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dc.contributor.authorTondo, María Lauraes
dc.contributor.authorde Pedro Jové, Rogeres
dc.contributor.authorVandecaveye, Agustinaes
dc.contributor.authorPiskulic, Lauraes
dc.contributor.authorOrellano, Elena G.es
dc.contributor.authorValls, Marces
dc.date.accessioned2021-06-08T18:02:52Z-
dc.date.available2021-06-08T18:02:52Z-
dc.date.issued2020-
dc.identifier.citationTondo, M.L. et al. KatE from the bacterial plant pathogen Ralstonia solanacearum is a monofunctional catalase controlled by HrpG that plays a major role in bacterial survival to hydrogen peroxide [en línea]. Frontiers in Plant Science. 2020. 11:1156. doi: 10.3389/fpls.2020.01156 Disponible en: https://repositorio.uca.edu.ar/handle/123456789/11602es
dc.identifier.issn1664-462X-
dc.identifier.urihttps://repositorio.uca.edu.ar/handle/123456789/11602-
dc.description.abstractAbstract: Ralstonia solanacearum is the causative agent of bacterial wilt disease on a wide range of plant species. Besides the numerous bacterial activities required for host invasion, those involved in the adaptation to the plant environment are key for the success of infection. R. solanacearum ability to cope with the oxidative burst produced by the plant is likely one of the activities required to grow parasitically. Among the multiple reactive oxygen species (ROS)-scavenging enzymes predicted in the R. solanacearum GMI1000 genome, a single monofunctional catalase (KatE) and two KatG bifunctional catalases were identified. In this work, we show that these catalase activities are active in bacterial protein extracts and demonstrate by gene disruption and mutant complementation that the monofunctional catalase activity is encoded by katE. Different strategies were used to evaluate the role of KatE in bacterial physiology and during the infection process that causes bacterial wilt. We show that the activity of the enzyme is maximal during exponential growth in vitro and this growth-phase regulation occurs at the transcriptional level. Our studies also demonstrate that katE expression is transcriptionally activated by HrpG, a central regulator of R. solanacearum induced upon contact with the plant cells. In addition, we reveal that even though both KatE and KatG catalase activities are induced upon hydrogen peroxide treatment, KatE has a major effect on bacterial survival under oxidative stress conditions and especially in the adaptive response of R. solanacearum to this oxidant. The katE mutant strain also exhibited differences in the structural characteristics of the biofilms developed on an abiotic surface in comparison to wild-type cells, but not in the overall amount of biofilm production. The role of catalase KatE during the interaction with its host plant tomato is also studied, revealing that disruption of this gene has no effect on R. solanacearum virulence or bacterial growth in leave tissues, which suggests a minor role for this catalase in bacterial fitness in planta. Our work provides the first characterization of the R. solanacearum catalases and identifies KatE as a bona fide monofunctional catalase with an important role in bacterial protection against oxidative stress.es
dc.formatapplication/pdfes
dc.language.isoenges
dc.publisherFrontierses
dc.rightsAcceso abierto*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.sourceFrontiers in Plant Science. 2020. 11:1156es
dc.subjectMARCHITEZes
dc.subjectRalstonia solanacearumes
dc.subjectCATALASASes
dc.subjectkatEes
dc.subjectBACTERIASes
dc.titleKatE from the bacterial plant pathogen Ralstonia solanacearum is a monofunctional catalase controlled by HrpG that plays a major role in bacterial survival to hydrogen peroxidees
dc.typeArtículoes
dc.identifier.doi10.3389/fpls.2020.01156-
dc.identifier.pmid32849714-
uca.disciplinaINGENIERIA AMBIENTALes
uca.issnrd1es
uca.affiliationFil: Tondo, María Laura. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Área Biología Molecular; Argentinaes
uca.affiliationFil: Tondo, María Laura. Pontificia Universidad Católica Argentina. Facultad de Química e Ingeniería del Rosario. Instituto de Ingeniería Ambiental, Química y Biotecnología Aplicada; Argentinaes
uca.affiliationFil: de Pedro Jové, Roger. Centre for Research in Agricultural Genomics; Españaes
uca.affiliationFil: de Pedro Jové, Roger. University of Barcelona. Department of Genetics; Españaes
uca.affiliationFil: Vandecaveye, Agustina. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología Molecular y Celular de Rosario; Argentinaes
uca.affiliationFil: Piskulic, Laura. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Área Estadística y Procesamiento de Datos; Argentinaes
uca.affiliationFil: Orellano, Elena G. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Área Estadística y Procesamiento de Datos; Argentinaes
uca.affiliationFil: Orellano, Elena G. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Área Biología Molecular; Argentinaes
uca.affiliationFil: Valls, Marc. Centre for Research in Agricultural Genomics; Españaes
uca.affiliationFil: Valls, Marc. University of Barcelona. Department of Genetics; Españaes
uca.versionpublishedVersiones
item.fulltextWith Fulltext-
item.grantfulltextopen-
item.languageiso639-1en-
crisitem.author.deptFacultad de Química e Ingeniería del Rosario-
crisitem.author.deptInstituto de Investigaciones en Ingeniería Ambiental, Química y Biotecnología Aplicada (INGEBIO)-
crisitem.author.parentorgPontificia Universidad Católica Argentina-
crisitem.author.parentorgFacultad de Química e Ingeniería del Rosario-
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