Copyright © 1985 Published by Elsevier B.V.
Research letters
Spermine promotes the translocation of phosphatidate phosphohydrolase from the cytosol to the microsomal fraction of rat liver and it enhances the effects of oleate in this respect
Paloma Martin-Sanz1, a, Roger Hopewella and David N. Brindley
, a
aDepartment of Biochemistry, University of Nottingham Medical School, Queen's Medical Centre, Nottingham NG7 2UH, England
Received 30 August 1984;
Abstract
Spermine (0.5–2 mM) promoted the translocation of phosphatidate phosphohydrolase from the soluble to the microsomal fraction in a cell-free system derived from rat liver. By contrast, spermidine (1 mM) and putrescine (1 mM) had no significant effect on the translocation when added alone. Spermine, and to a lesser extent, spermidine, enhanced the translocating action of oleate and increased its effectiveness in transferring the phosphohydrolase from the soluble ot the microsomal fraction. It is proposed that the phosphohydrolase becomes metabolically active when it combines with membranes and that polyamines might help to regulate this interaction. This could facilitate the action of fatty acids and enable cells to increase their capacity for triacylglycerol synthesis to match an increased availability of fatty acids.
Keywords: Fatty acid; L-α-Phosphatidate phosphohydrolase; Polyamine; Translocation; Triacylglycerol synthesis
References
To whom correspondence should be addressed.1 Permanent address: Institute de Bioquimica, Facultad de Farmacia, Universidad Complutense de Madrid, Madrid-3, Spain.







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