The allosteric activator fructose-2,6-bisphosphate (F2,6-BP) exerts its principal effect on which pair of enzymes in liver carbohydrate metabolism?
- A Activates glucokinase; inhibits pyruvate kinase
- B Activates phosphoglucomutase; inhibits glycogen phosphorylase
- C Activates glucose-6-phosphate dehydrogenase; inhibits transketolase
- D Activates phosphofructokinase-1; inhibits fructose-1,6-bisphosphatase ✓
Explanation
F2,6-BP is synthesised by phosphofructokinase-2 (bifunctional enzyme) in response to insulin/fed state. It potently activates PFK-1, driving glycolysis, while simultaneously inhibiting fructose-1,6-bisphosphatase, suppressing gluconeogenesis. Glucagon reverses this by activating cAMP-dependent phosphorylation of the bifunctional enzyme, switching it to bisphosphatase mode. This reciprocal control is a key hormonal switch in hepatic glucose metabolism.
Reference: Harper's Illustrated Biochemistry, 32nd ed.
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