Analysis of two polyhydroxyalkanoate synthases in Bradyrhizobium japonicum USDA 110
- Autores
- Quelas, Juan Ignacio; Mongiardini, Elías Javier; Pérez Giménez, Julieta; Parisi, Gustavo Daniel; Lodeiro, Aníbal Roberto
- Año de publicación
- 2013
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Bradyrhizobium japonicum USDA 110 has five polyhydroxyalkanoate (PHA) synthases (PhaC) annotated in its genome: bll4360 (phaC1), bll6073 (phaC2), blr3732 (phaC3), blr2885 (phaC4), and bll4548 (phaC5). All these proteins possess the catalytic triad and conserved amino acid residues of polyester synthases and are distributed into four different PhaC classes. We obtained mutants in each of these paralogs and analyzed phaC gene expression and PHA production in liquid cultures. Despite the genetic redundancy, only phaC1 and phaC2 were expressed at significant rates, while PHA accumulation in stationary-phase cultures was impaired only in the ΔphaC1 mutant. Meanwhile, the ΔphaC2 mutant produced more PHA than the wild type under this condition, and surprisingly, the phaC3 transcript increased in the ΔphaC2 background. A double mutant, the ΔphaC2 ΔphaC3 mutant, consistently accumulated less PHA than the ΔphaC2 mutant. PHA accumulation in nodule bacteroids followed a pattern similar to that seen in liquid cultures, being prevented in the ΔphaC1 mutant and increased in the ΔphaC2 mutant in relation to the level in the wild type. Therefore, we used these mutants, together with a ΔphaC1 ΔphaC2 double mutant, to study the B. japonicum PHA requirements for survival, competition for nodulation, and plant growth promotion. All mutants, as well as the wild type, survived for 60 days in a carbon-free medium, regardless of their initial PHA contents. When competing for nodulation against the wild type in a 1:1 proportion, the ΔphaC1 and ΔphaC1 ΔphaC2 mutants occupied only 13 to 15% of the nodules, while the ΔphaC2 mutant occupied 81%, suggesting that the PHA polymer is required for successful competitiveness. However, the bacteroid content of PHA did not affect the shoot dry weight accumulation.
Facultad de Ciencias Exactas
Instituto de Biotecnologia y Biologia Molecular - Materia
-
Ciencias Exactas
Bradyrhizobium japonicum
polyhydroxyalkanoate synthases - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by-nc-sa/4.0/
- Repositorio
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/85500
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Analysis of two polyhydroxyalkanoate synthases in Bradyrhizobium japonicum USDA 110Quelas, Juan IgnacioMongiardini, Elías JavierPérez Giménez, JulietaParisi, Gustavo DanielLodeiro, Aníbal RobertoCiencias ExactasBradyrhizobium japonicumpolyhydroxyalkanoate synthases<i>Bradyrhizobium japonicum</i> USDA 110 has five polyhydroxyalkanoate (PHA) synthases (PhaC) annotated in its genome: <i>bll4360</i> (<i>phaC1</i>), <i>bll6073</i> (<i>phaC2</i>), <i>blr3732</i> (<i>phaC3</i>), <i>blr2885</i> (<i>phaC4</i>), and <i>bll4548</i> (<i>phaC5</i>). All these proteins possess the catalytic triad and conserved amino acid residues of polyester synthases and are distributed into four different PhaC classes. We obtained mutants in each of these paralogs and analyzed phaC gene expression and PHA production in liquid cultures. Despite the genetic redundancy, only <i>phaC1</i> and <i>phaC2</i> were expressed at significant rates, while PHA accumulation in stationary-phase cultures was impaired only in the Δ<i>phaC1</i> mutant. Meanwhile, the Δ<i>phaC2</i> mutant produced more PHA than the wild type under this condition, and surprisingly, the <i>phaC3</i> transcript increased in the Δ<i>phaC2</i> background. A double mutant, the Δ<i>phaC2</i> Δ<i>phaC3</i> mutant, consistently accumulated less PHA than the Δ<i>phaC2</i> mutant. PHA accumulation in nodule bacteroids followed a pattern similar to that seen in liquid cultures, being prevented in the Δ<i>phaC1</i> mutant and increased in the Δ<i>phaC2</i> mutant in relation to the level in the wild type. Therefore, we used these mutants, together with a Δ<i>phaC1</i> Δ<i>phaC2</i> double mutant, to study the <i>B. japonicum</i> PHA requirements for survival, competition for nodulation, and plant growth promotion. All mutants, as well as the wild type, survived for 60 days in a carbon-free medium, regardless of their initial PHA contents. When competing for nodulation against the wild type in a 1:1 proportion, the Δ<i>phaC1</i> and Δ<i>phaC1</i> Δ<i>phaC2</i> mutants occupied only 13 to 15% of the nodules, while the Δ<i>phaC2</i> mutant occupied 81%, suggesting that the PHA polymer is required for successful competitiveness. However, the bacteroid content of PHA did not affect the shoot dry weight accumulation.Facultad de Ciencias ExactasInstituto de Biotecnologia y Biologia Molecular2013info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf3145-3155http://sedici.unlp.edu.ar/handle/10915/85500enginfo:eu-repo/semantics/altIdentifier/issn/0021-9193info:eu-repo/semantics/altIdentifier/doi/10.1128/JB.02203-12info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-03T10:48:46Zoai:sedici.unlp.edu.ar:10915/85500Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-03 10:48:47.057SEDICI (UNLP) - Universidad Nacional de La Platafalse |
dc.title.none.fl_str_mv |
Analysis of two polyhydroxyalkanoate synthases in Bradyrhizobium japonicum USDA 110 |
title |
Analysis of two polyhydroxyalkanoate synthases in Bradyrhizobium japonicum USDA 110 |
spellingShingle |
Analysis of two polyhydroxyalkanoate synthases in Bradyrhizobium japonicum USDA 110 Quelas, Juan Ignacio Ciencias Exactas Bradyrhizobium japonicum polyhydroxyalkanoate synthases |
title_short |
Analysis of two polyhydroxyalkanoate synthases in Bradyrhizobium japonicum USDA 110 |
title_full |
Analysis of two polyhydroxyalkanoate synthases in Bradyrhizobium japonicum USDA 110 |
title_fullStr |
Analysis of two polyhydroxyalkanoate synthases in Bradyrhizobium japonicum USDA 110 |
title_full_unstemmed |
Analysis of two polyhydroxyalkanoate synthases in Bradyrhizobium japonicum USDA 110 |
title_sort |
Analysis of two polyhydroxyalkanoate synthases in Bradyrhizobium japonicum USDA 110 |
dc.creator.none.fl_str_mv |
Quelas, Juan Ignacio Mongiardini, Elías Javier Pérez Giménez, Julieta Parisi, Gustavo Daniel Lodeiro, Aníbal Roberto |
author |
Quelas, Juan Ignacio |
author_facet |
Quelas, Juan Ignacio Mongiardini, Elías Javier Pérez Giménez, Julieta Parisi, Gustavo Daniel Lodeiro, Aníbal Roberto |
author_role |
author |
author2 |
Mongiardini, Elías Javier Pérez Giménez, Julieta Parisi, Gustavo Daniel Lodeiro, Aníbal Roberto |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
Ciencias Exactas Bradyrhizobium japonicum polyhydroxyalkanoate synthases |
topic |
Ciencias Exactas Bradyrhizobium japonicum polyhydroxyalkanoate synthases |
dc.description.none.fl_txt_mv |
<i>Bradyrhizobium japonicum</i> USDA 110 has five polyhydroxyalkanoate (PHA) synthases (PhaC) annotated in its genome: <i>bll4360</i> (<i>phaC1</i>), <i>bll6073</i> (<i>phaC2</i>), <i>blr3732</i> (<i>phaC3</i>), <i>blr2885</i> (<i>phaC4</i>), and <i>bll4548</i> (<i>phaC5</i>). All these proteins possess the catalytic triad and conserved amino acid residues of polyester synthases and are distributed into four different PhaC classes. We obtained mutants in each of these paralogs and analyzed phaC gene expression and PHA production in liquid cultures. Despite the genetic redundancy, only <i>phaC1</i> and <i>phaC2</i> were expressed at significant rates, while PHA accumulation in stationary-phase cultures was impaired only in the Δ<i>phaC1</i> mutant. Meanwhile, the Δ<i>phaC2</i> mutant produced more PHA than the wild type under this condition, and surprisingly, the <i>phaC3</i> transcript increased in the Δ<i>phaC2</i> background. A double mutant, the Δ<i>phaC2</i> Δ<i>phaC3</i> mutant, consistently accumulated less PHA than the Δ<i>phaC2</i> mutant. PHA accumulation in nodule bacteroids followed a pattern similar to that seen in liquid cultures, being prevented in the Δ<i>phaC1</i> mutant and increased in the Δ<i>phaC2</i> mutant in relation to the level in the wild type. Therefore, we used these mutants, together with a Δ<i>phaC1</i> Δ<i>phaC2</i> double mutant, to study the <i>B. japonicum</i> PHA requirements for survival, competition for nodulation, and plant growth promotion. All mutants, as well as the wild type, survived for 60 days in a carbon-free medium, regardless of their initial PHA contents. When competing for nodulation against the wild type in a 1:1 proportion, the Δ<i>phaC1</i> and Δ<i>phaC1</i> Δ<i>phaC2</i> mutants occupied only 13 to 15% of the nodules, while the Δ<i>phaC2</i> mutant occupied 81%, suggesting that the PHA polymer is required for successful competitiveness. However, the bacteroid content of PHA did not affect the shoot dry weight accumulation. Facultad de Ciencias Exactas Instituto de Biotecnologia y Biologia Molecular |
description |
<i>Bradyrhizobium japonicum</i> USDA 110 has five polyhydroxyalkanoate (PHA) synthases (PhaC) annotated in its genome: <i>bll4360</i> (<i>phaC1</i>), <i>bll6073</i> (<i>phaC2</i>), <i>blr3732</i> (<i>phaC3</i>), <i>blr2885</i> (<i>phaC4</i>), and <i>bll4548</i> (<i>phaC5</i>). All these proteins possess the catalytic triad and conserved amino acid residues of polyester synthases and are distributed into four different PhaC classes. We obtained mutants in each of these paralogs and analyzed phaC gene expression and PHA production in liquid cultures. Despite the genetic redundancy, only <i>phaC1</i> and <i>phaC2</i> were expressed at significant rates, while PHA accumulation in stationary-phase cultures was impaired only in the Δ<i>phaC1</i> mutant. Meanwhile, the Δ<i>phaC2</i> mutant produced more PHA than the wild type under this condition, and surprisingly, the <i>phaC3</i> transcript increased in the Δ<i>phaC2</i> background. A double mutant, the Δ<i>phaC2</i> Δ<i>phaC3</i> mutant, consistently accumulated less PHA than the Δ<i>phaC2</i> mutant. PHA accumulation in nodule bacteroids followed a pattern similar to that seen in liquid cultures, being prevented in the Δ<i>phaC1</i> mutant and increased in the Δ<i>phaC2</i> mutant in relation to the level in the wild type. Therefore, we used these mutants, together with a Δ<i>phaC1</i> Δ<i>phaC2</i> double mutant, to study the <i>B. japonicum</i> PHA requirements for survival, competition for nodulation, and plant growth promotion. All mutants, as well as the wild type, survived for 60 days in a carbon-free medium, regardless of their initial PHA contents. When competing for nodulation against the wild type in a 1:1 proportion, the Δ<i>phaC1</i> and Δ<i>phaC1</i> Δ<i>phaC2</i> mutants occupied only 13 to 15% of the nodules, while the Δ<i>phaC2</i> mutant occupied 81%, suggesting that the PHA polymer is required for successful competitiveness. However, the bacteroid content of PHA did not affect the shoot dry weight accumulation. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Articulo 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://sedici.unlp.edu.ar/handle/10915/85500 |
url |
http://sedici.unlp.edu.ar/handle/10915/85500 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/issn/0021-9193 info:eu-repo/semantics/altIdentifier/doi/10.1128/JB.02203-12 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) |
eu_rights_str_mv |
openAccess |
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http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) |
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