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Authentication of commercial processed Glehniae Radix (Beishashen) by DNA barcodes
BACKGROUND: The radix of Glehnia littoralis Fr. Schmidt ex Miq. (Beishashen), is often misidentified and adultered in Chinese medicine. Its seven common adulterants include Chuanminshen violaceum Sheh et Shan (Chuanmingshen), Changium smyrnioides Wolff (Mingdangshen), Sphallerocarpus gracilis (Bess....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4665842/ https://www.ncbi.nlm.nih.gov/pubmed/26628908 http://dx.doi.org/10.1186/s13020-015-0071-8 |
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author | Zhu, Xunzhi Zhang, Yuxi Liu, Xia Hou, Dianyun Gao, Ting |
author_facet | Zhu, Xunzhi Zhang, Yuxi Liu, Xia Hou, Dianyun Gao, Ting |
author_sort | Zhu, Xunzhi |
collection | PubMed |
description | BACKGROUND: The radix of Glehnia littoralis Fr. Schmidt ex Miq. (Beishashen), is often misidentified and adultered in Chinese medicine. Its seven common adulterants include Chuanminshen violaceum Sheh et Shan (Chuanmingshen), Changium smyrnioides Wolff (Mingdangshen), Sphallerocarpus gracilis (Bess.) K.-Pol. (Miguoqin), Adenophora polyantha Nakai (Shishashen), Silene tatarinowii Regel (Shishengyingzicao), Adenophora tetraphylla (Thunb.) Fisch (Lunyeshashen) and Adenophora stricta Miq. (Shashen). This study aims to evaluate the feasibility of the second internal transcribed spacer (ITS2) DNA barcoding to discriminate between Glehniae Radix and its common adulterants. METHODS: In this study, we collected 46 samples of G. littoralis and 59 samples of its seven common adulterants. Genomic DNA sequences were extracted from samples, including original plants and commercially processed crude drugs. The ITS2 of the ribosomal DNA sequences were amplified and sequenced bi-directionally. The sequences were assembled by CodonCode Aligner 3.5.7. The descriptive data analysis was conducted and neighbor-joining (NJ) phylogenetic tree was constructed by MEGA 5.0 in accordance with the kimura 2 -parameter (K2P) model. The identification efficiency was evaluated based on the BLAST1 methods. The ITS2 secondary structures were predicted and compared between Glehniae Radix and its adulterants by the ITS2 database. RESULTS: As the 46 ITS2 sequences of G. littoralis were identical to each other, the identification efficiency of the ITS2 region was 100 %. A NJ tree based on the ITS2 sequences, and the predicted secondary structures of ITS2, distinguished Glehniae Radix from its adulterants. CONCLUSION: DNA barcoding based on ITS2 distinguished commercial processed Glehniae Radix from common herbal adulterants. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13020-015-0071-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4665842 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46658422015-12-02 Authentication of commercial processed Glehniae Radix (Beishashen) by DNA barcodes Zhu, Xunzhi Zhang, Yuxi Liu, Xia Hou, Dianyun Gao, Ting Chin Med Research BACKGROUND: The radix of Glehnia littoralis Fr. Schmidt ex Miq. (Beishashen), is often misidentified and adultered in Chinese medicine. Its seven common adulterants include Chuanminshen violaceum Sheh et Shan (Chuanmingshen), Changium smyrnioides Wolff (Mingdangshen), Sphallerocarpus gracilis (Bess.) K.-Pol. (Miguoqin), Adenophora polyantha Nakai (Shishashen), Silene tatarinowii Regel (Shishengyingzicao), Adenophora tetraphylla (Thunb.) Fisch (Lunyeshashen) and Adenophora stricta Miq. (Shashen). This study aims to evaluate the feasibility of the second internal transcribed spacer (ITS2) DNA barcoding to discriminate between Glehniae Radix and its common adulterants. METHODS: In this study, we collected 46 samples of G. littoralis and 59 samples of its seven common adulterants. Genomic DNA sequences were extracted from samples, including original plants and commercially processed crude drugs. The ITS2 of the ribosomal DNA sequences were amplified and sequenced bi-directionally. The sequences were assembled by CodonCode Aligner 3.5.7. The descriptive data analysis was conducted and neighbor-joining (NJ) phylogenetic tree was constructed by MEGA 5.0 in accordance with the kimura 2 -parameter (K2P) model. The identification efficiency was evaluated based on the BLAST1 methods. The ITS2 secondary structures were predicted and compared between Glehniae Radix and its adulterants by the ITS2 database. RESULTS: As the 46 ITS2 sequences of G. littoralis were identical to each other, the identification efficiency of the ITS2 region was 100 %. A NJ tree based on the ITS2 sequences, and the predicted secondary structures of ITS2, distinguished Glehniae Radix from its adulterants. CONCLUSION: DNA barcoding based on ITS2 distinguished commercial processed Glehniae Radix from common herbal adulterants. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13020-015-0071-8) contains supplementary material, which is available to authorized users. BioMed Central 2015-11-30 /pmc/articles/PMC4665842/ /pubmed/26628908 http://dx.doi.org/10.1186/s13020-015-0071-8 Text en © Zhu et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Zhu, Xunzhi Zhang, Yuxi Liu, Xia Hou, Dianyun Gao, Ting Authentication of commercial processed Glehniae Radix (Beishashen) by DNA barcodes |
title | Authentication of commercial processed Glehniae Radix (Beishashen) by DNA barcodes |
title_full | Authentication of commercial processed Glehniae Radix (Beishashen) by DNA barcodes |
title_fullStr | Authentication of commercial processed Glehniae Radix (Beishashen) by DNA barcodes |
title_full_unstemmed | Authentication of commercial processed Glehniae Radix (Beishashen) by DNA barcodes |
title_short | Authentication of commercial processed Glehniae Radix (Beishashen) by DNA barcodes |
title_sort | authentication of commercial processed glehniae radix (beishashen) by dna barcodes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4665842/ https://www.ncbi.nlm.nih.gov/pubmed/26628908 http://dx.doi.org/10.1186/s13020-015-0071-8 |
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