ASSEMBLY OF LIPIDS INTO MEMBRANES IN ACANTHAMOEBA PALESTINENSIS I. Observations on the Specificity and Stability of Choline-1 4C and Glycerol-3H as Labels for Membrane Phospholipids

In order to determine the feasibility of using radioactive precursors as markers for membrane phospholipids in Acanthamoeba palestinensis, the characteristics of phospholipids labeled with choline-14 C and glycerol-3H were examined . Choline-14 C was found to be a specific label for phosphatidyl choline . There was a turnover of the radioactive moiety of phosphatidyl choline at a rate that varied with the concentration of nonradioactive choline added to the growth medium. Radioactivity was lost from labeled phosphatidyl choline into the acidsoluble intracellular pool and from the pool into the extracellular medium . This loss of radioactivity from cells leveled off and an equilibrium was reached between the label in the cells and in the medium . Radioactive choline was incorporated into phosphatidyl choline by cell-free microsomal suspensions . This incorporation leveled off with the attainment of an equilibrium between the choline14 C in the reaction mixture and the choline14C moiety of phosphatidyl choline in the microsomal membranes . Therefore, a choline exchange reaction may occur in cell-free membranes, as well as living A . palestinensis. In contrast to choline-14C, the apparent turnover of glycerol3H-labeled phospholipids was not affected by large concentrations of nonradioactive choline or glycerol in the medium . The radioactivity in lipids labeled with glycerol3H consisted of 33%o neutral lipids and 67% phospholipids . Phospholipids labeled with glycerol3H turned over slowly, with a concomitant increase in the percentage of label in neutral lipids, indicating a conversion of phospholipids to neutral lipids. Because most ('96 %) of the glycerol3H recovered from microsomal membranes was in phospholipids, whereas only a minor component (-2 0/,) of the glycerol-3H was in the phospholipids isolated from nonmembrane lipids, glycerol 3H was judged to be a specific marker for membrane phospholipids.