JBC Advanced Glycation Endproducts

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J Biol Chem, Vol. 274, Issue 42, 29786-29790, October 15, 1999

Phosphatidic Acid Synthesis in Mitochondria
TOPOGRAPHY OF FORMATION AND TRANSMEMBRANE MIGRATION

Tandra Roy Chakraborty, Ales Vancura, Vivekanand S. Balija, and Dipak Haldar

From the Department of Biological Sciences, St. John's University, Jamaica, New York 11439

The topography of formation and migration of phosphatidic acid (PA) in the transverse plane of rat liver mitochondrial outer membrane (MOM) were investigated. Isolated mitochondria and microsomes, incubated with sn-glycerol 3-phosphate and an immobilized substrate palmitoyl-CoA-agarose, synthesized both lyso-PA and PA. The mitochondrial and microsomal acylation of glycerophosphate with palmitoyl-CoA-agarose was 80-100% of the values obtained in the presence of free palmitoyl-CoA. In another series of experiments, both free polymyxin B and polymyxin B-agarose stimulated mitochondrial glycerophosphate acyltransferase activity approximately 2-fold. When PA loaded mitochondria were treated with liver fatty acid binding protein, a fifth of the phospholipid left the mitochondria. The amount of exportable PA reduced with the increase in the time of incubation. In another approach, PA-loaded mitochondria were treated with phospholipase A2. The amount of phospholipase A2-sensitive PA reduced when the incubation time was increased. Taken together, the results suggest that lysophosphatidic acid (LPA) and PA are synthesized on the outer surface of the MOM and that PA moves to the inner membrane presumably for cardiolipin formation.


Copyright © 1999 by The American Society for Biochemistry and Molecular Biology, Inc.
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