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Organogenesis from root explants of commercial populations of <Emphasis Type="Italic">Passiflora edulis</Emphasis> Sims and a wild passionfruit species, <Emphasis Type="Italic">P. cincinnata</Emphasis> Masters
Authors:Crislene Viana da Silva  Leandro Silva de Oliveira  Virgilio Adriano Pereira Loriato  Luzimar Campos da Silva  José Marcello Salabert de Campos  Lyderson Facio Viccini  Evelyn Jardim de Oliveira  Wagner Campos Otoni
Institution:1.Departamento de Biologia Vegetal,Laboratório de Cultura de Tecidos Vegetais/BIOAGRO,Vi?osa,Brazil;2.Departamento de Biologia Vegetal,Laboratório de Anatomia Vegetal,Vi?osa,Brazil;3.Departamento de Biologia,Laboratório de Genética, Instituto de Ciências Biológicas, Universidade Federal de Juiz de Fora,Juiz de Fora,Brazil;4.Plant Biology Department,Plant Tissue Culture Laboratory/BIOAGRO, Federal University of Vi?osa,Vi?osa,Brazil
Abstract:Root explants of a wild passionfruit species (Passiflora cincinnata) and three P. edulis commercial populations (‘FB 100’, ‘FB 200’, and ‘FB 300’) were incubated on Murashige and Skoog (MS) medium supplemented with 4.44 μM 6-benzyladenine (BA) to induce shoot organogenesis. Shoots elongated in liquid medium with 2.89 μM gibberellic acid (GA3) under agitation were rooted in coconut fiber and acclimatized followed by transfer to a greenhouse into pots containing mixture of coconut fiber and Plantmax® (1:1). Explant samples were collected during organogenesis and submitted to light and scanning electron microscopy (SEM). Root explants of P. cincinnata responded earlier than those of P. edulis. However, on the third assessment, at 90 days, the genotype ‘FB 200’ showed shoot number significantly higher than ‘FB 100’ and ‘FB 300’, not differing from P. cincinnata. Organogenesis in P. cincinnata and P. edulis occurred via direct pathway, which was confirmed by anatomical studies and SEM. Flow cytometric analysis revealed no variation in DNA content of regenerated plantlets among all genotypes. Nuclear DNA (2C) values (pg) in regenerants of P. cincinnata (2.99 pg) and P. edulis (3.26–3.28 pg) were consistent with DNA amounts of seed-derived control plants.
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