Abstract |
The fungal respiratory pathogen Histoplasma capsulatum evades the innate immune response and colonizes macrophages during infection. Although macrophage production of the antimicrobial effector nitric oxide (NO) restricts H. capsulatum growth, the pathogen is able to establish a persistent infection. H. capsulatum contains a P450 nitric oxide reductase homologue (NOR1) that may be important for detoxifying NO during infection. To characterize the activity of this putative P450 enzyme, a 404 amino acid fragment of Nor1p was expressed in Escherichia coli and purified to homogeneity. Spectral characterization of Nor1p indicated that it was similar to other fungal P450 nitric oxide reductases. Nor1p catalyzed the reduction of NO to N2O using NADH as the direct reductant. The K(M) for NO was determined to be 20 microM and the k(cat) to be 5000 min(-1). Together, these results provide evidence for a protective role of a P450 nitric oxide reductase against macrophage-derived NO.
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Authors | Lily Y Chao, Jasper Rine, Michael A Marletta |
Journal | Archives of biochemistry and biophysics
(Arch Biochem Biophys)
Vol. 480
Issue 2
Pg. 132-7
(Dec 15 2008)
ISSN: 1096-0384 [Electronic] United States |
PMID | 18804446
(Publication Type: Journal Article, Research Support, N.I.H., Extramural)
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Chemical References |
- Hemoglobins
- Membrane Transport Proteins
- SGE1 protein, S cerevisiae
- Saccharomyces cerevisiae Proteins
- Transcription Factors
- Nitric Oxide
- Oxidoreductases
- NADPH-Ferrihemoprotein Reductase
- nitric-oxide reductase
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Topics |
- Amino Acid Sequence
- Escherichia coli
(metabolism)
- Hemoglobins
(chemistry)
- Histoplasma
(enzymology)
- Kinetics
- Membrane Transport Proteins
- Models, Chemical
- Molecular Sequence Data
- NADPH-Ferrihemoprotein Reductase
(chemistry)
- Nitric Oxide
(chemistry, metabolism)
- Oxidation-Reduction
- Oxidoreductases
(chemistry)
- Plasmids
(metabolism)
- Saccharomyces cerevisiae Proteins
(chemistry)
- Sequence Homology, Amino Acid
- Spectrophotometry
(methods)
- Transcription Factors
(chemistry)
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