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Quantitative determination of Roundup Ready soybean (Glycine max) extracted from highly processed flour

机译:从高度加工的面粉中提取的抗农达大豆的定量测定

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Roundup Ready soybean powder has been subjected to different amounts of DNA fragmentation to assess the accuracy of real-time PCR on processed food. Certified reference material (CRM) containing 10 g kg−1 of Roundup Ready soybean (ERM-BF410d) prepared by a dry-mixing processing method was exposed to water at two temperatures, using three different mixing devices, or to baking temperature (250°C) for 30 min. The amount of DNA extracted from the different samples was quantified by fluorimetry. The amount of fragmentation of the extracted DNA was characterised by gel and capillary electrophoresis and the percentage of genetically modified (GM) soybean was determined by a double quantitative real-time PCR method. Measurement of the event GTS 40-3-2 (RUR) was possible in all the treated materials, because small amplicons were amplified. Correct RUR percentages could be measured for intact powders with little or no DNA fragmentation. For samples with a high level of DNA degradation, however, the accuracy of the measurement was found to depend on the method used for DNA extraction. Genomic DNA isolated by use of silica resin resulted in statistically significant overestimation of the amount of GM.
机译:综述农达大豆粉已经历了不同量的DNA片段化,以评估加工食品上实时PCR的准确性。通过干混工艺制备的含有10 g kg-1 的农达就绪大豆(ERM-BF410d)的认证参考物质(CRM)使用两种不同的混合设备在两个温度下暴露于水,或者进行烘烤温度(250°C)30分钟。从不同样品中提取的DNA量通过荧光定量。通过凝胶和毛细管电泳对提取的DNA片段的数量进行表征,并通过双定量实时PCR方法确定转基因(GM)大豆的百分比。在所有处理过的材料中都可以测量事件GTS 40-3-2(RUR),因为扩增了小的扩增子。对于完整的粉末,几乎没有或没有DNA碎片,可以测量正确的RUR百分比。但是,对于DNA降解程度较高的样品,发现测量精度取决于DNA提取方法。通过使用硅胶树脂分离的基因组DNA导致GM量的统计显着高估。

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