Plant regeneration from shoot apical meristems of Melia azedarach L. (Meliaceae)

A protocol was developed for plani regeneration of MeIia azedarach L. by in vitro culture of meristem (0.5 mm in length). The influence of six clones was investigated. The culture procedure comprised sequential steps: 1 lnduction of shoots by in vitro culture of axillary buds from adult trees (10-15...

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Detalles Bibliográficos
Autores: Vila, Silvia Karina, Scocchi, Adriana, Mroginski, Luis Amado
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2002
País:Argentina
Institución:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/45054
Acceso en línea:http://hdl.handle.net/11336/45054
Access Level:acceso abierto
Palabra clave:Meristem
Plant Regeneration
Genotype
Forestry
Melia Azedarach
https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
Descripción
Sumario:A protocol was developed for plani regeneration of MeIia azedarach L. by in vitro culture of meristem (0.5 mm in length). The influence of six clones was investigated. The culture procedure comprised sequential steps: 1 lnduction of shoots by in vitro culture of axillary buds from adult trees (10-15 years old) by culture on Murashige and Skoog (1962) medium (MS) supplemented with 0.5 mg.dm-3 BAP (6-benzylaminopurine), 0.1 mg.dm-3 IBA (indolebutyric acid), and 0,1 mg.dm-3 GA3 (gibberellic acid). The Multiplication of the regenerated shoots was achieved in MS + 0.5 mg.dm-3 BAP + 0.1 mg.dm-3 GA3. 2) In vitro culture of the apical meristems from the regenerated shoots in MS medium (0.7 %) supplemented with various combinations of BAP. Maximum shoot proliferation was obtained on MS medium supplemented with 0.5 mg.dm-3 BAP and 0.1 mg.dm-3 IBA. Regenerated shoots were rooted on MS + 3.5 mg.dm-3 IBA (4 days) followed by subculture on MS laking growth regulators (30 days). Complete plants were transferred to soil.