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  • Submitochondrial localization of 6-N-trimethyllysine dioxygenase - implications for carnitine biosynthesis.

Submitochondrial localization of 6-N-trimethyllysine dioxygenase - implications for carnitine biosynthesis.

The FEBS journal (2007-10-20)
Naomi van Vlies, Rob Ofman, Ronald J A Wanders, Frédéric M Vaz
ABSTRACT

The first enzyme of carnitine biosynthesis is the mitochondrial 6-N-trimethyllysine dioxygenase, which converts 6-N-trimethyllysine to 3-hydroxy-6-N-trimethyllysine. Using progressive membrane solubilization with digitonin and protease protection experiments, we show that this enzyme is localized in the mitochondrial matrix. Latency experiments with intact mitochondria showed that 3-hydroxy-6-N-trimethyllysine formation is limited by 6-N-trimethyllysine transport across the mitochondrial inner membrane. Because the subsequent carnitine biosynthesis enzymes are cytosolic, after production, 3-hydroxy-6-N-trimethyllysine must be transported out of the mitochondria by a putative mitochondrial 6-N-trimethyllysine/3-hydroxy-6-N-trimethyllysine transporter system. This transport system represents an additional step in carnitine biosynthesis that could have considerable implications for the regulation of carnitine biosynthesis.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Nε,Nε,Nε-Trimethyllysine hydrochloride, ≥97% (TLC)