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DNA Barcoding Identification of Kadsurae Caulis and Spatholobi Caulis Based on Internal Transcribed Spacer 2 Region and Secondary Structure Prediction

BACKGROUND: Kadsurae Caulis and Spatholobi Caulis have very similar Chinese names. Their commodities were hard to distinguish because their stems were very alike after dried and processed. These two herbal drugs were often mixed in clinical use. OBJECTIVE: Authenticity assurance is crucial for quali...

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Autores principales: Yu, Xiaoxue, Xie, Zhiyong, Wu, Junwei, Tao, Junfei, Xu, Xinjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4883074/
https://www.ncbi.nlm.nih.gov/pubmed/27279702
http://dx.doi.org/10.4103/0973-1296.182162
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author Yu, Xiaoxue
Xie, Zhiyong
Wu, Junwei
Tao, Junfei
Xu, Xinjun
author_facet Yu, Xiaoxue
Xie, Zhiyong
Wu, Junwei
Tao, Junfei
Xu, Xinjun
author_sort Yu, Xiaoxue
collection PubMed
description BACKGROUND: Kadsurae Caulis and Spatholobi Caulis have very similar Chinese names. Their commodities were hard to distinguish because their stems were very alike after dried and processed. These two herbal drugs were often mixed in clinical use. OBJECTIVE: Authenticity assurance is crucial for quality control of herbal drugs. Therefore, it is essential to establish a method for identifying the two herbs. MATERIALS AND METHODS: In this paper, we used the DNA barcoding technology, based on the internal transcribed spacer 2 (ITS2) regions, to differentiate Kadsurae Caulis and Spatholobi Caulis. RESULTS: The ITS2 of these two herbs were very different. They were successfully differentiated using the DNA barcoding technique. CONCLUSIONS: DNA barcoding was a promising and reliable tool for the identification of medicinal plants. It can be a powerful complementary method for traditional authentication. SUMMARY: The internal transcribed spacer 2 (ITS2) regions between Kadsurae Caulis and Spatholobi Caulis varied considerably, totally 139 variable sites. Sample 1 was not Kadsurae Caulis as it labeled, but it should be Spatholobi Caulis in fact based on ITS2 region. The secondary structure can also separate Kadsurae Caulis and Spatholobi Caulis effectively. DNA barcoding provided an accurate and strong prove to identify these two herbs. Abbreviations used: CTAB: hexadecyltrimethylammonium bromide, DNA: deoxyribonucleic acid, ITS2:internal transcribed spacer 2, PCR: polymerase chain reaction
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spelling pubmed-48830742016-06-08 DNA Barcoding Identification of Kadsurae Caulis and Spatholobi Caulis Based on Internal Transcribed Spacer 2 Region and Secondary Structure Prediction Yu, Xiaoxue Xie, Zhiyong Wu, Junwei Tao, Junfei Xu, Xinjun Pharmacogn Mag Original Article BACKGROUND: Kadsurae Caulis and Spatholobi Caulis have very similar Chinese names. Their commodities were hard to distinguish because their stems were very alike after dried and processed. These two herbal drugs were often mixed in clinical use. OBJECTIVE: Authenticity assurance is crucial for quality control of herbal drugs. Therefore, it is essential to establish a method for identifying the two herbs. MATERIALS AND METHODS: In this paper, we used the DNA barcoding technology, based on the internal transcribed spacer 2 (ITS2) regions, to differentiate Kadsurae Caulis and Spatholobi Caulis. RESULTS: The ITS2 of these two herbs were very different. They were successfully differentiated using the DNA barcoding technique. CONCLUSIONS: DNA barcoding was a promising and reliable tool for the identification of medicinal plants. It can be a powerful complementary method for traditional authentication. SUMMARY: The internal transcribed spacer 2 (ITS2) regions between Kadsurae Caulis and Spatholobi Caulis varied considerably, totally 139 variable sites. Sample 1 was not Kadsurae Caulis as it labeled, but it should be Spatholobi Caulis in fact based on ITS2 region. The secondary structure can also separate Kadsurae Caulis and Spatholobi Caulis effectively. DNA barcoding provided an accurate and strong prove to identify these two herbs. Abbreviations used: CTAB: hexadecyltrimethylammonium bromide, DNA: deoxyribonucleic acid, ITS2:internal transcribed spacer 2, PCR: polymerase chain reaction Medknow Publications & Media Pvt Ltd 2016-05 2016-05-11 /pmc/articles/PMC4883074/ /pubmed/27279702 http://dx.doi.org/10.4103/0973-1296.182162 Text en Copyright: © Pharmacognosy Magazine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution NonCommercial ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Yu, Xiaoxue
Xie, Zhiyong
Wu, Junwei
Tao, Junfei
Xu, Xinjun
DNA Barcoding Identification of Kadsurae Caulis and Spatholobi Caulis Based on Internal Transcribed Spacer 2 Region and Secondary Structure Prediction
title DNA Barcoding Identification of Kadsurae Caulis and Spatholobi Caulis Based on Internal Transcribed Spacer 2 Region and Secondary Structure Prediction
title_full DNA Barcoding Identification of Kadsurae Caulis and Spatholobi Caulis Based on Internal Transcribed Spacer 2 Region and Secondary Structure Prediction
title_fullStr DNA Barcoding Identification of Kadsurae Caulis and Spatholobi Caulis Based on Internal Transcribed Spacer 2 Region and Secondary Structure Prediction
title_full_unstemmed DNA Barcoding Identification of Kadsurae Caulis and Spatholobi Caulis Based on Internal Transcribed Spacer 2 Region and Secondary Structure Prediction
title_short DNA Barcoding Identification of Kadsurae Caulis and Spatholobi Caulis Based on Internal Transcribed Spacer 2 Region and Secondary Structure Prediction
title_sort dna barcoding identification of kadsurae caulis and spatholobi caulis based on internal transcribed spacer 2 region and secondary structure prediction
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4883074/
https://www.ncbi.nlm.nih.gov/pubmed/27279702
http://dx.doi.org/10.4103/0973-1296.182162
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