RESUMO
The kinetics of the reaction of baker's yeast glucose-6-phosphate dehydrogenase with excess 5,5'-dithiobis(2-nitrobenzoic acid) (DTNB) were studied at pH 8.5 and 30 degrees C and at constant ionic strength of 0.01 and in the absence and in the presence of NADP+ or glucose 6-phosphate. The reaction follows pseudo-first-order kinetics irrespective of whether these substrates are absent or present. The observed pseudo-first-order rate constant is reduced in the presence of NADP+ or glucose 6-phosphate but on a molar basis, glucose 6-phosphate is more effective than NADP+ in protecting the sulfhydryl groups of the enzyme against the reaction with DTNB. In the presence of NADP+, the observed pseudo-first-order rate constant decreases to a constant, but finite, value at a saturating coenzyme concentration. The effect of NADP+ on the rate constant is consistent with the presence of noninteracting coenzyme binding sites in baker's yeast glucose-6-phosphate dehydrogenase.
