Plant Physiol. Drug Metab Dispos
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Plant Physiology 86:1099-1103 (1988)
© 1988 American Society of Plant Biologists

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 Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
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 CrossRef
Right arrow Citing Articles via Web of Science (12)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Callaghan, T.
Right arrow Articles by Benziman, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Callaghan, T.
Right arrow Articles by Benziman, M.
Agricola
Right arrow Articles by Callaghan, T.
Right arrow Articles by Benziman, M.
Metabolism and Enzymology

{beta}-Glucoside Activators of Mung Bean UDP-Glucose: {beta}-Glucan Synthase 1

I. Identification of an Endogenous {beta}-Linked Glucolipid Activator

Theresa Callaghan2, Peter Ross, Patricia Weinberger-Ohana, Gwenn Garden and Moshe Benziman

Department of Biological Chemistry, Institute of Life Sciences, The Hebrew University of Jerusalem, 91904 Jerusalem, Israel

Heat-stable activators of membranous {beta}-glucan synthase have been isolated from the supernatant fraction of crude mung bean (Vigna radiata) extracts by DEAE-cellulose and silica-gel chromatography. One of the activators has been partially purified and characterized on the basis of susceptibility to various enzymes and by analysis of the products formed upon total acid hydrolysis, alkaline-methanolysis, and {beta}-glucosidase digestion. This activator has the characteristics of a 1,2-dioleoyl diglyceride containing {beta}-linked glucose residue(s) at the C-3 position. When expressed per mole of glucosyl residues, the maximal Ka value of the activator is estimated to be 25 micromolar. Both the intact glucosyl and fatty acid moiety are essential to the stimulatory effect of the activator.


2 Present address: Department of Molecular Genetics and Biochemistry, Institut Pasteur, 25 et 28 Rue du Docteur Roux, 75724 Paris-Cedex 15, France.

1 Supported by a grant from the Robert Szold Institute for Applied Science, Hebrew University, Jerusalem, and by Weyerhaeuser Company, Tacoma, WA.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY® THE PLANT CELL
Copyright © 1988 by the American Society of Plant Biologists