genes. The electrophoresis result shows that amplification products are 95 base pairs, 121 base pairs, and 139 base pairs; and all three genes are in accordance with the size of the in silico to third genes bacteria. In conclusion, the research has been successfully designed a specific detection tool to three foodborne pathogen bacteria genes. Further stages test and the uses of Real-time PCR in the detection are still in the trial process for better detection method.
机译:对食品安全有很多公众关注。最近食品安全案例,包括发达国家和发展中国家的许多食物中毒案例,被认为是涉及警察调查的国家安全威胁。快速准确的检测方法需要在同一时间处理患有大量患者的食物中毒病例。因此,该研究旨在为食源性病原体细菌开发特定,敏感和快速的结果分子检测工具。因此,我们提出了具有聚合酶链反应的基因组水平方法。该研究成功地生产了对FIM-C S.Typhi,大肠杆菌和PEF沙门氏菌的扩增的特异性引物。电泳结果表明,扩增产物是95个碱基对,121个碱基对和139个碱基对;并且所有三个基因都按照硅的大小为三种基因细菌。总之,该研究已经成功设计了三种食源性病原体细菌基因的特定检测工具。进一步的阶段测试和检测中的实时PCR的用途仍在试验过程中以获得更好的检测方法。

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