Recombinant human cytochrome P450 1B1 expression in Escherichia coli.

Shimada T, Wunsch RM, Hanna IH, Sutter TR, Guengerich FP, Gillam EM
Arch Biochem Biophys. 1998 357 (1): 111-20

PMID: 9721189 · DOI:10.1006/abbi.1998.0808

Human cytochrome P450 (P450) 1B1 was expressed in Escherichia coli at a level of 200 nmol/liter culture using a pCW vector by removal of codons 2-4 and modification of the nucleotide sequence of the resulting N-terminal seven codons; a similar level of expression was found with a bicistronic construct that also expressed human NADPH-P450 reductase. P450 1B1 was purified (from the monocistronic system) to electrophoretic homogeneity and a specific content of 9.2 nmol P450/mg protein using DEAE, CM, and hydroxylapatite chromatography. The absolute spectra showed a considerable fraction of high-spin iron and little cytochrome P420. The catalytic activity of the purified enzyme was considerably enhanced in the presence of cholate. Both reconstituted P450 1B1 and the bacterial membranes prepared from the bicistronic vector system had similar7-ethoxyresorufin O-deethylation activities; as expected, 17beta-estradiol was hydroxylated primarily at the 4-position. The ability of human P450 1B1 to activate several heterocyclic amines and polycyclic hydrocarbon dihydrodiols was confirmed with reconstituted P450 1B1 and the P450 1B1 membranes in which NADPH-P450 reductase was coexpressed.

Copyright 1998 Academic Press.

MeSH Terms (13)

Aryl Hydrocarbon Hydroxylases Carcinogens Catalysis Cell Membrane Cytochrome P-450 CYP1A1 Cytochrome P-450 CYP1A2 Cytochrome P-450 CYP1B1 Cytochrome P-450 Enzyme System Escherichia coli Genetic Vectors Humans Recombinant Proteins Spectrophotometry

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