Department of Food Science and Technology, Faculty of Biosciences and Landscape Architecture, University College Ghent, Ghent University Association, Schoonmeersstraat 52, 9000 Ghent, Belgium.
Anal Bioanal Chem. 2010 Mar;396(6):2003-22. doi: 10.1007/s00216-009-3343-2. Epub 2009 Dec 15.
The applicability of a DNA-based method for GMO detection and quantification depends on the quality and quantity of the DNA. Important food-processing conditions, for example temperature and pH, may lead to degradation of the DNA, rendering PCR analysis impossible or GMO quantification unreliable. This review discusses the effect of several food processes on DNA degradation and subsequent GMO detection and quantification. The data show that, although many of these processes do indeed lead to the fragmentation of DNA, amplification of the DNA may still be possible. Length and composition of the amplicon may, however, affect the result, as also may the method of extraction used. Also, many techniques are used to describe the behaviour of DNA in food processing, which occasionally makes it difficult to compare research results. Further research should be aimed at defining ingredients in terms of their DNA quality and PCR amplification ability, and elaboration of matrix-specific certified reference materials.
基于 DNA 的转基因生物检测和定量方法的适用性取决于 DNA 的质量和数量。一些重要的食品加工条件,如温度和 pH 值,可能导致 DNA 降解,从而使 PCR 分析变得不可能或无法可靠地进行转基因生物定量。本文综述了几种食品加工过程对 DNA 降解及随后的转基因生物检测和定量的影响。数据表明,尽管这些过程确实会导致 DNA 片段化,但扩增 DNA 仍然是可能的。然而,扩增子的长度和组成可能会影响结果,所使用的提取方法也是如此。此外,许多技术用于描述 DNA 在食品加工过程中的行为,这偶尔会使得比较研究结果变得困难。进一步的研究应旨在根据 DNA 质量和 PCR 扩增能力来定义成分,并制定基质特异性的认证参考物质。