Estabelecimento in vitro de Ceiba rubriflora Carv.-Sobr. e L. P. Queiroz: uma espécie endêmica do vale do rio São Francisco

Ceiba rubriflora is a native Brazilian species, critically endangered, from region of middle São Francisco River. C. rubriflora’s seed production is scarce because of its endemism. Therefore, the micropropagation is presented as a tool for its propagation and seedling production. Thus, the aim of th...

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Detalles Bibliográficos
Autores: Anna Luiza Mota Docha, Leandro Silva de Oliveira, Nayara dos Santos Souza, Gilvano Ebling Brondani
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2020
País:Brasil
Institución:Universidade Federal de Minas Gerais (UFMG)
Repositorio:Repositório Institucional da UFMG
Idioma:portugués
OAI Identifier:oai:repositorio.ufmg.br:1843/51871
Acceso en línea:https://doi.org/10.35699/2447-6218.2020.24029
http://hdl.handle.net/1843/51871
Access Level:acceso abierto
Palabra clave:Paineira rubi
Mata seca
Conservação de espécie
Micropropagação
Sementes
Brotos (Plantas)
Germinação
Descripción
Sumario:Ceiba rubriflora is a native Brazilian species, critically endangered, from region of middle São Francisco River. C. rubriflora’s seed production is scarce because of its endemism. Therefore, the micropropagation is presented as a tool for its propagation and seedling production. Thus, the aim of the present study was to evaluate the in vitro establishment of C. rubriflora seeds after disinfestation with different concentrations of active chlorine and testing the in vitro multiplication of apical shoots in different concentrations of 6-benzylaminopurine (BAP). The in vitro establishment of seeds was performed in MS culture medium, which were previously submitted to sodium hypochlorite (NaOCl) disinfection at concentrations of 0.0; 0.5; 1.0; 1.5; and 2.5% active chlorine. Apical shoots of in vitro germinated seedlings were used as explants for multiplication, in MS culture medium, supplemented with BAP in concentrations of 0.0; 1.0 and 2.0 mg L-1. The evaluations were related to seedling survival, fungal and bacterial contamination and number of shoots per explant. The in vitro germination of seeds was satisfactory, with survival rate higher than 98%. The percentage of in vitro contamination was only 2%, free from bacterial cultures. The apical shoots of C. rubriflora were not multiplied in a single subculture in vitro in BAP culture medium. The results demonstrate the viability of in vitro germination of C. rubriflora seeds for the introduction and subsequent micropropagation process, opening perspectives for further studies with the species.