Biosynthesis of a C21 steroid conjugate in an insect. The conversion of [14C]cholesterol to 5-[14C]pregnen-3 beta,20 beta-diol glucoside in the tobacco hornworm, Manduca sexta

J Biol Chem. 1985 Dec 15;260(29):15410-2.

Abstract

Following injection into Manduca sexta (L.) female pupae (day 16), [14C]cholesterol was converted to a C21 steroid conjugate, 5-[14C]pregnen-3 beta,20 beta-diol glucoside. The conjugate was isolated from ovaries and eggs and contained three glucose units at least one of which is attached to C-20. The distribution of the other two glucose units remains to be determined. Other than the dealkylation of C-24 alkane or alkene substituents, side-chain cleavage of sterols is uncommon to insects. Here we report the first definitive proof of the biosynthesis of a C21 steroid conjugate from cholesterol in an insect species. The capability of M. sexta to so readily convert cholesterol to a C21 steroid suggests a physiological role for 5-pregnen-3 beta,20 beta-diol in this species.

MeSH terms

  • Animals
  • Cholesterol / metabolism*
  • Female
  • Glucosides / metabolism*
  • Glycosides / metabolism*
  • Lepidoptera
  • Magnetic Resonance Spectroscopy
  • Pregnenes / metabolism*
  • Pregnenolone / analogs & derivatives
  • Pregnenolone / metabolism

Substances

  • Glucosides
  • Glycosides
  • Pregnenes
  • Pregnenolone
  • 5-pregnene-3,20-diol
  • Cholesterol
  • 5-pregnen-3,20-diol glucoside