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Adventitious plant regeneration on leaf explants from adult male kiwifruit and AFLP analysis of genetic variation
Authors:M. J. Prado  M. V. Gonzalez  S. Romo  M. T. Herrera
Affiliation:(1) Dpto. Fisiología Vegetal, Escuela Politécnica Superior, Campus de Lugo, 27002 Lugo, Spain;(2) Dpto. Biología Vegetal y Ciencia del Suelo, Facultad de Biología, Universidad de Vigo, Campus Universitario, 36310 Vigo, Pontevedra, Spain
Abstract:The present work reports on a study of plant regeneration carried out with callus from the leaf blades and petioles of field-grown male adult kiwifruit plants (Actinidia deliciosa (Chev.) Liang and Ferguson). The cultivars used were ‘Tomuri’ and clone A, a selected male plant grown in north western Spain. The best shoot induction conditions were obtained in ‘Tomuri’ leaf blades cultured in K(h) medium in the presence of 23 μM Zeatin and 0.1 μM NAA. Under these conditions, more than 80% of organogenic callus induction was observed, with an average of 14 new shoots in the second subculture. The initial length of the shoots affected shoot elongation, which was accomplished by culturing isolated shoots in K(h) medium with half-strength salts, supplemented with 0.4 μM Zeatin and 0.1 μM NAA. A possible detrimental long-term effect of cytokinins on shoot elongation can account for the results, since elongation was not observed until 1 month of culture in elongation medium. For rooting, shoots (1 cm in length) were basally immersed in a 5 mM IBA solution for 15 s, and transferred to half-strength K(h) basal medium. Regenerated plants were acclimated in a sterile peat:perlite substrate for 10 days, and then transferred to soil. AFLP analysis was accomplished with 15 primer combinations from which 13 showed reproducible and well-resolved bands, producing a total of 1321 fragments from which 1281 were polymorphic (97%). A dendrogram was constructed using both monomorphic and polymorphic bands, showing genetic variation among field-grown plants and tissue culture-derived regenerants.
Keywords:  Tomuri’     Actinidia deliciosa   Tissue culture  Somaclonal variation  Molecular markers
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