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dc.contributor.authorMaslin Osathanunkulen_US
dc.contributor.authorChatmongkon Suwannapoomen_US
dc.contributor.authorKitisak Osathanunkulen_US
dc.contributor.authorPanagiotis Madesisen_US
dc.contributor.authorHugo De Boeren_US
dc.date.accessioned2018-09-05T02:53:27Z-
dc.date.available2018-09-05T02:53:27Z-
dc.date.issued2016-02-15en_US
dc.identifier.issn1618095Xen_US
dc.identifier.issn09447113en_US
dc.identifier.other2-s2.0-84958174720en_US
dc.identifier.other10.1016/j.phymed.2015.11.018en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84958174720&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/55237-
dc.description.abstract© 2016 Elsevier GmbH. All rights reserved. Background Phytopharmaceuticals are increasingly popular as alternative medicines, but poorly regulated in many countries. The manufacturers of these products should be subject to strict controls regarding each product's quality and constituents. Routine testing and identification of raw materials should be performed to ensure that the raw materials used in pharmaceutical products are suitable for their intended use. Hypothesis/purpose We have applied DNA Barcoding - High Resolution Melting (Bar-HRM), an emerging method for identifying of medicinal plant species based on DNA dissociation kinetics and DNA barcoding, for the authentication of medicinal plant species. Study design Commonly commercialized Thai medicinal plants that are widely used for medicinal purposes were used in this study. Publicly available sequences of four plastid markers were used for universal primer design. Species discrimination efficiency of the designed primers was evaluated as single and multi-locus analyses by using the primers sets. Methods HRM analysis was performed in triplicate on each of the 26 taxa to establish the Tmfor each primer set (matK, rbcLA, rbcLB, rbcLC, rpoC1, and trnL). The shapes of the melting curves were analyzed to distinguish the different plant species. Bar-HRM species identification success rates were assessed for each single-locus as well as for multi-locus combinations to establish the optimal combination of primer sets. Results In single locus analysis the rpoC1 primer set gave the highest discrimination (58%), and in multi locus analysis this could be increased from 87% to 99% depending on the total number of regions included. Different combinations proved to be more or less effective at discrimination, depending on the genus or family examined. Conclusions Bar-HRM has proven to be a cost-effective and reliable method for the identification of species in this study of Thai medicinal plants, and results show an identification success rate of 99% among species in the test set.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleEvaluation of DNA barcoding coupled high resolution melting for discrimination of closely related species in phytopharmaceuticalsen_US
dc.typeJournalen_US
article.title.sourcetitlePhytomedicineen_US
article.volume23en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsKunming Institute of Zoology Chinese Academy of Sciencesen_US
article.stream.affiliationsUniversity of Phayaoen_US
article.stream.affiliationsMaejo Universityen_US
article.stream.affiliationsCenter For Research And Technology - Hellasen_US
article.stream.affiliationsEvolutionary Biology Centreen_US
article.stream.affiliationsUniversitetet i Osloen_US
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