ArticleJournal of natural medicines2020
DNA barcoding for identification of agarwood source species using trnL-trnF and matK DNA sequences.
Article in Journal of natural medicines, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed.
- DNA Barcoding Provides Taxonomic Clues for Identifying Five EndangeredPlants (Basel, Switzerland) · 2025Article
- Deciphering insights into commercial Myrrh species authenticity from the psbA-trsnH genetic region.PloS one · 2025Article
- Identification and classification ofPeerJ · 2025Article
- Comprehensive analysis using DNA metabarcoding, SCAR marker based PCR assay, and HPLC unveils the adulteration in Brahmi herbal products.Molecular biology reports · 2023Article
- Highly divergent regions in the complete plastome sequences of3 Biotech · 2023Article
- Comparison of phenolic compounds contained in Aquilaria leaves of different species.Journal of natural medicines · 2022Article
- Factors affecting 2-(2-phenylethyl)chromones in artificial agarwood.Journal of natural medicines · 2022Article
- Comparison of eight complete chloroplast genomes of the endangered Aquilaria tree species (Thymelaeaceae) and their phylogenetic relationships.Scientific reports · 2020Article
- Species identification of Indonesian agarwood using a DNA-barcoding method.Journal of natural medicines · 2020Article
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Agarwood is a type of resinous wood found in the trunks of Aquilaria, Gonystylus, and Gyrinops species [1]. High-quality agarwood is extraordinarily expensive and therefore its source plant species have become depleted due to exploitation. In 2005, these species were added to Appendix II of the Convention on International Trade in Endangered Species of Wild Fauna and Flora [1]. Because these wild agarwood resources have become depleted, commercial production of agarwood has long been a desirable goal. In addition, inauthentic agarwood is sometimes produced from non-agarwood species. Few reports have attempted to identify source species in order to distinguish genuine from false agarwood. In this study, DNA was extracted from putative agarwood samples collected from Japanese, Indonesian, Thai, and Vietnamese markets. The trnL-trnF region and matK gene were amplified from each sample by PCR to serve as DNA barcodes for identifying the plant species to which each sample belonged. One of the wood samples did not originate from a genuine agarwood species. Although some species were identified, sequence data for agarwood source species currently available in GenBank is insufficient to identify the species to which all of these putative agarwood samples belonged. Thus, positive identification of remaining samples will require further exploration.
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