Literature DB >> 3196351

[19-14C]androstenedione: a new substrate for assaying aromatase and studying its reaction mechanism.

D F Covey1, P C McMullan, L L Wixler, M Cabell.   

Abstract

[19-14C]Androstenedione has been prepared and utilized as a substrate for assaying microsomal human placental aromatase. Enzyme activity is determined by measuring the rate at which [14C]formate is produced by aromatization of this 14C-labeled steroid. Isotope ratio experiments using [19-14C]androstenedione and [1 beta-3H]androstenedione demonstrate that an apparent kinetic hydrogen isotope effect exists for the aromatization of the tritiated steroid with kH/kT approximately 1.09. Metabolic switching occurs to a minor extent (approximately 3%) during aromatization of [1 beta-3H]androstenedione, but not during the aromatization of [19-14C]androstenedione.

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Year:  1988        PMID: 3196351     DOI: 10.1016/s0006-291x(88)80014-7

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


  1 in total

1.  Structure-function studies of human aromatase by site-directed mutagenesis: kinetic properties of mutants Pro-308----Phe, Tyr-361----Phe, Tyr-361----Leu, and Phe-406----Arg.

Authors:  D J Zhou; D Pompon; S A Chen
Journal:  Proc Natl Acad Sci U S A       Date:  1991-01-15       Impact factor: 11.205

  1 in total

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