Global transcriptional profiles of the copper responses in the cyanobacterium synechocystis sp. PCC 6803

Copper is an essential element involved in fundamental processes like respiration and photosynthesis. However, it becomes toxic at high concentration, which has forced organisms to control its cellular concentration. We have recently described a copper resistance system in the cyanobacterium Synecho...

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Detalles Bibliográficos
Autores: Giner Lamia, Joaquín, López Maury, Luis, Florencio Bellido, Francisco Javier
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2014
País:España
Institución:Universidad de Sevilla (US)
Repositorio:idUS. Depósito de Investigación de la Universidad de Sevilla
OAI Identifier:oai:idus.us.es:11441/55940
Acceso en línea:http://hdl.handle.net/11441/55940
https://doi.org/10.1371/journal.pone.0108912
Access Level:acceso abierto
Palabra clave:Bacterial Proteins
Copper
Cytochromes c6
DNA-Binding Proteins
Environmental Pollutants
Gene Expression Profiling
Gene Expression Regulation
Molecular Sequence Annotation
Plastocyanin
Reactive Oxygen Species
Synechocystis
Transcriptome
Descripción
Sumario:Copper is an essential element involved in fundamental processes like respiration and photosynthesis. However, it becomes toxic at high concentration, which has forced organisms to control its cellular concentration. We have recently described a copper resistance system in the cyanobacterium Synechocystis sp. PCC 6803, which is mediated by the two-component system, CopRS, a RND metal transport system, CopBAC and a protein of unknown function, CopM. Here, we report the transcriptional responses to copper additions at non-toxic (0.3 μM) and toxic concentrations (3 μM) in the wild type and in the copper sensitive copR mutant strain. While 0.3 μM copper slightly stimulated metabolism and promoted the exchange between cytochrome c6 and plastocyanin as soluble electron carriers, the addition of 3 μM copper catalyzed the formation of ROS, led to a general stress response and induced expression of Fe-S cluster biogenesis genes. According to this, a double mutant strain copRsufR, which expresses constitutively the sufBCDS ope ron, tolerated higher copper concentration than the copR mutant strain, suggesting that Fe-S clusters are direct targets of copper toxicity in Synechocystis. In addition we have also demonstrated that InrS, a nickel binding transcriptional repressor that belong to the CsoR family of transcriptional factor, was involved in heavy metal homeostasis, including copper, in Synechocystis. Finally, global gene expression analysis of the copR mutant strain suggested that CopRS only controls the expression of copMRS and copBAC operons in response to copper.