Optimizing In Vitro Propagation of Haworthia truncata Schönland Using Leaf, Root, and Inflorescence.
Leila Soleimani1, Hassan Salehi1, Taras Pasternak2
1Department of Horticultural Science, School of Agriculture, Shiraz University, Shiraz 7144113131, Iran.
Plants (Basel, Switzerland)
|January 25, 2025
Summary
Mass propagation of Haworthia truncata via tissue culture is crucial due to its scarcity. This study optimized plant growth regulators and explant types for efficient regeneration of this unique succulent.
Area of Science:
- Plant Biotechnology
- Horticultural Science
- Plant Physiology
Background:
- Haworthia truncata, a South African native, faces limited growth and scarcity, leading to high production costs.
- Global trade of Haworthia species is significant, with China and Turkey as major exporters.
- Tissue culture presents a viable method for mass propagation of desirable succulent species like H. truncata.
Purpose of the Study:
- To optimize tissue culture protocols for efficient mass propagation of Haworthia truncata.
- To evaluate the effects of different plant growth regulators (IBA, NAA, BA) on callus induction and shoot proliferation.
- To determine the most effective explant types (leaf, root, inflorescence) for regeneration.
Main Methods:
- Murashige and Skoog (MS) basal media were supplemented with varying concentrations of indole-3-butyric acid (IBA), naphthaleneacetic acid (NAA), and benzylaminopurine (BA).
- Explants including leaf, root, and inflorescence were cultured on media with different plant growth regulators (PGRs) or without PGRs (control).
- Callus induction, shoot proliferation, and rooting percentages were assessed to determine optimal regeneration conditions.
Main Results:
- Inflorescence explants showed highest callus induction (1.5 mg/L IBA) and shoot proliferation (1 mg/L IBA).
- Leaf explants performed best with 0.05 mg/L NAA and 0.25 mg/L BA for callus induction, and 0.05 mg/L NAA and 1 mg/L BA for shoot proliferation.
- Root explants achieved maximum callus induction (0.25 mg/L BA and 0.25 mg/L NAA) and shoot proliferation (0.05 mg/L NAA and 1 mg/L BA).
- The highest rooting percentage of regenerated shoots was achieved on ½ MS medium supplemented with 1.5 mg/L IBA.
Conclusions:
- Specific combinations of plant growth regulators and explant types significantly influence the efficiency of Haworthia truncata regeneration.
- Optimized tissue culture protocols using selected PGRs and explants can facilitate mass propagation of Haworthia truncata.
- This research provides a foundation for the commercial-scale production of Haworthia truncata, addressing scarcity and high costs.
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