1990)" Non --random association between sex and 6-phosphogluconate dehydrogenase isozyme genotypes in Gelditsia triacanthos L".
5 4 Enzymes tried Esterase (EST), Glucose-6-phosphate dehydrogenase (G6PDH), Malate dehydrogenase (MDH), Malic enzyme (ME), 6-phosphogluconate dehydrogenase (6PGDH), phosphoglucoisomerase (PGI), phosphoglucomutase (PGM), menadione reductase (MR), shikimic acid dehydrogenase (SKDH).
Polymorphism among alleles of the 6-phosphogluconate
dehydrogenase gene from Leishmania major and Leishmania tropica.
Of the enzyme systems initially assayed, alcohol dehydrogenase (ADH); lactate dehydrogenase (LDH); malate dehydrogenase (MDH); phosphohexose isomerase (PHI/PGI); and 6-phosphogluconate
dehydrogenase (6-PGD) resolved consistently.
dehydrogenase (PGD) allele phylogeny is incongruent with a recent origin of polyploidization in some North American Sphaeriidae (Mollusca, Bivalvia).
The enzymes glucose-6-phosphate dehydrogenase and 6-phosphogluconate
dehydrogenase preserve glucose metabolism at a cost to ribose synthesis.
Specifically, G6PD catalyzes the first step in the hexose-monophosphate shunt of the glycolytic pathway by converting glucose-6-phosphate to 6-phosphogluconate
, with [NADP.
Enzyme System AAT Aspartate aminotransferase ACO Aconitate hydratase ALD Fructose-bisphosphate aldolase AP-1 Glycil-leucine peptidase ARK Arginine kinase DIA Dihydrolipoamide dehydrogenase EST Esterase [beta]-GAL [beta]-galactosidase GAPDH Glyceraldehide-3-phosphate dehydrogenase GPI Glucose-6-phosphate isomerase G3PDH Glycerol-3-phosphate dehydrogenase NAD (+) IDH Isocitrate dehydrogenase NADP (+) LAP-1 Leucine aminopeptidase-1 LAP-2 Leucine aminopeptidase-2 MDH Malate dehydrogenase ME Malate dehydrogenase NADP (+) MPI Mannose-6-phosphate isomerase ODH D-octopine dehydrogenase PGD 6-phosphogluconate
dehydrogenase PGM Phosphoglucomutase PP Phenyl-proline peptidase SOD Superoxide dismutase Abbr.
Further studies on the properties and assay of glucose 6-phosphate dehydrogenase and 6-phosphogluconate
dehydrogenase in rat liver.
Simultaneous automated determination of glucose 6-phosphate dehydrogenase and 6-phosphogluconate
dehydrogenase activities in whole blood.
The Beutler enzyme spot test utilizes the phosphoglucomutase, G6PD, and 6-phosphogluconate
dehydrogenase present naturally in RBCs as the enzyme reactions subsequent to the GALT enzyme.
The principle of all the tests involves the oxidation of glucose-6 phosphate to 6-phosphogluconate
, and the concomitant reduction of [NADP.