001     16085
005     20200423203019.0
024 7 _ |a pmid:21799779
|2 pmid
024 7 _ |a pmc:PMC3140484
|2 pmc
024 7 _ |a 10.1371/journal.pone.0022143
|2 DOI
024 7 _ |a WOS:000292931200027
|2 WOS
024 7 _ |a 2128/11178
|2 Handle
037 _ _ |a PreJuSER-16085
041 _ _ |a eng
082 _ _ |a 500
084 _ _ |2 WoS
|a Biology
100 1 _ |a Schelder, S.
|b 0
|u FZJ
|0 P:(DE-Juel1)VDB78945
245 _ _ |a The two-component signal transduction system CopRS of Corynebacterium glutamicum is required for adaptation to copper-excess stress
260 _ _ |a Lawrence, Kan.
|b PLoS
|c 2011
295 1 0 |a online available
300 _ _ |a e22143
336 7 _ |a Journal Article
|0 PUB:(DE-HGF)16
|2 PUB:(DE-HGF)
336 7 _ |a Output Types/Journal article
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336 7 _ |a Journal Article
|0 0
|2 EndNote
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a article
|2 DRIVER
440 _ 0 |a PLOS One
|x 1932-6203
|0 18181
|y 7
|v 6
500 _ _ |a Record converted from VDB: 12.11.2012
520 _ _ |a Copper is an essential cofactor for many enzymes but at high concentrations it is toxic for the cell. Copper ion concentrations ≥50 µM inhibited growth of Corynebacterium glutamicum. The transcriptional response to 20 µM Cu(2+) was studied using DNA microarrays and revealed 20 genes that showed a ≥ 3-fold increased mRNA level, including cg3281-cg3289. Several genes in this genomic region code for proteins presumably involved in the adaption to copper-induced stress, e. g. a multicopper oxidase (CopO) and a copper-transport ATPase (CopB). In addition, this region includes the copRS genes (previously named cgtRS9) which encode a two-component signal transduction system composed of the histidine kinase CopS and the response regulator CopR. Deletion of the copRS genes increased the sensitivity of C. glutamicum towards copper ions, but not to other heavy metal ions. Using comparative transcriptome analysis of the ΔcopRS mutant and the wild type in combination with electrophoretic mobility shift assays and reporter gene studies the CopR regulon and the DNA-binding motif of CopR were identified. Evidence was obtained that CopR binds only to the intergenic region between cg3285 (copR) and cg3286 in the genome of C. glutamicum and activates expression of the divergently oriented gene clusters cg3285-cg3281 and cg3286-cg3289. Altogether, our data suggest that CopRS is the key regulatory system in C. glutamicum for the extracytoplasmic sensing of elevated copper ion concentrations and for induction of a set of genes capable of diminishing copper stress.
536 _ _ |a Biotechnologie
|c PBT
|2 G:(DE-HGF)
|0 G:(DE-Juel1)FUEK410
|x 0
588 _ _ |a Dataset connected to Web of Science, Pubmed
650 _ 2 |2 MeSH
|a Adaptation, Physiological: drug effects
650 _ 2 |2 MeSH
|a Adaptation, Physiological: genetics
650 _ 2 |2 MeSH
|a Bacterial Proteins: genetics
650 _ 2 |2 MeSH
|a Bacterial Proteins: metabolism
650 _ 2 |2 MeSH
|a Base Sequence
650 _ 2 |2 MeSH
|a Binding Sites
650 _ 2 |2 MeSH
|a Copper: toxicity
650 _ 2 |2 MeSH
|a Corynebacterium glutamicum: cytology
650 _ 2 |2 MeSH
|a Corynebacterium glutamicum: drug effects
650 _ 2 |2 MeSH
|a Corynebacterium glutamicum: genetics
650 _ 2 |2 MeSH
|a Corynebacterium glutamicum: physiology
650 _ 2 |2 MeSH
|a DNA, Bacterial: genetics
650 _ 2 |2 MeSH
|a DNA, Bacterial: metabolism
650 _ 2 |2 MeSH
|a Gene Expression Regulation, Bacterial: drug effects
650 _ 2 |2 MeSH
|a Gene Expression Regulation, Bacterial: genetics
650 _ 2 |2 MeSH
|a Genes, Bacterial: genetics
650 _ 2 |2 MeSH
|a Homeostasis: drug effects
650 _ 2 |2 MeSH
|a Homeostasis: genetics
650 _ 2 |2 MeSH
|a Mutation
650 _ 2 |2 MeSH
|a Nucleotide Motifs: genetics
650 _ 2 |2 MeSH
|a Phosphorylation: drug effects
650 _ 2 |2 MeSH
|a Phosphorylation: genetics
650 _ 2 |2 MeSH
|a Protein Kinases: genetics
650 _ 2 |2 MeSH
|a Protein Kinases: metabolism
650 _ 2 |2 MeSH
|a Signal Transduction: drug effects
650 _ 2 |2 MeSH
|a Signal Transduction: genetics
650 _ 2 |2 MeSH
|a Stress, Physiological: drug effects
650 _ 2 |2 MeSH
|a Stress, Physiological: genetics
650 _ 7 |0 0
|2 NLM Chemicals
|a Bacterial Proteins
650 _ 7 |0 0
|2 NLM Chemicals
|a DNA, Bacterial
650 _ 7 |0 7440-50-8
|2 NLM Chemicals
|a Copper
650 _ 7 |0 EC 2.7.-
|2 NLM Chemicals
|a Protein Kinases
650 _ 7 |0 EC 2.7.3.-
|2 NLM Chemicals
|a protein-histidine kinase
650 _ 7 |a J
|2 WoSType
700 1 _ |a Zaade, D.
|b 1
|0 P:(DE-HGF)0
700 1 _ |a Litsanov, B.
|b 2
|u FZJ
|0 P:(DE-Juel1)VDB78944
700 1 _ |a Bott, M.
|b 3
|u FZJ
|0 P:(DE-Juel1)128943
700 1 _ |a Brocker, M.
|b 4
|u FZJ
|0 P:(DE-Juel1)VDB13864
773 _ _ |a 10.1371/journal.pone.0022143
|g Vol. 6, p. e22143
|p e22143
|q 6|0 PERI:(DE-600)2267670-3
|t PLoS one
|v 6
|y 2011
|x 1932-6203
856 7 _ |2 Pubmed Central
|u http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3140484
856 4 _ |u https://juser.fz-juelich.de/record/16085/files/journal.pone.0022143.pdf
|y OpenAccess
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856 4 _ |u https://juser.fz-juelich.de/record/16085/files/journal.pone.0022143.jpg?subformat=icon-700
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914 1 _ |y 2011
915 _ _ |a Creative Commons Attribution CC BY 3.0
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