Department of Veterinary Microbiology and the Department of Entomology, Walter Reed Army Institute of Research, Department of Biochemistry, School of Medicine, University of Pennsylvania, Washington, D.C.
Malaria-infected chicken erythrocytes exhibited a marked increase in the metabolism of 1-14C-glucose to 14CO2. Addition of the cofactors, TPN or ATP, to red cell and parasite total hemolysate usually accelerated CO2 production. Virtually all activity was confined to the supernatant fluid as compared to the stroma. A pentose phosphate pathway is apparently absent in Plasmodium gallinaceum, and the parasite apparently utilizes this pathway in the host erythrocyte.
Present Address: Division of Chemistry, U.S. Army Medical Research and Nutrition Laboratory, Fitssimons General Hospital, Denver, Colorado.
Present Address: Division of Metabolism, U.S. Army Medical Research and Nutrition Laboratory, Fitzsimons General Hospital, Denver, Colorado.
Request for reprints should be sent to: Robert H. Herman, Major, M.C., Chief, Division of Metabolism U.S. Army Medical Research and Nutrition Laboratory, Fitzsimons General Hospital, Denver, Colorado 80240.