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High Frequency Regeneration of Plantlets from Seedling Explants of Asteracantha longifolia (L.) NEES  

Mishra Ramya Ranjan (Plant Tissue Culture laboratory. Division of Biotechnology, Majhighariani Institute of Technology and Science)
Behera Motilal (Plant Tissue Culture laboratory. Division of Biotechnology, Majhighariani Institute of Technology and Science)
Kumar Deep Ratan (Plant Tissue Culture laboratory. Division of Biotechnology, Majhighariani Institute of Technology and Science)
Panigrahi Jogeswar (Plant Tissue Culture laboratory. Division of Biotechnology, Majhighariani Institute of Technology and Science)
Publication Information
Journal of Plant Biotechnology / v.8, no.1, 2006 , pp. 27-35 More about this Journal
Abstract
Plantlet regeneration in Asteracantha longifolia(L.) Nees (Acanthaceae), a medicinal herb has been achieved from seedling explants on basal MS medium. Three different seedling explants including node, internode and leaf segments on used. Of these three explant, leaf explants gave better response for both callus mediated organogenesis and direct multiple shoot induction. Number of explants showing differentiation of shout buds was higher on MS media supplemented with BA compared to kinetin. MS medium fortified with BA ($2.0mgl^{-1}$) and NAA ($0.5mgl^{-1}$) was found to be most suitable for both callus mediated organogenesis and elongation of shouts. The elongated shoots were successfully routed on MS medium fortified with NAA or IBA. Among them $0.1mgl^{-1}$ NAA or $0.2mgl^{-1}$ IBA provides better response for rhizogenesis. Regenerated plantlets were successfully established in soil where 85.4% or them developed into morphologically normal and fertile plants. RAPD profiling using four decamer primers confirmed the genetic uniformity of the regenerated plantlets and substantiated the efficacy and suitability of this protocol for in vitro propagation of A. longifolia.
Keywords
Callus; genetic fidelity; organogenesis; RAPD; shoot bud differentiation;
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