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Preserving Nature's Treasure: A Journey into the In Vitro Conservation and Micropropagation of the Endangered Medicinal Marvel— Podophyllum hexandrum Royle.

Authors :
Khan, Zahoor
Khan, Bushra
Shah, Syed Tanveer
Iqbal, Javaid
Basit, Abdul
Khan, Muhammad Suleman
Iqbal, Waleed
Elsadek, Mohamed Farouk
Jamal, Aftab
Ali, Mohammad Ajmal
Prisa, Domenico
Source :
Horticulturae; Aug2024, Vol. 10 Issue 8, p809, 21p
Publication Year :
2024

Abstract

Podophyllum hexandrum Royle, also known as Podophyllum emodi Wall, holds significant ecological, ornamental, and medicinal values. However, it has become endangered due to overexploitation, prolonged seed dormancy, slow natural regeneration, and climate change. This study developed an efficient in vitro protocol for callogenesis and micropropagation of P. hexandrum to conserve germplasm in in vitro conditions. Callus formation from various plant parts, including the leaf, stem, rhizome, radicle, and cotyledon, was induced using Murashige and Skoog (MS) medium supplemented with different plant growth regulators. The combination of benzyladenine at 1 mg L<superscript>−1</superscript> and 4-dichlorophenoxy acetic acid at 3 mg L<superscript>−1</superscript> was optimal for biomass production, yielding 215.88 ± 0.31 mg, with growth per gram at 8.32 ± 0.32 and a growth rate of 13.62 ± 0.25 mg/day on MS medium. For shoot proliferation, benzyladenine (3.5 mg L<superscript>−1</superscript>) and naphthalene acetic acid (0.5 mg L<superscript>−1</superscript>) combined with activated charcoal showed the highest shoot induction percentage per explant. For shoot regeneration from calluses, 6-benzylaminopurine (0.5 mg L<superscript>−1</superscript>) and thidiazuron (2 mg L<superscript>−1</superscript>) were most effective, producing superior shoot length, number of regenerations, and regeneration percentage. Root induction was successful with α-naphthalene acetic acid supplementation (0.5 to 1.5 mg L<superscript>−1</superscript>) in MS medium, resulting in the highest number per explant (4.08 ± 0.08), length (5.45 ± 0.15 cm), and rooting rate (87.00 ± 1.66%) of roots in plantlets. Subculturing for callus culture was performed every 28 days for up to four subcultures to prevent nutrient depletion and toxic metabolite accumulation, ensuring tissue health and viability. Continuous subculturing of callus on MS medium maintained healthy P. hexandrum germplasm in vitro. Overall, this micropropagation protocol provides a rapid system for conserving P. hexandrum germplasm. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
23117524
Volume :
10
Issue :
8
Database :
Complementary Index
Journal :
Horticulturae
Publication Type :
Academic Journal
Accession number :
179380957
Full Text :
https://doi.org/10.3390/horticulturae10080809