Suppr超能文献

基于数字多用光盘的食物过敏原多重 DNA 检测

Multiplex DNA detection of food allergens on a digital versatile disk.

机构信息

Centro de Reconocimiento Molecular y Desarrollo Tecnológico, IDM, Departamento de Química, Universitat Politècnica de València, Camino de Vera, E46022 Valencia, Spain.

出版信息

J Agric Food Chem. 2012 Jan 11;60(1):36-43. doi: 10.1021/jf2037032. Epub 2011 Dec 12.

Abstract

The development of a DNA microarray method on a digital versatile disk (DVD) is described for the simultaneous detection of traces of hazelnut ( Corylus avellana L.), peanut ( Arachis hypogaea ), and soybean ( Glycine max ) in foods. After DNA extraction, multiplex PCR was set up using 5'-labeled specific primers for Cor a 1, Ar h 2, and Le genes, respectively. Digoxin-labeled PCR products were detected by hybridization with 5'-biotinylated probes immobilized on a streptavidin-modified DVD surface. The reaction product attenuates the signal intensity of the laser that reached the DVD drive used as detector, correlating well with the amount of amplified sequence. Analytical performances showed a detection limit of 1 μg/g and good assay reproducibility (RSD 8%), suitable for the simultaneous detection of the three targeted allergens. The developed methodology was tested with several commercially available foodstuffs, demonstrating its applicability. The results were in good agreement, in terms of sensitivity and reproducibility, with those obtained with ELISA, PCR-gel agarose electrophoresis, and RT-PCR.

摘要

描述了一种在数字多功能光盘(DVD)上开发的 DNA 微阵列方法,用于同时检测食品中榛子( Corylus avellana L.)、花生( Arachis hypogaea )和大豆( Glycine max )的痕迹。在提取 DNA 后,使用分别针对 Cor a 1 、Ar h 2 和 Le 基因的 5'-标记特异性引物建立了多重 PCR。地高辛标记的 PCR 产物通过与固定在链霉亲和素修饰的 DVD 表面的 5'-生物素化探针杂交进行检测。反应产物会减弱到达用作检测器的 DVD 驱动器的激光信号强度,与扩增序列的量呈良好相关。分析性能显示检测限为 1μg/g,并且具有良好的测定重现性(RSD 8%),适合同时检测三种目标过敏原。该方法已用于几种市售食品的测试,证明了其适用性。在灵敏度和重现性方面,结果与 ELISA、PCR-琼脂糖电泳和 RT-PCR 获得的结果非常吻合。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验