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首页> 外文期刊>Czech Journal of Food Sciences >Reliability of PCR based screening for identification and quantification of GMOs
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Reliability of PCR based screening for identification and quantification of GMOs

机译:基于PCR的筛选对转基因生物进行鉴定和定量的可靠性

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Handling with genetically modified organisms (GMOs) is regulated namely in EC. Laboratories often use polymerase chain reaction (PCR) based screening methods to monitor the presence of GM particles in food commodities as a cost effective approach. The reliability was tested of such screening using 35S CaMV promoter as the target sequences. Soya grown from non-GM cultivar as declared by a seed company was investigated after the harvest, transport to the silo, and before processing. The results based on PCR and real-time PCR analysis clearly showed that, the contamination with debris of other species, dust during transport, storage, and other kind of handling led to contamination with detectable amounts of Cauliflower mosaic virus ( CaMV). Impurities are allowed by EC regulations but may, as we have shown, interfere with the analytical procedures based on PCR. The identification of 35S CaMV promoter and NOS terminator in food with uncertain history and no approved specific events may indicate unknown GMOs and perhaps emergency situation.
机译:转基因生物(GMO)的处理即在欧共体中受到规范。实验室通常使用基于聚合酶链反应(PCR)的筛选方法来监测食品中转基因颗粒的存在,这是一种经济高效的方法。使用35S CaMV启动子作为靶序列测试了这种筛选的可靠性。在收获,运输到筒仓之前和加工之前,对种子公司宣布的从非转基因品种中生长的大豆进行了调查。基于PCR和实时PCR分析的结果清楚地表明,其他物种的碎屑,运输,储存和其他处理方式中的灰尘污染导致可检测量的花椰菜花叶病毒(CaMV)污染。 EC法规允许使用杂质,但正如我们已经表明的那样,杂质可能会干扰基于PCR的分析程序。在历史不确定且没有批准的特定事件的食品中鉴定出35S CaMV启动子和NOS终止子可能表明未知的GMO以及紧急情况。

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