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
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/85500

id SEDICI_d8256551f71632d3093b10162040abde
oai_identifier_str oai:sedici.unlp.edu.ar:10915/85500
network_acronym_str SEDICI
repository_id_str 1329
network_name_str SEDICI (UNLP)
spelling 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
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
dc.format.none.fl_str_mv application/pdf
3145-3155
dc.source.none.fl_str_mv reponame:SEDICI (UNLP)
instname:Universidad Nacional de La Plata
instacron:UNLP
reponame_str SEDICI (UNLP)
collection SEDICI (UNLP)
instname_str Universidad Nacional de La Plata
instacron_str UNLP
institution UNLP
repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
repository.mail.fl_str_mv alira@sedici.unlp.edu.ar
_version_ 1842260363944394752
score 13.13397