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A novel NO‐responding regulator controls the reduction of nitric oxide in Ralstonia eutropha

Ralstonia eutropha H16 mediates the reduction of nitric oxide (NO) to nitrous oxide (N2O) with two isofunctional single component membrane‐bound NO reductases (NorB1 and NorB2). This reaction is integrated into the denitrification pathway that involves the successive reduction of nitrate to dinitrog...

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Published in:Molecular microbiology 2000-11, Vol.38 (3), p.626-638
Main Authors: Pohlmann, Anne, Cramm, Rainer, Schmelz, Karin, Friedrich, Bärbel
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description Ralstonia eutropha H16 mediates the reduction of nitric oxide (NO) to nitrous oxide (N2O) with two isofunctional single component membrane‐bound NO reductases (NorB1 and NorB2). This reaction is integrated into the denitrification pathway that involves the successive reduction of nitrate to dinitrogen. The norB1 gene is co‐transcribed with norA1 from a σ54 (RpoN)‐dependent promoter, located upstream of norA1. With the aid of norA1′–lacZ transcriptional fusions and the generation of regulatory mutants, it was shown that norB1 gene transcription requires a functional rpoN gene and the regulator NorR, a novel member of the NtrC family of response regulators. The regulator gene maps adjacent to norAB, is divergently transcribed and present in two copies on the megaplasmid pHG1 (norR1) and the chromosome (norR2). Transcription activation by NorR responds to the availability of NO. A nitrite reductase‐deficient mutant that is incapable of producing NO endogenously, showed a 70% decrease of norA1 expression. Addition of the NO‐donating agent sodium nitroprusside caused induction of norA1′–lacZ transcription. Truncation of the N‐terminal receiver domain of NorR1 interrupted the NO signal transduction and led to a constitutive expression of norA1′–lacZ. The results indicate that NorR controls the reductive conversion of NO in R. eutropha. This reaction is not strictly co‐ordinated on the regulatory level with the other nitrogen oxide‐reducing steps of the denitrification chain that are independent of NorR.
doi_str_mv 10.1046/j.1365-2958.2000.02157.x
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This reaction is integrated into the denitrification pathway that involves the successive reduction of nitrate to dinitrogen. The norB1 gene is co‐transcribed with norA1 from a σ54 (RpoN)‐dependent promoter, located upstream of norA1. With the aid of norA1′–lacZ transcriptional fusions and the generation of regulatory mutants, it was shown that norB1 gene transcription requires a functional rpoN gene and the regulator NorR, a novel member of the NtrC family of response regulators. The regulator gene maps adjacent to norAB, is divergently transcribed and present in two copies on the megaplasmid pHG1 (norR1) and the chromosome (norR2). Transcription activation by NorR responds to the availability of NO. A nitrite reductase‐deficient mutant that is incapable of producing NO endogenously, showed a 70% decrease of norA1 expression. Addition of the NO‐donating agent sodium nitroprusside caused induction of norA1′–lacZ transcription. Truncation of the N‐terminal receiver domain of NorR1 interrupted the NO signal transduction and led to a constitutive expression of norA1′–lacZ. The results indicate that NorR controls the reductive conversion of NO in R. eutropha. 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This reaction is integrated into the denitrification pathway that involves the successive reduction of nitrate to dinitrogen. The norB1 gene is co‐transcribed with norA1 from a σ54 (RpoN)‐dependent promoter, located upstream of norA1. With the aid of norA1′–lacZ transcriptional fusions and the generation of regulatory mutants, it was shown that norB1 gene transcription requires a functional rpoN gene and the regulator NorR, a novel member of the NtrC family of response regulators. The regulator gene maps adjacent to norAB, is divergently transcribed and present in two copies on the megaplasmid pHG1 (norR1) and the chromosome (norR2). Transcription activation by NorR responds to the availability of NO. A nitrite reductase‐deficient mutant that is incapable of producing NO endogenously, showed a 70% decrease of norA1 expression. Addition of the NO‐donating agent sodium nitroprusside caused induction of norA1′–lacZ transcription. Truncation of the N‐terminal receiver domain of NorR1 interrupted the NO signal transduction and led to a constitutive expression of norA1′–lacZ. The results indicate that NorR controls the reductive conversion of NO in R. eutropha. This reaction is not strictly co‐ordinated on the regulatory level with the other nitrogen oxide‐reducing steps of the denitrification chain that are independent of NorR.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>11069685</pmid><doi>10.1046/j.1365-2958.2000.02157.x</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
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ispartof Molecular microbiology, 2000-11, Vol.38 (3), p.626-638
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source Wiley-Blackwell Read & Publish Collection
subjects Amino Acid Sequence
Bacterial Proteins - chemistry
Bacterial Proteins - genetics
Bacterial Proteins - metabolism
Cupriavidus necator - genetics
Cupriavidus necator - growth & development
Cupriavidus necator - metabolism
DNA-Binding Proteins
DNA-Directed RNA Polymerases - genetics
DNA-Directed RNA Polymerases - metabolism
Gene Expression Regulation, Bacterial - genetics
Genes, Regulator - genetics
Genes, Regulator - physiology
lacZ gene
Molecular Sequence Data
Nitric Oxide - metabolism
nitric-oxide reductase
norA1 gene
norB1 gene
NorR protein
Oxidation-Reduction
Oxidoreductases - chemistry
Oxidoreductases - genetics
Oxidoreductases - metabolism
Physical Chromosome Mapping
Ralstonia eutropha
RNA Polymerase Sigma 54
rpoN gene
Sigma Factor - genetics
Sigma Factor - metabolism
Transcription, Genetic
title A novel NO‐responding regulator controls the reduction of nitric oxide in Ralstonia eutropha
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