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Research Article · Open access · Published 17 August 2019

In Vitro Callus Induction and Regeneration of Medicinal Plant Datura innoxia

Baan Munim Twaij1, Alaa Jabbar Taha1 & Md. Nazmul Hasan2

American Journal of Biochemistry and Biotechnology, Volume 15, Issue 3, pp. 150–156 · doi.org/10.3844/ajbbsp.2019.150.156

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Abstract

The present study indicate the possibility of the development of callus from stem cut, leaf and root explants and regeneration of Datura plant (Datura innoxia) on Murashige and Skoog (MS) media supplemented with different concentrations of 6-Benzylaminopurine (BA) and 1-Naphthaleneacetic (NAA). Sterilized explants were inoculated and incubated in culture shade under different conditions (light and dark). Data analysis showed that maximum percentage (83%) of calli were induced from stem cut explants on MS media supplemented with NAA and BA at 0.5 and 1.0 mg/l respectively under dark condition. Maximum fresh and dry weight was found 395.63 mg and 35.64 mg respectively with supplementation of 0.5 mg/l NAA and 1 mg/l BA. Stem cut derived calli were transfer to MS regeneration medium supplementing different concentrations of plant regulators (PGRs) under different conditions. Maximum regeneration (78%) was found on MS media supplementing 1 mg/l of BA and 1 mg/l off NAA under dark condition. The attempt for callus induction from the explants (stem, leaf, root) using MS media with supplementation of different combinations of 2, 4-Dichlorophenoxyacetic acid (2, 4-D), BA and NAA, Kinetin (kin) under both light and dark conditions were carried out but no significant results were found.

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Twaij, B. M., Taha, A. J. & Hasan, M. N. (2019). In Vitro Callus Induction and Regeneration of Medicinal Plant Datura innoxia. American Journal of Biochemistry and Biotechnology, 15(3), 150–156. https://doi.org/10.3844/ajbbsp.2019.150.156

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In Vitro Callus Induction and Regeneration of Medicinal Plant Datura innoxiaAmerican Journal of Biochemistry and Biotechnology · Volume 15, Issue 3 · pp. 150–156 · CC BY 3.0Download