Molecular discrimination and phylogenetic relationships of physalis species based on ITS2 and rbcL DNA barcode sequence

Show simple item record

dc.contributor.author Pere, Katherine
dc.contributor.author Mburu, Kenneth
dc.contributor.author Muge, Edward K.
dc.contributor.author Wagacha, John M.
dc.contributor.author Nyaboga, Evans N.
dc.date.accessioned 2023-12-06T12:10:52Z
dc.date.available 2023-12-06T12:10:52Z
dc.date.issued 2023-11-17
dc.identifier.citation Crops, 3 302–319 2023 en_US
dc.identifier.issn 2673-7655
dc.identifier.uri https://www.mdpi.com/2673-7655/3/4/27
dc.identifier.uri https://repository.seku.ac.ke/handle/123456789/7430
dc.description https://doi.org/10.3390/crops3040027 en_US
dc.description.abstract Plants of the genus Physalis are of economic interest because of their fleshy edible fruits with high nutritional value. Some species have high medicinal value with a long history of ethnomedicinal use to treat diverse diseases. There is therefore a need to correctly discriminate the different species of Physalis for proper utilization. Although most Physalis species have unique morphologies, their vegetative stages are identical, making it difficult to accurately identify them based on morphological characteristics. DNA barcoding has the potential to discriminate species accurately. In this study, ribulose bisphosphate carboxylase large (rbcL) and internal transcribed spacer 2 (ITS2) regions were used to discriminate Physalis species and to reveal their phylogenetic relationships and genetic diversity. Physalis plant samples were collected from seven counties in Kenya based on the availability of the germplasm. The voucher specimens were identified using the botanical taxonomy method and were deposited in the University of Nairobi herbarium. Genomic DNA was isolated from leaf samples of 64 Physalis accessions and used for PCR amplification and the sequencing of rbcL and ITS2 barcode regions. The discriminatory ability of the barcodes was based on BLASTn comparison, phylogenetic reconstruction and cluster analysis, and the determination of inter- and intra-specific distances. The nucleotide polymorphism, genetic diversity and distance of the identified Physalis species were determined using DnaSP and MEGA 11.0 software. Species discrimination was more robust using ITS2 sequences. The species identified and discriminated by ITS2 sequences were Physalis purpurea, Physalis peruviana and Physalis cordata. The rbcL sequences were only able to identify Physalis to the genus level. There was high interspecific and low intraspecific divergence within the identified Physalis species based on ITS2 sequences. The ITS2 barcode is an ideal DNA barcode for use in the discrimination of species, as well as in genetic diversity studies of Physalis accessions in Kenya. en_US
dc.language.iso en en_US
dc.publisher MDPI en_US
dc.subject DNA barcoding en_US
dc.subject Physalis en_US
dc.subject ITS2 en_US
dc.subject rbcL en_US
dc.subject species discrimination en_US
dc.title Molecular discrimination and phylogenetic relationships of physalis species based on ITS2 and rbcL DNA barcode sequence en_US
dc.type Article en_US


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search Dspace


Browse

My Account