A novel regeneration system for a wild passion fruit species (Passiflora cincinnata Mast.) based on somatic embryogenesis from mature zygotic embryos


Autoria(s): SILVA, Maurecilne Lemes da; PINTO, Daniela Lopes Paim; GUERRA, Miguel Pedro; FLOH, Eny Iochevet Segal; BRUCKNER, Claudio Horst; OTONI, Wagner Campos
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2009

Resumo

The objective of the present work was to induce somatic embryogenesis from zygotic embryos of Passiflora cincinnata Masters. Zygotic embryos formed calli on media with different concentrations of 2,4-dichlorophenoxyacetic acid (2,4-D) and 4.5 mu M benzyladenine (BA) after 30 days of in vitro culture. A concentration of 18.1 mu M 2,4-D resulted in the largest number of somatic embryos. Embryogenic calli were yellowish and friable, forming whitish proembryogenic masses. Morphologically, embryogenic cells were small and had large nuclei and dense cytoplasm, whereas non-embryogenic cells were elongated, with small nuclei and less dense cytoplasm. Calli cultured under white light on basal Murashige and Skoog`s medium with activated charcoal produced embryos in all developmental stages. There were differences among the treatments, with some leading to the production of calli with embryos and some only to callus formation. Some abnormalities were associated with somatic embryos, including fused axes, fused cotyledons and polycotyledonary embryos. Production of secondary somatic embryos occurred in the first cycle of primary embryo development. Secondary embryos differentiated from the surface of the protodermal layer of primary embryos with intense cell proliferation, successive mitotic divisions in the initial phase of embryoid development, and a vascular system formed with no connection to the parental tissue. This secondary embryogenic system of P. cincinnata is characterized by intense proliferation and maintenance of embryogenic competence after successive subcultures. This reproducible protocol opens new prospects for massive propagation and is an alternative to the current organogenesis-based transformation protocol.

FAPEMIG[CAG 1527/2005]

Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

CAPES

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

CNPq

Identificador

PLANT CELL TISSUE AND ORGAN CULTURE, v.99, n.1, p.47-54, 2009

0167-6857

http://producao.usp.br/handle/BDPI/27302

10.1007/s11240-009-9574-2

http://dx.doi.org/10.1007/s11240-009-9574-2

Idioma(s)

eng

Publicador

SPRINGER

Relação

Plant Cell Tissue and Organ Culture

Direitos

restrictedAccess

Copyright SPRINGER

Palavras-Chave #Morphogenesis #Passion fruit #Somatic embryogenesis #Wild species #Zygotic embryo #PLANT-REGENERATION #CULTURES #L. #CHARCOAL #CELLS #Biotechnology & Applied Microbiology #Plant Sciences
Tipo

article

original article

publishedVersion