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使用手持式聚合酶链反应(PCR)设备对食品样本中的抗草甘膦转基因大豆进行快速筛查。

Rapid screening of roundup ready soybean in food samples by a hand-held PCR device.

作者信息

Tung Hsiang-Yun, Wang Sue-Hong, Chiang Yu-Cheng, Tsai Ming-Shiun

机构信息

1College of Biotechnology and Bioresources, Da-Yeh University, Changhua, Taiwan, 51591 China.

Department of Biomedical Sciences, Chung Shan Medical University, Taichung, Taiwan, 402 China.

出版信息

Food Sci Biotechnol. 2016 Aug 31;25(4):1101-1107. doi: 10.1007/s10068-016-0177-5. eCollection 2016.

Abstract

Insulated isothermal PCR (iiPCR) method was recently available for rapid on-site detection of roundup ready soybean (RRS; event GTS40-3-2) in food materials and products. Performance of this method was evaluated in this study. The 100% detection endpoint for the RRS by iiPCR was found in samples containing 0.1% RRS, equivalent to the results of the reference real-time PCR (rtPCR). Analysis of nucleic acids of soybean-based processed food products indicated 95% agreement between the iiPCR and rtPCR for RRS detection. By testing soybean milk and tofu samples using simple pretreatment methods, we found that the agreements between iiPCR and rtPCR methods of the aforementioned samples were 80% and 90%, respectively. Replicated tests of all discrepant samples implied that these samples had trace amounts of RRS, suggesting that the iiPCR system is more sensitive than the rtPCR method. In conclusion, the iiPCR technology can be a useful point-of-need tool to help make a timely decision in the consumption of genetically modified organisms.

摘要

绝缘等温PCR(iiPCR)方法最近可用于快速现场检测食品原料和产品中的抗草甘膦转基因大豆(RRS;事件GTS40-3-2)。本研究对该方法的性能进行了评估。通过iiPCR检测RRS的100%检测终点在含有0.1%RRS的样品中发现,这与参考实时PCR(rtPCR)的结果相当。对大豆加工食品的核酸分析表明,iiPCR和rtPCR在检测RRS方面的一致性为95%。通过使用简单的预处理方法检测豆浆和豆腐样品,我们发现上述样品的iiPCR和rtPCR方法之间的一致性分别为80%和90%。对所有差异样品的重复测试表明,这些样品含有微量的RRS,这表明iiPCR系统比rtPCR方法更敏感。总之,iiPCR技术可以成为一种有用的现场需求工具,有助于在转基因生物消费方面及时做出决策。

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本文引用的文献

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