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Glucose breakdown and energy production are vital cellular processes. splits glucose into , while the further breaks down . These steps generate ATP and electron carriers for the .

The electron transport chain uses electron carriers to create a proton gradient. This gradient powers , producing most of the cell's ATP. reverses this process, making glucose from non-carbohydrate sources when needed.

Glycolysis and the Krebs Cycle

Steps and outcomes of glycolysis

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  • breaks down glucose into two pyruvate molecules through a 10-step process
    • ATP phosphorylates glucose forming (catalyzed by hexokinase)
    • ATP phosphorylates creating (catalyzed by )
    • Fructose-1,6-bisphosphate splits into (G3P) and (DHAP), two 3-carbon molecules
    • Oxidation and phosphorylation of G3P yields
    • Conversion of 1,3-bisphosphoglycerate to generates 2 ATP
    • 3-phosphoglycerate converts to
    • 2-phosphoglycerate converts to (PEP)
    • PEP converts to pyruvate generating 2 ATP
  • Glycolysis yields a net energy outcome of 2 ATP and 2 per glucose molecule (glucose to 2 pyruvate)

Pyruvate in the Krebs cycle

  • Pyruvate converts to releasing CO2 and generating 1 NADH (catalyzed by )
  • Acetyl-CoA combines with forming
  • Citrate converts to
  • Oxidation of isocitrate to releases CO2 and generates 1 NADH
  • Oxidation of α-ketoglutarate to releases CO2 and generates 1 NADH
  • Conversion of succinyl-CoA to generates 1 (or ATP)
  • Oxidation of succinate to generates 1
  • Fumarate undergoes hydration to
  • Oxidation of malate to oxaloacetate generates 1 NADH
  • Each pyruvate molecule yields 3 NADH, 1 FADH2, 1 GTP (or ATP), and 2 CO2 in the ()

Electron Transport Chain and ATP Synthesis

Electron flow in cellular respiration

  • The consists of protein complexes in the inner mitochondrial membrane
  • NADH and FADH2 from glycolysis and the Krebs cycle donate electrons to the ETC
    • Complex I receives electrons from NADH
    • Complex II receives electrons from FADH2
  • Electrons undergo redox reactions as they pass through ETC complexes (I, III, and IV)
  • Protons (H+) are pumped from the mitochondrial matrix into the intermembrane space during electron flow
  • The ETC-generated proton gradient drives ATP synthesis via oxidative phosphorylation
  • Oxygen acts as the final electron acceptor combining with protons to form water (cellular respiration)

Mechanism of oxidative phosphorylation

  • ATP synthase, an enzyme complex in the inner mitochondrial membrane, synthesizes ATP
  • The ETC-generated proton gradient drives protons back into the mitochondrial matrix through ATP synthase
  • Proton flow through ATP synthase causes conformational changes that catalyze ADP phosphorylation to ATP
  • links the proton gradient's chemical energy to ATP synthesis
  • The number of ATP molecules generated per NADH and FADH2 depends on the specific ETC complexes involved
    • NADH typically yields 2.5-3 ATP
    • FADH2 typically yields 1.5-2 ATP

Gluconeogenesis

Glucose production via gluconeogenesis

  • synthesizes new glucose molecules from non-carbohydrate precursors
  • Main gluconeogenic substrates include:
    • Amino acids (from protein catabolism)
    • Glycerol (from triglyceride breakdown)
    • Lactate (from anaerobic glycolysis in skeletal muscle)
  • The liver is the primary site of gluconeogenesis with minor contributions from the kidneys
  • Key gluconeogenic steps:
    1. carboxylates pyruvate to oxaloacetate
    2. decarboxylates and phosphorylates oxaloacetate forming phosphoenolpyruvate (PEP)
    3. converts fructose-1,6-bisphosphate to fructose-6-phosphate
    4. removes the phosphate from yielding free glucose
  • Hormones like and cortisol regulate gluconeogenesis promoting the process during fasting or stress (low blood glucose)

Additional Carbohydrate Metabolism Pathways

Glycogen metabolism

  • Glycogenesis: synthesis of glycogen from glucose for storage
  • : breakdown of glycogen to glucose-1-phosphate for energy production

Alternative glucose metabolism

  • : generates NADPH and ribose-5-phosphate for biosynthetic processes

Metabolic regulation

  • Allosteric regulation of key enzymes (e.g., phosphofructokinase) controls flux through metabolic pathways
  • Hormonal control (e.g., , ) coordinates carbohydrate metabolism with whole-body energy needs
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© 2024 Fiveable Inc. All rights reserved.
AP® and SAT® are trademarks registered by the College Board, which is not affiliated with, and does not endorse this website.

© 2024 Fiveable Inc. All rights reserved.
AP® and SAT® are trademarks registered by the College Board, which is not affiliated with, and does not endorse this website.
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