Chapter 17 - Gluconeogenesis Flashcards
What energetic barrier prevents glycolysis from simply running in reverse to synthesize glucose?
What is the energetic cost of overcoming this barrier?
The reverse of glycolysis is highly endergonic under cellular conditions.
The expenditure of six NTP molecules in gluconeogenesis renders gluconeogenesis exergonic
What reactions of glycolysis are not reversible under intracellular conditions?
How are these reactions bypassed in gluconeogenesis?
In glycolysis, the formation of pyruvate and ATP by pyruvate kinase is irreversible
This step is bypassed by two reactions in gluconeogenesis
(1) the formation of oxaloacetate from pyruvate and CO2 by pyruvate carboxylase
(2) the formation of phosphoenolpyruvate from oxaloacetate and GTP by phosphoenolpyruvate carboxykinase.
The formation of fructose 1,6-bisphosphate by phosphofructokinase is bypassed by fructose 1,6-bisphosphatase in gluconeogenesis, which catalyzes the conversion of fructose 1,6-bisphosphate into fructose 6-phosphate
The hexokinase-catalyzed formation of glucose 6-phosphate in glycolysis is bypassed by glucose 6-phosphatase, but only in the liver
Gluconeogenesis takes place during intense exercise, which seems counterintuitive. Why would an organism synthesize glucose and, at the same time, use glucose to generate energy?
When muscle is actively contracting, lactate is produced from glucose by glycolysis. The lactate is released into the blood and absorbed by the liver, where it is converted by gluconeogenesis onto glucose. The newly synthesized glucose is then released and taken up by the muscle for energy generation.
Interorgan cooperation
Liver is primarily a gluconeogenic tissue, whereas muscle is primarily glycolytic. Why does this division of labor make good physiological sense?
Muscle is likely to produce lactic acid during contraction. Lactic acid is a strong acid and must not accumulate in muscle or blood.
Liver removes the lactic acid from the blood and converts it into glucose. The glucose can be released into the blood or stored as glycogen for later use.
Why does the lack of glucose 6-phosphate activity in the brain and muscle make good physiological sense?
Glucose is an important energy source for both tissues and is essentially the only energy source for the brain. Consequently, these tissues should never release glucose. glucose release is prevented by the absence of glucose 6-phosphatase.
Compare the roles of lactate dehydrogenase in gluconeogenesis and in lactic acid fermentation
In gluconeogenesis, lactate dehydrogenase synthesizes pyruvate from lactate.
In lactic acid fermentation, the enzyme synthesizes lactate from pyruvate
In starvation, protein degradation takes place in muscle. Explain how this degradation might affect gluconeogenesis in the liver.
Some of the amino acids will be released into the blood. The liver will take up the amino acids and convert the carbon skeletons into glucose.
How many NTP molecules are required for the synthesis of one molecule of glucose from two molecules of pyruvte?
6 NTP (4 ATP and 2 GTP)
How many NADH molecules are required for the synthesis of one molecule of glucose from two molecules of pyruvate?
2 NADH
How many NTP molecules are required to synthesize glucose from Glucose 6-phosphate
None
How many NTP molecules are required to synthesize glucose from Fructose 1,6-biphosphate?
None
How many NTP molecules are required to synthesize glucose from two molecules of oxaloacetate?
4 (2 ATP and 2 GTP)
How many NTP molecules are required to synthesize glucose from two molecules of dihydroxyacetone phosphate?
none
What are the two potential substrate cycles in the glycolytic and gluconeogenic pathways?
One cycle would require the glycolytic enzyme phosphofructokinase and the gluconeogenic enzyme fructose 1,6-bisphosphatase.
The other cycle would require pyruvate kinase from glycolysis and pyruvate carboxylase and phosphoenolpyruvate carboxykinase from gluconeogenesis.
What is the regulatory role for the substrate cycles in glycolysis and gluconeogenesis?
The substrate cycles regulate flux on one or the other pathway by amplifying metabolic signals.