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Differentiation of the Chinese minority medicinal plant genus Berchemia spp. by evaluating three candidate barcodes

The genus Berchemia comprises important Chinese plants with considerable medicinal value; however, these plants are often misidentified in the herbal medicinal market. To differentiate the various morphotypes of Berchemia species, a proficient method employing the screening of universal DNA barcodes...

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Autores principales: Guo, Li-Cheng, Zhao, Ming-Ming, Sun, Wei, Teng, Hong-Li, Huang, Bi-Sheng, Zhao, Xiang-Pei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899350/
https://www.ncbi.nlm.nih.gov/pubmed/27347459
http://dx.doi.org/10.1186/s40064-016-2207-4
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author Guo, Li-Cheng
Zhao, Ming-Ming
Sun, Wei
Teng, Hong-Li
Huang, Bi-Sheng
Zhao, Xiang-Pei
author_facet Guo, Li-Cheng
Zhao, Ming-Ming
Sun, Wei
Teng, Hong-Li
Huang, Bi-Sheng
Zhao, Xiang-Pei
author_sort Guo, Li-Cheng
collection PubMed
description The genus Berchemia comprises important Chinese plants with considerable medicinal value; however, these plants are often misidentified in the herbal medicinal market. To differentiate the various morphotypes of Berchemia species, a proficient method employing the screening of universal DNA barcodes was used in this work. Three candidate barcoding loci, namely, psbA-trnH, rbcL, and the second internal transcribed spacer (ITS2), were used to identify an effective DNA barcode that can differentiate the various Berchemia species. Additionally, PCR amplification, efficient sequencing, intra- and inter-specific divergences, and DNA barcoding gaps were employed to assess the ability of each barcode to identify these diverse Berchemia plants authentically; the species were differentiated using the Kimura two-parameter and maximum composite likelihood methods. Sequence data analysis showed that the ITS2 region was the most suitable candidate barcode and exhibited the highest interspecific divergence among the three DNA-barcoding sequences. A clear differentiation was observed at the species level, in which a maximum distance of 0.264 was exhibited between dissimilar species. Clustal analysis also demonstrated that ITS2 clearly differentiated the test species in a more effective manner than that with the two other barcodes at both the hybrid and variety levels. Results indicate that DNA barcoding is ideal for species-level identification of Berchemia and provides a foundation for further identification at the molecular level of other Rhamnaceae medicinal plants.
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spelling pubmed-48993502016-06-24 Differentiation of the Chinese minority medicinal plant genus Berchemia spp. by evaluating three candidate barcodes Guo, Li-Cheng Zhao, Ming-Ming Sun, Wei Teng, Hong-Li Huang, Bi-Sheng Zhao, Xiang-Pei Springerplus Research The genus Berchemia comprises important Chinese plants with considerable medicinal value; however, these plants are often misidentified in the herbal medicinal market. To differentiate the various morphotypes of Berchemia species, a proficient method employing the screening of universal DNA barcodes was used in this work. Three candidate barcoding loci, namely, psbA-trnH, rbcL, and the second internal transcribed spacer (ITS2), were used to identify an effective DNA barcode that can differentiate the various Berchemia species. Additionally, PCR amplification, efficient sequencing, intra- and inter-specific divergences, and DNA barcoding gaps were employed to assess the ability of each barcode to identify these diverse Berchemia plants authentically; the species were differentiated using the Kimura two-parameter and maximum composite likelihood methods. Sequence data analysis showed that the ITS2 region was the most suitable candidate barcode and exhibited the highest interspecific divergence among the three DNA-barcoding sequences. A clear differentiation was observed at the species level, in which a maximum distance of 0.264 was exhibited between dissimilar species. Clustal analysis also demonstrated that ITS2 clearly differentiated the test species in a more effective manner than that with the two other barcodes at both the hybrid and variety levels. Results indicate that DNA barcoding is ideal for species-level identification of Berchemia and provides a foundation for further identification at the molecular level of other Rhamnaceae medicinal plants. Springer International Publishing 2016-06-03 /pmc/articles/PMC4899350/ /pubmed/27347459 http://dx.doi.org/10.1186/s40064-016-2207-4 Text en © The Author(s) 2016 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.
spellingShingle Research
Guo, Li-Cheng
Zhao, Ming-Ming
Sun, Wei
Teng, Hong-Li
Huang, Bi-Sheng
Zhao, Xiang-Pei
Differentiation of the Chinese minority medicinal plant genus Berchemia spp. by evaluating three candidate barcodes
title Differentiation of the Chinese minority medicinal plant genus Berchemia spp. by evaluating three candidate barcodes
title_full Differentiation of the Chinese minority medicinal plant genus Berchemia spp. by evaluating three candidate barcodes
title_fullStr Differentiation of the Chinese minority medicinal plant genus Berchemia spp. by evaluating three candidate barcodes
title_full_unstemmed Differentiation of the Chinese minority medicinal plant genus Berchemia spp. by evaluating three candidate barcodes
title_short Differentiation of the Chinese minority medicinal plant genus Berchemia spp. by evaluating three candidate barcodes
title_sort differentiation of the chinese minority medicinal plant genus berchemia spp. by evaluating three candidate barcodes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899350/
https://www.ncbi.nlm.nih.gov/pubmed/27347459
http://dx.doi.org/10.1186/s40064-016-2207-4
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