Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1176477 | Analytical Biochemistry | 2007 | 5 Pages |
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 230 nm 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.
Related Topics
Physical Sciences and Engineering
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Authors
Yanyan Li, Philippe Lopez, Philippe Durand, Jamal Ouazzani, Bernard Badet, Marie-Ange Badet-Denisot,