The intracellular location of various enzymes involved in the metabolism of phospholipids of Candida albicans was studied. Among the biosynthetic enzymes, phosphatidylserine synthetase was found to be localized in the microsomes; choline kinase and ethanolamine kinase were cytosolic; acyltransferase was localized in the paniculate fraction and glycerol kinase and phosphatidic acid phosphatase were distributed in both the microsomal and cytosolic fractions. Phospholipase A and phospholipase C were abundant in the microsomes and phospholipase C was also detected in the cytosol. Lysophospholipase and glycerophosphocholine diesterase were distributed mainly in the mitochondria. Lipase activity was also detected in this fungus. Based on the enzymes detected in this study we have postulated pathways of phospholipid metabolism in C. albicans.Phospholipids are vital structural and functional entities of biomembranes [6] and their metabolism is related to the formation and functions of membrane components [ 1 ]. Biosynthesis of phospholipids occurs mainly via the Kennedy and CDP-diacylglycerol pathways, in addition to alternate routes such as base exchange, methylation, acylation and deacylation reactions. Phospholipid degradation takes place by three main pathways. The first includes phospholipase A, lysophospholipase and glycerophosphocholine diesterase, the second involves phospholipase C, and the third involves phospholipase D and results in the formation of phosphatidic acid. Phosphatidic acid is used either to synthesize triglycerides, or is degraded by lipase for conversion to glycerol-3-phosphate by glycerol kinase. The presence of these pathways has been established in mammalian systems, and to some extent in fungi [8,12,23], but in Candida albicans the information is restricted to extracellular phospholipases [4,19]. This communication describes the identification and subcellular distribution of enzymes of phospholipid metabolism in C. albicans.
METHODS
ChemicalsRadiolabelled (3H)-glycerol (sp. act. 2-50 mCi mmol-1), (3H)-ethanolamine (sp. act.