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首页> 外文期刊>Journal of Food Research >Milk Adulteration: Detection of Bovine Milk in Caprine Dairy Products by Real Time PCR
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Milk Adulteration: Detection of Bovine Milk in Caprine Dairy Products by Real Time PCR

机译:牛奶掺假:通过实时PCR检测Caprine乳制品中的牛奶

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Milk adulteration is an international social problem.Consumption of adulterated milk may cause serious health problems and a great concern of the food industry has been raised.In this study, a method based on the polymerase chain reaction (PCR) principle was validated for detecting cow's milk in goat's dairy products.A total of 40 goat's dairy products commonly consumed in Greece, were tested.Various concentrations, from 0.01 to 90%, of cows' milk in goats' milk samples were prepared for DNA extraction and further PCR analysis.Selection of highly polymorphic regions within the cow and goat mitochondrial D-loops, showing low homology between the two species, allowed to choose specific primer pairs for detection of cow and goat DNA.After electrophoresis, cow DNA was characterised by the fragment of the size of 300 bp, goat DNA by the fragment of 444 bp.The detection limit of the PCR method was 0.01% while sensitivity and specificity of the method were both 100%.Goat dairy products samples were tested for the presence of cow DNA.Thirty six out of forty (90%) that were tested, were found to produce cow-specific PCR product in addition to goat PCR product while only two samples gave goat-specific product only.The results are disappointing in terms of the food labelling honesty but on the other hand PCR is again a quickly, easy and reliable method that could be used for extended adulteration screening.
机译:牛奶掺假是一个国际社会问题。掺假牛奶的额外可能导致严重的健康问题,并提出了一种很大的关注食品行业。本研究,验证了一种基于聚合酶链反应(PCR)原理的方法检测牛的方法山羊乳制品的牛奶。在希腊常见的山羊乳制品中共有40岁的牛奶店进行了测试。为DNA提取和进一步的PCR分析制备山羊牛奶样品的奶牛牛奶的0.01〜90%的浓度。在牛和山羊线粒体D圈内的高度多态性区域,显示两种物种之间的低同源性,允许选择特定的引物对进行牛和山羊DNA的检测。电泳,母牛DNA的特征是尺寸的片段300 bp,山羊DNA通过444 bp的片段。PCR方法的检测限为0.01%,而该方法的敏感性和特异性均为100%.goat乳制品样品已经测试了牛DNA的存在。测试的四十(90%)中的三十六个,除了山羊PCR产物外,还产生牛特异性PCR产物,而只有两个样品仅给出山羊特异性产品。结果在食品标签诚实方面令人失望,但另一方面,PCR再次是一种快速,简便,可靠的方法,可用于扩展掺假筛选。

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