Our Research & Scientific Contributions

This study establishes an efficient protocol for rapid in vitro propagation of the endangered glory lily (Gloriosa superba L.) through callus-mediated organogenesis using non-dormant corm explants. Treatment with 2.0 mg L⁻¹ BAP, 0.5 mg L⁻¹ NAA, 5 mg L⁻¹ CH, and 20% CW yielded a shooting response rate of 83.33%. The findings contribute to conserving this critically important medicinal plant species.

Evaluated the effect of plant growth regulators and sterilizing agents on in vitro propagation and micro-tuberization of endangered Gloriosa superba L. Treatment with 10% H₂O₂ for 5 min exhibited 82.14% viability and no contamination. Full-strength MS medium with 2.0 mg L⁻¹ BAP and 0.5 mg L⁻¹ NAA displayed 90.63% bud break with significant shoot elongation. 1009 accesses, 25 citations.

Sterilizing seeds with 0.15% mercuric chloride for 8 minutes effectively eliminated contamination, ensuring 100% seedling survival. MS medium with 1.5 mg·L⁻¹ GA₃ and 1.5 mg·L⁻¹ BAP along with 4% sucrose achieved the highest in vitro seed germination. The first systematic protocol addressing dual dormancy in this critically endangered tropical medicinal plant.

First report on a multi-plant approach for in vitro plant regeneration through direct organogenesis in Gloriosa superba L. The highest shoot induction rate of 91.7% was achieved from non-dormant corm explants with BAP and adenine sulfate. This multi-explant in vitro propagation approach is recommended for wider conservation efforts using plant tissue culture.

A comprehensive literature review (1952–2024) examining the interplay between climate change and biodiversity conservation as two of the most urgent challenges of the 21st century. Analyzes IPCC projections for 2030, 2050, and 2100 using conservative values across six official Assessment Reports between 1990 and 2022.

Investigates the phytochemical profile and alkaloid enhancement in callus cultures of Gloriosa superba using plant growth regulators and abiotic stress elicitors. The study advances understanding of secondary metabolite production in this medicinally valuable endangered species, supporting both conservation and pharmaceutical research goals.

Comprehensive assessment of alkaloid profiles — particularly colchicine and colchicoside — in callus cultures derived from Gloriosa superba L. The research evaluates biotechnological strategies to enhance yield of these high-value pharmaceutical alkaloids without harvesting from wild populations, directly supporting conservation and sustainable production goals.