Carnitine biosynthesis. Purification of gamma-butyrobetaine hydroxylase from rat liver

Adv Exp Med Biol. 1999:466:117-24.

Abstract

gamma-Butyrobetaine hydroxylase catalyse the last step in carnitine biosynthesis, the formation of L-carnitine from gamma-butyrobetaine, a reaction dependent on Fe2+, alpha-ketoglutarate, ascorbate and oxygen. Initial attempts to purify the protein from rat liver showed that gamma-butyrobetaine hydroxylase is unstable. We, therefore, determined the influence of various compounds on the stability of gamma-butyrobetaine hydroxylase at different storage temperatures. The enzyme activity was best conserved by storing the protein at 4 degrees C in the presence of 200 g/l glycerol and 10 mM DTT. We subsequently purified the enzyme from rat liver to apparent homogeneity by liquid chromatography.

MeSH terms

  • Animals
  • Carnitine / biosynthesis*
  • Chromatography
  • Chromatography, Ion Exchange
  • Durapatite
  • Enzyme Stability
  • Liver / enzymology*
  • Mixed Function Oxygenases / chemistry
  • Mixed Function Oxygenases / isolation & purification*
  • Mixed Function Oxygenases / metabolism*
  • Rats
  • gamma-Butyrobetaine Dioxygenase

Substances

  • Durapatite
  • Mixed Function Oxygenases
  • gamma-Butyrobetaine Dioxygenase
  • Carnitine