Literature DB >> 7887959

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

O Boutaud1, M Ceruti, L Cattel, F Schuber.   

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.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7887959     DOI: 10.1006/bbrc.1995.1302

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  2 in total

1.  Biosynthesis of the defensive alkaloid cicindeloine in Stenus solutus beetles.

Authors:  Andreas Schierling; Konrad Dettner; Jürgen Schmidt; Karlheinz Seifert
Journal:  Naturwissenschaften       Date:  2012-07-14

2.  Enzyme-catalyzed cationic epoxide rearrangements in quinolone alkaloid biosynthesis.

Authors:  Yi Zou; Marc Garcia-Borràs; Mancheng C Tang; Yuichiro Hirayama; Dehai H Li; Li Li; Kenji Watanabe; K N Houk; Yi Tang
Journal:  Nat Chem Biol       Date:  2017-01-23       Impact factor: 15.040

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.