Literature DB >> 6685296

Alcohol oxidation by isozyme 3a of liver microsomal cytochrome P-450.

M J Coon, D R Koop, E T Morgan.   

Abstract

Liver microsomes from rabbits treated chronically with ethanol were solubilized and fractionated to yield a new isozyme of cytochrome P-450 in a homogeneous state. This cytochrome, designated as isozyme 3a on the basis of its relative electrophoretic mobility, is distinct from the known terminal amino acid sequences. In addition, peptide mapping by high performance liquid chromatography following trypsinolysis indicates that form 3a is a unique gene product. This cytochrome has unusually high activity in the oxidation of ethanol and other alcohols to aldehydes and in the rho-hydroxylation of aniline as compared with the other isozymes of P-450. The ethanol-oxidizing activity of isozyme 3a, which requires the presence of NADPH and NADPH-cytochrome P-450 reductase and is stimulated by the presence of phosphatidylcholine, is not due to contamination by catalase or an NAD+-or NADP+-dependent alcohol dehydrogenase.

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Year:  1983        PMID: 6685296     DOI: 10.1016/0091-3057(83)90168-5

Source DB:  PubMed          Journal:  Pharmacol Biochem Behav        ISSN: 0091-3057            Impact factor:   3.533


  2 in total

1.  Effects of ethanol on the kinetics of methyl ethyl ketone in man.

Authors:  J Liira; V Riihimäki; K Engström
Journal:  Br J Ind Med       Date:  1990-05

2.  CYP2E1 substrate inhibition. Mechanistic interpretation through an effector site for monocyclic compounds.

Authors:  Samuel L Collom; Ryan M Laddusaw; Amber M Burch; Petr Kuzmic; Martin D Perry; Grover P Miller
Journal:  J Biol Chem       Date:  2007-12-04       Impact factor: 5.157

  2 in total

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