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

Author:

Khan Zahoor1,Khan Bushra1ORCID,Shah Syed Tanveer2,Iqbal Javaid3ORCID,Basit Abdul4,Khan Muhammad Suleman5ORCID,Iqbal Waleed6ORCID,Elsadek Mohamed Farouk7ORCID,Jamal Aftab8ORCID,Ali Mohammad Ajmal9,Prisa Domenico10ORCID

Affiliation:

1. Department of Environmental Sciences, University of Peshawar, Peshawar 25120, Pakistan

2. Department of Agriculture, Faculty of Biological and Health Sciences, Hazara University, Mansehra 21120, Pakistan

3. Department of Environmental Sciences, University of Lakki Marwat, Lakki Marwat 28420, Pakistan

4. Floricultural Biotechnology Lab, Department of Horticultural Science, Kyungpook National University, Daegu 41566, Republic of Korea

5. Department of Horticulture, Faculty of Crop Production Sciences, The University of Agriculture, Peshawar 25130, Pakistan

6. Department of Agronomy, Faculty of Crop Production Sciences, The University of Agriculture, Peshawar 25130, Pakistan

7. Department of Biochemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia

8. Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of the Yangtze River), Ministry of Agriculture, College of Resources and Environment, Huazhong Agricultural University, Wuhan 430070, China

9. Department of Botany and Microbiology, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia

10. CREA Research Centre for Vegetable and Ornamental Crops, Council for Agricultural Research and Economics, Via dei Fiori 8, 51012 Pescia, PT, Italy

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−1 and 4-dichlorophenoxy acetic acid at 3 mg L−1 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−1) and naphthalene acetic acid (0.5 mg L−1) combined with activated charcoal showed the highest shoot induction percentage per explant. For shoot regeneration from calluses, 6-benzylaminopurine (0.5 mg L−1) and thidiazuron (2 mg L−1) 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−1) 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.

Funder

King Saud University

Publisher

MDPI AG

Reference53 articles.

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