REVIEW: The Versatile and Complex Enzymology of Nitric Oxide Synthase

A. C. F. Gorren^* and B. Mayer

Institut für Pharmakologie und Toxikologie, Karl-Franzens-Universität Graz, Universitätsplatz 2, A-8010 Graz, Austria; fax: 43-316-380-9890; E-mail: antonius.gorren@kfunigraz.ac.at

^* To whom correspondence should be addressed.

Received August 8, 1997

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The biogenesis of nitric oxide is catalyzed by nitric oxide synthase (NOS) which forms L-citrulline and NO from L-arginine. Here we review the enzymology of NOS. We discuss its modular structure, its prosthetic groups and cofactors, and we provide a brief account of present knowledge regarding cellular targeting and regulation of the different isoforms. The various reactions which are catalyzed by NOS are reviewed, and an inventory of different inhibitor types is given. Special attention is paid to the role of the cofactor tetrahydrobiopterin (BH₄) and of the dimeric structure, and to the possibility that the main product of NOS catalysis under some conditions may not be NO. Based on a number of recent observations, we postulate that neuronal NOS with one equivalent of BH₄ per dimer (a state which may be physiologically relevant) catalyzes the concerted formation of peroxynitrite.

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KEY WORDS: nitric oxide synthase, enzymology, tetrahydrobiopterin, uncoupling, dimer, peroxynitrite

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