CALLOGENESIS AND RHIZOGENESIS IN MAHOGANY (Swietenia macrophylla King) EXPLANTS CULTURED in vitro

Detalhes bibliográficos
Autor(a) principal: Rocha, Silvana Cruz da
Data de Publicação: 2005
Outros Autores: Quoirin, Marguerite
Tipo de documento: Artigo
Idioma: por
Título da fonte: Ciência Florestal (Online)
Texto Completo: https://periodicos.ufsm.br/cienciaflorestal/article/view/1785
Resumo: The indiscriminate exploitation of tropical trees in a search for economically valuable species leads to the risk of extinction of several species. This is the case of mahogany (Swietenia macrophylla King) in Brazil. The establishment of a method of direct or indirect bud regeneration could help to produce a great number of plantlets and could constitute an alternative to sexual propagation. The latter is limited by the fact that mahogany seeds lose their germinative power soon after harvest. In this work, two kinds of explants were used: leaf and root fragments from in vitro cultured plants. After disinfection, the explants were cultured in petri dishes containing modified Murashige and Skoog (1962) culture medium, with three-quarters of salt concentration, vitamins, 30 g.L-1 sucrose and 7 g.L-1 agar. The combinations of growth substances were: naphthaleneacetic acid (ANA 0.11 mM and 0.54 mM) and one type of cytokinin, kinetin (CIN 1.2 mM, 2.3 mM, 4.7 mM and 9.3 mM), 6-benzylaminopurine (BA 2.2 mM, 4.4 mM and 8.8 mM) or 2-isopentenyladenine (2-iP 2.5 mM). The variables were the concentration and combinations of the growth regulators and the explant origin.The cultures were evaluated every 30 days, the number of explants forming calluses or roots was recorded and the callus consistency was observed. Calluses were formed in both kinds of explants. In leaf explants, 90% of explants formed callus when culture medium contained 4.4 mM BA with 0.54 mM ANA and 8.9 mM BA with 0.11 or 0.54 mM ANA. For root explants, the combination that gave the highest number of calluses was 2.2 mM BA and 0.54 mM ANA and 55% of them formed callus. Adventitious roots were regenerated from leaf calluses or directly from leaf lamina cultured in media containing CIN and ANA. However, adventitious buds were not obtained with the growth regulator combinations tested in these experiments.
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spelling CALLOGENESIS AND RHIZOGENESIS IN MAHOGANY (Swietenia macrophylla King) EXPLANTS CULTURED in vitroCalogênese e rizogênese em explantes de mogno (Swietenia macrophylla King) cultivados in vitro.in vitro tissue cultureMeliaceaeorganogenesistropical species.cultura in vitroespécie tropicalMeliaceaeorganogêneseThe indiscriminate exploitation of tropical trees in a search for economically valuable species leads to the risk of extinction of several species. This is the case of mahogany (Swietenia macrophylla King) in Brazil. The establishment of a method of direct or indirect bud regeneration could help to produce a great number of plantlets and could constitute an alternative to sexual propagation. The latter is limited by the fact that mahogany seeds lose their germinative power soon after harvest. In this work, two kinds of explants were used: leaf and root fragments from in vitro cultured plants. After disinfection, the explants were cultured in petri dishes containing modified Murashige and Skoog (1962) culture medium, with three-quarters of salt concentration, vitamins, 30 g.L-1 sucrose and 7 g.L-1 agar. The combinations of growth substances were: naphthaleneacetic acid (ANA 0.11 mM and 0.54 mM) and one type of cytokinin, kinetin (CIN 1.2 mM, 2.3 mM, 4.7 mM and 9.3 mM), 6-benzylaminopurine (BA 2.2 mM, 4.4 mM and 8.8 mM) or 2-isopentenyladenine (2-iP 2.5 mM). The variables were the concentration and combinations of the growth regulators and the explant origin.The cultures were evaluated every 30 days, the number of explants forming calluses or roots was recorded and the callus consistency was observed. Calluses were formed in both kinds of explants. In leaf explants, 90% of explants formed callus when culture medium contained 4.4 mM BA with 0.54 mM ANA and 8.9 mM BA with 0.11 or 0.54 mM ANA. For root explants, the combination that gave the highest number of calluses was 2.2 mM BA and 0.54 mM ANA and 55% of them formed callus. Adventitious roots were regenerated from leaf calluses or directly from leaf lamina cultured in media containing CIN and ANA. However, adventitious buds were not obtained with the growth regulator combinations tested in these experiments.A exploração de árvores tropicais realizada de forma indiscriminada, buscando espécies de alto valor econômico, tem levado várias espécies, como o mogno (Swietenia macrophylla King), ao perigo de extinção. O desenvolvimento de uma metodologia de regeneração de gemas, direta ou indireta, poderia auxiliar na obtenção de um grande número de mudas e constituir uma perspectiva à propagação sexuada. Essa última é limitada pelo fato das sementes perderem rapidamente a capacidade germinativa. No presente trabalho, foram utilizados dois tipos de explantes: fragmentos foliares e de raízes de plantas cultivadas in vitro. Após desinfestação, os explantes foram colocados em meio de cultura de Murashige e Skoog (1962) contendo três quartos da concentração de sais, vitaminas do mesmo meio, 30g.L-1 de sacarose, auxina (ácido naftaleno-acético, ANA, 0,11 µM e 0,54 µM), citocinina (cinetina, CIN, 1,2 µM, 2,3 µM, 4,7 µM e 9,3 µM; 6-benziladenina, BA, 2,2 µM, 4,4 µM e 8,8 µM ou 2-isopenteniladenina, 2-iP, 2,5 µM) e 7g.L-1 de ágar. As variáveis testadas foram a concentração e o tipo de regulador de crescimento e a origem dos explantes. A cada 30 dias, os explantes foram avaliados pela contagem do número de explantes formando calos ou raízes e a consistência dos calos. Foram obtidos calos a com base nos dois tipos de explantes. Nos explantes foliares, 90% deles formaram calos em meios de cultura contendo BA 4,4 µM com ANA 0,54 µM e BA 8,9 µM com ANA 0,11 ou 0,54 µM. Nos explantes de raízes, a maior percentagem de explantes com calos foi de 55%, no meio de cultura com BA 2,2 µMe ANA 0,54 µM. Raízes adventícias foram obtidas partindo de calos e do limbo dos explantes foliares, em meios de cultura com CIN e ANA. Não foi observada a formação de gemas adventícias. Universidade Federal de Santa Maria2005-03-30info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://periodicos.ufsm.br/cienciaflorestal/article/view/178510.5902/198050981785Ciência Florestal; Vol. 14 No. 1 (2004); 91-101Ciência Florestal; v. 14 n. 1 (2004); 91-1011980-50980103-9954reponame:Ciência Florestal (Online)instname:Universidade Federal de Santa Maria (UFSM)instacron:UFSMporhttps://periodicos.ufsm.br/cienciaflorestal/article/view/1785/1051Rocha, Silvana Cruz daQuoirin, Margueriteinfo:eu-repo/semantics/openAccess2017-05-16T18:23:09Zoai:ojs.pkp.sfu.ca:article/1785Revistahttp://www.ufsm.br/cienciaflorestal/ONGhttps://old.scielo.br/oai/scielo-oai.php||cienciaflorestal@ufsm.br|| cienciaflorestal@gmail.com|| cf@smail.ufsm.br1980-50980103-9954opendoar:2017-05-16T18:23:09Ciência Florestal (Online) - Universidade Federal de Santa Maria (UFSM)false
dc.title.none.fl_str_mv CALLOGENESIS AND RHIZOGENESIS IN MAHOGANY (Swietenia macrophylla King) EXPLANTS CULTURED in vitro
Calogênese e rizogênese em explantes de mogno (Swietenia macrophylla King) cultivados in vitro.
title CALLOGENESIS AND RHIZOGENESIS IN MAHOGANY (Swietenia macrophylla King) EXPLANTS CULTURED in vitro
spellingShingle CALLOGENESIS AND RHIZOGENESIS IN MAHOGANY (Swietenia macrophylla King) EXPLANTS CULTURED in vitro
Rocha, Silvana Cruz da
in vitro tissue culture
Meliaceae
organogenesis
tropical species.
cultura in vitro
espécie tropical
Meliaceae
organogênese
title_short CALLOGENESIS AND RHIZOGENESIS IN MAHOGANY (Swietenia macrophylla King) EXPLANTS CULTURED in vitro
title_full CALLOGENESIS AND RHIZOGENESIS IN MAHOGANY (Swietenia macrophylla King) EXPLANTS CULTURED in vitro
title_fullStr CALLOGENESIS AND RHIZOGENESIS IN MAHOGANY (Swietenia macrophylla King) EXPLANTS CULTURED in vitro
title_full_unstemmed CALLOGENESIS AND RHIZOGENESIS IN MAHOGANY (Swietenia macrophylla King) EXPLANTS CULTURED in vitro
title_sort CALLOGENESIS AND RHIZOGENESIS IN MAHOGANY (Swietenia macrophylla King) EXPLANTS CULTURED in vitro
author Rocha, Silvana Cruz da
author_facet Rocha, Silvana Cruz da
Quoirin, Marguerite
author_role author
author2 Quoirin, Marguerite
author2_role author
dc.contributor.author.fl_str_mv Rocha, Silvana Cruz da
Quoirin, Marguerite
dc.subject.por.fl_str_mv in vitro tissue culture
Meliaceae
organogenesis
tropical species.
cultura in vitro
espécie tropical
Meliaceae
organogênese
topic in vitro tissue culture
Meliaceae
organogenesis
tropical species.
cultura in vitro
espécie tropical
Meliaceae
organogênese
description The indiscriminate exploitation of tropical trees in a search for economically valuable species leads to the risk of extinction of several species. This is the case of mahogany (Swietenia macrophylla King) in Brazil. The establishment of a method of direct or indirect bud regeneration could help to produce a great number of plantlets and could constitute an alternative to sexual propagation. The latter is limited by the fact that mahogany seeds lose their germinative power soon after harvest. In this work, two kinds of explants were used: leaf and root fragments from in vitro cultured plants. After disinfection, the explants were cultured in petri dishes containing modified Murashige and Skoog (1962) culture medium, with three-quarters of salt concentration, vitamins, 30 g.L-1 sucrose and 7 g.L-1 agar. The combinations of growth substances were: naphthaleneacetic acid (ANA 0.11 mM and 0.54 mM) and one type of cytokinin, kinetin (CIN 1.2 mM, 2.3 mM, 4.7 mM and 9.3 mM), 6-benzylaminopurine (BA 2.2 mM, 4.4 mM and 8.8 mM) or 2-isopentenyladenine (2-iP 2.5 mM). The variables were the concentration and combinations of the growth regulators and the explant origin.The cultures were evaluated every 30 days, the number of explants forming calluses or roots was recorded and the callus consistency was observed. Calluses were formed in both kinds of explants. In leaf explants, 90% of explants formed callus when culture medium contained 4.4 mM BA with 0.54 mM ANA and 8.9 mM BA with 0.11 or 0.54 mM ANA. For root explants, the combination that gave the highest number of calluses was 2.2 mM BA and 0.54 mM ANA and 55% of them formed callus. Adventitious roots were regenerated from leaf calluses or directly from leaf lamina cultured in media containing CIN and ANA. However, adventitious buds were not obtained with the growth regulator combinations tested in these experiments.
publishDate 2005
dc.date.none.fl_str_mv 2005-03-30
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://periodicos.ufsm.br/cienciaflorestal/article/view/1785
10.5902/198050981785
url https://periodicos.ufsm.br/cienciaflorestal/article/view/1785
identifier_str_mv 10.5902/198050981785
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://periodicos.ufsm.br/cienciaflorestal/article/view/1785/1051
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
publisher.none.fl_str_mv Universidade Federal de Santa Maria
dc.source.none.fl_str_mv Ciência Florestal; Vol. 14 No. 1 (2004); 91-101
Ciência Florestal; v. 14 n. 1 (2004); 91-101
1980-5098
0103-9954
reponame:Ciência Florestal (Online)
instname:Universidade Federal de Santa Maria (UFSM)
instacron:UFSM
instname_str Universidade Federal de Santa Maria (UFSM)
instacron_str UFSM
institution UFSM
reponame_str Ciência Florestal (Online)
collection Ciência Florestal (Online)
repository.name.fl_str_mv Ciência Florestal (Online) - Universidade Federal de Santa Maria (UFSM)
repository.mail.fl_str_mv ||cienciaflorestal@ufsm.br|| cienciaflorestal@gmail.com|| cf@smail.ufsm.br
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