Journal
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS
Volume 480, Issue 2, Pages 132-137Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.abb.2008.09.001
Keywords
Histoplasma capsulatum; Nitric oxide; Nitric oxide detoxification; Cytochrome P450; Cytochrome P450 nitric oxide reductase; Flavohemoglobin
Categories
Funding
- NIGMS NIH HHS [GM31105, R01 GM035827-20, R37 GM031105-27, GM35827, R01 GM035827, R01 GM031105, R37 GM031105] Funding Source: Medline
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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 Nor1 p was expressed in Escherichia coli and purified to homogeneity. Spectral characterization of Nor1 p indicated that it was similar to other fungal P450 nitric oxide reductases. Nor1 p catalyzed the reduction of NO to N2O using NADH as the direct reductant. The K-m for NO was determined to be 20 mu M 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. (c) 2008 Elsevier Inc. All rights reserved.
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