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Cyanamide mediated syntheses under plausible primitive earth conditions

V. The Synthesis of Phosphatidic Acids

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Summary

A mixture of ammonium palmitate,14C-sn-glycero-1(3)-phosphate, cyanimide and imidazole when heated for several hours formed significant quantities of phospholipids. These reaction products were shown by chromatographic, chemical and enzymatic procedures to be monopalmitoylglycerophosphate (MPGP), dipalmitoylglycerophosphate (DPGP) and monopalmitoyl cyclic glycerophosphate (cMPGP). A portion of the MPGP and DPGP possessed the same steric configuration as naturally occurring lysophosphatidic acid and phosphatidic acid. The yield of total phospholipid was maximal at temperatures between 60° and 90° after 8 h. When ratios of reactants were varied, up to 45% of radioactive glycerophosphate was converted into phospholipids. The average proportions of individual phosphatidic acids were: 60% MPGP, 27% DPGP and 13% cMPGP. Evidence was obtained for a synergistic relationship between cyanamide and imidazole in promoting the formation of phosphatidic acids. These results suggest that phosphatidic acids, which are essential precursors for the biochemical synthesis of more complex membrane phospholipids, could have been produced on the primitive Earth.

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Abbreviations

LPA:

lysophosphatidic acid (1-acyl-sn-glycero-3-phosphate)

PA:

phosphatidic acid (1, 2-di-acyl-sn-glycero-3-phosphate)

MPGP:

monopalmitoylglycerophosphate

cMPGP:

monopalmitoyl cyclic glycerophosphate (1(3)-acyl-sn-glycero-2,3 (1,2)-cyclic phosphate)

DPGP:

dipalmitoylglycerophosphate

GP:

glycerophosphate

cGP:

cyclic glycerophosphate (sn-glycero-2,3 (1,2)-cyclic phosphate)

TLC:

thin layer chromatography

References

  • Bartlett, G. (1959). J. Biol. Chem.234, 466–468

    Google Scholar 

  • Beck, A., Lohrmann, R., Orgel, L.E. (1967). Science157, 952

    Google Scholar 

  • Blank, M.L., Snyder, F. (1970). Biochemistry9, 5034–5036

    Google Scholar 

  • Brockerhoff, H. (1963). J. Lipid Res.4, 96–99

    Google Scholar 

  • Dawson, R.M.C. (1960). Biochem. J.75, 45–53

    Google Scholar 

  • Eichberg, J. (1974). J. Biol. Chem.249, 3423–3429

    Google Scholar 

  • Eichberg, J., Sherwood, E., Epps, D.E., Oró, J. (1977). J. Mol. Evol.10, 221–230

    Google Scholar 

  • Ibanez, J.D., Kimball, A.P., Oró, J. (1971). Science173, 444–446

    Google Scholar 

  • Halmann, M. (1968). Arch. Biochem. Biophys.128, 808–810

    Google Scholar 

  • Hanes, C.S., Isherwood, F.A. (1959). Nature164, 1107–1112

    Google Scholar 

  • Hargreaves, W.R., Mulvihill, S.J., Deamer, D.W. (1977). Nature266, 78–80

    Google Scholar 

  • Kates, M., Sastry, P.S. (1969). Methods in Enzymology14, 197–203

    Google Scholar 

  • Khorana, H.G. (1953). J. Chem. Soc. 2257–2266

  • Knauth, L.P., Epstein, S. (1976). Geochim. Cosmochim. Acta40, 1095–1108

    Google Scholar 

  • Lands, W.E.M., Hart, P. (1965). J. Biol. Chem.240, 1905–1911

    Google Scholar 

  • Lapidot, Y., Barzilay, I., Hajdu, J. (1969). Chem. Phys. Lipids3, 125–134

    Google Scholar 

  • Nooner, D.W., Gibert, J.M., Gelpi, E., Oró, J. (1976). Geochim. Cosmochim Acta40, 915–924

    Google Scholar 

  • Nooner, D.W., Sherwood, E., More, M.A., Oró, J. (1977). J. Mol. Evol.10, 211–220

    Google Scholar 

  • Okuyama, H., Lands, D.E.M., Gunstone, F.D. (1969). J. Biol. Chem.244, 6514–6519

    Google Scholar 

  • Oró, J. (1963). Ann. N.Y. Acad. Sci.108, 464–481

    Google Scholar 

  • Schwartz, A.W. (1972). Biochem. Biophys. Acta281, 477–480

    Google Scholar 

  • Sherwood, E., Joshi, A., Oró, J. (1977). J. Mol. Evol.10, 193–210

    Google Scholar 

  • Sherwood, E., Oró, J. (1977). J. Mol. Evol.10, 183–192

    Google Scholar 

  • Steinman, G., Kenyon, D.H., Calvin, M. (1966). Biochem. Biophys. Acta124, 339–350

    Google Scholar 

  • Van Deenen, L.L.M., de Haas, G.H. (1963). Biochim. Biophys. Acta70, 538–553

    Google Scholar 

  • Vaskovsky, V.E., Kostetsky, E.Y. (1968). J. Lipid Res.9, 396–398

    Google Scholar 

  • Wells, M.A., Dittmer, J.D. (1965). Biochemistry4, 2459–2469

    Google Scholar 

  • Zabor-Behrens, G., Kako, K.J. (1976). Lipids11, 713–717

    Google Scholar 

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Epps, D.E., Sherwood, E., Eichberg, J. et al. Cyanamide mediated syntheses under plausible primitive earth conditions. J Mol Evol 11, 279–292 (1978). https://doi.org/10.1007/BF01733838

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  • DOI: https://doi.org/10.1007/BF01733838

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