Induction of haploid morphogenic calluses from in vitro cultured anthers

Detalhes bibliográficos
Autor(a) principal: Peixe, Augusto
Data de Publicação: 2004
Outros Autores: Barroso, João, Potes, Amely, Pais, Maria
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10174/1864
Resumo: Apricot (Prunus armeniaca) ‘Harcot’ anthers were cultured in vitro for the production of haploid plants. The best androgenic response was achieved with Nitsch and Nitsch (1969) medium, supplemented with 4.52 microM 2,4-D, 4.52 micoM zeatin, 2.85 microM IAA and 40 g l−1 sucrose. Cultures were maintained in the dark for 8 days, at 28 ◦C, followed by transfer to a 16-h photoperiod, with 35 micro mm−2 s−1 light intensity and 24/22 ◦C day/night temperature. The androgenic response was correlated with the floral bud size, its phenologic stage and the level of microspore evolution. Anthers containing microspores at the tetrade/uninucleate stage were the most appropriate. The ploidy level of the calluses was evaluated by flow cytometry revealing that they range from haploid to octaploid. Mixoploid calluses have also been identified. Histological studies showed that the haploid calluses have their origin in the microspores. Nodular structures consisting of cells with dense cytoplasm and differentiated xylem elements were observed and were surrounded by an auto-fluorescent layer, probably due to cutin deposition.
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spelling Induction of haploid morphogenic calluses from in vitro cultured anthersandrogenesis, apricot, flow cytometry, haploidization, stone fruitsApricot (Prunus armeniaca) ‘Harcot’ anthers were cultured in vitro for the production of haploid plants. The best androgenic response was achieved with Nitsch and Nitsch (1969) medium, supplemented with 4.52 microM 2,4-D, 4.52 micoM zeatin, 2.85 microM IAA and 40 g l−1 sucrose. Cultures were maintained in the dark for 8 days, at 28 ◦C, followed by transfer to a 16-h photoperiod, with 35 micro mm−2 s−1 light intensity and 24/22 ◦C day/night temperature. The androgenic response was correlated with the floral bud size, its phenologic stage and the level of microspore evolution. Anthers containing microspores at the tetrade/uninucleate stage were the most appropriate. The ploidy level of the calluses was evaluated by flow cytometry revealing that they range from haploid to octaploid. Mixoploid calluses have also been identified. Histological studies showed that the haploid calluses have their origin in the microspores. Nodular structures consisting of cells with dense cytoplasm and differentiated xylem elements were observed and were surrounded by an auto-fluorescent layer, probably due to cutin deposition.Kluwer Academic Publishers2009-12-09T10:05:03Z2009-12-092004-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article203708 bytesapplication/pdfhttp://hdl.handle.net/10174/1864http://hdl.handle.net/10174/1864eng35-41Plant Cell, Tissue and Organ Culture77livreICAAMapeixe@uevora.ptndndnd582Peixe, AugustoBarroso, JoãoPotes, AmelyPais, Mariainfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-01-03T18:37:47Zoai:dspace.uevora.pt:10174/1864Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T00:57:40.030610Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Induction of haploid morphogenic calluses from in vitro cultured anthers
title Induction of haploid morphogenic calluses from in vitro cultured anthers
spellingShingle Induction of haploid morphogenic calluses from in vitro cultured anthers
Peixe, Augusto
androgenesis, apricot, flow cytometry, haploidization, stone fruits
title_short Induction of haploid morphogenic calluses from in vitro cultured anthers
title_full Induction of haploid morphogenic calluses from in vitro cultured anthers
title_fullStr Induction of haploid morphogenic calluses from in vitro cultured anthers
title_full_unstemmed Induction of haploid morphogenic calluses from in vitro cultured anthers
title_sort Induction of haploid morphogenic calluses from in vitro cultured anthers
author Peixe, Augusto
author_facet Peixe, Augusto
Barroso, João
Potes, Amely
Pais, Maria
author_role author
author2 Barroso, João
Potes, Amely
Pais, Maria
author2_role author
author
author
dc.contributor.author.fl_str_mv Peixe, Augusto
Barroso, João
Potes, Amely
Pais, Maria
dc.subject.por.fl_str_mv androgenesis, apricot, flow cytometry, haploidization, stone fruits
topic androgenesis, apricot, flow cytometry, haploidization, stone fruits
description Apricot (Prunus armeniaca) ‘Harcot’ anthers were cultured in vitro for the production of haploid plants. The best androgenic response was achieved with Nitsch and Nitsch (1969) medium, supplemented with 4.52 microM 2,4-D, 4.52 micoM zeatin, 2.85 microM IAA and 40 g l−1 sucrose. Cultures were maintained in the dark for 8 days, at 28 ◦C, followed by transfer to a 16-h photoperiod, with 35 micro mm−2 s−1 light intensity and 24/22 ◦C day/night temperature. The androgenic response was correlated with the floral bud size, its phenologic stage and the level of microspore evolution. Anthers containing microspores at the tetrade/uninucleate stage were the most appropriate. The ploidy level of the calluses was evaluated by flow cytometry revealing that they range from haploid to octaploid. Mixoploid calluses have also been identified. Histological studies showed that the haploid calluses have their origin in the microspores. Nodular structures consisting of cells with dense cytoplasm and differentiated xylem elements were observed and were surrounded by an auto-fluorescent layer, probably due to cutin deposition.
publishDate 2004
dc.date.none.fl_str_mv 2004-01-01T00:00:00Z
2009-12-09T10:05:03Z
2009-12-09
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10174/1864
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 35-41
Plant Cell, Tissue and Organ Culture
77
livre
ICAAM
apeixe@uevora.pt
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nd
nd
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publisher.none.fl_str_mv Kluwer Academic Publishers
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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