Cells utilize various molecules generated from the breakdown of sugars and fats to create organic molecules.
Discussion of ATP production mechanisms is deferred until Chapter 14.
Oxidizing glucose directly to CO2 and H2O would release excessive energy at once, making it unrecoverable. Instead, cells use enzymes for controlled oxidation.
Enzymatic breakdown occurs in steps, yielding energy in small amounts captured by activated carriers (e.g., ATP, NADH).
ATP can be synthesized through:
Direct coupling of exergonic reactions to ATP formation.
Oxidative phosphorylation, detailed in Chapter 14.
Food molecule breakdown occurs in three stages:
Stage 1: Breakdown of macromolecules to simple subunits.
Stage 2: Conversion of simple subunits to acetyl CoA, producing limited ATP and NADH.
Stage 3: Complete oxidation of acetyl CoA, generating significant ATP.
Stage 1: Conversion of polymers (proteins, polysaccharides, fats) into monomeric subunits (amino acids, sugars, fatty acids).
Stage 2: Glycolysis splits glucose into pyruvate, producing ATP and NADH in the cytosol. Pyruvate enters the mitochondria for further processing.
Stage 3: Acetyl CoA enters the citric acid cycle within the mitochondrial matrix, driving further oxidation and ATP production via oxidative phosphorylation.
Glycolysis is a ten-step process crucial for breaking down glucose:
Investment: Initial steps cost two ATP to prepare glucose for breakdown.
Payoff: Subsequent steps yield four ATP and produce NADH, leading to a net gain of two ATP per glucose.
Each reaction in glycolysis is catalyzed by a specific enzyme.
ATP formation occurs through substrate-level phosphorylation in glycolysis, where phosphate groups are directly transferred from substrate to ADP.
NADH generated in glycolysis contributes to ATP production when electrons are transferred to the electron-transport chain during oxidative phosphorylation.
Under anaerobic conditions, glycolysis can occur without oxygen, leading to fermentation, which generates limited ATP while converting pyruvate to lactate or ethanol, thus regenerating NAD+.
Anaerobic microorganisms use a different final electron acceptor in anaerobic respiration, contrasting with fermentation by utilizing the electron-transport chain.
ATP and NADH generated in catabolic processes are critical for driving biosynthetic reactions and maintaining cellular functions.
Pyruvate produced from glycolysis is converted to acetyl CoA and subsequently processed in the citric acid cycle generating NADH, FADH2, and GTP, primarily within the mitochondrial matrix.
Fatty acids are also converted to acetyl CoA, enhancing energy extraction during catabolism within mitochondria.
NADH and FADH2 donate high-energy electrons to the electron-transport chain, triggering ATP synthesis through chemiosmosis.
Oxygen is vital as it serves as the terminal electron acceptor in mitochondrial respiration, producing water.
Cellular metabolism is tightly regulated through feedback mechanisms, allowing cells to adapt and maintain energy balance.
Gluconeogenesis is regulated to synthesize glucose in response to energy needs, utilizing specific bypass enzymes for irreversible steps in glycolysis.
Cells store glucose as glycogen and fats as triacylglycerols for future energy needs, mobilizing energy in response to hormonal signals during fasting or strenuous activity.
Glycogen serves as a readily available glucose source for brief energy demands, while fats provide a denser energy reserve over prolonged periods.
Food breakdown is organized in distinct cellular compartments.
Processes of glycolysis, citric acid cycle, and oxidative phosphorylation underlie cellular energy metabolism.
Regulated feedback controls allocate resources between energy production and storage, shaping cellular responses to fluctuating energy supply.