Tissue Culture

Electronic Journal of Biotechnology ISSN: 0717-3458 Vol. 9 No. 3, Special Issue, 2006
© 2006 by Pontificia Universidad Católica de Valparaíso -- Chile  
DOI: 10.2225/vol9-issue3-fulltext-13  
RESEARCH ARTICLE

An alternative pathway for plant in vitro regeneration of chinaberry -tree Melia azedarach L. derived from the induction of somatic embryogenesis

Sandra Sharry*
Centro Experimental de Propagación Vegetativa (C.E.Pro.Ve)
Facultad de Ciencias Agrarias y Forestales
Universidad Nacional de La Plata
C.C 31, (1900), La Plata
Buenos Aires, Argentina
Tel: 54 221 423 6616
Fax: 54 221 425 2346
E-mail: ceprove@ceres.agro.unlp.edu.ar

José Luis Cabrera Ponce
Unidad Irapuato
Departamento de Genética
Centro de Estudios Avanzados
Instituto Politécnico Nacional (CINVESTAV-IPN)
Tel: 52 462 623 9606
Fax: 52 462 624 5846
E-mail: jlcabrera@ira.cinvestav.mx

Luis Herrera Estrella
Centro de Estudios Avanzados del IPN (CINVESTAV-IPN)
Unidad Irapuato
Departamento de Genética
Tel: 52 462 623 9606
Fax: 52 462 624 5846
E-mail: lherrera@ira.cinvestav.mx

Rosa María Rangel Cano
Centro de EstudiosAvanzados del IPN (CINVESTAV-IPN)
Unidad Irapuato
Departamento de Genética
Tel: 52 462 623 9606
Fax: 52 462 624 5846
E-mail: rrangel@ira.cinvestav.mx

Silvia Lede
Centro Experimental de Propagación Vegetativa (C.E.Pro.Ve)
Facultad de Ciencias Agrarias y Forestales
Universidad Nacional de La Plata
C.C 31, (1900), La Plata
Buenos Aires, Argentina
Tel: 54 221 423 6616
Fax: 54 221 425 2346
E-mail: ceprove@ceres.agro.unlp.edu.ar 

Walter Abedini
Centro Experimental de Propagación Vegetativa (C.E.Pro.Ve)
Facultad de Ciencias Agrarias y Forestales
Universidad Nacional de La Plata
C.C 31, (1900), La Plata
Buenos Aires, Argentina
Tel: 54 221 423 6616
Fax: 54 221 425 2346
E-mail: ceprove@ceres.agro.unlp.edu.ar

*Corresponding author

Financial support: Comisión de Investigaciones Científicas de la Provincia de Buenos Aires (CICPBA).

Keywords: callus induction, clonal forestry, embryos conversion, micropropagation, persian lilac, somatic embryos.

Abbreviations:

2,4-D: 2, 4 Diclorophenoxyacetic acid
Ade: Adenine
AG3: Giberellic acid
BAP: N6- Benzylaminopurine
HC: Hydrolized Casein
IAA: Indole-3-acetic acid
IBA: Indole-3- butyric acid
MS: Murashige and Skoog's medium
NAA: 1-Naphtaleneacetic acid
NaOCl: sodium chloride
PGR: plant growth regulator
Put: Putrescine
SE: Somatic embryogenesis

Abstract   Reprint (PDF)

A highly efficient somatic embryogenesis system and subsequent plant regeneration of chinaberry (Melia azedarach L.) was developed. Plants were regenerated from indirect somatic embryogenesis induction. Novel features of this improved protocol, include: a) Embryogenic callus induction with no addition of 2, 4-D in the culture media; b) Somatic embryos differentiation was achieved by using high concentration of cytokinins (BAP 10 mg/L) and adenine; c) 100% conversion of somatic embryos to plants was practically obtained and 100% of plants survived under greenhouse conditions; d) Addition of putrescine improved somatic embryos germination. The amount of somatic embryos produced by the pathway of indirect somatic embryogenesis was 447 per gram of fresh weight callus. Regenerated plants were phenotypically normal. The developed protocol established the potential to produce plantlets from cotyledon explants through somatic embryogenesis. It also presents itself as a highly efficient method for mass clonal propagation and conservation of Melia azedarach.

Supported by UNESCO / MIRCEN network