Erythrocytic glucose-6-phosphate dehydrogenase measured by a differential pH technique

Clin Chem. 1987 Apr;33(4):579-82.

Abstract

We propose a new quantitative electrochemical method for determining glucose-6-phosphate dehydrogenase (EC 1.1.1.49) activity in purified erythrocytes or in whole blood, based on measurement of the pH change caused by oxidation of glucose 6-phosphate to 6-phosphogluconic acid, with simultaneous reduction of NADP+ to NADPH + H+. No sample pretreatment (e.g., preparation of hemolysate) is needed, and the automatic correction for sample blanks obviates interference from 6-phosphogluconate dehydrogenase (EC 1.1.1.44). The method is simple and fast, and the standard curve is linear to at least 2200 U/L at 37 degrees C. The within-day CV was 3.9% for activities in healthy individuals (mean value 1204 U/L), and 10% for deficient ones (classified as belonging to class II, mean value 407 U/L). Results (y) correlated well with those obtained with the WHO-recommended method (x): y = 1.13x + 0.02 (r = 0.971) for purified erythrocytes. Normal reference intervals are reported for the enzyme in purified erythrocytes and in whole blood.

MeSH terms

  • Erythrocytes / enzymology*
  • Glucosephosphate Dehydrogenase / blood*
  • Humans
  • Hydrogen-Ion Concentration
  • Mathematics
  • Methods
  • NADP
  • Phosphogluconate Dehydrogenase / blood
  • Reference Values

Substances

  • NADP
  • Phosphogluconate Dehydrogenase
  • phosphogluconate dehydrogenase (decarboxylating)
  • Glucosephosphate Dehydrogenase