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开发和实验室间评估用于多重定量检测 15 种转基因大豆品系的液滴数字 PCR 分析方法。

Development and inter-laboratory assessment of droplet digital PCR assays for multiplex quantification of 15 genetically modified soybean lines.

机构信息

Department of Biotechnology and Systems Biology, National Institute of Biology, Večna pot 111, SI-1000, Ljubljana, Slovenia.

Josef Stefan International Postgraduate School, Jamova 39, SI-1000, Ljubljana, Slovenia.

出版信息

Sci Rep. 2017 Aug 17;7(1):8601. doi: 10.1038/s41598-017-09377-w.

Abstract

Quantification of genetically modified organisms (GMOs) in food and feed products is often required for their labelling or for tolerance thresholds. Standard-curve-based simplex quantitative polymerase chain reaction (qPCR) is the prevailing technology, which is often combined with screening analysis. With the rapidly growing number of GMOs on the world market, qPCR analysis becomes laborious and expensive. Innovative cost-effective approaches are therefore urgently needed. Here, we report the development and inter-laboratory assessment of multiplex assays to quantify GMO soybean using droplet digital PCR (ddPCR). The assays were developed to facilitate testing of foods and feed for compliance with current GMO regulations in the European Union (EU). Within the EU, the threshold for labelling is 0.9% for authorised GMOs per ingredient. Furthermore, the EU has set a technical zero tolerance limit of 0.1% for certain unauthorised GMOs. The novel multiplex ddPCR assays developed target 11 GMO soybean lines that are currently authorised, and four that are tolerated, pending authorisation in the EU. Potential significant improvements in cost efficiency are demonstrated. Performance was assessed for the critical parameters, including limits of detection and quantification, and trueness, repeatability, and robustness. Inter-laboratory performance was also determined on a number of proficiency programme and real-life samples.

摘要

定量检测食品和饲料产品中的转基因生物体(GMOs)通常是为了进行标签标注或达到耐受阈值。基于标准曲线的单重聚合酶链式反应(qPCR)定量检测是目前主流技术,通常与筛选分析相结合。随着世界市场上转基因生物数量的快速增长,qPCR 分析变得繁琐且昂贵。因此,急需创新的具有成本效益的方法。在这里,我们报告了使用液滴数字 PCR(ddPCR)定量检测转基因大豆的多重分析方法的开发和实验室间评估。这些分析方法旨在促进食品和饲料的检测,以符合欧盟(EU)当前的转基因生物法规。在欧盟,对于每种成分,授权的转基因生物的标记阈值为 0.9%。此外,欧盟为某些未经授权的转基因生物设定了 0.1%的技术零容忍限量。新开发的多重 ddPCR 分析方法针对目前在欧盟授权的 11 种转基因大豆品系和 4 种有待授权的品系进行检测。证明了在成本效率方面有显著的改进。对包括检测限和定量限以及准确性、重复性和稳健性在内的关键参数进行了性能评估。还在一些能力验证计划和实际样品上确定了实验室间的性能。

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