Abstract
Choline accumulation and phosphatidylcholine biosynthesis were investigated in the choline-requiring anaerobic protozoon Entodinium caudatum by incubating whole cells or subcellular fractions with [14C] choline, phosphoryl [14C] choline and CDP-[14C] choline. 2. All membrane fractions contained choline kinase (EC 2.7.1.32) and CDP-choline-1,2-diacylglycerol cholinephosphotransferase (EC 2.7.8.2), although the specific activities were less in the cell-envelope fraction. Choline phosphate cytidylyltransferase (EC 2.7.7.15) was limited to the supernatant, and this enzyme was rate-limiting for phosphatidylcholine synthesis in the whole cell. 3. Synthesis of phosphatidylcholine from free choline by membranes was only possible in the presence of supernatant. Such reconstituted systems required ATP (2.5 mM), CTP (1 mM) and Mg2+ (5 mM) for maximum synthesis of the phospholipid. CTP and Mg2+ were absolute requirements. 4. Hemicholinium-3 prevented choline uptake by the cells and was strongly inhibitory towards choline kinase; the other enzymes involved in phosphatidylcholine synthesis were minimally affected. 5. Ca2+ ions (0.5 mM) substantially inhibited CDP-choline-1,2-diacylglycerol cholinephosphotransferase in the presence of 15 mM-Mg2+, but choline phosphate cytidylyltransferase and choline kinase were less affected. 6. No free choline could be detected intact cells even after short (10-180s) incubations or at temperatures down to 10 degrees C. The [14C] choline entering was mainly present as phosphorylcholine and to a lesser extent as phosphatidylcholine. 7. It is suggested that choline kinase effectively traps any choline within the cell, thus ensuring a supply of the base for future growth. At low choline concentrations the activity of choline kinase is rate-limiting for choline uptake, and the enzyme might possibly play an active role in the transport phenomenon. Thus the choline uptake by intact cells and choline kinase have similar Km values and show similar responses to temperature and hemicholinium-3.
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- Ansell G. B., Spanner S. G. The inhibition of brain choline kinase by hemicholinium-3. J Neurochem. 1974 Jun;22(6):1153–1155. doi: 10.1111/j.1471-4159.1974.tb04352.x. [DOI] [PubMed] [Google Scholar]
- BORKENHAGEN L. F., KENNEDY E. P. The enzymatic synthesis of cytidine diphosphate choline. J Biol Chem. 1957 Aug;227(2):951–962. [PubMed] [Google Scholar]
- Broad T. E., Dawson R. M. Phospholipid biosynthesis in the anaerobic protozoon Entodinium caudatum. Biochem J. 1975 Feb;146(2):317–328. doi: 10.1042/bj1460317. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Broad T. E., Dawson R. M. Role of choline in the nutrition of the rumen protozoon Entodinium caudatum. J Gen Microbiol. 1976 Feb;92(2):391–397. doi: 10.1099/00221287-92-2-391. [DOI] [PubMed] [Google Scholar]
- Bygrave F. L., Dawson R. M. Phosphatidylcholine biosynthesis in the anaerobic protozoon Entodinium caudatum. Biochem Soc Trans. 1975;3(5):740–741. doi: 10.1042/bst0030740. [DOI] [PubMed] [Google Scholar]
- COLEMAN G. S. The cultivation of sheep rumen oligotrich protozoa in vitro. J Gen Microbiol. 1960 Apr;22:555–563. doi: 10.1099/00221287-22-2-555. [DOI] [PubMed] [Google Scholar]
- Dawson R. M., Kemp P. The aminoethylphosphonate-containing lipids of rumen protozoa. Biochem J. 1967 Nov;105(2):837–842. doi: 10.1042/bj1050837. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Diamond I., Kennedy E. P. Carrier-mediated transport of choline into synaptic nerve endings. J Biol Chem. 1969 Jun 25;244(12):3258–3263. [PubMed] [Google Scholar]
- Diamond I., Milfay D. Uptake of ( 3 H-methyl)choline by microsomal, synaptosomal, mitochondrial and synaptic vesicle fractions of rat brain. The effects of hemicholinium. J Neurochem. 1972 Aug;19(8):1899–1909. doi: 10.1111/j.1471-4159.1972.tb01478.x. [DOI] [PubMed] [Google Scholar]
- Fiscus W. G., Schneider W. C. The role of phospholipids in stimulating phosphorylcholine cytidyltransferase activity. J Biol Chem. 1966 Jul 25;241(14):3324–3330. [PubMed] [Google Scholar]
- Haeffner E. W. Studies on choline permeation through the plasma membrane and its incorporation into phosphatidyl choline of Ehrlich-Lettré-ascites tumor cells in vitro. Eur J Biochem. 1975 Feb 3;51(1):219–228. doi: 10.1111/j.1432-1033.1975.tb03922.x. [DOI] [PubMed] [Google Scholar]
- KENNEDY E. P., WEISS S. B. The function of cytidine coenzymes in the biosynthesis of phospholipides. J Biol Chem. 1956 Sep;222(1):193–214. [PubMed] [Google Scholar]
- Kano H., Ono K. Utilization of endogenous phospholipids by the backreaction of CDP-choline (-ethanolamine): 1,2-diglyceride choline (ethanolamine)-phosphotransferase in rat liver microsomes. Biochim Biophys Acta. 1973 May 24;306(2):203–217. [PubMed] [Google Scholar]
- LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
- Martin K. Extracellular cations and the movement of choline across the erythrocyte membrane. J Physiol. 1972 Jul;224(1):207–230. doi: 10.1113/jphysiol.1972.sp009890. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McCaman R. E., Cook K. Intermediary metabolism of phospholipids in brain tissue. 3. Phosphocholine-glyceride transferase. J Biol Chem. 1966 Jul 25;241(14):3390–3394. [PubMed] [Google Scholar]
- McMurray W. C., Dawson R. M. Phospholipid exchange reactions within the liver cell. Biochem J. 1969 Mar;112(1):91–108. doi: 10.1042/bj1120091. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miller E. K., Dawson R. M. Exchange of phospholipids between brain membranes in vitro. Biochem J. 1972 Feb;126(4):823–835. doi: 10.1042/bj1260823. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Plagemann P. G. Choline metabolism and membrane formation in rat hepatoma cells grown in suspension culture. 3. Choline transport and uptake by simple diffusion and lack of direct exchange with phosphatidylcholine. J Lipid Res. 1971 Nov;12(6):715–724. [PubMed] [Google Scholar]
- Plagemann P. G., Roth M. F. Permeation as the rate-limiting step in the phosphorylation of uridine and choline and their incorporation into macromolecules by Novikoff hepatoma cells. Competitive inhibition by phenethyl alcohol, persantin, and adenosine. Biochemistry. 1969 Dec;8(12):4782–4789. doi: 10.1021/bi00840a020. [DOI] [PubMed] [Google Scholar]
- Roberts J. B., Bygrave F. L. Influence of mitochondria on phospholipid synthesis in preparations from rat liver. Biochem J. 1973 Nov;136(3):467–475. doi: 10.1042/bj1360467. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smith J. D., Law J. H. Phosphatidylcholine biosynthesis in Tetrahymena pyriformis. Biochim Biophys Acta. 1970 Feb 10;202(1):141–152. doi: 10.1016/0005-2760(70)90225-0. [DOI] [PubMed] [Google Scholar]
- Stahl W. L., Trams E. G. Synthesis of lipids by liver plasma membranes. Incorporation of acyl-coenzyme A derivatives into membrane lipids in vitro. Biochim Biophys Acta. 1968 Dec 10;163(4):459–471. doi: 10.1016/0005-2736(68)90075-8. [DOI] [PubMed] [Google Scholar]
- Stoffel W., Schiefer H. G. Biosynthesis and composition of phosphatides in outer and inner mitochondrial membranes. Hoppe Seylers Z Physiol Chem. 1968 Aug;349(8):1017–1026. doi: 10.1515/bchm2.1968.349.2.1017. [DOI] [PubMed] [Google Scholar]
- Weinhold P. A., Rethy V. B. The separation, purification, and characterization of ethanolamine kinase and choline kinase from rat liver. Biochemistry. 1974 Dec 3;13(25):5135–5141. doi: 10.1021/bi00722a013. [DOI] [PubMed] [Google Scholar]