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Plant Regeneration via Somatic Embryogenesis from Leaf and Floral Explants of ‘Chancellor’ Wine Grape

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dc.contributor.author Mulwa, Richard M.S.
dc.contributor.author Norton, Margaret M.A.
dc.contributor.author Skirvin, Robert M.
dc.date.issued 2006
dc.date.accessioned 2021-05-21T07:34:04Z
dc.date.available 2021-05-21T07:34:04Z
dc.identifier.uri http://41.89.96.81:8080/xmlui/handle/123456789/2551
dc.description.abstract Abundant embryogenic callus was obtained from leaf and floral explants of ʺChancellorʺ grape by continuous culture for 12 weeks on Nitsch and Nitsch basal medium supplemented with 9 μM 2, 4‐D + 17 μM IASP + either 1 μM BA or 1 μM TDZ (ECIM) in darkness. They were successfully maintained by a five to six week subculture interval on NN medium containing 2 μM 2, 4‐D + 0.2 μM TDZ + 4 μM IASP (LTMM). Near synchronous embryo developed from embryogenic callus on medium containing 10 μM IASP + 8 μM NOA + 1 μM TDZ + 1 μM ABA + 2.5 g/l AC (EDMM). Individually separated somatic embryos were germinated on both NN and half strength of MS containing 0.5 μM BA + 0.025 μM NAA, respectively; normal plantlet conversion from embryos was low (35%). Whole fruiting plants were obtained. Aberrant embryo development was characterized by failure to form functional shoot meristems following the initial cotyledon expansion during germination. These observations indicate that the embryo conversion stage of the regeneration is difficult and remains a limiting factor requiring more empirical experimentation for improvement in grape tissue culture. en_US
dc.language.iso en en_US
dc.publisher Egerton University en_US
dc.subject Chancellor grape en_US
dc.subject Regeneration en_US
dc.subject Somatic embryogenesis en_US
dc.title Plant Regeneration via Somatic Embryogenesis from Leaf and Floral Explants of ‘Chancellor’ Wine Grape en_US
dc.type Other en_US


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