Crystal Structure of Naphthalene Dioxygenase: Side-on Binding of Dioxygen to Iron

Author:

Karlsson Andreas1,Parales Juanito V.2,Parales Rebecca E.2,Gibson David T.2,Eklund Hans1,Ramaswamy S.3

Affiliation:

1. Department of Molecular Biology, Swedish University of Agricultural Sciences, Box 590, Biomedical Center, 75124 Uppsala, Sweden.

2. Department of Microbiology and Center for Biocatalysis and Bioprocessing,

3. Department of Biochemistry, University of Iowa, Iowa City, IA 52242, USA.

Abstract

Binding of oxygen to iron is exploited in several biological and chemical processes. Although computational and spectroscopic results have suggested side-on binding, only end-on binding of oxygen to iron has been observed in crystal structures. We have determined structures of naphthalene dioxygenase that show a molecular oxygen species bound to the mononuclear iron in a side-on fashion. In a complex with substrate and dioxygen, the dioxygen molecule is lined up for an attack on the double bond of the aromatic substrate. The structures reported here provide the basis for a reaction mechanism and for the high stereospecificity of the reaction catalyzed by naphthalene dioxygenase.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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