首页> 外文期刊>Food Control >Detecting Satureja montana L. and Origanum majorana L. by means of SCAR-PCR in commercial samples of Mediterranean oregano.
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Detecting Satureja montana L. and Origanum majorana L. by means of SCAR-PCR in commercial samples of Mediterranean oregano.

机译:通过SCAR-PCR检测地中海牛至的商业样品中的大头菜(Satureja montana)和大牛至(Origanum majorana)。

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摘要

A recent pharmacognostic survey of the European market highlighted a high frequency of adulteration of commercial Mediterranean oregano with species of the Lamiaceae family (Satureja montana L. and Origanum majorana L.) having a similar appearance and a superimposing essential oil profile. When performed by skilled adulterators, this dilution can only be detected by pharmacognostic assays or phytochemical analyses, which can be either extremely laborious, expensive and time consuming when multiple batches of oregano have to be evaluated, or can produce inconclusive results. Sequence-Characterized Amplified Regions markers (SCARs) specific for these adulterants were developed from Random Amplified Polymorphic DNA (RAPD) markers, in order to support results of pharmacognostic or chemical analyses and/or to speed up the primary screening of oregano batches and allow the pre-emptive rejection of suspect samples, thus narrowing the number of samples to be subjected to further tests. The SCAR primers gave rise to the amplification of specific bands of expected sizes which allowed the detection of down to 0.5% of adulterating plants, despite the small genetic distance between the species involved. A specific protocol for DNA extraction was set up. In addiction, the relatively small size of these amplicons is suitable for the analysis of potentially degraded DNA obtained from dried and stored commercial material.
机译:最近对欧洲市场的药理学调查显示,商业化的地中海牛至与唇形科(Samija montana L.和 Origanum majorana L.)掺假的频率很高。类似的外观和叠加的精油轮廓。当由熟练的掺假者进行时,这种稀释只能通过药理学分析或植物化学分析来检测,当必须评估多批牛至时,这可能是非常费力,昂贵和费时的,或者会产生不确定的结果。从随机扩增多态性DNA(RAPD)标记中开发出了针对这些掺假品的序列特征性扩增区域标记(SCAR),以支持药理学或化学分析的结果和/或加快牛至批次的初步筛选并允许抢先拒绝可疑样品,从而缩小了要进行进一步测试的样品数量。尽管所涉及物种之间的遗传距离很小,但SCAR引物引起了预期大小的特定条带的扩增,从而允许检出低至0.5%的掺假植物。建立了DNA提取的特定协议。在成瘾中,这些扩增子的相对较小的尺寸适合于分析从干燥和储存的商业材料获得的潜在降解的DNA。

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