Cellular-Respiration-Aerobic-Respiration
Major Steps in Aerobic Respiration
Pyruvate Oxidation
Krebs Cycle/Tricarboxylic Acid Cycle/Citric Acid Cycle
Oxidative Phosphorylation (Electron Transport Chain & Chemiosmosis)
Pyruvate Oxidation
Converts each pyruvate molecule from glycolysis to a 2-carbon molecule (acetyl CoA) in the mitochondrial matrix.
Known as a “link reaction,” it connects glycolysis and the citric acid cycle.
NADH Management
Importance of NAD+: Essential for glycolysis; without it, glycolysis halts.
Regeneration of NAD+:
When oxygen is present, NADH donates electrons to the electron transport chain, regenerating NAD+.
In absence of oxygen, cells use fermentation, a simpler pathway where NADH donates its electrons to another molecule, regenerating NAD+ without producing ATP.
Krebs Cycle/Citric Acid Cycle/Tricarboxylic Acid Cycle
Takes place in the mitochondrial fluid matrix.
Pyruvic acid is restructured to acetyl CoA, which enters the cycle.
Produces NADH, CO2, and hydrogen through various enzymatic reactions.
Discovered by biochemist Hans Adolf Krebs.
Steps in Krebs Cycle
Step 1
Acetyl CoA combines with oxaloacetate (4-carbon) to form citrate (6-carbon); catalyzed by Citrate synthase.
Step 2
Citrate is converted to isocitrate via two steps:
Dehydration to form cis-aconitate
Hydration of cis-aconitate to form isocitrate, catalyzed by aconitase.
Step 3
Isocitrate oxidizes, releasing CO2, forming α-ketoglutarate (5-carbon); NAD+ is reduced to NADH, catalyzed by isocitrate dehydrogenase.
Step 4
α-ketoglutarate oxidizes, releasing CO2 and reducing NAD+ to NADH; forms succinyl CoA, catalyzed by α-ketoglutarate dehydrogenase.
Step 5
In succinyl-CoA, CoA is replaced by a phosphate, transferring to GDP to form GTP, resulting in succinate (4-carbon); catalyzed by succinyl-CoA synthetase.
Step 6
Succinate oxidized to fumarate (4-carbon); forms FADH2; catalyzed by succinate dehydrogenase.
Step 7
Water is added to fumarate to form malate (4-carbon); catalyzed by fumarase.
Step 8
Malate oxidizes to regenerate oxaloacetate; reduces NAD+ to NADH, catalyzed by malate dehydrogenase.
Overview of Reactions in Krebs Cycle
Condensation
Dehydration & Hydration
Oxidative Decarboxylation
Substrate-level Phosphorylation
Dehydrogenation
Hydration
Dehydrogenation
Products of the Krebs Cycle
For one turn:
2 carbons from acetyl CoA enter
2 CO2 released
3 NADH and 1 FADH2 produced
1 ATP or GTP produced
Multiply by 2 for glucose breakdown.
Electron Transport Chain + Chemiosmosis
Composed of protein complexes that couple redox reactions to proton pumping, generating an electrochemical gradient.
Purpose
ATP production; located in the inner mitochondrial membrane.
Characteristics
Electrons from metabolism are transported to O2, the final electron acceptor.
Maximally utilizes body’s oxygen and functions as a final common pathway of metabolism.
Components of the Electron Transport Chain
Complexes Overview
Complex I - NADH Dehydrogenase
Collects electrons from NADH; releases 4 H+ ions.
Complex II - Succinate Dehydrogenase
Receives FADH2; transfers its electrons to CoQ; does not release protons.
Coenzyme Q (CoQ)
Lipid soluble, non-protein component of ETC; mobile.
Complex III - Cytochrome Reductase
Releases 4 H+ and transfers electrons to cytochrome c.
Complex IV - Cytochrome Oxidase
Releases 2 H+; final electron acceptor oxygen splits into water.
ATP Synthase
Uses the proton gradient generated by the electron transport chain to synthesize ATP.
Consists of two domains: F0 (membrane spanning) and F1 (extramembranous).
Inhibitors of ETC
Compounds that block electron passage, inhibiting ATP synthesis.
Total ATP Yield per Glucose
Overall yield from glycolysis to aerobic respiration:
Glycolysis: 4 ATP (2 net) + 2 NADH (yielding 4 ATP)
Pyruvate Conversion: 2 NADH (yielding 6 ATP)
Krebs Cycle: 2 ATP + 2 FADH2 (yielding 3-4 ATP) + 6 NADH (yielding 15-18 ATP)
Total: 38 ATP per glucose (32-38 depending on NADH/FADH2 conversion rates).