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Unfertilized ovary: a novel explant for coconut (Cocos nucifera L.) somatic embryogenesis
Authors:Prasanthi I. P. Perera  Valerie Hocher  Jean Luc Verdeil  Sylvie Doulbeau  Deepthi M. D. Yakandawala  L. Kaushalya Weerakoon
Affiliation:(1) Tissue Culture Division, Coconut Research Institute, 61150 Lunuwila, Sri Lanka;(2) Institute for Research and Development (IRD), UMR 1098 BEPC, IRD, BP 64501-911 Avenue Agropolis, 34394 Montpellier Cedex 1, France;(3) CIRAD, TA40/02 Avenue Agropolis, 34398 Montpellier Cedex 5, France;(4) Department of Botany, Faculty of Science, University of Peradeniya, Peradeniya, Sri Lanka
Abstract:Unfertilized ovaries isolated from immature female flowers of coconut (Cocos nucifera L.) were tested as a source of explants for callogenesis and somatic embryogenesis. The correct developmental stage of ovary explants and suitable in vitro culture conditions for consistent callus production were identified. The concentration of 2,4-dichlorophenoxyacetic acid (2,4-D) and activated charcoal was found to be critical for callogenesis. When cultured in a medium containing 100 μM 2,4-D and 0.1% activated charcoal, ovary explants gave rise to 41% callusing. Embryogenic calli were sub-cultured into somatic embryogenesis induction medium containing 5 μM abscisic acid, followed by plant regeneration medium (with 5 μM 6-benzylaminopurine). Many of the somatic embryos formed were complete with shoot and root poles and upon germination they gave rise to normal shoots. However, some abnormal developments were also observed. Flow cytometric analysis revealed that all the calli tested were diploid. Through histological studies, it was possible to study the sequence of the events that take place during somatic embryogenesis including orientation, polarization and elongation of the embryos.
Keywords:Somatic embryogenesis  Coconut (Cocos nucifera L.)  Ovary culture  Histology  Flow cytometry
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