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dc.contributor.authorIndieka, Abwao S.-
dc.contributor.authorOdee, David W.-
dc.contributor.authorMuluvi, G.M.-
dc.date.accessioned2014-04-22T08:34:25Z-
dc.date.available2014-04-22T08:34:25Z-
dc.date.issued2007-
dc.identifier.urihttp://10.10.20.22:8080//handle/123456789/559-
dc.description.abstractExperiments were conducted to study plant regeneration through direct somatic embryogenesis using mature zygotic embryo and cotyledonary explants from seeds of Melia volkensii stored for <3 and >12 months. Explants were cultured on Murashige and Skoog (MS) medium supplemented with BAP, NAA and 2,4-0 (0.5,1.0 and 2.0 mg rl) alone, and BAP (0.5, 1.0, 2.0 and 4.0 mg I-I) in combination with 2,4-0 or NAA (0.2 and 0.5 mg 1-1). After 4 weeks in culture, up to 60% of cotyledonary explants from the seeds stored for <3 months produced direct somatic embryos on BAP (0.5-4.0 mg I-I) in combination with 2,4-0 (0.2 mg rl). The number of somatic embryos ranged from 5 to 14 per explant in BAP (0.5 mg rl ) and 2,4-0 (0.2 mg 1-1) combination. Only 20% of cotyledonary explants from seeds stored for >12 months produced somatic embryos. Mature zygotic embryos failed to produce any somatic embryos. Subcultures of somatic embryos from cotyledonary explants of seeds stored for <3 months formed clusters of shootlets on semi solid MS and 1/2 MS media. After 6 weeks of subculture on multiplication MS media augmented with BAP (0.5 mg I-I) and IAA (0.2 mg rl ), 70% of the shoot tips formed 4-7 shoots per explant. Up to 33% of the multiplied shoots were rooted in MSen_US
dc.description.sponsorshipSpringer/KEFRIen_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.relation.ispartofseriesNew forests;Vol.34: 73-81-
dc.subjectCotyledonen_US
dc.subjectmass-propagationen_US
dc.subjectseed storageen_US
dc.subjectsomatic embryosen_US
dc.subjectzygotic embryosen_US
dc.titleRegeneration of Melia volkensii Gurke (Meliaceae) through direct somatic embryogenesisen_US
dc.typePreprinten_US
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