Somatic embryogenesis in Acrocomia aculeata Jacq. (Lodd.) ex Mart using the thin cell layer technique

Detalhes bibliográficos
Autor(a) principal: Padilha,João Henrique Delfrate
Data de Publicação: 2015
Outros Autores: Ribas,Luciana Lopes Fortes, Amano,Érika, Quoirin,Marguerite
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Acta Botanica Brasilica
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-33062015000400516
Resumo: Considering the necessity of Acrocomia aculeata propagation for large-scale production, the aim of this study was to establish a somatic embryogenesis protocol using the thin cell layer (TCL) technique. Aerial parts of in vitro plants were transversally cut at the base into eight TCLs and placed in a culture medium for callus induction. The induction medium was composed of Y3 salts and Morel´s vitamins and supplemented with 150, 300 or 600 μM picloram. After 12 weeks the calli were transferred to a medium supplemented with BAP or 2-iP (12.5 or 25 μM). After 18 weeks, the somatic embryo clusters were transferred to a conversion medium (plant growth regulator-free medium). Primary callus induction rate was higher in the first three TCLs and in media containing 150 or 300 µM picloram. The best maturation results were obtained in medium containing 12.5 μM 2-iP or 12.5 μM BAP. Few somatic embryos converted into plants. The histological analyses showed that callus induction started adjacent to vascular bundles after two days of culture, and somatic embryos arose in the periphery of nodular calli. This study showed that the TCL embryogenesis protocol is promising for in vitro multiplication of A. aculeata.
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spelling Somatic embryogenesis in Acrocomia aculeata Jacq. (Lodd.) ex Mart using the thin cell layer technique2-iPcallus inductionhistologymacaw palmpicloramConsidering the necessity of Acrocomia aculeata propagation for large-scale production, the aim of this study was to establish a somatic embryogenesis protocol using the thin cell layer (TCL) technique. Aerial parts of in vitro plants were transversally cut at the base into eight TCLs and placed in a culture medium for callus induction. The induction medium was composed of Y3 salts and Morel´s vitamins and supplemented with 150, 300 or 600 μM picloram. After 12 weeks the calli were transferred to a medium supplemented with BAP or 2-iP (12.5 or 25 μM). After 18 weeks, the somatic embryo clusters were transferred to a conversion medium (plant growth regulator-free medium). Primary callus induction rate was higher in the first three TCLs and in media containing 150 or 300 µM picloram. The best maturation results were obtained in medium containing 12.5 μM 2-iP or 12.5 μM BAP. Few somatic embryos converted into plants. The histological analyses showed that callus induction started adjacent to vascular bundles after two days of culture, and somatic embryos arose in the periphery of nodular calli. This study showed that the TCL embryogenesis protocol is promising for in vitro multiplication of A. aculeata.Sociedade Botânica do Brasil2015-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-33062015000400516Acta Botanica Brasilica v.29 n.4 2015reponame:Acta Botanica Brasilicainstname:Sociedade Botânica do Brasil (SBB)instacron:SBB10.1590/0102-33062015abb0109info:eu-repo/semantics/openAccessPadilha,João Henrique DelfrateRibas,Luciana Lopes FortesAmano,ÉrikaQuoirin,Margueriteeng2015-12-09T00:00:00Zoai:scielo:S0102-33062015000400516Revistahttps://www.scielo.br/j/abb/ONGhttps://old.scielo.br/oai/scielo-oai.phpacta@botanica.org.br||acta@botanica.org.br|| f.a.r.santos@gmail.com1677-941X0102-3306opendoar:2015-12-09T00:00Acta Botanica Brasilica - Sociedade Botânica do Brasil (SBB)false
dc.title.none.fl_str_mv Somatic embryogenesis in Acrocomia aculeata Jacq. (Lodd.) ex Mart using the thin cell layer technique
title Somatic embryogenesis in Acrocomia aculeata Jacq. (Lodd.) ex Mart using the thin cell layer technique
spellingShingle Somatic embryogenesis in Acrocomia aculeata Jacq. (Lodd.) ex Mart using the thin cell layer technique
Padilha,João Henrique Delfrate
2-iP
callus induction
histology
macaw palm
picloram
title_short Somatic embryogenesis in Acrocomia aculeata Jacq. (Lodd.) ex Mart using the thin cell layer technique
title_full Somatic embryogenesis in Acrocomia aculeata Jacq. (Lodd.) ex Mart using the thin cell layer technique
title_fullStr Somatic embryogenesis in Acrocomia aculeata Jacq. (Lodd.) ex Mart using the thin cell layer technique
title_full_unstemmed Somatic embryogenesis in Acrocomia aculeata Jacq. (Lodd.) ex Mart using the thin cell layer technique
title_sort Somatic embryogenesis in Acrocomia aculeata Jacq. (Lodd.) ex Mart using the thin cell layer technique
author Padilha,João Henrique Delfrate
author_facet Padilha,João Henrique Delfrate
Ribas,Luciana Lopes Fortes
Amano,Érika
Quoirin,Marguerite
author_role author
author2 Ribas,Luciana Lopes Fortes
Amano,Érika
Quoirin,Marguerite
author2_role author
author
author
dc.contributor.author.fl_str_mv Padilha,João Henrique Delfrate
Ribas,Luciana Lopes Fortes
Amano,Érika
Quoirin,Marguerite
dc.subject.por.fl_str_mv 2-iP
callus induction
histology
macaw palm
picloram
topic 2-iP
callus induction
histology
macaw palm
picloram
description Considering the necessity of Acrocomia aculeata propagation for large-scale production, the aim of this study was to establish a somatic embryogenesis protocol using the thin cell layer (TCL) technique. Aerial parts of in vitro plants were transversally cut at the base into eight TCLs and placed in a culture medium for callus induction. The induction medium was composed of Y3 salts and Morel´s vitamins and supplemented with 150, 300 or 600 μM picloram. After 12 weeks the calli were transferred to a medium supplemented with BAP or 2-iP (12.5 or 25 μM). After 18 weeks, the somatic embryo clusters were transferred to a conversion medium (plant growth regulator-free medium). Primary callus induction rate was higher in the first three TCLs and in media containing 150 or 300 µM picloram. The best maturation results were obtained in medium containing 12.5 μM 2-iP or 12.5 μM BAP. Few somatic embryos converted into plants. The histological analyses showed that callus induction started adjacent to vascular bundles after two days of culture, and somatic embryos arose in the periphery of nodular calli. This study showed that the TCL embryogenesis protocol is promising for in vitro multiplication of A. aculeata.
publishDate 2015
dc.date.none.fl_str_mv 2015-12-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-33062015000400516
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-33062015000400516
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/0102-33062015abb0109
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Botânica do Brasil
publisher.none.fl_str_mv Sociedade Botânica do Brasil
dc.source.none.fl_str_mv Acta Botanica Brasilica v.29 n.4 2015
reponame:Acta Botanica Brasilica
instname:Sociedade Botânica do Brasil (SBB)
instacron:SBB
instname_str Sociedade Botânica do Brasil (SBB)
instacron_str SBB
institution SBB
reponame_str Acta Botanica Brasilica
collection Acta Botanica Brasilica
repository.name.fl_str_mv Acta Botanica Brasilica - Sociedade Botânica do Brasil (SBB)
repository.mail.fl_str_mv acta@botanica.org.br||acta@botanica.org.br|| f.a.r.santos@gmail.com
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