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pubmed-article:10514455pubmed:abstractTextThe 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 A(2). The amount of phospholipase A(2)-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.lld:pubmed
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pubmed-article:10514455pubmed:articleTitlePhosphatidic acid synthesis in mitochondria. Topography of formation and transmembrane migration.lld:pubmed
pubmed-article:10514455pubmed:affiliationDepartment of Biological Sciences, St. John's University, Jamaica, New York 11439, USA.lld:pubmed
pubmed-article:10514455pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:10514455pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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