An enzyme-coupled assay for amidotransferase activity of glucosamine-6-phosphate synthase

Anal Biochem. 2007 Nov 15;370(2):142-6. doi: 10.1016/j.ab.2007.07.031. Epub 2007 Aug 9.

Abstract

An assay for glucosamine-6-phosphate synthase using a yeast glucosamine-6-phosphate N-acetyltransferase 1 (GNA1) as coupling enzyme was developed. GNA1 transfers the acetyl moiety from acetyl-coenzyme A (CoA) to glucosamine-6-phosphate, releasing coenzyme A. The assay measures the production of glucosamine-6-phosphate by either following the consumption of acetyl-CoA spectrophotometrically at 230nm or quantifying the free thiol with 5,5'-dithio-bis(2-nitrobenzoic acid) (Ellman's reagent) in a discontinuous manner. This method is simple to perform and can be adapted to a 96-well microtiter plate format, which will facilitate high-throughput inhibitor screening and mechanistic studies using purified GlmS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Glutamine-Fructose-6-Phosphate Transaminase (Isomerizing) / metabolism*
  • Kinetics
  • Polymerase Chain Reaction
  • Saccharomyces cerevisiae / enzymology
  • Saccharomyces cerevisiae Proteins / metabolism
  • Substrate Specificity
  • Transaminases / metabolism*

Substances

  • Saccharomyces cerevisiae Proteins
  • Transaminases
  • Glutamine-Fructose-6-Phosphate Transaminase (Isomerizing)