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萘双加氧酶的晶体结构:双氧与铁的侧位结合

Crystal structure of naphthalene dioxygenase: side-on binding of dioxygen to iron.

作者信息

Karlsson Andreas, Parales Juanito V, Parales Rebecca E, Gibson David T, Eklund Hans, Ramaswamy S

机构信息

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

出版信息

Science. 2003 Feb 14;299(5609):1039-42. doi: 10.1126/science.1078020.

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.

摘要

氧与铁的结合在多个生物和化学过程中都有应用。尽管计算和光谱结果表明存在侧基结合,但在晶体结构中仅观察到氧与铁的端基结合。我们已经确定了萘双加氧酶的结构,该结构显示分子氧以侧基方式与单核铁结合。在与底物和双加氧的复合物中,双加氧分子排列好以进攻芳香底物的双键。本文报道的结构为萘双加氧酶催化反应的反应机制和高立体特异性提供了基础。

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