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Journal of Lipid Research, Vol 18, 53-58, Copyright © 1977 by Lipid Research, Inc.
A Radominska-Pyrek, J Strosznajder, Z Dabrowiecki, G Goracci, T Chojnacki and LA Horrocks
The formation of product by ethanolamine phosphotransferases (EC 2.7.8.1)
and cholinephosphotransferases (EC 2.7.8.2) in microsomal fractions from
brains and livers of mature rats is increased several fold by
1,2-diacyl-sn-glycerols. With the addition of 1-alkyl-2-acyl-sn- glycerols,
we have found an 11-fold increase with brain microsomes and a 20-fold
increase with lvier microsomes in the synthesis of choline ether lipids
(1-alkyl-2-acyl- and 1-alk-1'-enyl-2-acyl-sn-glycero-3-
phosphorylcholines). For the synthesis of ethanolamine ether lipids (1-
alkyl-2-acyl and 1-alk-1'-enyl-2-acyl-sn-glycero-3-
phosphorylethanolamines), the stimulation of alkylacylglycerols was 7- fold
for brain microsomes and 18-fold for liver microsomes. The alkylacyl
glycerols (8 mM) also inhibited the synthesis of diacyl phosphoglycerides
by 44 to 65%, indicating that the same ethanolaminephosphotransferases and
cholinephosphotransferases are utilized for the synthesis of alkylacyl
phosphoglycerides and diacyl phosphoglycerides. A desaturation of the alkyl
groups may take place in the same reaction mixture. The rate of
incorporation of phosphorylcholine into alkenylacyl
glycerophosphorylcholines (choline plasmalogens) with alkylacylglycerols,
cytidine diphosphate choline, and liver microsomes was 15 nmoles per mg
protein per hour. The in vitro synthesis of choline plasmalogens with
alkylacylglycerols had not been observed previously. The corresponding rate
of incorporation of phosphorylethanolamine into ethanolamine plasmalogens
was 10 nmoles per mg protein per hour, a value greater than any of the
previously reported values for ethanolamine plasmalogen formation from
alkylacyl glycerophosphorylethanolamines.
ARTICLES
Enzymic synthesis of ether types of choline and ethanolamine phosphoglycerides by microsomal fractions from rat brain and liver
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