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The Gene MT3-B Can Differentiate Palm Oil from Other Oil Samples

机译:Gene MT3-B可以将棕榈油与其他油样品区分开来

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The practice of blending cheap palm oil with more expensive oils is currently rampant owing to the increased global price of oil and the price gap between types of oils. This adulteration poses a serious threat to the trade of edible oil and negatively affects consumers. The aim of this study was to identify the presence of palm oil as an additive in more expensive oils using a PCR-based technique. A taxon-specific gene, MT3-B, was found by searching the GenBank database. MT3-B showed high oil palm (Elaeis guineensis Jacq.) specificity, low intraspecies variability, and a low copy number. On the basis of the MT3-B sequence, conventional and real-time PCR assays were established to detect palm oil contamination by amplifying an amplicon of 109 bp. The lowest copy number that the conventional PCR method could detect was five haploid copies;the limit of detection (LOD) for the real-time PCR assay was estimated to be five haploid copies. Experimental results demonstrated that the PCR-based methods were specific, sensitive, and reliable and could successfully detect the palm oil component of mixed oil samples.
机译:由于增加了石油的全球价格以及油类类型之间的价格差距,目前猖獗将廉价的棕榈油混合廉价的棕榈油。这种掺假对食用油的贸易构成了严重的威胁,对消费者产生负面影响。本研究的目的是使用基于PCR的技术识别作为更昂贵的油中的添加剂作为添加剂的棕榈油的存在。通过搜索Genbank数据库发现了一个分类的特异性基因MT3-B。 MT3-B显示出高油棕(Elaeis Guineensis Jacq。)特异性,低的内部变异性和低拷贝数。在MT3-B序列的基础上,建立常规和实时PCR测定以通过扩增109bp的扩增子来检测棕榈油污染。常规PCR方法可以检测的最低拷贝数为五倍倍增拷贝;估计实时PCR测定的检测极限(LOD)是五倍体拷贝。实验结果表明,基于PCR的方法是特异性,敏感的,可靠的,并且可以成功地检测混合油样的棕榈油组分。

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