Preliminary results for genetic transformation of shoot tip of Eucalyptus saligna Sm. via Agrobacterium tumefaciens

Detalhes bibliográficos
Autor(a) principal: Silva, André Luis Lopes da
Data de Publicação: 2011
Outros Autores: Oliveira, Yohana, Costa, Jefferson da Luz, Mudry, Clarissa de Souza, Scheidt, Gessiel Newton, Brondani, Gilvano Ebling
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFLA
Texto Completo: http://repositorio.ufla.br/jspui/handle/1/37285
Resumo: The regeneration of transgenic plants of Eucalypt is the largest difficulty for the genetic transformation of this genus; in addition a low rate of transformed plants is reached. The aim of this research was to evaluate acetosyringone (3',5'-Dimethoxy-4'-hydroxyacetophenone) on the co-culture medium during genetic transformation of shoot tips of Eucalyptus saligna via Agrobacterium tumefaciens and to promote the explants selection supposedly transformed. Shoot tip from multiple shoots was used as explants. These explants were pre-cultured during two days before the transformation. Strain EHA105 of A. tumefaciens harboring the plasmid pBI121 was used. The treatments were: 0 and 100 μM acetosyringone added to the co-culture, after co-culture the explants were cultured in multiplication medium supplemented with 250 mg.L-1 Cefotaxime® and each sub-culture the kanamycin levels were increased from 50 to 150 mg.L-1. The transient expression of the uidA gene in shoot tips was evaluated after the end of the co-culture (fifth day) and after seven days of culture on medium containing kanamycin. The presence of 100 μM acetosyringone at the co-culture of shoot tips of Eucalyptus saligna promoted higher transient expression of the uidA gene and retards toxic effects caused by kanamycin.
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spelling Preliminary results for genetic transformation of shoot tip of Eucalyptus saligna Sm. via Agrobacterium tumefaciensStrain EHA105GUS geneEucalyptβ-glucuronidaseThe regeneration of transgenic plants of Eucalypt is the largest difficulty for the genetic transformation of this genus; in addition a low rate of transformed plants is reached. The aim of this research was to evaluate acetosyringone (3',5'-Dimethoxy-4'-hydroxyacetophenone) on the co-culture medium during genetic transformation of shoot tips of Eucalyptus saligna via Agrobacterium tumefaciens and to promote the explants selection supposedly transformed. Shoot tip from multiple shoots was used as explants. These explants were pre-cultured during two days before the transformation. Strain EHA105 of A. tumefaciens harboring the plasmid pBI121 was used. The treatments were: 0 and 100 μM acetosyringone added to the co-culture, after co-culture the explants were cultured in multiplication medium supplemented with 250 mg.L-1 Cefotaxime® and each sub-culture the kanamycin levels were increased from 50 to 150 mg.L-1. The transient expression of the uidA gene in shoot tips was evaluated after the end of the co-culture (fifth day) and after seven days of culture on medium containing kanamycin. The presence of 100 μM acetosyringone at the co-culture of shoot tips of Eucalyptus saligna promoted higher transient expression of the uidA gene and retards toxic effects caused by kanamycin.A regeneração de plantas transgênicas de eucalipto representa a maior dificuldade para a transformação genética de plantas do gênero Eucalyptus, além de que taxas baixas de plantas transformadas são alcançadas. O objetivo desse trabalho foi avaliar a acetosiringona no meio de co-cultura durante a transformação genética de ápices caulinares de Eucalyptus saligna via Agrobacterium tumefaciens e promover a seleção dos supostos explantes transformados. Ápices caulinares originados de brotações múltiplas foram usados como explantes. Estes explantes foram pré-cultivados por dois dias antes da transformação. A linhagem EHA105 de A. tumefaciens contendo o plasmídeo pBI120 foi utilizada. Os tratamentos foram: 0 e 100 μM de acetosiringona adicionada ao meio de co-cultura, após a co-cultura os explantes foram cultivados em meio de multiplicação suplementado com 250 mg.L-1 de cefotaxima e a cada subcultivo a concentração de canamicina foi aumentada, de 50 até 150 mg.L-1. A expressão transiente do gene uidA nos ápices caulinares foi avaliada no final da co-cultura e após sete dias em meio com canamicina (agente seletivo). A presença de 100 μM de acetosiringona no meio de co-cultura dos ápices caulinares de Eucalyptus saligna promoveu maior expressão transiente do gene uidA e retardou a ação tóxica causada pela canamicina.Universidade Federal do Tocantins2019-10-17T18:48:38Z2019-10-17T18:48:38Z2011-02info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfSILVA, A. L. L. da et al. Preliminary results for genetic transformation of shoot tip of Eucalyptus saligna Sm. via Agrobacterium tumefaciens. Journal of Biotechnology and Biodiversity, [S.l.], v. 2, n. 1, p. 1-6, Feb. 2011.http://repositorio.ufla.br/jspui/handle/1/37285Journal of Biotechnology and Biodiversityreponame:Repositório Institucional da UFLAinstname:Universidade Federal de Lavras (UFLA)instacron:UFLAAttribution-NonCommercial 4.0 Internationalhttp://creativecommons.org/licenses/by-nc/4.0/info:eu-repo/semantics/openAccessSilva, André Luis Lopes daOliveira, YohanaCosta, Jefferson da LuzMudry, Clarissa de SouzaScheidt, Gessiel NewtonBrondani, Gilvano Eblingeng2019-10-17T18:49:30Zoai:localhost:1/37285Repositório InstitucionalPUBhttp://repositorio.ufla.br/oai/requestnivaldo@ufla.br || repositorio.biblioteca@ufla.bropendoar:2019-10-17T18:49:30Repositório Institucional da UFLA - Universidade Federal de Lavras (UFLA)false
dc.title.none.fl_str_mv Preliminary results for genetic transformation of shoot tip of Eucalyptus saligna Sm. via Agrobacterium tumefaciens
title Preliminary results for genetic transformation of shoot tip of Eucalyptus saligna Sm. via Agrobacterium tumefaciens
spellingShingle Preliminary results for genetic transformation of shoot tip of Eucalyptus saligna Sm. via Agrobacterium tumefaciens
Silva, André Luis Lopes da
Strain EHA105
GUS gene
Eucalypt
β-glucuronidase
title_short Preliminary results for genetic transformation of shoot tip of Eucalyptus saligna Sm. via Agrobacterium tumefaciens
title_full Preliminary results for genetic transformation of shoot tip of Eucalyptus saligna Sm. via Agrobacterium tumefaciens
title_fullStr Preliminary results for genetic transformation of shoot tip of Eucalyptus saligna Sm. via Agrobacterium tumefaciens
title_full_unstemmed Preliminary results for genetic transformation of shoot tip of Eucalyptus saligna Sm. via Agrobacterium tumefaciens
title_sort Preliminary results for genetic transformation of shoot tip of Eucalyptus saligna Sm. via Agrobacterium tumefaciens
author Silva, André Luis Lopes da
author_facet Silva, André Luis Lopes da
Oliveira, Yohana
Costa, Jefferson da Luz
Mudry, Clarissa de Souza
Scheidt, Gessiel Newton
Brondani, Gilvano Ebling
author_role author
author2 Oliveira, Yohana
Costa, Jefferson da Luz
Mudry, Clarissa de Souza
Scheidt, Gessiel Newton
Brondani, Gilvano Ebling
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Silva, André Luis Lopes da
Oliveira, Yohana
Costa, Jefferson da Luz
Mudry, Clarissa de Souza
Scheidt, Gessiel Newton
Brondani, Gilvano Ebling
dc.subject.por.fl_str_mv Strain EHA105
GUS gene
Eucalypt
β-glucuronidase
topic Strain EHA105
GUS gene
Eucalypt
β-glucuronidase
description The regeneration of transgenic plants of Eucalypt is the largest difficulty for the genetic transformation of this genus; in addition a low rate of transformed plants is reached. The aim of this research was to evaluate acetosyringone (3',5'-Dimethoxy-4'-hydroxyacetophenone) on the co-culture medium during genetic transformation of shoot tips of Eucalyptus saligna via Agrobacterium tumefaciens and to promote the explants selection supposedly transformed. Shoot tip from multiple shoots was used as explants. These explants were pre-cultured during two days before the transformation. Strain EHA105 of A. tumefaciens harboring the plasmid pBI121 was used. The treatments were: 0 and 100 μM acetosyringone added to the co-culture, after co-culture the explants were cultured in multiplication medium supplemented with 250 mg.L-1 Cefotaxime® and each sub-culture the kanamycin levels were increased from 50 to 150 mg.L-1. The transient expression of the uidA gene in shoot tips was evaluated after the end of the co-culture (fifth day) and after seven days of culture on medium containing kanamycin. The presence of 100 μM acetosyringone at the co-culture of shoot tips of Eucalyptus saligna promoted higher transient expression of the uidA gene and retards toxic effects caused by kanamycin.
publishDate 2011
dc.date.none.fl_str_mv 2011-02
2019-10-17T18:48:38Z
2019-10-17T18:48:38Z
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 SILVA, A. L. L. da et al. Preliminary results for genetic transformation of shoot tip of Eucalyptus saligna Sm. via Agrobacterium tumefaciens. Journal of Biotechnology and Biodiversity, [S.l.], v. 2, n. 1, p. 1-6, Feb. 2011.
http://repositorio.ufla.br/jspui/handle/1/37285
identifier_str_mv SILVA, A. L. L. da et al. Preliminary results for genetic transformation of shoot tip of Eucalyptus saligna Sm. via Agrobacterium tumefaciens. Journal of Biotechnology and Biodiversity, [S.l.], v. 2, n. 1, p. 1-6, Feb. 2011.
url http://repositorio.ufla.br/jspui/handle/1/37285
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv Attribution-NonCommercial 4.0 International
http://creativecommons.org/licenses/by-nc/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Attribution-NonCommercial 4.0 International
http://creativecommons.org/licenses/by-nc/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal do Tocantins
publisher.none.fl_str_mv Universidade Federal do Tocantins
dc.source.none.fl_str_mv Journal of Biotechnology and Biodiversity
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
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