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A tricistronic human adrenodoxin reductase-adrenodoxin-cytochrome P450 27A1 vector system for substrate hydroxylation in Escherichia coli.

Salamanca-Pinzón SG, Guengerich FP
Protein Expr Purif. 2011 79 (2): 231-6

PMID: 21621619 · PMCID: PMC3155662 · DOI:10.1016/j.pep.2011.05.008

Cytochrome P450 (P450) 27A1 catalyzes 27-hydroxylation of cholesterol and 25-hydroxylation of vitamin D(3), serving as an important component for the maintenance of lipid homeostasis. In eukaryotic cells P450 27A1 is a membrane-bound protein located on the inner mitochondrial membrane and requires two auxiliary reduction partners, adrenodoxin (Adx) and NADPH-adrenodoxin reductase (Adr), for catalysis in the bile acid biosynthesis pathway. A strategy was developed for the functional coexpression of P450 27A1 with Adr and Adx in a tricistronic fashion (single RNA, three proteins) in Escherichia coli, mimicking the mitochondrial P450 system. Intact bacterial cells coexpressing the P450 vector (pTC27A1) efficiently hydroxylated cholesterol at the 27 position as well as vitamin D(3) at the 25 position when supplemented with glycerol as a carbon source. Thus, E. coli containing pTC27A1 is able to hydroxylate cholesterol in a self-sufficient fashion and is suitable for further applications of protein interaction, drug discovery, and inhibitor evaluation and for the study of other mitochondrial P450s and oxysterol production in microorganisms without a need for membrane reconstitution, membrane simulation by detergents, or purification of the components.

Copyright © 2011 Elsevier Inc. All rights reserved.

MeSH Terms (20)

Adrenodoxin Animals Blotting, Western Cattle Cholecalciferol Cholesterol Chromatography, Liquid Cytochrome P-450 Enzyme System Escherichia coli Ferredoxin-NADP Reductase Genetic Vectors Humans Hydroxylation Mitochondria NADP Protein Binding Protein Engineering Recombinant Fusion Proteins Spectrometry, Mass, Electrospray Ionization Tandem Mass Spectrometry

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