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
.jpg)
- Institución
- Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
- OAI Identificador
- paperaa:paper_03781097_v284_n2_p218_RaigerIustman
Ver los metadatos del registro completo
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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 |
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article |
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publishedVersion |
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http://hdl.handle.net/20.500.12110/paper_03781097_v284_n2_p218_RaigerIustman |
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http://hdl.handle.net/20.500.12110/paper_03781097_v284_n2_p218_RaigerIustman |
| dc.language.none.fl_str_mv |
eng |
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eng |
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info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar |
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openAccess |
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http://creativecommons.org/licenses/by/2.5/ar |
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application/pdf |
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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 |
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Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales |
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