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The combination of ITS2 and psbA-trnH region is powerful DNA barcode markers for authentication of medicinal Terminalia plants from Thailand

机译:ITS2和PSBA-TRNH区域的组合是强大的DNA条形码标记,用于认证泰国的药物终端植物

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The dried fruits of Terminalia plant (Combretaceae) called "Samo" have been used as herbal medicine in Thai traditional medicine. Four "Samo" crude drugs, namely, Samo thai, Samo thed, Samo dee-ngu, and Samo phiphek, are used as the main ingredients in Triphala and Trisamo recipes. Their commercial products are available in processed and powdered form, but are difficult to authenticate by conventional methods. In this study, we aimed to discriminate species of genus Terminalia for the identification of their crude drugs by a DNA barcoding technique. A total of 208 closely related nucleotide sequences were obtained from nine Terminalia species collected from Thailand and the DDBJ/EMBL/GenBank database. An effective DNA barcode marker was selected from six DNA loci (matK, rbcL, psbA-trnH, ITS, ITS1, and ITS2) and their two-locus combination. All sequences were analyzed by three major methods: (1) BLAST search; (2) the genetic divergence method using Kimura 2-parameter (K2P) distance matrices; and (3) tree topology analysis based on the neighbor-joining method. Comparison of the six candidate DNA loci indicated that ITS identified Terminalia with 100% accuracy at the species and genus levels in the BLAST1 method. ITS2 showed the highest K2P variability. The data from the single markers and the two-locus combinations revealed that only the two-locus combinations, namely, the combinations of rbcL, ITS, ITS1, and ITS2 with psbA-trnH, clearly discriminated all the species. From the results of DNA sequence analysis and the three methods, ITS2 is recommended for the identification of Terminalia species to supplement psbA-trnH.
机译:往来称为“萨摩”的末端植物(梳子岩)的干果已被用作泰国传统医学中的草药。四个“SAMO”粗药,即Samo Thai,Somo The,Samo Dee-Ngu和Samo Phiphek,用作三哈拉和三萨莫食谱的主要成分。他们的商业产品可用于加工和粉状形式,但难以通过常规方法进行验证。在这项研究中,我们旨在通过DNA条形码技术鉴定终端炎属植物的种类来鉴定其粗药物。从从泰国和DDBJ / EMBL / GENBANK数据库收集的九种末端IIES获得了总共208个密切相关的核苷酸序列。有效的DNA条形码标记物选自六个DNA基因座(MATK,RBCL,PSBA-TRNH,ITS1和ITS2)及其两基因座组合。通过三种主要方法分析所有序列:(1)BLAST搜索; (2)使用Kimura 2参数(K2P)距离矩阵的遗传分解方法; (3)基于邻近加入方法的树拓扑分析。六个候选DNA基因座的比较表明,其鉴定的终体趋势具有100%的血液和BERT1方法中的物种和属级别的精度。 ITS2显示了最高的K2P变异性。来自单个标记的数据和两个轨迹组合揭示了只有双轨组合,即RBCL,ITS1和ITS2与PSBA-TRNH的组合明确区分了所有物种。从DNA序列分析的结果和三种方法,建议鉴定终端度物种以补充PSBA-TRNH。

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