Purification and properties of 5-enolpyruvylshikimate 3-phosphate synthase from seedlings of Pisum sativum L. 1984

D M Mousdale, and J R Coggins
Department of Biochemistry, University of Glasgow, G12 8QQ, Glasgow, UK.

5-Enolpyruvylshikimate 3-phosphate synthase (3-phosphoshikimate 1-carboxyvinyltransferase; EC 2.5.1.19) from shoot tissue of pea seedlings was purified to apparent homogeneity by sequential ammonium-sulphate precipitation, ion-exchange and hydrophobic-interaction chromatography and substrate elution from cellulose phosphate. Gel electrophoresis and gel-permeation chromatography showed that the purified enzyme was monomeric with molecular weight 50,000. The herbicide glyphosate was a potent inhibitor of the forward enzyme-catalyzed reaction.

UI MeSH Term Description Entries

Related Publications

D M Mousdale, and J R Coggins
July 1983, The Biochemical journal,
D M Mousdale, and J R Coggins
September 1984, European journal of biochemistry,
D M Mousdale, and J R Coggins
April 2003, Protein expression and purification,
D M Mousdale, and J R Coggins
December 1985, Journal of molecular biology,
D M Mousdale, and J R Coggins
January 1975, Methods in enzymology,
D M Mousdale, and J R Coggins
September 1998, Biochemistry,
Copied contents to your clipboard!