Nitric oxide, nitrite, and Fnr regulation of hmp (flavohemoglobin) gene expression in Escherichia coli K-12
- 1 September 1996
- journal article
- research article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 178 (18) , 5487-5492
- https://doi.org/10.1128/jb.178.18.5487-5492.1996
Abstract
Escherichia coli possesses a soluble flavohemoglobin, with an unknown function, encoded by the hmp gene. A monolysogen containing an hmp-lacZ operon fusion was constructed to determine how the hmp promoter is regulated in response to heme ligands (O2, NO) or the presence of anaerobically utilized electron acceptors (nitrate, nitrite). Expression of the phi (hmp-lacZ)1 fusion was similar during aerobic growth in minimal medium containing glucose, glycerol, maltose, or sorbitol as a carbon source. Mutations in cya (encoding adenylate cyclase) or changes in medium pH between 5 and 9 were without effect on aerobic expression. Levels of aerobic and anaerobic expression in glucose-containing minimal media were similar; both were unaffected by an arcA mutation. Anaerobic, but not aerobic, expression of phi (hmp-lacZ)1 was stimulated three- to four-fold by an fnr mutation; an apparent Fnr-binding site is present in the hmp promoter. Iron depletion of rich broth medium by the chelator 2'2'-dipyridyl (0.1 mM) enhanced hmp expression 40-fold under anaerobic conditions, tentatively attributed to effects on Fnr. At a higher chelator concentration (0.4 mM), hmp expression was also stimulated aerobically. Anaerobic expression was stimulated 6-fold by the presence of nitrate and 25-fold by the presence of nitrite. Induction by nitrate or nitrite was unaffected by narL and/or narP mutations, demonstrating regulation of hmp by these ions via mechanisms alternative to those implicated in the regulation of other respiratory genes. Nitric oxide (10 to 20 microM) stimulated aerobic phi (hmp-lacZ)1 activity by up to 19-fold; soxS and soxR mutations only slightly reduced the NO effect. We conclude that hmp expression is negatively regulated by Fnr under anaerobic conditions and that additional regulatory mechanisms are involved in the responses to oxygen, nitrogen compounds, and iron availability. Hmp is implicated in reactions with small nitrogen compounds.Keywords
This publication has 54 references indexed in Scilit:
- The flavohaemoglobin (HMP) of Escherichia coli generates superoxide in vitro and causes oxidative stress in vivoFEBS Letters, 1996
- Oxygen-Dependent Regulation of Vitreoscilla Globin Gene: Evidence for Positive Regulation by FNRBiochemical and Biophysical Research Communications, 1994
- Reactions of the Escherichia coli flavohaemoglobin (Hmp) with oxygen and reduced nicotinamide adenine dinucleotide: evidence for oxygen switching of flavin oxidoreduction and a mechanism for oxygen sensingProceedings Of The Royal Society B-Biological Sciences, 1994
- Ferric Reductases in Escherichia coli: The Contribution of the Hemoglobin-like ProteinBiochemical and Biophysical Research Communications, 1994
- Activation of FNR-dependent transcription by iron: An in vitro switch for FNRFEMS Microbiology Letters, 1993
- Oxygen-regulated gene expression in Escherichia coli: (Delivered at the 122nd Ordinary Meeting of the Society for General Microbiology, 25 March 1992)Journal of General Microbiology, 1992
- The haemoglobin‐like protein (HMP) of Escherichia coli has ferrisiderophore reductase activity and its C‐terminal domain shares homology with ferredoxin NADP+ reductasesFEBS Letters, 1992
- Iron content and FNR-dependent gene regulation inEscherichia coliFEMS Microbiology Letters, 1991
- Properties of the two terminal oxidases of Escherichia coliBiochemistry, 1991
- Kinetics of the reactions of trioxodinitrate and nitrite ions with cytochrome d in Escherichia coliBiochimica et Biophysica Acta (BBA) - Bioenergetics, 1991