The alternative sigma factor, σS, affects polyhydroxyalkanoate metabolism in Pseudomonas putida

Autores
Raiger-Iustman, L.J.; Ruiz, J.A.
Año de publicación
2008
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
To determine whether the stationary sigma factor, σS, influences polyhydroxyalkanoate metabolism in Pseudomonas putida KT2440, an rpoS-negative mutant was constructed to evaluate polyhydroxyalkanoate accumulation and expression of a translational fusion to the promoter region of the genes that code for polyhydroxyalkanoate synthase 1 (phaC1) and polyhydroxyalkanoate depolymerase (phaZ). By comparison with the wild-type, the rpoS mutant showed a higher polyhydroxyalkanoate degradation rate and increased expression of the translational fusion during the stationary growth phase. These results suggest that σS might control the genes involved in polyhydroxyalkanoate metabolism, possibly in an indirect manner. In addition, survival and oxidative stress assays performed under polyhydroxyalkanoate- and nonpolyhydroxyalkanoate- accumulating conditions demonstrated that the accumulated polyhydroxyalkanoate increased the survival and stress tolerance of the rpoS mutant. According to this, polyhydroxyalkanoate accumulation would help cells to overcome the adverse conditions encountered during the stationary phase in the strain that lacks RpoS. © 2008 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. All rights reserved.
Fil:Raiger-Iustman, L.J. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Ruiz, J.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fuente
FEMS Microbiol. Lett. 2008;284(2):218-224
Materia
Polyhydroxyalkanoate
Pseudomonas putida
Regulation
RpoS
Stress resistance
bacterial enzyme
polyhydroxyalkanoate depolymerase
polyhydroxyalkanoate synthase
polyhydroxyalkanoate synthase 1
polyhydroxyalkanoic acid
sigma factor
sigma factor RpoS
article
bacterial metabolism
bacterial strain
bacterial survival
controlled study
degradation
gene inactivation
nonhuman
oxidative stress
priority journal
promoter region
protein expression
Pseudomonas putida
Bacterial Proteins
Cloning, Molecular
Gene Expression Regulation, Bacterial
Gene Silencing
Hydrogen Peroxide
Microbial Viability
Oxidative Stress
Plasmids
Polyhydroxyalkanoates
Promoter Regions (Genetics)
Pseudomonas putida
Recombinant Fusion Proteins
Sigma Factor
Time
Pseudomonas putida
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/2.5/ar
Repositorio
Biblioteca Digital (UBA-FCEN)
Institución
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
OAI Identificador
paperaa:paper_03781097_v284_n2_p218_RaigerIustman

id BDUBAFCEN_a5d400103b5f1cb8b6c63f46e796fe47
oai_identifier_str paperaa:paper_03781097_v284_n2_p218_RaigerIustman
network_acronym_str BDUBAFCEN
repository_id_str 1896
network_name_str Biblioteca Digital (UBA-FCEN)
spelling The alternative sigma factor, σS, affects polyhydroxyalkanoate metabolism in Pseudomonas putidaRaiger-Iustman, L.J.Ruiz, J.A.PolyhydroxyalkanoatePseudomonas putidaRegulationRpoSStress resistancebacterial enzymepolyhydroxyalkanoate depolymerasepolyhydroxyalkanoate synthasepolyhydroxyalkanoate synthase 1polyhydroxyalkanoic acidsigma factorsigma factor RpoSarticlebacterial metabolismbacterial strainbacterial survivalcontrolled studydegradationgene inactivationnonhumanoxidative stresspriority journalpromoter regionprotein expressionPseudomonas putidaBacterial ProteinsCloning, MolecularGene Expression Regulation, BacterialGene SilencingHydrogen PeroxideMicrobial ViabilityOxidative StressPlasmidsPolyhydroxyalkanoatesPromoter Regions (Genetics)Pseudomonas putidaRecombinant Fusion ProteinsSigma FactorTimePseudomonas putidaTo determine whether the stationary sigma factor, σS, influences polyhydroxyalkanoate metabolism in Pseudomonas putida KT2440, an rpoS-negative mutant was constructed to evaluate polyhydroxyalkanoate accumulation and expression of a translational fusion to the promoter region of the genes that code for polyhydroxyalkanoate synthase 1 (phaC1) and polyhydroxyalkanoate depolymerase (phaZ). By comparison with the wild-type, the rpoS mutant showed a higher polyhydroxyalkanoate degradation rate and increased expression of the translational fusion during the stationary growth phase. These results suggest that σS might control the genes involved in polyhydroxyalkanoate metabolism, possibly in an indirect manner. In addition, survival and oxidative stress assays performed under polyhydroxyalkanoate- and nonpolyhydroxyalkanoate- accumulating conditions demonstrated that the accumulated polyhydroxyalkanoate increased the survival and stress tolerance of the rpoS mutant. According to this, polyhydroxyalkanoate accumulation would help cells to overcome the adverse conditions encountered during the stationary phase in the strain that lacks RpoS. © 2008 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. All rights reserved.Fil:Raiger-Iustman, L.J. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Ruiz, J.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.2008info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://hdl.handle.net/20.500.12110/paper_03781097_v284_n2_p218_RaigerIustmanFEMS Microbiol. Lett. 2008;284(2):218-224reponame:Biblioteca Digital (UBA-FCEN)instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesinstacron:UBA-FCENenginfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/2.5/ar2025-10-23T11:18:24Zpaperaa:paper_03781097_v284_n2_p218_RaigerIustmanInstitucionalhttps://digital.bl.fcen.uba.ar/Universidad públicaNo correspondehttps://digital.bl.fcen.uba.ar/cgi-bin/oaiserver.cgiana@bl.fcen.uba.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:18962025-10-23 11:18:26.214Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesfalse
dc.title.none.fl_str_mv The alternative sigma factor, σS, affects polyhydroxyalkanoate metabolism in Pseudomonas putida
title The alternative sigma factor, σS, affects polyhydroxyalkanoate metabolism in Pseudomonas putida
spellingShingle The alternative sigma factor, σS, affects polyhydroxyalkanoate metabolism in Pseudomonas putida
Raiger-Iustman, L.J.
Polyhydroxyalkanoate
Pseudomonas putida
Regulation
RpoS
Stress resistance
bacterial enzyme
polyhydroxyalkanoate depolymerase
polyhydroxyalkanoate synthase
polyhydroxyalkanoate synthase 1
polyhydroxyalkanoic acid
sigma factor
sigma factor RpoS
article
bacterial metabolism
bacterial strain
bacterial survival
controlled study
degradation
gene inactivation
nonhuman
oxidative stress
priority journal
promoter region
protein expression
Pseudomonas putida
Bacterial Proteins
Cloning, Molecular
Gene Expression Regulation, Bacterial
Gene Silencing
Hydrogen Peroxide
Microbial Viability
Oxidative Stress
Plasmids
Polyhydroxyalkanoates
Promoter Regions (Genetics)
Pseudomonas putida
Recombinant Fusion Proteins
Sigma Factor
Time
Pseudomonas putida
title_short The alternative sigma factor, σS, affects polyhydroxyalkanoate metabolism in Pseudomonas putida
title_full The alternative sigma factor, σS, affects polyhydroxyalkanoate metabolism in Pseudomonas putida
title_fullStr The alternative sigma factor, σS, affects polyhydroxyalkanoate metabolism in Pseudomonas putida
title_full_unstemmed The alternative sigma factor, σS, affects polyhydroxyalkanoate metabolism in Pseudomonas putida
title_sort The alternative sigma factor, σS, affects polyhydroxyalkanoate metabolism in Pseudomonas putida
dc.creator.none.fl_str_mv Raiger-Iustman, L.J.
Ruiz, J.A.
author Raiger-Iustman, L.J.
author_facet Raiger-Iustman, L.J.
Ruiz, J.A.
author_role author
author2 Ruiz, J.A.
author2_role author
dc.subject.none.fl_str_mv Polyhydroxyalkanoate
Pseudomonas putida
Regulation
RpoS
Stress resistance
bacterial enzyme
polyhydroxyalkanoate depolymerase
polyhydroxyalkanoate synthase
polyhydroxyalkanoate synthase 1
polyhydroxyalkanoic acid
sigma factor
sigma factor RpoS
article
bacterial metabolism
bacterial strain
bacterial survival
controlled study
degradation
gene inactivation
nonhuman
oxidative stress
priority journal
promoter region
protein expression
Pseudomonas putida
Bacterial Proteins
Cloning, Molecular
Gene Expression Regulation, Bacterial
Gene Silencing
Hydrogen Peroxide
Microbial Viability
Oxidative Stress
Plasmids
Polyhydroxyalkanoates
Promoter Regions (Genetics)
Pseudomonas putida
Recombinant Fusion Proteins
Sigma Factor
Time
Pseudomonas putida
topic Polyhydroxyalkanoate
Pseudomonas putida
Regulation
RpoS
Stress resistance
bacterial enzyme
polyhydroxyalkanoate depolymerase
polyhydroxyalkanoate synthase
polyhydroxyalkanoate synthase 1
polyhydroxyalkanoic acid
sigma factor
sigma factor RpoS
article
bacterial metabolism
bacterial strain
bacterial survival
controlled study
degradation
gene inactivation
nonhuman
oxidative stress
priority journal
promoter region
protein expression
Pseudomonas putida
Bacterial Proteins
Cloning, Molecular
Gene Expression Regulation, Bacterial
Gene Silencing
Hydrogen Peroxide
Microbial Viability
Oxidative Stress
Plasmids
Polyhydroxyalkanoates
Promoter Regions (Genetics)
Pseudomonas putida
Recombinant Fusion Proteins
Sigma Factor
Time
Pseudomonas putida
dc.description.none.fl_txt_mv To determine whether the stationary sigma factor, σS, influences polyhydroxyalkanoate metabolism in Pseudomonas putida KT2440, an rpoS-negative mutant was constructed to evaluate polyhydroxyalkanoate accumulation and expression of a translational fusion to the promoter region of the genes that code for polyhydroxyalkanoate synthase 1 (phaC1) and polyhydroxyalkanoate depolymerase (phaZ). By comparison with the wild-type, the rpoS mutant showed a higher polyhydroxyalkanoate degradation rate and increased expression of the translational fusion during the stationary growth phase. These results suggest that σS might control the genes involved in polyhydroxyalkanoate metabolism, possibly in an indirect manner. In addition, survival and oxidative stress assays performed under polyhydroxyalkanoate- and nonpolyhydroxyalkanoate- accumulating conditions demonstrated that the accumulated polyhydroxyalkanoate increased the survival and stress tolerance of the rpoS mutant. According to this, polyhydroxyalkanoate accumulation would help cells to overcome the adverse conditions encountered during the stationary phase in the strain that lacks RpoS. © 2008 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. All rights reserved.
Fil:Raiger-Iustman, L.J. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Ruiz, J.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
description To determine whether the stationary sigma factor, σS, influences polyhydroxyalkanoate metabolism in Pseudomonas putida KT2440, an rpoS-negative mutant was constructed to evaluate polyhydroxyalkanoate accumulation and expression of a translational fusion to the promoter region of the genes that code for polyhydroxyalkanoate synthase 1 (phaC1) and polyhydroxyalkanoate depolymerase (phaZ). By comparison with the wild-type, the rpoS mutant showed a higher polyhydroxyalkanoate degradation rate and increased expression of the translational fusion during the stationary growth phase. These results suggest that σS might control the genes involved in polyhydroxyalkanoate metabolism, possibly in an indirect manner. In addition, survival and oxidative stress assays performed under polyhydroxyalkanoate- and nonpolyhydroxyalkanoate- accumulating conditions demonstrated that the accumulated polyhydroxyalkanoate increased the survival and stress tolerance of the rpoS mutant. According to this, polyhydroxyalkanoate accumulation would help cells to overcome the adverse conditions encountered during the stationary phase in the strain that lacks RpoS. © 2008 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. All rights reserved.
publishDate 2008
dc.date.none.fl_str_mv 2008
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/20.500.12110/paper_03781097_v284_n2_p218_RaigerIustman
url http://hdl.handle.net/20.500.12110/paper_03781097_v284_n2_p218_RaigerIustman
dc.language.none.fl_str_mv eng
language eng
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/2.5/ar
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/2.5/ar
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv FEMS Microbiol. Lett. 2008;284(2):218-224
reponame:Biblioteca Digital (UBA-FCEN)
instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron:UBA-FCEN
reponame_str Biblioteca Digital (UBA-FCEN)
collection Biblioteca Digital (UBA-FCEN)
instname_str Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron_str UBA-FCEN
institution UBA-FCEN
repository.name.fl_str_mv Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
repository.mail.fl_str_mv ana@bl.fcen.uba.ar
_version_ 1846784878847197184
score 12.982451