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Methods used to determine the structure of the oxygenase component of naphthalene 1,2 dioxygenase.
Subramanian, Ramaswamy.
Afiliación
  • Subramanian R; Department of Biological Sciences, Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN, United States. Electronic address: subram68@purdue.edu.
Methods Enzymol ; 704: 27-38, 2024.
Article en En | MEDLINE | ID: mdl-39300651
ABSTRACT
Rieske non-heme iron oxygenases are ubiquitously expressed in prokaryotes. These enzymes catalyze a wide variety of reactions, including cis-dihydroxylation, mono-hydroxylation, sulfoxidation, and demethylation. They contain a Rieske-type [2Fe-2S] cluster and an active site with a mono-nuclear iron bound to a 2-His carboxylate triad. Naphthalene 1,2 dioxygenase, a representative of this family, catalyzes the conversion of naphthalene to (+)-cis-(1R,2S)-dihydroxy-1,2-dihydronaphthalene. This transformation requires naphthalene, two electrons, and an oxygen molecule. The first structure of the terminal oxygenase component of a Rieske non-heme iron oxygenase to be determined was naphthalene 1,2 dioxygenase (NDO-O). In this article, we describe in detail the methods used to recombinantly express and purify NDO-O in rich and minimal salts media, the crystallization of NDO-O for structure determination by X-ray crystallography, the challenges faced, and the methods used for the preparation of enzyme ligand complexes. The methods used here resulted in the determination of several NDO-O complexes with aromatic substrates, nitric oxide, oxygen molecule, and products, leading to an initial understanding of the mechanism of enzyme catalysis and the molecular determinants of the regio- and stereo-specificity of this class of enzymes.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Dioxigenasas Idioma: En Revista: Methods Enzymol Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Dioxigenasas Idioma: En Revista: Methods Enzymol Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos