J. Lipid Res.  Neurobiology of Lipids (ISSN1683-5506)
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Holub, B. J.
Right arrow Articles by Thompson, W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Holub, B. J.
Right arrow Articles by Thompson, W.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

Journal of Lipid Research, Vol. 11, 558-564, November 1970
Copyright © 1970 by Lipid Research, Inc.

Molecular species of mono-, di-, and triphosphoinositides of bovine brain

B. J. Holub , A. Kuksis , and W. Thompson

Department of Biochemistry and the Banting and Best Department of Medical Research, University of Toronto, Toronto, Ontario, Canada

The mono-, di-, and triphosphoinositides of bovine brain were isolated by chromatography on columns of DEAE-cellulose, alumina, and silicic acid. The major molecular species in each phosphoinositide class were identified and quantitatively estimated by combined thin-layer and gas-liquid chromatography of the component diglycerides, which were released by hydrolysis with a specific brain phosphodiesterase. The diglycerides were treated with pancreatic lipase, and the positional distribution of the fatty acids was determined.

Over 27 molecular species were identified, and these accounted for about 95% of each phosphoinositide class, but the 1-stearate 2-arachidonate derivative contributed more than 40% of the total in each class. The other molecular species also were qualitatively and quantitatively similar in the three phosphoinositide classes. All the long-chain and polyunsaturated acids were confined to the 2-position and were preferentially paired with stearic acid in the 1-position. Oleic acid in the 2-position was about equally divided between species with palmitic and stearic acids in the 1-position.

These results suggest that the mono-, di-, and triphosphoinositides of the bovine brain have similar compositions and that the various molecular species may be metabolically related.

Supplementary key words fatty acids • positional distribution • diglycerides • diglyceride acetates

Submitted on March 30, 1970
Accepted on August 5, 1970


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
Biophys. JHome page
J. A. Szule, N. L. Fuller, and R. P. Rand
The Effects of Acyl Chain Length and Saturation of Diacylglycerols and Phosphatidylcholines on Membrane Monolayer Curvature
Biophys. J., August 1, 2002; 83(2): 977 - 984.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
Y Nishizuka
Intracellular signaling by hydrolysis of phospholipids and activation of protein kinase C
Science, October 23, 1992; 258(5082): 607 - 614.
[Abstract] [PDF]


Home page
ScienceHome page
Y Nishizuka
Studies and perspectives of protein kinase C
Science, July 18, 1986; 233(4761): 305 - 312.
[Abstract] [PDF]


Home page
ScienceHome page
Y Nishizuka
Turnover of inositol phospholipids and signal transduction
Science, September 21, 1984; 225(4668): 1365 - 1370.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 All ASBMB Journals   Journal of Biological Chemistry 
 Molecular and Cellular Proteomics   ASBMB Today 
Copyright © 1970 by the American Society for Biochemistry and Molecular Biology.