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Induction of somatic embryogenesis and caulogenesis from cotyledon and leaf protoplast-derived colonies of melon (Cucumis melo L.)
Authors:Isabelle Debeaujon  Michel Branchard
Institution:(1) Laboratoire de Génétique Végétale, CNRS-URA 115, Université de Paris-XI, Bât. 360, F-91405 Orsay Cedex, France;(2) Laboratoire de Biotechnologie et Amélioration des Végétaux, Faculté des Sciences et Techniques, Université de Bretagne Occidentale, 6 avenue Victor Le Gorgeu, F-29287 Brest Cedex, France
Abstract:Summary A procedure leading to the regeneration of whole plants from protoplasts of melon is described. Protoplasts were isolated from cotyledons and leaves of plants grown in vitro. After 14 days of culture, average viability and division rates were respectively 60% and 30% for the two organs, considering total initial protoplasts plated. The manipulation of the exogenous auxin / cytokinin balance in regeneration media enabled to direct morphogenesis towards somatic embryogenesis (1 mg·l–1 2,4-dichlorophenoxyacetic acid and 0.1 mg·l–1 6-benzylaminopurine) or caulogenesis (0.5 mg·l–1 6-benzylaminopurine and 0.5 mg·l–1 kinetin). Contrary to division ability, regeneration capacity was genotype-dependent under our conditions, but the two organs expressed similar division and regeneration capacities. Maltose was superior to sucrose for the development of caulogenic nodules into buds. Some plants were transplanted to soil, where they appeared to be fertile and produced seeds.Abbreviations BAP 6-benzylaminopurine - CPW Cell and Protoplast Washing medium - KIN kinetin - MES 2-(N-morpholino) ethanesulfonic acid - MS Murashige and Skoog (1962) - NAA 1 — naphthaleneacetic acid - PAS H (staining), Periodic Acid-Schiff / Hematoxylin - 2,4-D 2,4-dichlorophenoxyacetic acid
Keywords:Melon  Protoplasts  Somatic embryogenesis  Caulogenesis  Maltose
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