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Questions and Answers
How many ATP are produced from the complete oxidation of one acetyl CoA in the Krebs Cycle?
How many ATP are produced from the complete oxidation of one acetyl CoA in the Krebs Cycle?
Which of the following molecules is a stimulator of citrate synthase in the Krebs Cycle?
Which of the following molecules is a stimulator of citrate synthase in the Krebs Cycle?
Which inhibitor regulates isocitrate dehydrogenase (ICDH) in the Krebs Cycle?
Which inhibitor regulates isocitrate dehydrogenase (ICDH) in the Krebs Cycle?
From glucose degradation via glycolysis and the Krebs Cycle, how much ATP is produced from complete oxidation of one glucose?
From glucose degradation via glycolysis and the Krebs Cycle, how much ATP is produced from complete oxidation of one glucose?
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What effect does ATP concentration have on the energy level in cells affecting the Krebs Cycle?
What effect does ATP concentration have on the energy level in cells affecting the Krebs Cycle?
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Which reaction converts pyruvate to oxaloacetate in the context of anaplerosis?
Which reaction converts pyruvate to oxaloacetate in the context of anaplerosis?
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Which of the following molecules stimulates the α-ketoglutarate dehydrogenase complex?
Which of the following molecules stimulates the α-ketoglutarate dehydrogenase complex?
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What is the main regulatory factor for the Krebs Cycle concerning energy levels?
What is the main regulatory factor for the Krebs Cycle concerning energy levels?
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What happens to pyruvate when aerobic conditions are present?
What happens to pyruvate when aerobic conditions are present?
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Which of the following best describes the purpose of the TCA cycle?
Which of the following best describes the purpose of the TCA cycle?
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Which coenzymes are reduced during the TCA cycle?
Which coenzymes are reduced during the TCA cycle?
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What distinguishes the TCA cycle from glycolysis?
What distinguishes the TCA cycle from glycolysis?
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Which of the following is a result of each turn of the TCA cycle for one acetyl-CoA?
Which of the following is a result of each turn of the TCA cycle for one acetyl-CoA?
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Which molecules serve as electron acceptors in the TCA cycle?
Which molecules serve as electron acceptors in the TCA cycle?
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What is one of the roles of intermediates in the TCA cycle?
What is one of the roles of intermediates in the TCA cycle?
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What happens under anaerobic conditions regarding energy production?
What happens under anaerobic conditions regarding energy production?
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Study Notes
Krebs Cycle Overview
- The Krebs cycle, also known as the citric acid cycle or TCA cycle, is a crucial metabolic process.
- It's named after Hans Krebs, who received a Nobel Prize in 1953 for his work on it.
- The cycle is aerobic, meaning it requires oxygen.
- Pyruvate from glycolysis is oxidized completely to CO2 and H2O.
- Oxygen acts as the final electron acceptor.
- If the cell is under anaerobic conditions, energy production is less efficient (6%).
Krebs Cycle Energy Production
- The cycle produces reduced coenzymes (NADH and FADH2).
- Oxidative phosphorylation utilizes these coenzymes to create ATP (adenosine triphosphate).
- The cycle is amphibolic, meaning it has both catabolic and anabolic functions.
Krebs Cycle Two Purposes
- Oxidize acetyl-CoA: To CO2 releasing energy (ATP/GTP).
- Produce reducing power: (NADH, FADH2).
- Involved in the aerobic degradation of carbohydrates, lipids, and amino acids.
Krebs Cycle Intermediates
- The cycle's intermediates can be used for biosynthetic reactions.
- Supply precursors for the synthesis of carbohydrates, lipids, amino acids, nucleotides, and porphyrins.
- Intermediates can be shared with other metabolic pathways.
- Reactions feeding into the cycle replenish the cycle's intermediates.
Glycolysis vs. Krebs Cycle
- Glycolysis is a linear pathway occurring in the cytosol that doesn't require oxygen.
- The Krebs cycle is a cyclic pathway located in the mitochondrial matrix that requires oxygen.
Krebs Cycle Summary
- For each acetyl-CoA entering, two CO2 molecules are released.
- Coenzymes NAD+ and FAD are reduced.
- One GDP (or ADP) is phosphorylated.
- The initial acceptor (oxaloacetate) is reformed.
Krebs Cycle Energy Yield
- Each acetyl CoA entering the cycle produces 3 NADH, 1 FADH2 and 1 GTP (or ATP).
ATP Calculation
- Oxidation of one NADH yields 2.5 ATP.
- Oxidation of one FADH2 yields 1.5 ATP.
- Complete oxidation of one acetyl CoA yields 10 ATP.
- Complete oxidation of one glucose yields 32 ATP.
Krebs Cycle Regulation
- Regulation depends on the energy level of the cell (ATP, NADH, FADH2).
- High energy levels slow down the Krebs cycle.
- The reverse is also true; low energy levels increase activity.
Pathway Control Mechanisms
Control mechanisms include:
- Small molecule modulators (cycle products can inhibit).
- Covalent modification of cycle enzymes.
- Supply of acetyl-CoA.
Regulation of specific Krebs enzymes
- Citrate synthase
- Inhibitors: NADH, ATP, succinyl-CoA, citrate
- Stimulators: ADP
- Isocitrate dehydrogenase
- Inhibitors: NADH, ATP
- Stimulators: NAD+, ADP and Ca2+
- α-ketoglutarate dehydrogenase complex
- Inhibitors: NADH, ATP and succinyl-CoA
- Stimulators: NAD+, ADP, AMP
Anaplerotic Reactions
- Anaplerotic reactions replenish the Krebs cycle intermediates.
- Pyruvate carboxylase converts pyruvate to oxaloacetate, activated by acetyl-CoA.
- Degradation of odd-numbered fatty acids produces succinyl-CoA.
- Degradation of amino acids produces other intermediates.
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Description
Explore the intricacies of the Krebs cycle, or citric acid cycle, a fundamental metabolic pathway that plays a vital role in energy production. Learn about its aerobic nature, its importance in oxidizing acetyl-CoA, and the production of key coenzymes like NADH and FADH2. This overview includes the cycle's catabolic and anabolic functions, and its intermediates.