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Expression of nitrite reductase in Nitrosomonas europaea involves NsrR, a novel nitrite‐sensitive transcription repressor
Author(s) -
Beaumont Hubertus J. E.,
Lens Sylvia I.,
Reijnders Willem N. M.,
Westerhoff Hans V.,
Van Spanning Rob J. M.
Publication year - 2004
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1111/j.1365-2958.2004.04248.x
Subject(s) - nitrosomonas europaea , biology , nitrite reductase , denitrifying bacteria , repressor , nitrite , bacteria , nitrifying bacteria , transcription (linguistics) , microbiology and biotechnology , biochemistry , nitrification , gene , gene expression , genetics , denitrification , chemistry , nitrate , ecology , linguistics , philosophy , organic chemistry , nitrogen
Summary Production of nitric oxide (NO) and nitrous oxide (N 2 O) by ammonia (NH 3 )‐oxidizing bacteria in natural and man‐made habitats is thought to contribute to the undesirable emission of NO and N 2 O into the earth's atmosphere. The NH 3 ‐oxidizing bacterium Nitrosomonas europaea expresses nitrite reductase (NirK), an enzyme that has so far been studied predominantly in heterotrophic denitrifying bacteria where it is involved in the production of these nitrogenous gases. The finding of nirK homologues in other NH 3 ‐oxidizing bacteria suggests that NirK is widespread among this group; however, its role in these nitrifying bacteria remains unresolved. We identified a gene, nsrR , which encodes a novel nitrite (NO 2 – )‐sensitive transcription repressor that plays a pivotal role in the regulation of NirK expression in N. europaea . NsrR is a member of the Rrf2 family of putative transcription regulators. NirK was expressed aerobically in response to increasing concentrations of NO 2 – and decreasing pH. Disruption of nsrR resulted in the constitutive expression of NirK. NsrR repressed transcription from the nirK gene cluster promoter (P nir ), the activity of which correlated with NirK expression. Reconstruction of the NsrR‐P nir system in Escherichia coli revealed that repression by NsrR was reversed by NO 2 – in a pH‐dependent manner. The findings are consistent with the hypothesis that N. europaea expresses NirK as a defence against the toxic NO 2 – that is produced during nitrification.