In vitro regeneration of Camellia sinensis (L.) O. Kuntze by somatic embryogenesis

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dc.contributor.author Wachira, Francis N.
dc.date.accessioned 2017-01-13T07:04:44Z
dc.date.available 2017-01-13T07:04:44Z
dc.date.issued 1995-04
dc.identifier.citation Plant Cell Reports April 1995, Volume 14, Issue 7, pp 463–466 en_US
dc.identifier.issn 0721-7714
dc.identifier.uri http://link.springer.com/article/10.1007/BF00234056
dc.identifier.uri http://repository.seku.ac.ke/handle/123456789/2913
dc.description DOI: 10.1007/BF00234056 en_US
dc.description.abstract Within 3 weeks of culture, excised cotyledon expiants of Camellia sinensis (L.) O. Kuntze produced somatic embryos without intermediate callus when cultured in Murashige and Skoog's basal medium with 30 g−1 sucrose. In medium without plant growth regulators, up to 60% of the cultures developed somatic embryos. Embryogenic competence was reduced by increasing concentrations of plant growth regulators tested (i.e. kinetin, 6-benzylaminopurine, and indole butyric acid). The somatic embryos developed, grew to maturity without being subcultured within 6–8 weeks. Secondary embryogenesis was not observed. Germination of isolated mature somatic embryos was low in medium without plant growth regulators. Up to 53% and 60% germination occurred when medium impregnated with kinetin at 1.8 mgl−1 or 1.0 mgl−1 6-benzylaminopurine were used respectively. Callus was also routinely produced when cotyledons were cultured in MS basal medium with auxins (2,4-dichlorophenoxyacetic acid and indole acetic acid). Callus induction was however, also achieved in plant growth regulator free medium. Indirect somatic embryogenesis was not induced in the present study. en_US
dc.language.iso en en_US
dc.publisher Springer Verlag en_US
dc.title In vitro regeneration of Camellia sinensis (L.) O. Kuntze by somatic embryogenesis en_US
dc.type Article en_US


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