Authenticity testing and detection of Eurycoma longifolia in commercial herbal products using bar-high resolution melting analysis

• Published in: Genes
• Main Author: Fadzil N.F.; Wagiran A.; Salleh F.M.; Abdullah S.; Izham N.H.M.
• Format: Article
• Language: English
• Published: MDPI AG 2018
• Online Access: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85052628199&doi=10.3390%2fgenes9080408&partnerID=40&md5=955e36d5b13e573dbbd13668c53c19cd

The present study demonstrated High Resolution Melting (HRM) analysis combined with DNA barcode (Bar-HRM) as a fast and highly sensitive technique for detecting adulterants in Eurycoma longifolia commercial herbal products. Targeting the DNA barcoding of the chloroplastic region-ribulose biphosphate carboxylase large chain (rbcL) and the nuclear ribosomal region-internal transcribed spacer 2 (ITS2), PCR amplification and HRM analysis using saturated Eva green dye as the source of fluorescence signals, was accomplished by employing a real-time cycler. The results were further validated by sequencing to identify unknown sequence from Genbank database and to generate phylogenetic tree using neighbour joint (NJ) analysis. Both of the DNA markers exhibited a distinguishable melting temperature and shape of the normalised curve between the reference and the adulterants. In the case of species identification, ITS2 was more successful in differentiating between species. Additionally, detection of admixture sample containing small traces of targeted E. longifolia DNA (w/v) can be detected as low as 5% for rbcL and less than 1% for ITS2, proving the sensitivity and versatility of the HRM analysis. In conclusion, the Bar-HRM analysis is a fast and reliable technique that can effectively detect adulterants in herbal products. Therefore, this will be beneficial for regulatory agencies in order to regulate food safety issues. © 2018 by the authors. Licensee MDPI, Basel, Switzerland.