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Somatic embryogenesis in Citrus SPP.: Carbohydrate stimulation and histodifferentiation
Authors:Márcio L. Tomaz  Beatriz M. Januzzi Mendes  francisco De Assis A. Mourão Filho  Clarice G. B. Demétrio  Naratip Jansakul  Adriana P. Martinelli Rodriguez
Affiliation:(1) Escola Superior de Agricultura ‘Luiz de Queiroz’, 13418-900 Piracicaba/SP, Brazil;(2) Laboratório de Biotecnologia Vegetal, Centro de Energia Nuclear na Agricultura/USP, Av. Centenário 303, 13416-970 Piracicaba/SP, Brazil;(3) University of Exeter, Exeter, UK
Abstract:Summary Somatic embryogenesis from nucellus-derived callus cultures of five cultivars, including three (Caipira, Seleta Vermelha, and Valencia) of sweet oranges (C. sinesis L. Osbeck), Rangpur lime (C. limonia L. Osbeck), and Cleopatra mandarin (C. reticulata Blanco) (lines I and II), were studied. Callus lines maintained on MT medium supplemented with 50 g l−1 sucrose were transferred to MT medium supplemented with different carbohydrate sources: galactose, glucose, lactose, maltose, or sucrose at 18, 37, 75, 110, or 150 mM, or glycerol at 6, 12, 24, 36, or 50 mM. Globular embryos were observed after approximately 4 wk, in several treatments. Cultures of Valencia and Caipira sweet oranges and Cleopatra mandarin (line I) showed high numbers of embryos on medium containing galactose, lactose, and maltose. Histological studies showed somatic embryos in all developmental stages with a normal histodiffeentiation pattern. The other two cultivars (Rangpur lime and Cleopatra mandarin, line II) formed very few embryos, which did not develop further following the globular stage. Some of the abnormalities observed were lack or dedifferentiation of protoderm and absence of apical meristems and procambial strands. Embryos that followed the normal sequence of development were easily converted into plants. Non-embryogenic cultures continued as proliferating callus cultures, eventually forming a few embryos which did not convert into plants. Statistical analyses of the callus response to carbohydrate treatments was done using an overdispersion Poisson model.
Keywords:galactose  generalized linear models  histology  maltose  overdispersion
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