Indirect Regeneration and Somatic Embryogenesis from Leaf and Stem Explants of Crassula ovata (Mill.) Druce – An Ornamental Medicinal Plant
Commenced in January 2007
Frequency: Monthly
Edition: International
Paper Count: 32807
Indirect Regeneration and Somatic Embryogenesis from Leaf and Stem Explants of Crassula ovata (Mill.) Druce – An Ornamental Medicinal Plant

Authors: A. B. A. Ahmed, Amar, D. I., R. M. Taha

Abstract:

This research aims to investigate callus induction, somatic embryogenesis and indirect plant regeneration of Crassula ovata (Mill.) Druce – the famous ornamental plant. Experiment no.1: Callus induction was obtained from leaf and stem explants on Murashige and Skoog (MS) medium supplemented with various plant growth regulators (PGRs). Effects of different PGRs, plant regeneration and subsequent plantlet conversion were also assessed. Indirect plant regeneration was achieved from the callus of stem explants by the addition of 1.5 mg/L Kinetin (KN) alone. Best shoot induction was achieved (6.5 shoots/per explant) after 60 days. For successful rooting, regenerated plantlets were sub-cultured on the same MS media supplemented with 1.5 mg/L KN alone. The rooted plantlets were acclimatized and the survival rate was 90%. Experiment no.2: Results revealed that 0.5 mg/L 2,4-D alone and in combination with 1.0 mg/L 6-Benzyladenine (BA) gave 89.8% callus from the stem explants as compared to leaf explants. Callus proliferation and somatic embryo formation were also evaluated by ‘Double Staining Method’ and different stages of somatic embryogenesis were revealed by scanning electron microscope. Full Strength MS medium produced the highest number (49.6%) of cotyledonary stage somatic embryos (SEs). Mature cotyledonary stage SEs developed into plantlets after 12 weeks of culture. Wellrooted plantlets were successfully acclimatized at the survival rate of 85%. Indirectly regenerated plants did not show any detectable variation in morphological and growth characteristics when compared with the donor plant.

Keywords: Callus induction, Crassula ovata, Double Staining, Indirect plant regeneration, Somatic embryogenesis.

Digital Object Identifier (DOI): doi.org/10.5281/zenodo.1096954

Procedia APA BibTeX Chicago EndNote Harvard JSON MLA RIS XML ISO 690 PDF Downloads 2708

References:


[1] WHO/Acadia, Rapport de la Journe Internationale de, diabetes, 1992, 14 Octobre.
[2] H. Lucy, and J. D. Edgar, “Medicinal Plants: a re-emerging Health aid” Plant Biotechnology, 2, 1999, 3-8.
[3] A. B. A. Ahmed, A. S. Rao, M. V. Rao, and R. M. Taha, “Effect of picloram, additives and plant growth regulators on somatic embryogenesis of Phyla nodiflora”, Brazilian Archives Biology and Technology, 54, 2011, 7-13.
[4] T. Murashige, and F. A. Skoog, “Revised media for rapid growth and bioassay with tobacco tissue cultures”, Physiology plant, 15, 1962, 473- 497.
[5] K. A. Gomez, and A. A. Gomez, “Statistical procedures for agricultural research with emphasis on rice”, International Rice Research Institute, Los Bans, Philippines, IRRI Publication, 1976, p. 264.
[6] A. B. A. Ahmed, A. S. Rao, M. V. Rao, and R. M. Taha, “Optimized conditions for callus induction, plant regeneration and alkaloids accumulation in stem and shoot tip explants of Phyla nodiflora”, Spanish Journal of Agricultural Research, 9, 2011, 1262-1270.