Peroxisomal acyl-CoA synthetases

Biochim Biophys Acta. 2012 Sep;1822(9):1411-20. doi: 10.1016/j.bbadis.2012.02.010. Epub 2012 Feb 17.

Abstract

Peroxisomes carry out many essential lipid metabolic functions. Nearly all of these functions require that an acyl group-either a fatty acid or the acyl side chain of a steroid derivative-be thioesterified to coenzyme A (CoA) for subsequent reactions to proceed. This thioesterification, or "activation", reaction, catalyzed by enzymes belonging to the acyl-CoA synthetase family, is thus central to cellular lipid metabolism. However, despite our rather thorough understanding of peroxisomal metabolic pathways, surprisingly little is known about the specific peroxisomal acyl-CoA synthetases that participate in these pathways. Of the 26 acyl-CoA synthetases encoded by the human and mouse genomes, only a few have been reported to be peroxisomal, including ACSL4, SLC27A2, and SLC27A4. In this review, we briefly describe the primary peroxisomal lipid metabolic pathways in which fatty acyl-CoAs participate. Then, we examine the evidence for presence and functions of acyl-CoA synthetases in peroxisomes, much of which was obtained before the existence of multiple acyl-CoA synthetase isoenzymes was known. Finally, we discuss the role(s) of peroxisome-specific acyl-CoA synthetase isoforms in lipid metabolism.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Acyl Coenzyme A / biosynthesis
  • Acyl Coenzyme A / metabolism
  • Amino Acid Sequence
  • Animals
  • Coenzyme A Ligases / chemistry
  • Coenzyme A Ligases / metabolism*
  • Coenzyme A Ligases / physiology
  • Conserved Sequence
  • Fatty Acids / metabolism
  • Humans
  • Lipid Metabolism
  • Molecular Sequence Data
  • Oxidation-Reduction
  • Peroxisomal Disorders / enzymology
  • Peroxisomal Disorders / metabolism
  • Peroxisomes / enzymology*
  • Peroxisomes / metabolism

Substances

  • Acyl Coenzyme A
  • Fatty Acids
  • Coenzyme A Ligases