Please use this identifier to cite or link to this item: http://repo.lib.jfn.ac.lk/ujrr/handle/123456789/930
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dc.contributor.authorValentine, O.N.-
dc.contributor.authorThirukkumaran, G.-
dc.contributor.authorShunsuke, I.-
dc.contributor.authorMasahiro, M.-
dc.date.accessioned2016-08-04T08:26:31Z-
dc.date.accessioned2022-06-24T07:22:34Z-
dc.date.available2016-08-04T08:26:31Z-
dc.date.available2022-06-24T07:22:34Z-
dc.date.issued2009-
dc.identifier.urihttp://repo.lib.jfn.ac.lk/ujrr/handle/123456789/930-
dc.description.abstractPlant regeneration protocol of ‘‘Egusi’’ melon (Colocynthis citrullus L.) was established using three local (‘‘Ejagham’’, ‘‘Sewere’’ and ‘‘Barablackedge’’) and one improved (NHC1-130) cultivars. Cotyledonary explants of different lengths (1/2, 1/4 and 1/6) excised from 4- or 8-day-old seedlings germinated in vitro were cultured on MS medium supplemented with different concentrations of 6-benzylaminopurine (BA). The best results were obtained when cotyledons from 4-day-old seedlings were cut into 2 (1/2) halves. Plant regeneration was optimal on medium containing 5 mg/l BA, yielding 86.3%, 77.0% and 76.3% shoot induction frequencies amongst the three local cultivars of ‘‘Ejagham’’, ‘‘Sewere’’ and ‘‘Barablackedge’’, respectively. In NHC1-130, the highest shoot induction frequency (85%) was obtained on medium containing 2 mg/l BA. Adventitious shoots were elongated on medium containing 0.1 mg/l BA and successfully rooted on hormone-free MS medium. Flow cytometric analysis revealed 70% of the plants to be diploid.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectEgusien_US
dc.subjectRegenerationen_US
dc.subjectOrganogenesisen_US
dc.subjectBAen_US
dc.subjectPloidyen_US
dc.titleEfficient plant regeneration via organogenesis in ‘‘Egusi’’ melon (Colocynthis citrullus L.)en_US
dc.typeArticleen_US
Appears in Collections:Agricultural Biology

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