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J. Biol. Chem., Vol. 262, Issue 16, 7635-7638, Jun, 1987
H Inoue, M Moriyasu and N Hamasaki
The concentration of 3-phosphoglyceroyl phosphate in erythrocytes was
increased by more than 100-fold when red cells were incubated with
extracellular phosphoenolpyruvate at 37 degrees C. Since these elevated
levels were maintained for 60 min, the metabolism of 3-phosphoglyceroyl
phosphate and related compounds could be investigated in
phosphoenolpyruvate-treated erythrocytes. 2,3-Bisphosphoglycerate synthesis
was not affected by intracellular pH when the 3- phosphoglyceroyl phosphate
level was constant but did vary with 3- phosphoglyceroyl phosphate
concentration. On the other hand, the relationship between the rate of
2,3-bisphosphoglycerate synthesis and 3-phosphoglyceroyl phosphate
concentration was not straightforward. At relatively low concentrations of
3-phosphoglyceroyl phosphate, the observed rate of 2,3-bisphosphoglycerate
synthesis agreed with a rate calculated from a formula incorporating
kinetic parameters of purified 2,3-bisphosphoglycerate synthase (Rose, Z.B.
(1973) Arch. Biochem. Biophys. 158, 903-910). However, at high
concentrations of 3- phosphoglyceroyl phosphate, the observed rate of 2,3-
bisphosphoglycerate synthesis was lower than the calculated value. The
concentration of glucose 1,6-bisphosphate did not increase even when 3-
phosphoglyceroyl phosphate was elevated to 200 microM. Elevated levels of
intracellular 2,3-bisphosphoglycerate did not inhibit glycolytic activity
in these erythrocytes. These results suggest that incubation of
erythrocytes with phosphoenolpyruvate is a useful technique to investigate
the effect of metabolic perturbations at the intermediate stages of
glycolysis.
Metabolism of 3-phosphoglyceroyl phosphate in phosphoenolpyruvate- enriched human erythrocytes
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