Evidence map›Paper›PMID 37306873›Full record

ArticleMolecular biology reports2023

Development of species-specific ISSR-derived SCAR marker for early discrimination between Cinnamomum verum and Cinnamomum cassia.

Himanshi Gangwar, Vijay Gahlaut, Ramesh Chauhan, Satbeer Singh, Vandana Jaiswal

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Article in Molecular biology reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Himanshi GangwarBiotechnology, Division, CSIR-Institute of Himalayan Bioresource Technology, Palampur, Himachal Pradesh, 176061, India.
Vijay GahlautBiotechnology, Division, CSIR-Institute of Himalayan Bioresource Technology, Palampur, Himachal Pradesh, 176061, India.
Ramesh ChauhanAcademy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India.
Satbeer SinghAcademy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India.
Vandana JaiswalBiotechnology, Division, CSIR-Institute of Himalayan Bioresource Technology, Palampur, Himachal Pradesh, 176061, India. vandana@ihbt.res.in.ORCID http://orcid.org/0000-0001-8620-7595

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCinnamomum verum (true cinnamon) and Cinnamomum cassia (cassia cinnamon) are two important species belonging to family Lauraceae. These species are recognized by morphological, chemical composition and essential oil contents. The appropriate identification of species would be considerably improved by a genetic method. The main objective of the present study was to develop molecular markers distinguishing between C. verum and C. cassia. METHODS AND

resultsA total 71 ISSR (Inter simple sequence repeat) and four universal barcoding (ITS, rbcL, matK, and psbA-trnH) genes were used to distinguish both the species. No sequence variation was observed between the two species for any DNA barcode gene. However, one ISSR i.e. ISSR-37 showed a clear distinction between the species and produced 570 bp and 746 bp amplicons in C. verum and C. cassia, respectively. The polymorphic bands were converted into species-specific SCAR markers. The SCAR-CV was specific to C. verum and amplified 190 bp band, however there was no amplification seen in the C. cassia samples.

conclusionThe SCAR marker generated in this study can be employed as efficient, economical, and reliable molecular tool for the identification of C. verum.

Indexed as

Cinnamomum aromaticumLauraceaeOils, VolatileCinnamomum zeylanicumDNA Barcoding, TaxonomicOils, VolatileCinnamonDNA barcodePCRSequence variationSpecies identification

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