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Nitrous oxide production via enzymatic nitroxyl from the nitrifying archaeon Nitrosopumilus maritimus .
- Source :
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Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2025 Jan 21; Vol. 122 (3), pp. e2416971122. Date of Electronic Publication: 2025 Jan 17. - Publication Year :
- 2025
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Abstract
- Ammonia oxidizing archaea (AOA) are among the most abundant microorganisms on earth and are known to be a major source of nitrous oxide (N <subscript>2</subscript> O) emissions, although biochemical origins of this N <subscript>2</subscript> O remain unknown. Enzymological details of AOA nitrogen metabolism are broadly unavailable. We report the recombinant expression, purification, and characterization of a multicopper oxidase, Nmar&#95;1354, from the AOA Nitrosopumilus maritimus . We show that Nmar&#95;1354 selectively produces nitroxyl (HNO) by coupling the oxidation of the obligate nitrification intermediate hydroxylamine (NH <subscript>2</subscript> OH) to dioxygen (O <subscript>2</subscript> ) reduction. This HNO undergoes several downstream reactions, although the major fates are production of N <subscript>2</subscript> via reaction with NH <subscript>2</subscript> OH and dimerization with itself to yield N <subscript>2</subscript> O. These results afford one plausible enzymatic origin for N <subscript>2</subscript> O release by AOA. Moreover, these results reveal a physiologically relevant enzymatic reaction for producing HNO, an enigmatic nitrogen oxide speculated to be operative in cellular signaling and in energy transduction.<br />Competing Interests: Competing interests statement:The authors declare no competing interest.
- Subjects :
- Oxidoreductases metabolism
Oxidoreductases genetics
Archaea metabolism
Archaea genetics
Archaea enzymology
Hydroxylamine metabolism
Archaeal Proteins metabolism
Archaeal Proteins genetics
Ammonia metabolism
Oxygen metabolism
Nitrogen Oxides metabolism
Nitrous Oxide metabolism
Nitrification
Oxidation-Reduction
Subjects
Details
- Language :
- English
- ISSN :
- 1091-6490
- Volume :
- 122
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Publication Type :
- Academic Journal
- Accession number :
- 39823305
- Full Text :
- https://doi.org/10.1073/pnas.2416971122