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In vitro culture and plant regeneration of large flowered purslane
Authors:Badr-Din Rossi-Hassani  Jean-Pierre Zryd
Institution:(1) Laboratoire de Phytogénétique Cellulaire, Université de Lausanne, 1015 Lausanne, Switzerland;(2) Present address: Laboratoire de Biochimie & Biologie Moléculaire, Faculté des Sciences-Dhar Mehraz, Fès B.P. 1796, Morocco
Abstract:Culture conditions were established for callus induction from a range of Portulaca grandiflora Hook tissues. Rapidly growing calli were obtained on Murashige and Skoog medium with stem-, leaf- and sepal-derived explants. Plant regeneration via organogenesis was explant-origin dependent with hypocotyl tissues giving the highest shooting frequency. Light conditions, pH and carbon source had a pronounced effect on the percentage of explants regenerating buds and the number of buds formed. It was possible to establish stable regenerated plants in the glasshouse.Abbreviations BA 6-benzyladenine - 2,4-D 2,4-dichlorophenoxyacetic acid - NAA 1-naphthaleneacetic acid - IAA indoleacetic acid - MS Murashige and Skoog (1962) medium
Keywords:callus culture  hypocotyl  regenerants  Portulaca grandiflora
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