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Molecular identification of the traditional herbal medicines, Arisaematis Rhizoma and Pinelliae Tuber, and common adulterants via universal DNA barcode sequences

机译:通过通用DNA条形码序列对传统草药Arisaematis Rhizoma和Pinelliae Tuber以及常见的掺假品进行分子鉴定

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Methods to identify Pinelliae Tuber and Arisaematis Rhizoma are required because of frequent reciprocal substitution between these two herbal medicines and the existence of several closely related plant materials. As a result of the morphological similarity of dried tubers, correct discrimination of authentic herbal medicines is difficult by conventional methods. Therefore, we analyzed DNA barcode sequences to identify each herbal medicine and the common adulterants at a species level. To verify the identity of these herbal medicines, we collected five authentic species (Pinellia ternata for Pinelliae Tuber, and Arisaema amurense, A. amurense var. serratum, A. erubescens, and A. heterophyllum for Arisaematis Rhizoma) and six common adulterant plant species. Maturase K (matK) and ribulose-1,5-bisphosphate carboxylase/oxygenase large subunit (rbcL) genes were then amplified using universal primers. In comparative analyses of two DNA barcode sequences, we obtained 45 species-specific nucleotides sufficient to identify each species (except A. erubescens with matK) and 28 marker nucleotides for each species (except P. pedatisecta with rbcL). Sequence differences at corresponding positions of the two combined DNA barcodes provided genetic marker nucleotides that could be used to identify specimens of the correct species among the analyzed medicinal plants. Furthermore, we generated a phylogenetic tree showing nine distinct groups depending on the species. These results can be used to authenticate Pinelliae Tuber and Arisaematis Rhizoma from their adulterants and to identify each species. Thus, comparative analyses of plant DNA barcode sequences identified useful genetic markers for the authentication of Pinelliae Tuber and Arisaematis Rhizoma from several adulterant herbal materials.
机译:由于这两种草药之间经常相互替换,并且存在几种密切相关的植物材料,因此需要鉴定半夏和半夏的方法。由于干块茎的形态相似,传统方法很难正确鉴别正宗草药。因此,我们分析了DNA条码序列,以在种类级别上识别每种草药和常见掺假物。为了验证这些草药的身份,我们收集了五个正宗物种(半夏块茎的Pinellia ternata和Arisaema amurense,锯齿曲霉A. erubescens和A. erubescens的南芥)和六个常见的掺假植物物种。 。然后使用通用引物扩增成熟酶K(matK)和核糖-1,5-双磷酸羧化酶/加氧酶大亚基(rbcL)基因。在两个DNA条形码序列的比较分析中,我们获得了足以识别每个物种的45种特定于物种的核苷酸(除了带有matK的芥菜)和每种物种的28个标记核苷酸(除了具有rbcL的ped.sec。pedatisecta)。两个组合的DNA条形码对应位置的序列差异提供了遗传标记核苷酸,可用于在分析的药用植物中鉴定正确物种的标本。此外,我们生成了一个系统进化树,根据树种显示了九个不同的组。这些结果可用于从掺假物中鉴别半夏块茎和南芥(Arisaematis Rhizoma)并鉴定每个物种。因此,对植物DNA条形码序列的比较分析从几种掺假草药材料中鉴定出了鉴别半夏和半夏的有用的遗传标记。

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