Cultivo e conservação in vitro de sempre vivas

Detalhes bibliográficos
Autor(a) principal: Moreira, Fernanda da Conceição
Data de Publicação: 2015
Tipo de documento: Tese
Idioma: por
Título da fonte: Repositório Institucional da UFLA
Texto Completo: http://repositorio.ufla.br/jspui/handle/1/56399532
Resumo: Comanthera bisulcata (Eriocaulaceae) and Xyris cipoensis (Xyridaceae) are ornamental species, occurring in campos rupestres environments and are on the endangered list species. The aim of this study were: (i) in vitro establishment, control of senescence and the multiplication of Comanthera bisulcata seedlings. (ii) micropropagation and (iii) conservation in vitro of Xyris cipoensis. To establish in vitro C. bisulcata was performed seeds sterilization at different times immersed in NaOCl. The germination and growth of seedlings were evaluated in WPM medium with different pH. For the control of senescence were tested 0, 0.2, 2 and 20 µM AgNO3 and the oxidation control was tested from 0 to 400 mg L-1 of polyvinylpyrrolidone (PVP). The multiplication was tested 2.68 µM NAA + 2.27 µM TDZ, 2.22 µM BA or 2.32 μM KIN. Subsequently, an experiment was conducted comparing the semi-solid system and the temporary immersion system (Plantform®). The Xyris cipoensis seeds were decontaminated in different exposure times NaOCl. The WPM medium with different sucrose concentrations was tested. The seeds were stored in liquid nitrogen. Thawing was performed at different times. Subsequently, the seeds were dried at different times, cryopreserved and thawed for 60 seconds. In C. bisulcata the highest percentage of disinfestation (96%) and germination (54%) of the seeds was observed in five minutes immersion in NaOCl. Seedlings grown at pH 4.4 showed higher average root length (1 cm) and greater average height (2.8 cm) of seedlings. During the proliferation phase, the seedlings senescence can be reduced with 0.2 M AgNO3 and the oxidation with 400 mg L-1 antioxidant polyvinylpyrrolidone and 2.68 µM NAA + 2.27 uM TDZ was suitable to induce shoots. The relative growth rate (RGR) and average values average weight of seedlings demonstrated the superiority of temporary immersion system liquid (Plantform®) comparing to the semi-solid system during micropropagation C. bisulcata. The highest percentage of decontamination and germination (90% and 84%) was observed after five minutes of exposure to NaOCl and using 15g L-1 sucrose, respectively. An efficient protocol for the in vitro propagation was obtained and increased post-thaw viability of cryopreserved seed was reached after thawing for 60 seconds. Survival seeds increased when seeds were dehydrated before cryopreservation process.
id UFLA_1e784d32eb56754096571bafcbf4e939
oai_identifier_str oai:localhost:1/28532
network_acronym_str UFLA
network_name_str Repositório Institucional da UFLA
repository_id_str
spelling Cultivo e conservação in vitro de sempre vivasEspécie endêmicaSistema de imersão temporária (Plantform®)MicropropagaçãoCriopreservaçãoCampo RupestreBiorreatorEndemic speciesNative speciesTemporary immersion system (Plantform®)In vitro conservationCryopreservationBiorreactorFisiologia VegetalComanthera bisulcata (Eriocaulaceae) and Xyris cipoensis (Xyridaceae) are ornamental species, occurring in campos rupestres environments and are on the endangered list species. The aim of this study were: (i) in vitro establishment, control of senescence and the multiplication of Comanthera bisulcata seedlings. (ii) micropropagation and (iii) conservation in vitro of Xyris cipoensis. To establish in vitro C. bisulcata was performed seeds sterilization at different times immersed in NaOCl. The germination and growth of seedlings were evaluated in WPM medium with different pH. For the control of senescence were tested 0, 0.2, 2 and 20 µM AgNO3 and the oxidation control was tested from 0 to 400 mg L-1 of polyvinylpyrrolidone (PVP). The multiplication was tested 2.68 µM NAA + 2.27 µM TDZ, 2.22 µM BA or 2.32 μM KIN. Subsequently, an experiment was conducted comparing the semi-solid system and the temporary immersion system (Plantform®). The Xyris cipoensis seeds were decontaminated in different exposure times NaOCl. The WPM medium with different sucrose concentrations was tested. The seeds were stored in liquid nitrogen. Thawing was performed at different times. Subsequently, the seeds were dried at different times, cryopreserved and thawed for 60 seconds. In C. bisulcata the highest percentage of disinfestation (96%) and germination (54%) of the seeds was observed in five minutes immersion in NaOCl. Seedlings grown at pH 4.4 showed higher average root length (1 cm) and greater average height (2.8 cm) of seedlings. During the proliferation phase, the seedlings senescence can be reduced with 0.2 M AgNO3 and the oxidation with 400 mg L-1 antioxidant polyvinylpyrrolidone and 2.68 µM NAA + 2.27 uM TDZ was suitable to induce shoots. The relative growth rate (RGR) and average values average weight of seedlings demonstrated the superiority of temporary immersion system liquid (Plantform®) comparing to the semi-solid system during micropropagation C. bisulcata. The highest percentage of decontamination and germination (90% and 84%) was observed after five minutes of exposure to NaOCl and using 15g L-1 sucrose, respectively. An efficient protocol for the in vitro propagation was obtained and increased post-thaw viability of cryopreserved seed was reached after thawing for 60 seconds. Survival seeds increased when seeds were dehydrated before cryopreservation process.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Comanthera bisulcata (Eriocaulaceae) e Xyris cipoensis (Xyridaceae) são espécies ornamentais que ocorrem em ambientes de Campo Rupestre e encontram-se na lista de espécies ameaçadas de extinção. Objetivou-se realizar o (i) estabelecimento in vitro, o controle da senescência e a multiplicação de plântulas de Comanthera bisulcata. (ii) micropropagação e a (iii) conservação in vitro de Xyris cipoensis. Para o estabelecimento in vitro de C. bisulcata foi realizada a desinfestação de sementes em diferentes tempos de imersão ao NaOCl. A germinação e o crescimento de plântulas foram avaliados em meio WPM com diferentes pHs. Para o controle de senescência em plântulas foram testadas 0, 0,2, 2 e 20 µM de AgNO3 e, para controle de oxidação em plântulas, foram estudadas 0 e 400 mg L-1 de polivinilpirrolidona (PVP). Para a multiplicação, testaram-se 2,68 µM de ANA, combinado com 2,27 µM de TDZ, 2,22 µM de BAP ou 2,32 µM de KIN. Posteriormente, foi realizado um experimento comparando o sistema semissólido e o sistema de imersão temporária líquida (Plantform®). Para Xyris cipoensis as sementes foram descontaminadas em diferentes tempos de exposição ao NaOCl. Para a germinação em meio WPM, testaram-se diferentes concentrações de sacarose. As sementes foram armazenadas em nitrogênio líquido. O descongelamento foi realizado em diferentes períodos. Sementes foram desidratadas em diferentes tempos, criopreservadas e descongeladas. Em C. bisulcata, verificou-se a maior porcentagem de desinfestação (96%) e de germinação (54%) de sementes em cinco minutos de imersão ao NaOCl. As plântulas cultivadas em pH 4,4 apresentaram maior comprimento médio de raízes (1 cm) e maior altura média (2,8 cm) de plântulas. Durante a fase de multiplicação, a senescência de plântulas pôde ser reduzida com 0,2 µM de AgNO3 e a oxidação com 400 mg L-1 de PVP. Para indução de brotações, melhores resultados foram obtidos com 2,68 µM de ANA + 2,27 µM de TDZ. A taxa de crescimento relativo e peso médio de plântulas demonstraram superioridade do sistema de imersão líquida temporária (Plantform®) em relação ao sistema semissólido durante a micropropagação de C. bisulcata. Em X. cipoensis, a maior porcentagem de descontaminação (90%) e de germinação (84%) foi observada após cinco minutos de exposição ao NaOCl com 15g L-1 de sacarose. Um protocolo para o estabelecimento in vitro foi obtido e uma maior viabilidade pós-descongelamento das sementes criopreservados foi alcançada após o descongelamento por 60 segundos. A sobrevivência aumentou quando as sementes foram desidratadas antes da criopreservação.Universidade Federal de LavrasPrograma de Pós-Graduação em Fisiologia VegetalUFLAbrasilDepartamento de BiologiaPaiva, RenatoNery, Fernanda CarlotaSantos, Breno RégisCarvalho, Milene Alves de FigueiredoRodrigues, Leonardo Augusto ZebralMoreira, Fernanda da Conceição2018-02-05T16:32:02Z2018-02-05T16:32:02Z2018-02-052015-07-31info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisapplication/pdfMOREIRA, F. da C. Cultivo e conservação in vitro de sempre vivas. 2015. 102 p. Tese (Doutorado em Fisiologia Vegetal) – Universidade Federal de Lavras, Lavras, 2015.http://repositorio.ufla.br/jspui/handle/1/56399532porinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFLAinstname:Universidade Federal de Lavras (UFLA)instacron:UFLA2023-05-09T13:31:25Zoai:localhost:1/28532Repositório InstitucionalPUBhttp://repositorio.ufla.br/oai/requestnivaldo@ufla.br || repositorio.biblioteca@ufla.bropendoar:2023-05-09T13:31:25Repositório Institucional da UFLA - Universidade Federal de Lavras (UFLA)false
dc.title.none.fl_str_mv Cultivo e conservação in vitro de sempre vivas
title Cultivo e conservação in vitro de sempre vivas
spellingShingle Cultivo e conservação in vitro de sempre vivas
Moreira, Fernanda da Conceição
Espécie endêmica
Sistema de imersão temporária (Plantform®)
Micropropagação
Criopreservação
Campo Rupestre
Biorreator
Endemic species
Native species
Temporary immersion system (Plantform®)
In vitro conservation
Cryopreservation
Biorreactor
Fisiologia Vegetal
title_short Cultivo e conservação in vitro de sempre vivas
title_full Cultivo e conservação in vitro de sempre vivas
title_fullStr Cultivo e conservação in vitro de sempre vivas
title_full_unstemmed Cultivo e conservação in vitro de sempre vivas
title_sort Cultivo e conservação in vitro de sempre vivas
author Moreira, Fernanda da Conceição
author_facet Moreira, Fernanda da Conceição
author_role author
dc.contributor.none.fl_str_mv Paiva, Renato
Nery, Fernanda Carlota
Santos, Breno Régis
Carvalho, Milene Alves de Figueiredo
Rodrigues, Leonardo Augusto Zebral
dc.contributor.author.fl_str_mv Moreira, Fernanda da Conceição
dc.subject.por.fl_str_mv Espécie endêmica
Sistema de imersão temporária (Plantform®)
Micropropagação
Criopreservação
Campo Rupestre
Biorreator
Endemic species
Native species
Temporary immersion system (Plantform®)
In vitro conservation
Cryopreservation
Biorreactor
Fisiologia Vegetal
topic Espécie endêmica
Sistema de imersão temporária (Plantform®)
Micropropagação
Criopreservação
Campo Rupestre
Biorreator
Endemic species
Native species
Temporary immersion system (Plantform®)
In vitro conservation
Cryopreservation
Biorreactor
Fisiologia Vegetal
description Comanthera bisulcata (Eriocaulaceae) and Xyris cipoensis (Xyridaceae) are ornamental species, occurring in campos rupestres environments and are on the endangered list species. The aim of this study were: (i) in vitro establishment, control of senescence and the multiplication of Comanthera bisulcata seedlings. (ii) micropropagation and (iii) conservation in vitro of Xyris cipoensis. To establish in vitro C. bisulcata was performed seeds sterilization at different times immersed in NaOCl. The germination and growth of seedlings were evaluated in WPM medium with different pH. For the control of senescence were tested 0, 0.2, 2 and 20 µM AgNO3 and the oxidation control was tested from 0 to 400 mg L-1 of polyvinylpyrrolidone (PVP). The multiplication was tested 2.68 µM NAA + 2.27 µM TDZ, 2.22 µM BA or 2.32 μM KIN. Subsequently, an experiment was conducted comparing the semi-solid system and the temporary immersion system (Plantform®). The Xyris cipoensis seeds were decontaminated in different exposure times NaOCl. The WPM medium with different sucrose concentrations was tested. The seeds were stored in liquid nitrogen. Thawing was performed at different times. Subsequently, the seeds were dried at different times, cryopreserved and thawed for 60 seconds. In C. bisulcata the highest percentage of disinfestation (96%) and germination (54%) of the seeds was observed in five minutes immersion in NaOCl. Seedlings grown at pH 4.4 showed higher average root length (1 cm) and greater average height (2.8 cm) of seedlings. During the proliferation phase, the seedlings senescence can be reduced with 0.2 M AgNO3 and the oxidation with 400 mg L-1 antioxidant polyvinylpyrrolidone and 2.68 µM NAA + 2.27 uM TDZ was suitable to induce shoots. The relative growth rate (RGR) and average values average weight of seedlings demonstrated the superiority of temporary immersion system liquid (Plantform®) comparing to the semi-solid system during micropropagation C. bisulcata. The highest percentage of decontamination and germination (90% and 84%) was observed after five minutes of exposure to NaOCl and using 15g L-1 sucrose, respectively. An efficient protocol for the in vitro propagation was obtained and increased post-thaw viability of cryopreserved seed was reached after thawing for 60 seconds. Survival seeds increased when seeds were dehydrated before cryopreservation process.
publishDate 2015
dc.date.none.fl_str_mv 2015-07-31
2018-02-05T16:32:02Z
2018-02-05T16:32:02Z
2018-02-05
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv MOREIRA, F. da C. Cultivo e conservação in vitro de sempre vivas. 2015. 102 p. Tese (Doutorado em Fisiologia Vegetal) – Universidade Federal de Lavras, Lavras, 2015.
http://repositorio.ufla.br/jspui/handle/1/56399532
identifier_str_mv MOREIRA, F. da C. Cultivo e conservação in vitro de sempre vivas. 2015. 102 p. Tese (Doutorado em Fisiologia Vegetal) – Universidade Federal de Lavras, Lavras, 2015.
url http://repositorio.ufla.br/jspui/handle/1/56399532
dc.language.iso.fl_str_mv por
language por
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 Lavras
Programa de Pós-Graduação em Fisiologia Vegetal
UFLA
brasil
Departamento de Biologia
publisher.none.fl_str_mv Universidade Federal de Lavras
Programa de Pós-Graduação em Fisiologia Vegetal
UFLA
brasil
Departamento de Biologia
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFLA
instname:Universidade Federal de Lavras (UFLA)
instacron:UFLA
instname_str Universidade Federal de Lavras (UFLA)
instacron_str UFLA
institution UFLA
reponame_str Repositório Institucional da UFLA
collection Repositório Institucional da UFLA
repository.name.fl_str_mv Repositório Institucional da UFLA - Universidade Federal de Lavras (UFLA)
repository.mail.fl_str_mv nivaldo@ufla.br || repositorio.biblioteca@ufla.br
_version_ 1807835169015463936