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GMO detection in food and feed through screening by visual loop-mediated isothermal amplification assays

机译:通过视觉回路介导的等温扩增测定法筛选食品和饲料中的转基因生物

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摘要

Isothermal DNA/RNA amplification techniques are the primary methodology for developing on-spot rapid nucleic acid amplification assays, and the loop-mediated isothermal amplification (LAMP) technique has been developed and applied in the detection of foodborne pathogens, plant/animal viruses, and genetically modified (GM) food/feed contents. In this study, one set of LAMP assays targeting on eight frequently used universal elements, marker genes, and exogenous target genes, such as CaMV35S promoter, FMV35S promoter, NOS, bar, cry1Ac, CP4 epsps, pat, and NptII, were developed for visual screening of GM contents in plant-derived food samples with high efficiency and accuracy. For these eight LAMP assays, their specificity was evaluated by testing commercial GM plant events and their limits of detection were also determined, which are 10 haploid genome equivalents (HGE) for FMV35S promoter, cry1Ac, and pat assays, as well as five HGE for CaMV35S promoter, bar, NOS terminator, CP4 epsps, and NptII assays. The screening applicability of these LAMP assays was further validated successfully using practical canola, soybean, and maize samples. The results suggested that the established visual LAMP assays are applicable and cost-effective for GM screening in plant-derived food samples.
机译:等温DNA / RNA扩增技术是开发现场快速核酸扩增测定的主要方法,环介导等温扩增(LAMP)技术已经开发并应用于食源性病原体,植物/动物病毒和转基因食品/饲料含量。在这项研究中,针对以下八个常用通用元素,标记基因和外源靶基因(例如CaMV35S启动子,FMV35S启动子,NOS,bar,cry1Ac,CP4 epsps,pat和NptII)的一组LAMP分析被开发用于高效,准确地目测植物来源食品样品中的转基因含量。对于这八种LAMP分析,通过测试商业转基因植物事件评估了它们的特异性,并确定了其检出限,它们分别是FMV35S启动子,cry1Ac和pat分析的10个单倍体基因组当量(HGE),以及5个用于HMV检测的HGE。 CaMV35S启动子,bar,NOS终止子,CP4 epsps和NptII分析。使用实际的低芥酸菜籽,大豆和玉米样品进一步成功验证了这些LAMP分析的筛选适用性。结果表明,已建立的可视LAMP测定法适用于植物来源的食品样品中的GM筛选,并且具有成本效益。

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