A site-directed mutagenesis study of human placental aromatase

J Biol Chem. 1992 Jan 15;267(2):762-8.

Abstract

Aromatase, a cytochrome P-450, catalyzes the formation of aromatic C18 estrogenic steroids from C19 androgens. Using the x-ray structure of cytochrome P-450cam as the model, seven mutants of human aromatase were designed and expressed in Chinese hamster ovary cells by a stable expression method. They are His-128----Gln, His-128----Ala, Cys-299----Ala, Glu-302----Leu, Asp-309----Asn, Asp-309----Ala, and Ser-312----Cys. The presence of the aromatase mutants in the transfected Chinese hamster ovary cells were confirmed by immunoprecipitation analysis. The kinetic parameters of these mutants using [1 beta,2 beta-3H] androstenedione (or [1 beta-3H]androstenedione), and [1 beta,2 beta-3H]testosterone as substrates were determined. In addition, inhibition profiles for these mutants with two aromatase inhibitors, 4-hydroxyandrostenedione and aminoglutethimide were obtained. Furthermore, the reactions catalyzed by these mutants were examined by evaluating the levels of the product estrone, and two intermediates, 19-hydroxyandrostenedione and 19-oxoandrostenedione by reverse phase high performance liquid chromatography using [7-3H]androstenedione as the substrate. Our results indicate that among the positions we modified, Asp-309 appears to be very important for the enzyme catalysis.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aminoglutethimide / pharmacology
  • Animals
  • Aromatase / genetics*
  • Aromatase / metabolism
  • Aromatase Inhibitors
  • Base Sequence
  • Binding Sites
  • Chromatography, High Pressure Liquid
  • Computer Simulation
  • Cricetinae
  • Cricetulus
  • Female
  • Humans
  • Kinetics
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed*
  • Placenta / enzymology*
  • Precipitin Tests
  • Pregnancy
  • Transfection

Substances

  • Aromatase Inhibitors
  • Aminoglutethimide
  • Aromatase