Induction of somatic embryogenesis in two cultivars of anthurium analysed by scanning electron microscopy

Detalhes bibliográficos
Autor(a) principal: dos Santos Melo, Priscila Bezerra
Data de Publicação: 2019
Outros Autores: Portugal Pinto de Carvalho, Ana Cristina, Campos de Magalhães Bertini, Cândida Hermínia, Muniz, Celli Rodrigues, Rossetti, Adroaldo Guimarães
Tipo de documento: Artigo
Idioma: por
Título da fonte: Agro@mbiente on-line
Texto Completo: https://revista.ufrr.br/agroambiente/article/view/5333
Resumo: Somatic embryogenesis is an advantageous tool in the commercial production of micropropagated anthurium plantlets. As such, the aim of this study was to establish a protocol for the induction of somatic embryogenesis in Jureia and Luau cultivars. Defoliated nodal segments, 1.0 cm in length and containing one bud, were used as explants. The experimental design was completely randomised, in a 2 x 3 x 5 factorial scheme (cultivar: Jureia and Luau x auxin: 2,4-D, NAA and Picloram x concentration: 0, 2.5, 5.0, 7.5, and 10.0 μM), with 30 treatments in a scheme of plots split over time (15, 30, 45, 60, 75 and 90 days). The anatomy and percentage of embryogenic callus formation were analysed. The structures formed, analysed by scanning electron microscopy, corresponded to embryogenic calli. The Luau cultivar was superior in forming embryogenic calli. For the two cultivars, among the auxins under study, NAA demonstrated a greater induction potential for somatic embryogenesis, with the concentration of 7.5 μM giving the highest mean values. The 90-day evaluation period showed the maximum formation of embryogenic calli; however, mean values were fairly similar to the 75-day evaluation period. To induce embryogenic calli, therefore, it is suggested that the nodal segments be inoculated into a culture medium with added NAA growth regulator at a concentration of 7.5 μM, and that the explants remain in this medium for 75 days after inoculation.
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spelling Induction of somatic embryogenesis in two cultivars of anthurium analysed by scanning electron microscopyAnálise microestrutural. Calos embriogênicos. Micropropagação. Morfogênese in vitro.Somatic embryogenesis is an advantageous tool in the commercial production of micropropagated anthurium plantlets. As such, the aim of this study was to establish a protocol for the induction of somatic embryogenesis in Jureia and Luau cultivars. Defoliated nodal segments, 1.0 cm in length and containing one bud, were used as explants. The experimental design was completely randomised, in a 2 x 3 x 5 factorial scheme (cultivar: Jureia and Luau x auxin: 2,4-D, NAA and Picloram x concentration: 0, 2.5, 5.0, 7.5, and 10.0 μM), with 30 treatments in a scheme of plots split over time (15, 30, 45, 60, 75 and 90 days). The anatomy and percentage of embryogenic callus formation were analysed. The structures formed, analysed by scanning electron microscopy, corresponded to embryogenic calli. The Luau cultivar was superior in forming embryogenic calli. For the two cultivars, among the auxins under study, NAA demonstrated a greater induction potential for somatic embryogenesis, with the concentration of 7.5 μM giving the highest mean values. The 90-day evaluation period showed the maximum formation of embryogenic calli; however, mean values were fairly similar to the 75-day evaluation period. To induce embryogenic calli, therefore, it is suggested that the nodal segments be inoculated into a culture medium with added NAA growth regulator at a concentration of 7.5 μM, and that the explants remain in this medium for 75 days after inoculation.UFRR2019-05-03info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://revista.ufrr.br/agroambiente/article/view/533310.18227/1982-8470ragro.v13i0.5333AGRO@MBIENTE ON-LINE JOURNALRAGR; Vol. 13 (2019): Edição Continuada; 1-13REVISTA AGRO@MBIENTE ON-LINE; Vol. 13 (2019): Edição Continuada; 1-13REVISTA AGRO@MBIENTE ON-LINE; v. 13 (2019): Edição Continuada; 1-131982-8470reponame:Agro@mbiente on-lineinstname:Universidade Federal de Roraima (UFRR)instacron:UFRRporhttps://revista.ufrr.br/agroambiente/article/view/5333/2613Copyright (c) 2019 REVISTA AGRO@MBIENTE ON-LINEinfo:eu-repo/semantics/openAccessdos Santos Melo, Priscila BezerraPortugal Pinto de Carvalho, Ana CristinaCampos de Magalhães Bertini, Cândida HermíniaMuniz, Celli RodriguesRossetti, Adroaldo Guimarães2019-12-06T15:37:15Zoai:oai.revista.ufrr.br:article/5333Revistahttps://revista.ufrr.br/index.php/agroambientePUBhttps://revista.ufrr.br/index.php/agroambiente/oai||scpuchoa@dsi.ufrr.br|| arcanjoalves@oi.com.br1982-84701982-8470opendoar:2019-12-06T15:37:15Agro@mbiente on-line - Universidade Federal de Roraima (UFRR)false
dc.title.none.fl_str_mv Induction of somatic embryogenesis in two cultivars of anthurium analysed by scanning electron microscopy
title Induction of somatic embryogenesis in two cultivars of anthurium analysed by scanning electron microscopy
spellingShingle Induction of somatic embryogenesis in two cultivars of anthurium analysed by scanning electron microscopy
dos Santos Melo, Priscila Bezerra
Análise microestrutural. Calos embriogênicos. Micropropagação. Morfogênese in vitro.
title_short Induction of somatic embryogenesis in two cultivars of anthurium analysed by scanning electron microscopy
title_full Induction of somatic embryogenesis in two cultivars of anthurium analysed by scanning electron microscopy
title_fullStr Induction of somatic embryogenesis in two cultivars of anthurium analysed by scanning electron microscopy
title_full_unstemmed Induction of somatic embryogenesis in two cultivars of anthurium analysed by scanning electron microscopy
title_sort Induction of somatic embryogenesis in two cultivars of anthurium analysed by scanning electron microscopy
author dos Santos Melo, Priscila Bezerra
author_facet dos Santos Melo, Priscila Bezerra
Portugal Pinto de Carvalho, Ana Cristina
Campos de Magalhães Bertini, Cândida Hermínia
Muniz, Celli Rodrigues
Rossetti, Adroaldo Guimarães
author_role author
author2 Portugal Pinto de Carvalho, Ana Cristina
Campos de Magalhães Bertini, Cândida Hermínia
Muniz, Celli Rodrigues
Rossetti, Adroaldo Guimarães
author2_role author
author
author
author
dc.contributor.author.fl_str_mv dos Santos Melo, Priscila Bezerra
Portugal Pinto de Carvalho, Ana Cristina
Campos de Magalhães Bertini, Cândida Hermínia
Muniz, Celli Rodrigues
Rossetti, Adroaldo Guimarães
dc.subject.por.fl_str_mv Análise microestrutural. Calos embriogênicos. Micropropagação. Morfogênese in vitro.
topic Análise microestrutural. Calos embriogênicos. Micropropagação. Morfogênese in vitro.
description Somatic embryogenesis is an advantageous tool in the commercial production of micropropagated anthurium plantlets. As such, the aim of this study was to establish a protocol for the induction of somatic embryogenesis in Jureia and Luau cultivars. Defoliated nodal segments, 1.0 cm in length and containing one bud, were used as explants. The experimental design was completely randomised, in a 2 x 3 x 5 factorial scheme (cultivar: Jureia and Luau x auxin: 2,4-D, NAA and Picloram x concentration: 0, 2.5, 5.0, 7.5, and 10.0 μM), with 30 treatments in a scheme of plots split over time (15, 30, 45, 60, 75 and 90 days). The anatomy and percentage of embryogenic callus formation were analysed. The structures formed, analysed by scanning electron microscopy, corresponded to embryogenic calli. The Luau cultivar was superior in forming embryogenic calli. For the two cultivars, among the auxins under study, NAA demonstrated a greater induction potential for somatic embryogenesis, with the concentration of 7.5 μM giving the highest mean values. The 90-day evaluation period showed the maximum formation of embryogenic calli; however, mean values were fairly similar to the 75-day evaluation period. To induce embryogenic calli, therefore, it is suggested that the nodal segments be inoculated into a culture medium with added NAA growth regulator at a concentration of 7.5 μM, and that the explants remain in this medium for 75 days after inoculation.
publishDate 2019
dc.date.none.fl_str_mv 2019-05-03
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
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dc.identifier.uri.fl_str_mv https://revista.ufrr.br/agroambiente/article/view/5333
10.18227/1982-8470ragro.v13i0.5333
url https://revista.ufrr.br/agroambiente/article/view/5333
identifier_str_mv 10.18227/1982-8470ragro.v13i0.5333
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://revista.ufrr.br/agroambiente/article/view/5333/2613
dc.rights.driver.fl_str_mv Copyright (c) 2019 REVISTA AGRO@MBIENTE ON-LINE
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2019 REVISTA AGRO@MBIENTE ON-LINE
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv UFRR
publisher.none.fl_str_mv UFRR
dc.source.none.fl_str_mv AGRO@MBIENTE ON-LINE JOURNALRAGR; Vol. 13 (2019): Edição Continuada; 1-13
REVISTA AGRO@MBIENTE ON-LINE; Vol. 13 (2019): Edição Continuada; 1-13
REVISTA AGRO@MBIENTE ON-LINE; v. 13 (2019): Edição Continuada; 1-13
1982-8470
reponame:Agro@mbiente on-line
instname:Universidade Federal de Roraima (UFRR)
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instname_str Universidade Federal de Roraima (UFRR)
instacron_str UFRR
institution UFRR
reponame_str Agro@mbiente on-line
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repository.name.fl_str_mv Agro@mbiente on-line - Universidade Federal de Roraima (UFRR)
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