@article {2287,
	title = {A new CuZ active form in the catalytic reduction of N(2)O by nitrous oxide reductase from Pseudomonas nautica},
	journal = {J Biol Inorg Chem},
	volume = {15},
	number = {6},
	year = {2010},
	note = {<p>1432-1327 (Electronic)0949-8257 (Linking)Journal ArticleResearch Support, Non-U.S. Gov{\textquoteright}t</p>
},
	month = {Aug},
	pages = {967-76},
	abstract = {<p>The final step of bacterial denitrification, the two-electron reduction of N(2)O to N(2), is catalyzed by a multi-copper enzyme named nitrous oxide reductase. The catalytic centre of this enzyme is a tetranuclear copper site called CuZ, unique in biological systems. The in vitro reconstruction of the activity requires a slow activation in the presence of the artificial electron donor, reduced methyl viologen, necessary to reduce CuZ from the resting non-active state (1Cu(II)/3Cu(I)) to the fully reduced state (4Cu(I)), in contrast to the turnover cycle, which is very fast. In the present work, the direct reaction of the activated form of Pseudomonas nautica nitrous oxide reductase with stoichiometric amounts of N(2)O allowed the identification of a new reactive intermediate of the catalytic centre, CuZ degrees , in the turnover cycle, characterized by an intense absorption band at 680 nm. Moreover, the first mediated electrochemical study of Ps. nautica nitrous oxide reductase with its physiological electron donor, cytochrome c-552, was performed. The intermolecular electron transfer was analysed by cyclic voltammetry, under catalytic conditions, and a second-order rate constant of (5.5 +/- 0.9) x 10(5) M(-1 )s(-1) was determined. Both the reaction of stoichiometric amounts of substrate and the electrochemical studies show that the active CuZ degrees species, generated in the absence of reductants, can rearrange to the resting non-active CuZ state. In this light, new aspects of the catalytic and activation/inactivation mechanism of the enzyme are discussed.</p>
},
	keywords = {*Biocatalysis, *Catalytic Domain, Copper/*metabolism, Cytochrome c Group/metabolism, Electrochemistry, Electron Spin Resonance Spectroscopy, Electron Transport, Enzyme Activation, Kinetics, Nitrous Oxide/*metabolism, Oxidoreductases/*chemistry/*metabolism, Pseudomonas/*enzymology},
	url = {http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve\&db=PubMed\&dopt=Citation\&list_uids=20422435 },
	author = {Dell{\textquoteright}Acqua, S. and Pauleta, S. R. and Paes de Sousa, P. M. and Monzani, E. and Casella, L. and Moura, J. J. and Moura, I.}
}
