Micropropagação de espécies de fisális com potencial econômico
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Tipo de documento: | Dissertação |
Idioma: | por |
Título da fonte: | Biblioteca Digital de Teses e Dissertações do UNIOESTE |
Texto Completo: | http://tede.unioeste.br/handle/tede/4819 |
Resumo: | In vitro cultivation techniques, such as micropropagation, have been considered promising tools for the production of quality seedlings on a large scale. The objective of this work was evaluate asepsis protocols, composition and concentration of culture media in the in vitro establishment of physalis species. Four experiments were conducted in vitro. In experiment I, seeds of 3 species of physalis (Physalis peruviana, P. ixocarpa and P. minima) were used x 3 asepsis protocols (I = Twin 20 solution for 5 minutes + 70% alcohol for 30 seconds + sodium hypochlorite for 3 minutes, II = 70% alcohol for 30 seconds + sodium hypochlorite for 3 minutes, III = 70% alcohol for 3 minutes + sodium hypochlorite for 10 minutes). For 30 days, fungal and bacterial contamination and the percentage of germination were evaluated every 4 days. In experiment II, 3 culture media (MS, Knudson and WPM) and explants 3 species of fisális (Physalis peruviana, P. ixocarpa and P. minima) were used. In experiment III, explants of 2 species of physalis (Physalis peruviana and P. minima) x 4 concentrations of MS culture medium (0, 50, 75 and 100%) were used. In experiment IV, explants of 2 species of physalis (Physalis peruviana and P. minima) x 4 sucrose concentrations (0, 15, 30 and 60 L-1) were used. For experiments II, III and IV after 30 days were evaluated: number of seedlings, shoots, leaves and roots, length of the largest root (cm) and aerial part of plant (cm), fresh and dry seedling biomass (g). The experimental design was completely randomized, in a 3 x 3 (experiments I and II) and 2 x 4 (experiments III and IV) factorial scheme, containing 5 repetitions, 1 glass per repetition and 5 seeds per glass. Protocols II and III were appropriate for P. peruviana germination, and I and III for P. minima, the three protocols were efficient for controlling fungi and bacteria. Sucrose concentrations close to 50 g L-1 favored the establishment of P. peruviana of approximately 20 g L-1 favored the establishment of P. minima. The culture medium MS is the most suitable for the in vitro establishment of P. peruviana, P. minima and P. ixocarpa. The culture medium at 100% concentration obtained better values in the in vitro development parameters evaluated for the species P. peruviana and P. minima. |
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Villa, Fabíolahttp://lattes.cnpq.br/1043592167112136Fogaça, Luciana Alveshttp://lattes.cnpq.br/1052718598551568Rorato, Daniele Guarientihttp://lattes.cnpq.br/6780331506626816Stefanello, Suzanahttp://lattes.cnpq.br/0157777453041078Silva, Daniel Fernandes dahttp://lattes.cnpq.br/6562731599312560http://lattes.cnpq.br/2920787798631249Silva, Luciana Sabini da2020-07-03T22:57:34Z2020-02-20SILVA, Luciana Sabini da. Micropropagação de espécies de fisális com potencial econômico. 2020. 28 f. Dissertação (Mestrado em Agronomia) - Universidade Estadual do Oeste do Paraná, Marechal Cândido Rondon, 2020.http://tede.unioeste.br/handle/tede/4819In vitro cultivation techniques, such as micropropagation, have been considered promising tools for the production of quality seedlings on a large scale. The objective of this work was evaluate asepsis protocols, composition and concentration of culture media in the in vitro establishment of physalis species. Four experiments were conducted in vitro. In experiment I, seeds of 3 species of physalis (Physalis peruviana, P. ixocarpa and P. minima) were used x 3 asepsis protocols (I = Twin 20 solution for 5 minutes + 70% alcohol for 30 seconds + sodium hypochlorite for 3 minutes, II = 70% alcohol for 30 seconds + sodium hypochlorite for 3 minutes, III = 70% alcohol for 3 minutes + sodium hypochlorite for 10 minutes). For 30 days, fungal and bacterial contamination and the percentage of germination were evaluated every 4 days. In experiment II, 3 culture media (MS, Knudson and WPM) and explants 3 species of fisális (Physalis peruviana, P. ixocarpa and P. minima) were used. In experiment III, explants of 2 species of physalis (Physalis peruviana and P. minima) x 4 concentrations of MS culture medium (0, 50, 75 and 100%) were used. In experiment IV, explants of 2 species of physalis (Physalis peruviana and P. minima) x 4 sucrose concentrations (0, 15, 30 and 60 L-1) were used. For experiments II, III and IV after 30 days were evaluated: number of seedlings, shoots, leaves and roots, length of the largest root (cm) and aerial part of plant (cm), fresh and dry seedling biomass (g). The experimental design was completely randomized, in a 3 x 3 (experiments I and II) and 2 x 4 (experiments III and IV) factorial scheme, containing 5 repetitions, 1 glass per repetition and 5 seeds per glass. Protocols II and III were appropriate for P. peruviana germination, and I and III for P. minima, the three protocols were efficient for controlling fungi and bacteria. Sucrose concentrations close to 50 g L-1 favored the establishment of P. peruviana of approximately 20 g L-1 favored the establishment of P. minima. The culture medium MS is the most suitable for the in vitro establishment of P. peruviana, P. minima and P. ixocarpa. The culture medium at 100% concentration obtained better values in the in vitro development parameters evaluated for the species P. peruviana and P. minima.Técnicas de cultivo in vitro, como a micropropagação, têm sido consideradas ferramentas promissoras à produção de mudas de qualidade em larga escala. Este estudo teve como objetivo avaliar protocolos de assepsia, bem como a composição e concentração de meios de cultivo no estabelecimento e multiplicação in vitro de espécies de fisális. Quatro experimentos foram conduzidos in vitro. No experimento I foram utilizadas sementes de 3 espécies de fisális (Physalis peruviana, P. ixocarpa e P. minima) x 3 protocolos de assepsia (I = solução Twin 20 por 5 minutos + álcool 70% por 30 segundos + hipoclorito de sódio por 3 minutos, II = álcool 70% por 30 segundos + hipoclorito de sódio por 3 minutos, III = álcool 70% por 3 minutos + hipoclorito de sódio por 10 minutos). Durante 30 dias avaliou-se a cada 4 dias a contaminação fúngica e bacteriana e a porcentagem de germinação. No experimento II foram utilizados explantes de 2 espécies de fisális (Physalis peruviana e P. minima) x 4 concentrações de sacarose (0, 15, 30 e 60 L-1). No experimento III foram utilizados 3 meios de cultura (MS, Knudson e WPM) e explantes 3 espécies de fisális (Physalis peruviana, P. ixocarpa e P. minima). O experimento IV foi realizado com explantes de 2 espécies de fisális (Physalis peruviana e P. minima) x 4 concentrações de meio de cultura MS (0, 50, 75 e 100%). Para os experimentos II, III e IV após 30 dias foram avaliados: número de plântulas regeneradas, brotações, folhas e raízes, comprimento da maior raiz (cm) e parte aérea (cm), biomassa fresca e seca das plântulas (g). Todos os protocolos de assepsia foram eficientes para o controle de fungo e bactéria. A germinação de P. ixocarpa não teve interferência pelo protocolo utilizado, P. peruviana obteve maiores valores de germinação quanto realizados os protocolos I e II e P. minima quando usados os protocolos I e III. As concentrações de sacarose próximas a 50 g L-1 favoreceram o estabelecimento de P. peruviana de aproximadamente 20 g L-1 favoreceram o estabelecimento de P. minima. O meio de cultura MS é o mais indicado para o estabelecimento in vitro de P. peruviana, P. minima e P. ixocarpa. O meio de cultivo na concentração de 100% obteve melhores valores nos parâmetros de desenvolvimento in vitro avaliados para as espécies P. peruviana e P. minima.Submitted by Helena Bejio (helena.bejio@unioeste.br) on 2020-07-03T22:57:34Z No. of bitstreams: 2 Dissertação.Luciana Sabini da Silva-1.pdf: 1019248 bytes, checksum: a1708e464d9e95c11779bd086fe4b1ae (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5)Made available in DSpace on 2020-07-03T22:57:34Z (GMT). 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dc.title.por.fl_str_mv |
Micropropagação de espécies de fisális com potencial econômico |
title |
Micropropagação de espécies de fisális com potencial econômico |
spellingShingle |
Micropropagação de espécies de fisális com potencial econômico Silva, Luciana Sabini da Physalis sp Cultura de tecidos Assepsia Meios de cultura Sacarose CIÊNCIAS AGRÁRIAS:AGRONOMIA |
title_short |
Micropropagação de espécies de fisális com potencial econômico |
title_full |
Micropropagação de espécies de fisális com potencial econômico |
title_fullStr |
Micropropagação de espécies de fisális com potencial econômico |
title_full_unstemmed |
Micropropagação de espécies de fisális com potencial econômico |
title_sort |
Micropropagação de espécies de fisális com potencial econômico |
author |
Silva, Luciana Sabini da |
author_facet |
Silva, Luciana Sabini da |
author_role |
author |
dc.contributor.advisor1.fl_str_mv |
Villa, Fabíola |
dc.contributor.advisor1Lattes.fl_str_mv |
http://lattes.cnpq.br/1043592167112136 |
dc.contributor.advisor-co1.fl_str_mv |
Fogaça, Luciana Alves |
dc.contributor.advisor-co1Lattes.fl_str_mv |
http://lattes.cnpq.br/1052718598551568 |
dc.contributor.referee1.fl_str_mv |
Rorato, Daniele Guarienti |
dc.contributor.referee1Lattes.fl_str_mv |
http://lattes.cnpq.br/6780331506626816 |
dc.contributor.referee2.fl_str_mv |
Stefanello, Suzana |
dc.contributor.referee2Lattes.fl_str_mv |
http://lattes.cnpq.br/0157777453041078 |
dc.contributor.referee3.fl_str_mv |
Silva, Daniel Fernandes da |
dc.contributor.referee3Lattes.fl_str_mv |
http://lattes.cnpq.br/6562731599312560 |
dc.contributor.authorLattes.fl_str_mv |
http://lattes.cnpq.br/2920787798631249 |
dc.contributor.author.fl_str_mv |
Silva, Luciana Sabini da |
contributor_str_mv |
Villa, Fabíola Fogaça, Luciana Alves Rorato, Daniele Guarienti Stefanello, Suzana Silva, Daniel Fernandes da |
dc.subject.por.fl_str_mv |
Physalis sp Cultura de tecidos Assepsia Meios de cultura Sacarose |
topic |
Physalis sp Cultura de tecidos Assepsia Meios de cultura Sacarose CIÊNCIAS AGRÁRIAS:AGRONOMIA |
dc.subject.cnpq.fl_str_mv |
CIÊNCIAS AGRÁRIAS:AGRONOMIA |
description |
In vitro cultivation techniques, such as micropropagation, have been considered promising tools for the production of quality seedlings on a large scale. The objective of this work was evaluate asepsis protocols, composition and concentration of culture media in the in vitro establishment of physalis species. Four experiments were conducted in vitro. In experiment I, seeds of 3 species of physalis (Physalis peruviana, P. ixocarpa and P. minima) were used x 3 asepsis protocols (I = Twin 20 solution for 5 minutes + 70% alcohol for 30 seconds + sodium hypochlorite for 3 minutes, II = 70% alcohol for 30 seconds + sodium hypochlorite for 3 minutes, III = 70% alcohol for 3 minutes + sodium hypochlorite for 10 minutes). For 30 days, fungal and bacterial contamination and the percentage of germination were evaluated every 4 days. In experiment II, 3 culture media (MS, Knudson and WPM) and explants 3 species of fisális (Physalis peruviana, P. ixocarpa and P. minima) were used. In experiment III, explants of 2 species of physalis (Physalis peruviana and P. minima) x 4 concentrations of MS culture medium (0, 50, 75 and 100%) were used. In experiment IV, explants of 2 species of physalis (Physalis peruviana and P. minima) x 4 sucrose concentrations (0, 15, 30 and 60 L-1) were used. For experiments II, III and IV after 30 days were evaluated: number of seedlings, shoots, leaves and roots, length of the largest root (cm) and aerial part of plant (cm), fresh and dry seedling biomass (g). The experimental design was completely randomized, in a 3 x 3 (experiments I and II) and 2 x 4 (experiments III and IV) factorial scheme, containing 5 repetitions, 1 glass per repetition and 5 seeds per glass. Protocols II and III were appropriate for P. peruviana germination, and I and III for P. minima, the three protocols were efficient for controlling fungi and bacteria. Sucrose concentrations close to 50 g L-1 favored the establishment of P. peruviana of approximately 20 g L-1 favored the establishment of P. minima. The culture medium MS is the most suitable for the in vitro establishment of P. peruviana, P. minima and P. ixocarpa. The culture medium at 100% concentration obtained better values in the in vitro development parameters evaluated for the species P. peruviana and P. minima. |
publishDate |
2020 |
dc.date.accessioned.fl_str_mv |
2020-07-03T22:57:34Z |
dc.date.issued.fl_str_mv |
2020-02-20 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
format |
masterThesis |
status_str |
publishedVersion |
dc.identifier.citation.fl_str_mv |
SILVA, Luciana Sabini da. Micropropagação de espécies de fisális com potencial econômico. 2020. 28 f. Dissertação (Mestrado em Agronomia) - Universidade Estadual do Oeste do Paraná, Marechal Cândido Rondon, 2020. |
dc.identifier.uri.fl_str_mv |
http://tede.unioeste.br/handle/tede/4819 |
identifier_str_mv |
SILVA, Luciana Sabini da. Micropropagação de espécies de fisális com potencial econômico. 2020. 28 f. Dissertação (Mestrado em Agronomia) - Universidade Estadual do Oeste do Paraná, Marechal Cândido Rondon, 2020. |
url |
http://tede.unioeste.br/handle/tede/4819 |
dc.language.iso.fl_str_mv |
por |
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por |
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5624066117035054290 |
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600 600 600 |
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2075167498588264571 |
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http://creativecommons.org/licenses/by/4.0/ info:eu-repo/semantics/openAccess |
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http://creativecommons.org/licenses/by/4.0/ |
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openAccess |
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application/pdf |
dc.publisher.none.fl_str_mv |
Universidade Estadual do Oeste do Paraná Marechal Cândido Rondon |
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Programa de Pós-Graduação em Agronomia |
dc.publisher.initials.fl_str_mv |
UNIOESTE |
dc.publisher.country.fl_str_mv |
Brasil |
dc.publisher.department.fl_str_mv |
Centro de Ciências Agrárias |
publisher.none.fl_str_mv |
Universidade Estadual do Oeste do Paraná Marechal Cândido Rondon |
dc.source.none.fl_str_mv |
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MD5 MD5 MD5 MD5 MD5 |
repository.name.fl_str_mv |
Biblioteca Digital de Teses e Dissertações do UNIOESTE - Universidade Estadual do Oeste do Paraná (UNIOESTE) |
repository.mail.fl_str_mv |
biblioteca.repositorio@unioeste.br |
_version_ |
1811723427238641664 |