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Difficulties in the assay of phosphatidate phosphohydrolase activity. Influence of ionic strength, detergent, and selection of substrate
Author(s) -
Stark Margareta,
Humble Elisabet
Publication year - 1996
Publication title -
lipids
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.601
H-Index - 120
eISSN - 1558-9307
pISSN - 0024-4201
DOI - 10.1007/bf02522468
Subject(s) - substrate (aquarium) , lipidology , selection (genetic algorithm) , chemistry , substrate specificity , phosphatidate , clinical chemistry , ionic strength , chromatography , biochemistry , biophysics , enzyme , biology , diacylglycerol kinase , organic chemistry , computer science , ecology , protein kinase c , aqueous solution , artificial intelligence
In the present paper, problems in connection with assay of the activity of magnesium‐dependent rat liver phosphatidate phosphohydrolase (PAP) are discussed. PAP activity is usually measured by following the production of diacylglycerol or inorganic phosphate from the substrate phosphatidate. These two methods may give widely different results due to a number of factors that may affect the assay. One such factor is the composition of the substrate. Higher apparent enzyme activity was observed with dioleoyl‐phosphatidate than with dipalmitoyl‐phosphatidate. This substrate‐dependent difference in apparent PAP activity was 2‐2.5‐fold in the absence and 10‐fold in the presence of Triton X‐100, respectively. Triton X‐100 reduced the activity as measured with the dipalmitoyl‐phosphatidate substrate. In contrast, the activity of PAP as measured with dioleoyl‐phosphatidate was stimulated by Triton X‐100 The stimulatory effect of Triton was reduced or abolished when the ionic strength in the assay mixture was increased. Assays based on 32 P‐labeled substrate are rapid and sensitive. It is shown here that 33 P can be used as an alternative. This radionuclide has a longer half‐life and also emits particles with lower energy, thus posing less potential health hazards for the user.