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Retention of the label during the conversion of [3-3H] squalene into (3S)-2,3-oxidosqualene catalyzed by mammalian squalene oxidase.

作者信息

Boutaud O, Ceruti M, Cattel L, Schuber F

机构信息

Laboratoire de Chimie Bioorganique (URA CNRS 1386), Faculté de Pharmacie, Strasbourg-Illkirch, France.

出版信息

Biochem Biophys Res Commun. 1995 Mar 8;208(1):42-7. doi: 10.1006/bbrc.1995.1302.

Abstract

Squalene epoxidase is the only known flavoprotein that catalyzes the epoxidation of an olefin. In order to test the possibility of a catalytic non-heme metal-based mechanism, the conversion of chemically synthesized [3-3H]squalene into [3H]2,3-oxidosqualene, by partially purified pig liver squalene epoxidase, was studied. No exchange of the labeled hydrogen could be observed, ruling out a mechanism involving, e.g., an iron carbene type species at C-3.

摘要

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