Induction of haploid morphogenic calluses from in vitro cultured anthers
Autor(a) principal: | |
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Data de Publicação: | 2004 |
Outros Autores: | , , |
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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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 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10174/1864 http://hdl.handle.net/10174/1864 |
url |
http://hdl.handle.net/10174/1864 |
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 nd nd nd 582 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
203708 bytes application/pdf |
dc.publisher.none.fl_str_mv |
Kluwer Academic Publishers |
publisher.none.fl_str_mv |
Kluwer Academic Publishers |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
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1799136460979306496 |