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Development of nucleic acid isolation by non-silica-based nanoparticles and real-time PCR kit for edible vegetable oil traceability

机译:通过基于非二氧化硅的纳米颗粒分离核酸和实时PCR试剂盒开发可食用植物油的可追溯性

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For efficient extraction of amplifiable DNA from edible vegetable oils, we developed a novel DNA extraction approach based on the non-silica-based dipolar nanocomposites. The nanoparticle comprises a hydrophilic polymethyl methacrylate core with abundant capillaries, hydrophilic vesicles decorated with molecules having DNA affinity and a coating hydrophobic polystyrene layer. The nanoparticles are soluble in oil, adsorb the DNA from the aqueous phase and gave a high DNA recovery ratio. All DNA extracts from fully refined vegetable oil soybean, peanut, rapeseed, and cottonseed oils, including their blends, were sufficiently pure to be amplified by real-time PCR targeting the chloroplast ribulose-1,5-bisphosphate gene (rbcL), therefore, the species of origin and their ratios in mixed vegetable oils blended from two or three oil-species could be determined. These results indicate that the novel DNA isolation and real-time PCR kit is a simple, sensitive and efficient tool for the species identification and traceability in refined vegetable oils.
机译:为了从食用植物油中有效提取可扩增的DNA,我们开发了一种基于非二氧化硅的偶极纳米复合材料的新颖DNA提取方法。纳米颗粒包括具有丰富毛细管的亲水性聚甲基丙烯酸甲酯核,装饰有具有DNA亲和力的分子的亲水性囊泡和疏水性聚苯乙烯涂层。纳米粒子可溶于油,从水相中吸收DNA,并具有较高的DNA回收率。从完全精制的植物油大豆油,花生油,菜籽油和棉籽油中提取的所有DNA提取物(包括其混合物)都具有足够的纯度,可以通过针对叶绿体-1,5-双磷酸核糖体基因(rbcL)的实时PCR进行扩增,因此,可以确定两种或三种油种类混合的混合植物油中的起源物种及其比例。这些结果表明,新颖的DNA分离和实时PCR试剂盒是一种用于精制植物油中物种鉴定和追溯的简单,灵敏和有效的工具。

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