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从两种适用于聚合酶链反应检测鉴定的食品添加剂中分离DNA的新方法。

New method of DNA isolation from two food additives suitable for authentication in polymerase chain reaction assays.

作者信息

Urdiaín Mercedes, Doménech-Sánchez Antonio, Albertí Sebastián, Benedí V Javier, Rosselló Josep A

机构信息

Microbiologia, Departament de Biología, Universitat de les Illes Balears, E-07071 Palma de Mallorca, Spain.

出版信息

J Agric Food Chem. 2005 May 4;53(9):3345-7. doi: 10.1021/jf0482919.

Abstract

Locust bean gum and guar gum are galactomannans used as additives (E 410 and E 412, respectively) in the food industry as stabilizing agents. Analytical discrimination between the two additives in gums and foods is now feasible by molecular techniques. However, only complex and time-consuming DNA isolation protocols are available to date. We have developed simple improved protocols to obtain enough DNA suitable for PCR amplification from a few milligrams of commercial E 410 and E 412 additives (containing more than 75% polysaccharides). The suspension of additives in water or 10 mM Tris-HCl, pH 8.5, efficiently recovers DNA suitable for authentication in PCR assays. However, the Tris method was much more efficient for the extraction of DNA from E 410 than for E 412 additives. Conversely, the water method was the most suitable for detecting DNA extracted from E 412 or from E 410/E 412 mixtures. Combined with the use of the two specific ribosomal primer pairs previously designed, our methods are well-suited for a fast and simple high-throughput sample treatment of commercial gums for molecular certification.

摘要

刺槐豆胶和瓜尔豆胶是半乳甘露聚糖,在食品工业中分别用作添加剂(分别为E 410和E 412)作为稳定剂。目前,通过分子技术可以对胶类和食品中的这两种添加剂进行分析鉴别。然而,迄今为止,只有复杂且耗时的DNA分离方案。我们已经开发出简单的改进方案,能够从几毫克商业E 410和E 412添加剂(含有超过75%的多糖)中获得足够用于PCR扩增的DNA。添加剂在水或10 mM Tris-HCl(pH 8.5)中的悬浮液能有效回收适合PCR检测鉴定的DNA。然而,Tris方法从E 410中提取DNA比从E 412添加剂中提取DNA效率更高。相反,水方法最适合检测从E 412或E 410/E 412混合物中提取的DNA。结合之前设计的两对特异性核糖体引物对的使用,我们的方法非常适合对商业胶类进行快速、简单的高通量样品处理以进行分子认证。

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