New vectors derives from pUC 18 for clonig and thermal-induced expression in Escherichia coli
Autor(a) principal: | |
---|---|
Data de Publicação: | 2009 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Brazilian Journal of Microbiology |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822009000400007 |
Resumo: | We report the construction of two vectors for Escherichia coli: pUC72, for molecular cloning, and pPLT7, for thermal-induced expression. The main feature of pUC72 is a novel polylinker region that includes restriction sites for Nde I and Nco I which provide an ATG codon for proper translation initiation of expressed genes. Vector pPLT7 is ideal for thermo-inducible expression in host cells that carry the cI857 repressor gene. The use of pPLT7 was validated by the successful expression of the genes encoding carp and porcine growth hormones. These vectors provide novel cloning possibilities in addition to simple, non-expensive, high level expression of recombinant proteins in E. coli. |
id |
SBM-1_172586af412c30128c352ea068423b9f |
---|---|
oai_identifier_str |
oai:scielo:S1517-83822009000400007 |
network_acronym_str |
SBM-1 |
network_name_str |
Brazilian Journal of Microbiology |
repository_id_str |
|
spelling |
New vectors derives from pUC 18 for clonig and thermal-induced expression in Escherichia coliHeterologous expressionEscherichia colimolecular cloninginduced expressionWe report the construction of two vectors for Escherichia coli: pUC72, for molecular cloning, and pPLT7, for thermal-induced expression. The main feature of pUC72 is a novel polylinker region that includes restriction sites for Nde I and Nco I which provide an ATG codon for proper translation initiation of expressed genes. Vector pPLT7 is ideal for thermo-inducible expression in host cells that carry the cI857 repressor gene. The use of pPLT7 was validated by the successful expression of the genes encoding carp and porcine growth hormones. These vectors provide novel cloning possibilities in addition to simple, non-expensive, high level expression of recombinant proteins in E. coli.Sociedade Brasileira de Microbiologia2009-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822009000400007Brazilian Journal of Microbiology v.40 n.4 2009reponame:Brazilian Journal of Microbiologyinstname:Sociedade Brasileira de Microbiologia (SBM)instacron:SBM10.1590/S1517-83822009000400007info:eu-repo/semantics/openAccessXavier,Mauro Aparecido SouzaKipnis,AndréTorres,Fernando Araripe GonçalvesAstofi-Filho,Spartacoeng2009-10-06T00:00:00Zoai:scielo:S1517-83822009000400007Revistahttps://www.scielo.br/j/bjm/ONGhttps://old.scielo.br/oai/scielo-oai.phpbjm@sbmicrobiologia.org.br||mbmartin@usp.br1678-44051517-8382opendoar:2009-10-06T00:00Brazilian Journal of Microbiology - Sociedade Brasileira de Microbiologia (SBM)false |
dc.title.none.fl_str_mv |
New vectors derives from pUC 18 for clonig and thermal-induced expression in Escherichia coli |
title |
New vectors derives from pUC 18 for clonig and thermal-induced expression in Escherichia coli |
spellingShingle |
New vectors derives from pUC 18 for clonig and thermal-induced expression in Escherichia coli Xavier,Mauro Aparecido Souza Heterologous expression Escherichia coli molecular cloning induced expression |
title_short |
New vectors derives from pUC 18 for clonig and thermal-induced expression in Escherichia coli |
title_full |
New vectors derives from pUC 18 for clonig and thermal-induced expression in Escherichia coli |
title_fullStr |
New vectors derives from pUC 18 for clonig and thermal-induced expression in Escherichia coli |
title_full_unstemmed |
New vectors derives from pUC 18 for clonig and thermal-induced expression in Escherichia coli |
title_sort |
New vectors derives from pUC 18 for clonig and thermal-induced expression in Escherichia coli |
author |
Xavier,Mauro Aparecido Souza |
author_facet |
Xavier,Mauro Aparecido Souza Kipnis,André Torres,Fernando Araripe Gonçalves Astofi-Filho,Spartaco |
author_role |
author |
author2 |
Kipnis,André Torres,Fernando Araripe Gonçalves Astofi-Filho,Spartaco |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Xavier,Mauro Aparecido Souza Kipnis,André Torres,Fernando Araripe Gonçalves Astofi-Filho,Spartaco |
dc.subject.por.fl_str_mv |
Heterologous expression Escherichia coli molecular cloning induced expression |
topic |
Heterologous expression Escherichia coli molecular cloning induced expression |
description |
We report the construction of two vectors for Escherichia coli: pUC72, for molecular cloning, and pPLT7, for thermal-induced expression. The main feature of pUC72 is a novel polylinker region that includes restriction sites for Nde I and Nco I which provide an ATG codon for proper translation initiation of expressed genes. Vector pPLT7 is ideal for thermo-inducible expression in host cells that carry the cI857 repressor gene. The use of pPLT7 was validated by the successful expression of the genes encoding carp and porcine growth hormones. These vectors provide novel cloning possibilities in addition to simple, non-expensive, high level expression of recombinant proteins in E. coli. |
publishDate |
2009 |
dc.date.none.fl_str_mv |
2009-12-01 |
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=S1517-83822009000400007 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822009000400007 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S1517-83822009000400007 |
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 |
Sociedade Brasileira de Microbiologia |
publisher.none.fl_str_mv |
Sociedade Brasileira de Microbiologia |
dc.source.none.fl_str_mv |
Brazilian Journal of Microbiology v.40 n.4 2009 reponame:Brazilian Journal of Microbiology instname:Sociedade Brasileira de Microbiologia (SBM) instacron:SBM |
instname_str |
Sociedade Brasileira de Microbiologia (SBM) |
instacron_str |
SBM |
institution |
SBM |
reponame_str |
Brazilian Journal of Microbiology |
collection |
Brazilian Journal of Microbiology |
repository.name.fl_str_mv |
Brazilian Journal of Microbiology - Sociedade Brasileira de Microbiologia (SBM) |
repository.mail.fl_str_mv |
bjm@sbmicrobiologia.org.br||mbmartin@usp.br |
_version_ |
1752122202617020416 |