Somatic embryogenesis and ploidy stability in cassava (Manihot esculenta Crantz) cultivars regenerated by in vitro culture of young leaves.

Detalhes bibliográficos
Autor(a) principal: MELO, N. F. de
Data de Publicação: 2002
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)
Texto Completo: http://www.alice.cnptia.embrapa.br/alice/handle/doc/137733
Resumo: The regeneration and cytogenetic analysis of 7 cassava (Manihot esculenta Crantz) cultivars obtained by organogenesis and somatic embryogenesis were investigated. In the first phase, callus formation was induced in young leaves using MS medium supplemented with 1.0, 5.0, 10.0, 15.0 and 20.0 mg/l of 2,4-D or without a growth regulator (control). In the second phase (development), the calli obtained in the above treatments were transferred to MS medium supplemented with factorial combinations of GA3 and BAP at 0, 0.5, 1.0, 1.5 and 2.0 mg/l. Results of the first phase showed that 2,4-D induced the formation of both friable and compact calli. The compact calli displayed root and shoot formation, whilst somatic embryos were obtained only from friable calli in the medium with 1.0 mg/l GA3. Plants obtained from somatic embryos were regenerated in MS medium supplemented with 0.04 mg/l NAA and 0.05 mg/l GA3. Cytogenetic analysis in 167 regenerated plants from somatic embryogenesis and 176 from organogenesis showed 2n= 36 as a normal diploid chromosome number.
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spelling Somatic embryogenesis and ploidy stability in cassava (Manihot esculenta Crantz) cultivars regenerated by in vitro culture of young leaves.AnáliseCaloCitogenética VegetalEmbriogéneseMandiocaManihot EsculentaMicropropagaçãoVariedadeThe regeneration and cytogenetic analysis of 7 cassava (Manihot esculenta Crantz) cultivars obtained by organogenesis and somatic embryogenesis were investigated. In the first phase, callus formation was induced in young leaves using MS medium supplemented with 1.0, 5.0, 10.0, 15.0 and 20.0 mg/l of 2,4-D or without a growth regulator (control). In the second phase (development), the calli obtained in the above treatments were transferred to MS medium supplemented with factorial combinations of GA3 and BAP at 0, 0.5, 1.0, 1.5 and 2.0 mg/l. Results of the first phase showed that 2,4-D induced the formation of both friable and compact calli. The compact calli displayed root and shoot formation, whilst somatic embryos were obtained only from friable calli in the medium with 1.0 mg/l GA3. Plants obtained from somatic embryos were regenerated in MS medium supplemented with 0.04 mg/l NAA and 0.05 mg/l GA3. Cytogenetic analysis in 167 regenerated plants from somatic embryogenesis and 176 from organogenesis showed 2n= 36 as a normal diploid chromosome number.NATONIEL FRANKLIN DE MELO, CPATSA.MELO, N. F. de2018-05-15T00:33:28Z2018-05-15T00:33:28Z2003-03-1420022018-05-15T00:33:28Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleCytologia, Tpkyo, v. 67, n. 4, p. 337-341, 2002.http://www.alice.cnptia.embrapa.br/alice/handle/doc/137733enginfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)instname:Empresa Brasileira de Pesquisa Agropecuária (Embrapa)instacron:EMBRAPA2018-05-15T00:33:34Zoai:www.alice.cnptia.embrapa.br:doc/137733Repositório InstitucionalPUBhttps://www.alice.cnptia.embrapa.br/oai/requestopendoar:21542018-05-15T00:33:34falseRepositório InstitucionalPUBhttps://www.alice.cnptia.embrapa.br/oai/requestcg-riaa@embrapa.bropendoar:21542018-05-15T00:33:34Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) - Empresa Brasileira de Pesquisa Agropecuária (Embrapa)false
dc.title.none.fl_str_mv Somatic embryogenesis and ploidy stability in cassava (Manihot esculenta Crantz) cultivars regenerated by in vitro culture of young leaves.
title Somatic embryogenesis and ploidy stability in cassava (Manihot esculenta Crantz) cultivars regenerated by in vitro culture of young leaves.
spellingShingle Somatic embryogenesis and ploidy stability in cassava (Manihot esculenta Crantz) cultivars regenerated by in vitro culture of young leaves.
MELO, N. F. de
Análise
Calo
Citogenética Vegetal
Embriogénese
Mandioca
Manihot Esculenta
Micropropagação
Variedade
title_short Somatic embryogenesis and ploidy stability in cassava (Manihot esculenta Crantz) cultivars regenerated by in vitro culture of young leaves.
title_full Somatic embryogenesis and ploidy stability in cassava (Manihot esculenta Crantz) cultivars regenerated by in vitro culture of young leaves.
title_fullStr Somatic embryogenesis and ploidy stability in cassava (Manihot esculenta Crantz) cultivars regenerated by in vitro culture of young leaves.
title_full_unstemmed Somatic embryogenesis and ploidy stability in cassava (Manihot esculenta Crantz) cultivars regenerated by in vitro culture of young leaves.
title_sort Somatic embryogenesis and ploidy stability in cassava (Manihot esculenta Crantz) cultivars regenerated by in vitro culture of young leaves.
author MELO, N. F. de
author_facet MELO, N. F. de
author_role author
dc.contributor.none.fl_str_mv NATONIEL FRANKLIN DE MELO, CPATSA.
dc.contributor.author.fl_str_mv MELO, N. F. de
dc.subject.por.fl_str_mv Análise
Calo
Citogenética Vegetal
Embriogénese
Mandioca
Manihot Esculenta
Micropropagação
Variedade
topic Análise
Calo
Citogenética Vegetal
Embriogénese
Mandioca
Manihot Esculenta
Micropropagação
Variedade
description The regeneration and cytogenetic analysis of 7 cassava (Manihot esculenta Crantz) cultivars obtained by organogenesis and somatic embryogenesis were investigated. In the first phase, callus formation was induced in young leaves using MS medium supplemented with 1.0, 5.0, 10.0, 15.0 and 20.0 mg/l of 2,4-D or without a growth regulator (control). In the second phase (development), the calli obtained in the above treatments were transferred to MS medium supplemented with factorial combinations of GA3 and BAP at 0, 0.5, 1.0, 1.5 and 2.0 mg/l. Results of the first phase showed that 2,4-D induced the formation of both friable and compact calli. The compact calli displayed root and shoot formation, whilst somatic embryos were obtained only from friable calli in the medium with 1.0 mg/l GA3. Plants obtained from somatic embryos were regenerated in MS medium supplemented with 0.04 mg/l NAA and 0.05 mg/l GA3. Cytogenetic analysis in 167 regenerated plants from somatic embryogenesis and 176 from organogenesis showed 2n= 36 as a normal diploid chromosome number.
publishDate 2002
dc.date.none.fl_str_mv 2002
2003-03-14
2018-05-15T00:33:28Z
2018-05-15T00:33:28Z
2018-05-15T00:33:28Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv Cytologia, Tpkyo, v. 67, n. 4, p. 337-341, 2002.
http://www.alice.cnptia.embrapa.br/alice/handle/doc/137733
identifier_str_mv Cytologia, Tpkyo, v. 67, n. 4, p. 337-341, 2002.
url http://www.alice.cnptia.embrapa.br/alice/handle/doc/137733
dc.language.iso.fl_str_mv eng
language eng
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instname:Empresa Brasileira de Pesquisa Agropecuária (Embrapa)
instacron:EMBRAPA
instname_str Empresa Brasileira de Pesquisa Agropecuária (Embrapa)
instacron_str EMBRAPA
institution EMBRAPA
reponame_str Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)
collection Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)
repository.name.fl_str_mv Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) - Empresa Brasileira de Pesquisa Agropecuária (Embrapa)
repository.mail.fl_str_mv cg-riaa@embrapa.br
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