Plant regeneration and Agrobacterium-mediated transformation of Achyranthes bidentata using cotton EREBP gene
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Brazilian Archives of Biology and Technology |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132013000300001 |
Resumo: | The aim of this work was to study the plant regeneration and Agrobacterium-mediated transformation of Achyranthes bidentata using cotton EREBP gene. Results showed that the callus induction rate of stems from A. bidentata was the highest (100%) and bud was in approximately 70% of calli from stems. However bud differentiation rate of the callus from leaves and petioles was very low. Compared with ceftriaxone, 200mg/L cefotaxime could completely control Agrobacterium tumefaciens and had relatively less toxic action on the stems of A. bidentata. In addition, the induction rate of callus resistant to hygromycin was the highest when infected for 3 min and co-cultivated for 3 d. Six positive transgenic plants transformed with pCAMBIA1304-GhEREB2 expression vector were obtained and confirmed by PCR. The expression of target gene GhEREB2 was detected in five transgenic plants by RT-PCR. In brief, an efficient system of genetic transformation and plant regeneration was established for A. bidentata. |
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Plant regeneration and Agrobacterium-mediated transformation of Achyranthes bidentata using cotton EREBP geneAchyranthes bidentataEREBP geneAgrobacterium tumefaciensgenetic transformationThe aim of this work was to study the plant regeneration and Agrobacterium-mediated transformation of Achyranthes bidentata using cotton EREBP gene. Results showed that the callus induction rate of stems from A. bidentata was the highest (100%) and bud was in approximately 70% of calli from stems. However bud differentiation rate of the callus from leaves and petioles was very low. Compared with ceftriaxone, 200mg/L cefotaxime could completely control Agrobacterium tumefaciens and had relatively less toxic action on the stems of A. bidentata. In addition, the induction rate of callus resistant to hygromycin was the highest when infected for 3 min and co-cultivated for 3 d. Six positive transgenic plants transformed with pCAMBIA1304-GhEREB2 expression vector were obtained and confirmed by PCR. The expression of target gene GhEREB2 was detected in five transgenic plants by RT-PCR. In brief, an efficient system of genetic transformation and plant regeneration was established for A. bidentata.Instituto de Tecnologia do Paraná - Tecpar2013-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132013000300001Brazilian Archives of Biology and Technology v.56 n.3 2013reponame:Brazilian Archives of Biology and Technologyinstname:Instituto de Tecnologia do Paraná (Tecpar)instacron:TECPAR10.1590/S1516-89132013000300001info:eu-repo/semantics/openAccessDuan,Hong YingDing,Xiao ShengSong,Jian YingHe,Yun LongZhou,Yan Qingeng2013-07-12T00:00:00Zoai:scielo:S1516-89132013000300001Revistahttps://www.scielo.br/j/babt/https://old.scielo.br/oai/scielo-oai.phpbabt@tecpar.br||babt@tecpar.br1678-43241516-8913opendoar:2013-07-12T00:00Brazilian Archives of Biology and Technology - Instituto de Tecnologia do Paraná (Tecpar)false |
dc.title.none.fl_str_mv |
Plant regeneration and Agrobacterium-mediated transformation of Achyranthes bidentata using cotton EREBP gene |
title |
Plant regeneration and Agrobacterium-mediated transformation of Achyranthes bidentata using cotton EREBP gene |
spellingShingle |
Plant regeneration and Agrobacterium-mediated transformation of Achyranthes bidentata using cotton EREBP gene Duan,Hong Ying Achyranthes bidentata EREBP gene Agrobacterium tumefaciens genetic transformation |
title_short |
Plant regeneration and Agrobacterium-mediated transformation of Achyranthes bidentata using cotton EREBP gene |
title_full |
Plant regeneration and Agrobacterium-mediated transformation of Achyranthes bidentata using cotton EREBP gene |
title_fullStr |
Plant regeneration and Agrobacterium-mediated transformation of Achyranthes bidentata using cotton EREBP gene |
title_full_unstemmed |
Plant regeneration and Agrobacterium-mediated transformation of Achyranthes bidentata using cotton EREBP gene |
title_sort |
Plant regeneration and Agrobacterium-mediated transformation of Achyranthes bidentata using cotton EREBP gene |
author |
Duan,Hong Ying |
author_facet |
Duan,Hong Ying Ding,Xiao Sheng Song,Jian Ying He,Yun Long Zhou,Yan Qing |
author_role |
author |
author2 |
Ding,Xiao Sheng Song,Jian Ying He,Yun Long Zhou,Yan Qing |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Duan,Hong Ying Ding,Xiao Sheng Song,Jian Ying He,Yun Long Zhou,Yan Qing |
dc.subject.por.fl_str_mv |
Achyranthes bidentata EREBP gene Agrobacterium tumefaciens genetic transformation |
topic |
Achyranthes bidentata EREBP gene Agrobacterium tumefaciens genetic transformation |
description |
The aim of this work was to study the plant regeneration and Agrobacterium-mediated transformation of Achyranthes bidentata using cotton EREBP gene. Results showed that the callus induction rate of stems from A. bidentata was the highest (100%) and bud was in approximately 70% of calli from stems. However bud differentiation rate of the callus from leaves and petioles was very low. Compared with ceftriaxone, 200mg/L cefotaxime could completely control Agrobacterium tumefaciens and had relatively less toxic action on the stems of A. bidentata. In addition, the induction rate of callus resistant to hygromycin was the highest when infected for 3 min and co-cultivated for 3 d. Six positive transgenic plants transformed with pCAMBIA1304-GhEREB2 expression vector were obtained and confirmed by PCR. The expression of target gene GhEREB2 was detected in five transgenic plants by RT-PCR. In brief, an efficient system of genetic transformation and plant regeneration was established for A. bidentata. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-06-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132013000300001 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132013000300001 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S1516-89132013000300001 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Instituto de Tecnologia do Paraná - Tecpar |
publisher.none.fl_str_mv |
Instituto de Tecnologia do Paraná - Tecpar |
dc.source.none.fl_str_mv |
Brazilian Archives of Biology and Technology v.56 n.3 2013 reponame:Brazilian Archives of Biology and Technology instname:Instituto de Tecnologia do Paraná (Tecpar) instacron:TECPAR |
instname_str |
Instituto de Tecnologia do Paraná (Tecpar) |
instacron_str |
TECPAR |
institution |
TECPAR |
reponame_str |
Brazilian Archives of Biology and Technology |
collection |
Brazilian Archives of Biology and Technology |
repository.name.fl_str_mv |
Brazilian Archives of Biology and Technology - Instituto de Tecnologia do Paraná (Tecpar) |
repository.mail.fl_str_mv |
babt@tecpar.br||babt@tecpar.br |
_version_ |
1750318275640688640 |