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By W. W. Christie

This can be the 3rd quantity of an occasional sequence of books facing facets of lipid methodology.  The individuals speak about and learn positional isomers of glycerolipids, long-chain acyl-coenzyme A esters, 31P nuclear magnetic resonance profiling of phospholipids and a few very important references in lipid method.

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J. Am. Oil Chem. , 70, 1161-1171 (1993). 54. Laakso,P. , J. Am. Oil Chem. , 70, 1173-1176 ( 1993). 55. , in The Lipid Handbook, pp. D. L. B. Padley, Chapman and Hall, London). 56. D. , Lipids, 25, 313-317 (1988). 57. Lehner,R. ,J. Biol. , 268, 8781-8786 (1993). 58. , Kuksis,A. , Lipids, 28, 29-34 (1993). 59. , Raclot,T. , Lipids, 28, 279-284 (1993). 60. , Analysis of Triglycerides, Academic Press, New York, 1972. 61. Lohninger,A. , J. , 192, 185-192 (1980). 62. , Receuil. J. Roy. Neth. Chem. , 98, 92-95 (1979).

Presumably, the two phosphomonoesters of the phosphatidylinositol bisphosphate, PIP 2, would exhibit a weak acid pHdependence of the monoester chemical shifts also). The ionization curve exhibits the typical features of such data [26,76]. There are two well-defined endpoints, corresponding to the monoprotonated acid, at pH values< 7, and the conjugate dianionic base, at pH values > 10, and a single transition segment between these two extremes. 44 is rather basic for a simple orthophosphate monoester [24,26,27].

J. Am. Oil Chem. , 70, 629-631 (1993). 64. J. , Biol. , 21, 541-547 (1992). 65. , Odham,G. , J. , 350, 417-426 (1985). 66. E. , Lipids, 5, 48-53 (1990). 67. , Buchnea,D. ,J. Biol. , 250, 3414-3418 (1975). 68. , In Handbook of Lipid Research, Vol. 1, Fatty Acids and Gklycerides, pp. 123-196 (1978) (edited by A. Kuksis, Plenum Press, Inc, New York). 69. J. , Can. J. , 57, 117-124 (1979). 70. , Marai,L. , Anal. , 50, 557-561 (1978). 71. , Yang,L-Y. , Biochem. , 65, 811-821 ( 1987). 72. N. , Lipids, 25, 33-39 (1990).

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