The zoospores of Blastocladiella emersonii, when derived from cultures grown on solid media, contain about 11% total lipid. This lipid was separated chromatographically on silicic acid into neutral lipid (46.6%), glycolipid (15.8%), and phospholipid (37.6%). Each class was fractionated further on columns of silicic acid, Florisil, or diethylaminoethyl-cellulose, and monitored by thin-layer chromatography. Triglycerides were the major neutral lipids, mono-and diglycosyldiglycerides were the major glycolipids, and phosphatidylcholine and phosphatidylethanolamine were the major phospholipids. Other neutral lipids and phospholipids detected were: hydrocarbons, free fatty acids, free sterols, sterol esters, diglycerides, monoglycerides, lysophosphatidylcholine, lysophos: phatidylethanolamine, phosphatidic acid, phosphatidylserine, and phosphatidylinositol. Palmitic, palmitoleic, stearic, oleic, y-linolenic, and arachidonic acids were the most frequently occurring fatty acids. When B. emersonii was grown in "C-labeled liquid media, lipid again accounted for 11% of both Production of plants and zoospores in liquid media. PYG broth cultures were prepared, inoculated, and induced to release zoospores at 22 C, by the method of Myers and Cantino (26). [1,2-'4C]sodium acetate (New England Nuclear Corp.; 50 pCi) was added 9 h after inoculation, the final concentration being 5 x 10-I M. For studies of zoosporangial lipid, thalli were harvested either just before zoospore cleavage or after zoospores had been cleaved but not released (ca. 23 h after. inoculation); for studies of zoospore lipid, spores were collected about 1 h later.Extraction of lipid. Spore pellets were washed with water, sedimented, sonically treated (30 s, 80 W), and extracted at room temperature with chloro-192 on August 1, 2020 by guest