Synthesis of CDP-diglyceride from phosphatidylinositol and CMP

A reaction in which CDP-diglyceride and inositol are formed from 1-stearoyl, 2-arachidonoyl phosphatidylinositol and CMP occurs readily in dialyzed microsomal preparations from the mouse pancreas. The reaction is Mn 2+-dependent, and it is inhibited by each of the two products, CDP-diglyceride and m...

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Veröffentlicht in:Biochemical and biophysical research communications 1977-09, Vol.78 (1), p.364-371
Hauptverfasser: Hokin-Neaverson, Mabel, Sadeghian, Kenneth, Harris, Douglas W., Merrin, James S.
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container_issue 1
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container_title Biochemical and biophysical research communications
container_volume 78
creator Hokin-Neaverson, Mabel
Sadeghian, Kenneth
Harris, Douglas W.
Merrin, James S.
description A reaction in which CDP-diglyceride and inositol are formed from 1-stearoyl, 2-arachidonoyl phosphatidylinositol and CMP occurs readily in dialyzed microsomal preparations from the mouse pancreas. The reaction is Mn 2+-dependent, and it is inhibited by each of the two products, CDP-diglyceride and myoinositol. It is presumed to involve the back-reaction of CDP-diglyceride: inositol phosphatidyltransferase (phosphatidyl-inositol synthetase, EC.2.7.8.11.)
doi_str_mv 10.1016/0006-291X(77)91263-3
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ispartof Biochemical and biophysical research communications, 1977-09, Vol.78 (1), p.364-371
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Animals
Cytidine Diphosphate Diglycerides - biosynthesis
Cytidine Monophosphate - metabolism
Cytosine Nucleotides - metabolism
Magnesium - pharmacology
Manganese - pharmacology
Mice
Microsomes - metabolism
Nucleoside Diphosphate Sugars - biosynthesis
Pancreas - metabolism
Phosphatidylinositols - metabolism
Phosphotransferases - metabolism
Ribonucleotides - pharmacology
title Synthesis of CDP-diglyceride from phosphatidylinositol and CMP
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