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Khushwaha, J.

Publications and source records attributed to Khushwaha, J..

2 recordsLinked to original sources

DNA barcoding and species delimitation based on four Chloroplast loci to identify species within the Elaeocarpaceae family

AbstractDNA barcoding is an indispensable taxonomic tool for plant species identification. The present research successfully amplified the four coding regions of plastid namely; matK, rpoB, ndhJ, and accD, sequenced, and submitted it to NCBI Genbank after verification. This study evaluated the significance of single (matK, rpoB, ndhJ, and accD) and two-locus plastid loci (rpoB+matK, ndhJ+matK, accD+matK) and examined their abilities for species identification and phylogenetic construction of Elaeocarpaceae plants. The average aligned length for matK, rpoB, ndhJ, accD, ndhJ+matK, rpoB+matK, and accD+matK was 395 bp, 538 bp, 477 bp, 254 bp, 872 bp, 937 bp, and 649 bp, respectively. The highest substitution rate was recorded in the rpoB (18.47%), followed by ndhJ (17.38%), accD (14.00%), and matK (11.23%). The number of variable sites, segregating sites (S), nucleotide diversity (Pi), and mutations (Eta) were observed to be highest in the matK region. Evolutionary relationship based on the Neighbor-joining method demonstrated that candidate barcode sequences were competent for identifying Crinodendron, Elaeocarpus, Sloanea, and Vallea species. A significant barcoding gap was identified in two barcoding regions (matK and ndhJ+matK). The species-specific barcodes for the genus Elaeocarpus were generated based on Single Nucleotide Polymorphism (SNP) analysis. This study offers novel strategies for effectively identifying species within Elaeocarpaceae and lays the foundation for germplasm conservation and utilization.

bioinformatics↗

Phytochemical Characterization of Bio-active Compounds in Hydroethanolic Extract of Elaeocarpus ganitrus leaves using HPLC, LC-MS, and HPTLC Analyses

Bioactive compounds have various applications in different industries, including food, pharmaceutical, and cosmetic industries, demonstrating the need to identify the best-standardized technique to screen the phytochemical profile of medicinal plants. This study aimed to characterize the bioactive compounds in the hydroethanolic extracts of Elaeocarpus ganitrus leaves using various analytical techniques: HPLC, LC-MS, and HPTLC. Air-dried leaves of E. ganitrus were extracted with 70% ethanol. The phytochemical composition of crude extracts was analyzed by the High performance liquid chromatography (HPLC) method, and a total of 93 compounds, including 46 flavonoids, 17 phenols, 14 polyphenols, 3 phenolic acid, 3 phenolic glycosides, 2 flavonoid glycosides, 2 glycosides, 2 phenylpropanoid glycoside, 1 hydroxycinnamic acid, 1 lignan, 1 tannin, and 1 terpene glycoside were detected and quantified. The Liquid chromatography mass spectrometry (LC-MS) analyses identified 11 major eleven compounds: quercetin (803.0215 {micro}g/L), gallic acid (726.13 {micro}g/L), ferulic acid (652.34 {micro}g/L), chlorogenic acid (651.021{micro}g/L), pinocembrin (264.11 {micro}g/L), p-aminobenzoic acid (251.021 {micro}g/L), epicatechin (246.02 {micro}g/L), catechin (161.51 {micro}g/L), caffeic acid (123.31 {micro}g/L), syringaldehyde (116.31 {micro}g/L), and naringenin (106.31 {micro}g/L). The chemical fingerprinting was carried out by high performance thin layer chromatography (HPTLC), and HPTLC fingerprint qualitatively revealed a predominant amount of gallic acid (48.64 %), curcumin (15.21 %), caffeic acid (12.19 %) and cinnamic acid (6.50 %). A significant amount of bioactive constituents in a hydroethanolic extract of E. ganitrus leaves indicates the plants therapeutic potential, including antioxidant, anti-inflammatory, antidiabetic, anticancer, neuroprotective, and cardio-protective activities.

biochemistry↗