Utilization of different fatty acyl-CoA thioesters by serine palmitoyltransferase from rat brain

J Lipid Res. 1984 Feb;25(2):185-8.

Abstract

Serine palmitoyltransferase (EC 2.3.1.50) catalyzes the first unique reaction of sphingolipid biosynthesis. Activities were determined with different fatty acyl-CoA substrates to describe the range of long-chain bases that could be made by rat brain microsomes. The activities were greatest with palmitoyl-CoA and palmitelaidoyl-CoA, followed by fully saturated homologs differing from these by only one carbon atom, and diminished considerably as the alkyl-chain length increased or decreased, or with the presence of a cis-double bond. These characteristics explain the predominance of long-chain bases with 18 carbon atoms in brain sphingolipids, and account for the minor variants such as the C17- and C20-long chain bases.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acyl Coenzyme A / metabolism*
  • Acyltransferases / metabolism*
  • Animals
  • Brain / enzymology
  • Brain / metabolism*
  • Female
  • Microsomes / enzymology
  • Microsomes / metabolism*
  • Palmitoyl Coenzyme A / metabolism
  • Rats
  • Rats, Inbred BUF
  • Serine C-Palmitoyltransferase
  • Sphingolipids / biosynthesis

Substances

  • Acyl Coenzyme A
  • Sphingolipids
  • oleoyl-coenzyme A
  • Palmitoyl Coenzyme A
  • stearoyl-coenzyme A
  • Acyltransferases
  • Serine C-Palmitoyltransferase