Direct Somatic Embryogenesis in Gloriosa superba L. An Endangered Medicinal Plant of India

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Published: 2008-01-02

Page: 7-12


Manju Madhavan *

Centre for Research and Post Graduate Studies, Department of Botany Sacred Heart College, Thevara, Kochi- 682013

Joy P. Joseph

Centre for Research and Post Graduate Studies, Department of Botany Sacred Heart College, Thevara, Kochi- 682013.

*Author to whom correspondence should be addressed.


Abstract

Gloriosa superba L., is a valuable endangered medicinal plant where the corms are used for in vivo multiplication. One corm gives only one or at the maximum two plants a year. The present study reports that somatic embryogenesis directly from leaf explants when cultured on basal Murashige and Skoog medium supplemented with 2 mg/l Naphthaleneacetic acid and l mg/l 6-benzylaminopurine. In leaf and internodal cultures where the supplements were 2 mg/l Naphthaleneacetic acid and 0.05-0.15 mg/l l-phenyl-3-(1.2,3-thidiazol-5-yl-urea), root tubers or microcorms were initiated. These root tubers upon transfer to an induction medium containing 2 mg/l Naphthaleneacetic acid and 0.5-1.5 mg/1 6-benzylaminopurine somatic embryos were induced. Transfer of root tubers to Naphthaleneacetic acid and 6-benzylaminopurine combination resulted in the induction of somatic embryos. Maturation of somatic embryos occurred in medium containing 2 mg/l Naphthaleneacetic acid and 0.5 mg/l 6, benzylaminopurine. Abscisic acid at 0.5-1 mg/1 when added resulted in the enhanced recovery of mature embryos. Complete plantlet development occurred in MS medium without growth regulators. The plantlets were hardened and transferred to soil.

Keywords: Colchicine, Embryogenesis, In vitro, Plant growth regulator, Roots tubers


How to Cite

Madhavan, Manju, and Joy P. Joseph. 2008. “Direct Somatic Embryogenesis in Gloriosa Superba L. An Endangered Medicinal Plant of India”. PLANT CELL BIOTECHNOLOGY AND MOLECULAR BIOLOGY 9 (1-2):7-12. https://www.ikprress.org/index.php/PCBMB/article/view/2292.

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