Not available outside of the UK & Ireland.
Analysis Note
Absorbance of purified enzyme: 1.15 (1 mg enzyme/ml, 280.5 nm)
Application
Component of cofactor recycling systems for NADPH.
It was used in enzymatic determination of C6 phosphorylation of glycogen.
General description
Glucose-6-Phosphate Dehydrogenase (G6PD) is a ubiquitous enzyme which acts as a catalyst in producing pentose. It also produces NADPH for various biosynthetic and detoxification reactions. Sometimes G6PD provides an alternative to main glycolytic pathway for glucose utilization. It also has its application as DNA markers on X-chromosome.1
Other Notes
For life science research only. Not for use in diagnostic procedures.
Physical form
Solution of 1,000 U in 1 ml 3.2 M ammonium sulfate, pH approximately 6
Preparation Note
Activator: HCO3- (≤ 0.3 M) activates slightly.
Quality
Contaminants: ﹤0.001% CK, ﹤0.01% GR and PGI each, ﹤0.02% “NADH oxidase”, ﹤0.05% HK, ﹤0.001% 6-PGDH
Specificity
Specificity: At pH 7.8, 25 °C: G6P-DH from Leuconostoc (LG6PDH) is highly specific for D-glucose-6-phosphate (Km = 36 μM, NADP as coenzyme; 64 μM, NAD as coenzyme), but will use either NADP (Km = 7.4 μM; relative rate 1.0) or NAD (Km = 115 μM; relative rate 1.8) as coenzyme.LG6P-DH does not react with fructose-6-phosphate, fructose-1,6-biphosphate, glucose-1-phosphate or ribose-1-phosphate. LG6P-DG will oxidize 2-deoxy-glucose-6-phosphate with NADP, but not with NAD as coenzyme. There is a slow reaction with D-glucose.Heat inactivation: The ammonium sulfate suspension is not inactivated when heated to temperatures ≤ 50 °C for 10 minutes. At temperatures > 60 °C the enzyme is rapidly inactivated.
Unit Definition
Unit Conversion: One unit (U) [+25 °C] ≈ 1.18 U [+30 °C] ≈ 1.45 U [+37 °C], all with NAD as coenzymeUnit Definition: One unit (U) LG6P-DH oxidizes 1 mol of glucose-6-phosphate and reduces 1 mol of NAD in 1 minute at +25 °C and pH 7.8.
This product has met the following criteria: