Metabolism and Energy Concepts
Metabolism: All chemical reactions within a cell.
Catabolism: Breakdown of molecules, releasing energy (exergonic).
Anabolism: Building of molecules, requiring energy (endergonic).
Exergonic: Reactions that release energy (e.g., cellular respiration).
Endergonic: Reactions that absorb energy (e.g., protein synthesis).
Hydrolysis: Breaking molecules by adding water (e.g., ATP → ADP + Pi).
Dehydration Synthesis: Building molecules by removing water (e.g., forming proteins).
Denature: Structural change in a protein (e.g., enzyme) that inhibits function.
Activation Energy: Minimum energy needed to start a chemical reaction.
Heterotrophs: Organisms that consume organic molecules for carbon.
Autotrophs: Organisms that use CO₂ as their carbon source.
Phototrophs: Obtain energy from light.
Chemotrophs: Obtain energy from chemical compounds.
Oxidative Phosphorylation: Produces ATP via the electron transport chain (ETC).
Aerobic Respiration: Uses oxygen as the final electron acceptor in the ETC.
Anaerobic Respiration: Uses a non-oxygen molecule (e.g., nitrate, sulfate) as the final electron acceptor.
Law: Energy cannot be created or destroyed, only transformed.
Biochemical Pathways: Cells convert chemical energy in nutrients into usable energy (ATP) through pathways like cellular respiration and photosynthesis.
Structure: Composed of adenine, ribose, and three phosphate groups.
Energy Storage: Energy is stored in high-energy phosphate bonds.
Energy Transfer: When ATP is hydrolyzed to ADP + Pi, energy is released (exergonic reaction).
Energy Release: Drives cellular work (e.g., muscle contraction, biosynthesis).
Energy Storage: When energy is required, ADP + Pi are converted back to ATP (endergonic reaction).
Oxidation: Loss of electrons.
Reduction: Gain of electrons.
Role in ETC: As electrons are passed through the electron transport chain, energy is released and used to pump H⁺ ions, generating a proton gradient.
Location: Cytoplasm.
Inputs: Glucose, 2 ATP, 2 NAD⁺.
Outputs: 2 Pyruvate, 4 ATP (net 2 ATP), 2 NADH.
Location: Mitochondrial matrix (eukaryotes) / Cytoplasm (prokaryotes).
Inputs: 2 Pyruvate, 2 NAD⁺.
Outputs: 2 Acetyl-CoA, 2 CO₂, 2 NADH.
Location: Mitochondrial matrix (eukaryotes) / Cytoplasm (prokaryotes).
Inputs: 2 Acetyl-CoA, 6 NAD⁺, 2 FAD.
Outputs: 4 CO₂, 2 ATP, 6 NADH, 2 FADH₂.
Location:
Eukaryotes: Inner mitochondrial membrane.
Prokaryotes: Plasma membrane.
Process:
Electron carriers (NADH, FADH₂) donate electrons to the ETC.
H⁺ ions are pumped across the membrane, creating a proton gradient.
ATP synthase uses this gradient to convert ADP + Pi to ATP.
Final Electron Acceptor:
Aerobic: Oxygen, producing H₂O.
Anaerobic: Other molecules (e.g., nitrate, sulfate).
Location: Cytoplasm.
Process: Generates ATP through glycolysis alone, regenerating NAD⁺ for glycolysis.
When: Occurs when oxygen (or final electron acceptor) is not available.
Inputs: Glucose.
Outputs: Lactic acid, 2 ATP.
Example: Muscle cells, Lactobacillus bacteria.
Inputs: Glucose.
Outputs: Ethanol, CO₂, 2 ATP.
Example: Yeast, used in bread and alcohol production.
Respiration (Aerobic): Produces ~38 ATP per glucose.
Fermentation: Produces only 2 ATP per glucose.
Carbohydrates: Enter as glucose in glycolysis.
Lipids: Broken down to glycerol (enters glycolysis) and fatty acids (enter Krebs cycle via β-oxidation).
Proteins: Broken down to amino acids, deaminated, and enter glycolysis or Krebs cycle.
Made of proteins, sometimes with cofactors (e.g., vitamins, metal ions).
Substrate: The reactant that binds to the enzyme's active site.
Product: The result of the enzymatic reaction.
Active Site: The region on the enzyme where the substrate binds.
Activation Energy: Enzymes lower the activation energy, allowing reactions to occur faster.
Each enzyme works with a specific substrate.
Example: Lactase only acts on lactose.
Temperature:
Optimal range: Too high or too low denatures the enzyme.
pH:
Each enzyme has an optimal pH. Extreme pH can denature enzymes.
Substrate Concentration:
Increasing substrate increases activity until the enzyme is saturated.
Inhibitors:
Competitive Inhibitors: Bind to the active site, blocking the substrate.
Non-Competitive Inhibitors: Bind elsewhere, changing enzyme shape.
This structured breakdown covers essential concepts, pathways, and mechanisms needed for a solid understanding of metabolism and enzyme activity. Would you like more details on specific metabolic pathways or enzyme examples?