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Detection of Listeria monocytogenes in foods by SYBR Green I melting curve

机译:Sybr Green I熔化曲线检测食品中李斯特里亚单核细胞增生

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Two pairs of specific primers were composited based on the hlyA gene of L.monocytogenes and the 16sRNA gene of the genus Listeria. Optimal reaction system and condition of the SYBR Greenlfluorescent PCR were established, respectively, which could detect two specific genes. The reaction solution was verified by the method of gel electrophoresis. The results showed that two target fragments possessed different sizes and Tm valves which were amplfied corresponding two separate peaks. The standard curve based on the L.monocytogenes hlyA gene was established and the correlation coefficient was 0.996. The minimal detection limit was 89CFU/mL. Moreover, suspicious strain isolated from white clams was tested by using this method so as to study the feasibility. The positive result was evaluated with the National Standard Methods (GB 4789.30-2010). The verified result indicated that the positive result of SYBR Greenlfluorescent PCR matched with the GB 4789.30-2010 exactly.
机译:基于L.Monocytogenes的Hlya基因和Genus histeria的16SRNA基因进行两对特异性引物。建立了最佳反应系统和SYBR GreenlflorescencePCR的条件,分别可以检测到两个特定基因。通过凝胶电泳的方法验证反应溶液。结果表明,两个靶碎片具有不同尺寸和TM阀,其被放大相应的两个单独的峰。建立了基于L.MONOCYTOGOLESHLYA基因的标准曲线,相关系数为0.996。最小检测限为89cfu / ml。此外,通过使用该方法测试从白色蛤隔离的可疑菌株,以研究可行性。用国家标准方法(GB 4789.30-2010)评估阳性结果。经过验证的结果表明,Sybr Greenlflorescence PCR的正面结果与GB 4789.30-2010恰好。

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