The Semireduced Mechanism for Nitric Oxide Reduction by Non-Heme Diiron Complexes: Modeling Flavodiiron Nitric Oxide Reductases
Abstract
Flavodiiron nitric oxide reductases (FNORs) are a subclass of Favodiiron proteins (FDPs) capable of preferential binding and subsequent reduction of NO to N2O. FNORs are found in certain pathogenic bacteria, equipping them with resistance to nitrosative stress, generated as a part of the immune defense in humans, and allowing them to proliferate. Here, we report the spectroscopic characterization and detailed reactivity studies of the diiron dinitrosyl model complex [Fe2(BPMP)(OPr)(NO)2](OTf)2 for the FNOR active site that is capable of reducing NO to N2O [Zheng et al., J. Am. Chem. Soc. 2013, 135, 4902-4905]. Using UV-vis spectroscopy, cyclic voltammetry, and spectro-electrochemis- try, we show that one reductive equivalent is in fact sufficient for the quantitative generation of N2O, following a semi-reduced reaction mechanism. This reaction is very efficient and produces N2O with a first-order rate constant k > 102 s-1. Further isotope labeling studies confirm an intramolecular N-N coupling mechanism, consistent with the rapid time scale of the reduction and a very low barrier for N-N bond formation. Accordingly, the reaction proceeds at -80 °C, allowing for the direct observation of the mixed-valent product of the reaction. At higher temperatures, the initial reaction product is unstable and decays, ultimately generating the diferrousmore »
- Authors:
-
- Univ. of Michigan, Ann Arbor, MI (United States). Dept. of Chemistry
- Univ. of Göttingen, Göttingen (Germany). Inst. für Anorganische Chemie
- Argonne National Lab. (ANL), Argonne, IL (United States). Advanced Photon Source (APS)
- Publication Date:
- Research Org.:
- Argonne National Lab. (ANL), Argonne, IL (United States)
- Sponsoring Org.:
- National Science Foundation (NSF); USDOE Office of Science (SC)
- OSTI Identifier:
- 1461298
- Grant/Contract Number:
- AC02-06CH11357; CHE-0840456
- Resource Type:
- Accepted Manuscript
- Journal Name:
- Journal of the American Chemical Society
- Additional Journal Information:
- Journal Volume: 140; Journal Issue: 7; Journal ID: ISSN 0002-7863
- Publisher:
- American Chemical Society (ACS)
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 59 BASIC BIOLOGICAL SCIENCES
Citation Formats
White, Corey J., Speelman, Amy L., Kupper, Claudia, Demeshko, Serhiy, Meyer, Franc, Shanahan, James P., Alp, E. Ercan, Hu, Michael, Zhao, Jiyong, and Lehnert, Nicolai. The Semireduced Mechanism for Nitric Oxide Reduction by Non-Heme Diiron Complexes: Modeling Flavodiiron Nitric Oxide Reductases. United States: N. p., 2018.
Web. doi:10.1021/jacs.7b11464.
White, Corey J., Speelman, Amy L., Kupper, Claudia, Demeshko, Serhiy, Meyer, Franc, Shanahan, James P., Alp, E. Ercan, Hu, Michael, Zhao, Jiyong, & Lehnert, Nicolai. The Semireduced Mechanism for Nitric Oxide Reduction by Non-Heme Diiron Complexes: Modeling Flavodiiron Nitric Oxide Reductases. United States. https://doi.org/10.1021/jacs.7b11464
White, Corey J., Speelman, Amy L., Kupper, Claudia, Demeshko, Serhiy, Meyer, Franc, Shanahan, James P., Alp, E. Ercan, Hu, Michael, Zhao, Jiyong, and Lehnert, Nicolai. Fri .
"The Semireduced Mechanism for Nitric Oxide Reduction by Non-Heme Diiron Complexes: Modeling Flavodiiron Nitric Oxide Reductases". United States. https://doi.org/10.1021/jacs.7b11464. https://www.osti.gov/servlets/purl/1461298.
@article{osti_1461298,
title = {The Semireduced Mechanism for Nitric Oxide Reduction by Non-Heme Diiron Complexes: Modeling Flavodiiron Nitric Oxide Reductases},
author = {White, Corey J. and Speelman, Amy L. and Kupper, Claudia and Demeshko, Serhiy and Meyer, Franc and Shanahan, James P. and Alp, E. Ercan and Hu, Michael and Zhao, Jiyong and Lehnert, Nicolai},
abstractNote = {Flavodiiron nitric oxide reductases (FNORs) are a subclass of Favodiiron proteins (FDPs) capable of preferential binding and subsequent reduction of NO to N2O. FNORs are found in certain pathogenic bacteria, equipping them with resistance to nitrosative stress, generated as a part of the immune defense in humans, and allowing them to proliferate. Here, we report the spectroscopic characterization and detailed reactivity studies of the diiron dinitrosyl model complex [Fe2(BPMP)(OPr)(NO)2](OTf)2 for the FNOR active site that is capable of reducing NO to N2O [Zheng et al., J. Am. Chem. Soc. 2013, 135, 4902-4905]. Using UV-vis spectroscopy, cyclic voltammetry, and spectro-electrochemis- try, we show that one reductive equivalent is in fact sufficient for the quantitative generation of N2O, following a semi-reduced reaction mechanism. This reaction is very efficient and produces N2O with a first-order rate constant k > 102 s-1. Further isotope labeling studies confirm an intramolecular N-N coupling mechanism, consistent with the rapid time scale of the reduction and a very low barrier for N-N bond formation. Accordingly, the reaction proceeds at -80 °C, allowing for the direct observation of the mixed-valent product of the reaction. At higher temperatures, the initial reaction product is unstable and decays, ultimately generating the diferrous complex [Fe2(BPMP)(OPr)2](OTf) and an unidentified ferric product. Finally, these results combined offer deep insight into the mechanism of NO reduction by the relevant model complex [Fe2(BPMP)(OPr)(NO)2]2+ and provide direct evidence that the semireduced mechanism would constitute a highly efficient pathway to accomplish NO reduction to N2O in FNORs and in synthetic catalysts.},
doi = {10.1021/jacs.7b11464},
journal = {Journal of the American Chemical Society},
number = 7,
volume = 140,
place = {United States},
year = {Fri Jan 19 00:00:00 EST 2018},
month = {Fri Jan 19 00:00:00 EST 2018}
}
Web of Science
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