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  4. Plant regeneration of Dimocarpus scandens (Winit & Kerr) Boonsuk & Chantar. (Lamyai-Thao) by tissue culture technique
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Plant regeneration of Dimocarpus scandens (Winit & Kerr) Boonsuk & Chantar. (Lamyai-Thao) by tissue culture technique

Author(s)
Jitwetkul, A.
Poeaim, A.
Pongtongkam, P.
Chareonsap, P. P.
Poeaim, S.
Date Issued
May 1, 2025
Type
Article
DOI
10.63369/ijat.2025.21.3.879-890
Abstract
The minimum contamination percentage (25%) was recorded in the experiment using 0.2% mercuric chloride (HgCl2) for 20 min, which was observed to be a 50% germination rate after 2 weeks of culture. The maximum germination rate (68%) was obtained on Murashige and Skoog (MS) solid medium supplemented with 1.0 mg/L 6-benzylaminopurine (BAP), giving a shoot length of 48.00 mm. and root length of 31.40 mm. The optimal condition of nodal segment sterilization was recorded in the experiment using 0.1% HgCl2 for 10 min, which gave 80% survival explants. For shoot induction, it was worked on MS solid medium with 0.5 mg/L 6-benzylaminopurine (BAP) that induced the highest average length of 11.31 mm. The highest root formation frequency (50%) and root length (3.0 mm) were achieved on an MS medium containing 2.0 mg/L indole-3-butyric acid (IBA). The plantlets were acclimatized and established in the soil.
Citation
International Journal of Agricultural Technology, 21(3), 879-890, 2025
Subjects

Dimocarpus scandens

Plant induction

Seed germination

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