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DENTAL BIOCHEMISTRY 2015 LECTURE 10 GLUCONEOGENESIS

DENTAL BIOCHEMISTRY 2015 LECTURE 10 GLUCONEOGENESIS. Michael Lea. Lecture Outline. Function of gluconeogenesis and tissue distribution Reaction sequence Rate-limiting steps Energy requirement Substrates and regulation of gluconeogenesis

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DENTAL BIOCHEMISTRY 2015 LECTURE 10 GLUCONEOGENESIS

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  1. DENTAL BIOCHEMISTRY 2015LECTURE 10GLUCONEOGENESIS Michael Lea

  2. Lecture Outline • Function of gluconeogenesis and tissue distribution • Reaction sequence • Rate-limiting steps • Energy requirement • Substrates and regulation of gluconeogenesis • Suggested reading: Lippincott’s Biochemistry, 6th edition, pages 117-123

  3. Function of gluconeogenesis and tissue distribution • Gluconeogenesis is the synthesis of glucose from three carbon precursors including lactate, pyruvate and glycerol • Gluconeogenesis occurs in the liver and kidney

  4. Reaction sequence • The conversion of pyruvate to glucose occurs in a series of eleven reactions. • Seven of the reactions are catalyzed by enzymes that are also used in glycolysis. • The conversion of pyruvate to phosphenolpyruvate occurs in two steps catalyzed by pyruvate carboxylase and phosphoenolpyruvate carboxykinase. • Two specific phosphatases catalyze the hydrolysis of fructose 1,6-bisphosphate and glucose 6-phosphate.

  5. Rate-limiting Steps in Gluconeogenesis • Hormonal and dietary regulation is exerted on the enzymes whose function is restricted to gluconeogenesis : pyruvate carboxylase, phosphoenolpyruvate carboxykinase, fructose 1,6-bisphosphatase and glucose 6-phosphatase. • Activation of pyruvate carboxylase by acetyl coenzyme A is an important regulatory mechanism.

  6. Energy Requirement • The conversion of two moles of pyruvate to one mole of glucose requires the equivalent of 6 moles of ATP and two moles of NADH.

  7. ADP ATP X

  8. Substrates for Gluconeogenesis • Major substrates include lactate, pyruvate and glycerol. • Most amino acids can be metabolized to form precursors for gluconeogenesis.

  9. Reciprocal Control of Glycolysis and Gluconeogenesis • Insulin increases glycolysis and decreases gluconeogenesis • Glucocorticoids and glucagon increase gluconeogenesis and decrease glycolysis.

  10. Reciprocal Control of Glycolysis and Gluconeogenesis by Fructose 2,6-bisphosphate • Fructose 2,6-bisphosphate (F26BP) is a switch molecule that increases glycolysis by activating phosphofructokinase 1 and inhibiting fructose 1,6-bisphosphatase. • F26BP levels are controlled by an enzyme with 2 active sites. The un-phosphorylated enzyme has phosphofructokinase 2 activity and yields F26BP. The phosphorylated enzyme has fructose 2,6-bisphosphatase activity and lowers the concentration of F26BP.

  11. ADP ATP X X

  12. Gluconeogenesis and Diabetes • In diabetes mellitus there is impaired uptake of glucose, particularly in muscle and adipose tissue. • The body responds as in starvation with an increase in gluconeogenesis. This results in a further elevation of blood glucose levels that may exceed the renal glucose threshold resulting in significant glucose in urine.

  13. Lecture Objectives • After studying this lecture material you should be able to • Describe the function of gluconeogenesis • Identify where gluconeogenesis occurs • Distinguish the enzyme catalyzed reactions common to glycolysis and gluconeogenesis and those unique to gluconeogenesis • Identify the energy requirement for gluconeogenesis • Describe the substrates and regulation of gluconeogenesis

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