Melika Vahdani , Mohammad Ali Sahari , Mehrnaz Tanavar
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引用次数: 0
摘要
本研究的目的是开发一种基于 DNA 的食用油鉴定和追踪方法,这对健康管理非常重要。研究人员采用三种不同的 DNA 提取方法(CTAB、MBST 试剂盒和人工正己烷法)从粗制和精制大豆油、玉米油和菜籽油中提取高纯度 DNA。然后使用特定引物进行聚合酶链反应,以确定是否存在与每种油类相关的基因,并评估转基因性。结果表明,DNA 存在于粗油和精炼油中,但含量很低。不过,使用方法 3 提取 DNA 可以为成功的 PCR 扩增提供足够数量和质量的 DNA。研究得出结论,从油类中提取 DNA 的主要挑战是 PCR 抑制剂的存在,而使用基于正己烷的手动方法可以克服这一问题。此外,使用 SDS-PAGE 对油脂中的蛋白质含量进行检测也没有发现任何蛋白质条带。
Quantitative and qualitative analysis of three DNA extraction methods from soybean, maize, and canola oils and investigation of the presence of genetically modified organisms (GMOs)
The objective of this study was to develop a DNA-based method for the identification and tracking of edible oils, which is important for health management. Three different DNA extraction methods (CTAB, MBST kit, and manual hexane-based method) were used to obtain high-purity DNA from crude and refined soybean, maize, and canola oils. PCR was then conducted using specific primers to identify the presence of genes related to each oil type and to assess transgenicity. The results showed that DNA was present in crude and refined oils, but in very low amounts. However, using method 3 for DNA extraction provided sufficient quantity and quality of DNA for successful PCR amplification. The study concluded that the main challenge in DNA extraction from oils is the presence of PCR inhibitors, which can be overcome using the manual hexane-based method. Also, the examination of protein presence in the oils using SDS-PAGE did not indicate any protein bands.