Phase 1: Glycolysis
10 reactions converting glucose (6 carbon) into two pyruvate (3 carbon) molecules.
Minimal energy is released; no CO2 or water are produced.
Potential energy remains in the food molecules.
Phase 2: Pyruvate Oxidation and Krebs Cycle (Citric Acid Cycle)
Pyruvate is oxidized and CO2 is produced.
Energy extraction continues as carbons are fully respired out (breathing out).
Key reactions occur in the mitochondria.
Phase 3: Electron Transport Chain and Chemiosmosis
Oxygen serves as the terminal electron acceptor, combining with protons and electrons, producing water.
ATP synthesis primarily occurs through oxidative phosphorylation.
Electron transport chains are crucial for creating proton gradients, not directly for ATP production.
Substrate Level Phosphorylation
Accounts for some ATP production during glycolysis and Krebs cycle but less efficient
Oxidative Phosphorylation
Major ATP production method derived from the electrochemical gradient created by the electron transport chain.
ATP synthase (machine) synthesizes ATP from ADP and inorganic phosphate through chemiosmosis.
Functional Importance of Enzymes
Enzymes are regulated based on the availability of substrates and the need for product.
Allosteric regulation allows enzymes to either ramp up or decrease their activity based on the cellular conditions.
Fermentation Process
Occurs when oxygen (terminal electron acceptor) is limited, primarily after glycolysis.
No ATP is produced during fermentation; its purpose is to regenerate NAD+ from NADH to keep glycolysis operational.
Fermentation can increase glycolysis rates significantly—10 to 20 times faster.
Alcoholic Fermentation
Performed by yeast (e.g., brewer's yeast) producing ethanol and CO2.
Exploited in brewing and baking industries.
Lactic Acid Fermentation
Occurs in human muscle cells when oxygen is scarce, producing lactic acid.
Responsible for muscle fatigue during strenuous activity; lactic acid is eventually transported to the liver for processing.
Humans can utilize carbohydrates, fats, and proteins for energy.
Amino acids from proteins can enter metabolic pathways after deamination, connecting to glycolysis or Krebs cycle.
Fatty acids are converted into acetyl CoA, feeding directly into the Krebs cycle, showcasing metabolic efficiency without needing separate extensive pathways for each type.
Without oxygen, aerobic organisms can only rely on glycolysis, reducing ATP yield significantly (36 to 2 ATP per glucose).
Rapid glycolysis may deplete food and result in cell death if oxygen is not restored.
Allosteric Regulation
Regulatory molecules bind to allosteric sites, changing conformational shape, either activating or inhibiting enzyme functionalities.
Feedback inhibition occurs when the end product of a metabolic pathway inhibits an upstream process to maintain balance.
Fructose-1,6-bisphosphate formation represents regulatory point:
High ATP levels signal to slow down glycolysis, while high ADP levels stimulate activity, illustrating the balance of energy needs in cell metabolism.