Oxidative phosphorylation begins the process of synthesizing ATP using electrons from mitochondrial oxidation.
Crucial for activities requiring sustained ATP production, such as running.
Key players: NADH and FADH2 donate electrons to the electron transport chain (ETC) located in the inner mitochondrial membrane.
Electron Transport Chain (ETC):
Electrons pass through a series of carriers, releasing energy used to pump protons (H+) across the inner membrane.
Establishes a proton gradient, essential for ATP synthesis.
ATP Synthase:
Protons flow back into the matrix through ATP synthase, driving ATP production from ADP and inorganic phosphate (Pi).
Mitochondria have two membranes:
Outer Membrane: Contains porins that allow the transit of small molecules.
Inner Membrane: Highly folded (cristae) to increase surface area for ETC and ATP synthase.
Matrix: Contains enzymes for the citric acid cycle (CAC) and fatty acid oxidation.
The inner membrane lacks pores and selectively transports metabolites.
Mitochondria likely evolved from bacterial endosymbionts, forming a symbiotic relationship with larger host cells.
They contain their own DNA, a remnant from their bacterial ancestors, coding for some mitochondrial proteins.
Two main components:
Electron Transport: Electrons from NADH and FADH2 drive the reduction of oxygen to water.
ATP Synthesis: Proton gradient created by electron transport powers ATP synthesis.
Electron transfer potential is characterized by standard reduction potentials (E°'):
NADH E°': -0.32 volts (good electron donor)
Oxygen E°': +0.82 volts (strong oxidizing agent)
Change in standard reduction potential (ΔE°') for electron flow results in a significant free energy change, enabling ATP synthesis.
Electrons flow through complexes
Complex I (NADH-Q Oxidoreductase): accepts electrons from NADH.
Complex II (Succinate-Q Reductase): accepts electrons from FADH2.
Complex III (Q-Cytochrome c Oxidoreductase): transfers electrons to cytochrome c.
Complex IV (Cytochrome c Oxidase): reduces oxygen to water and pumps protons across the membrane.
Ubiquinone (Coenzyme Q) and cytochrome c function as mobile electron carriers between the complexes.
Complex I:
Contains FMN and iron-sulfur clusters; accepts electrons from NADH and reduces ubiquinone (Q) to QH2.
Pumps 4 protons across the membrane.
Complex II:
Receives electrons from FADH2, does not pump protons.
Complex III:
Uses QH2 to transfer electrons to cytochrome c; pumps 4 protons across the membrane.
Complex IV:
Accepts electrons from cytochrome c, reduces oxygen to water; pumps 2 protons across the membrane.
NADH generates approximately 2.5 ATP; FADH2 generates approximately 1.5 ATP.
Total ATP yield from glucose breakdown varies:
Glycolysis: 2 ATP (net gain) and 2 NADH
CAC: Generates 6 NADH and 2 FADH2 from glucose through 2 acetyl CoA, producing ATP through substrate-level phosphorylation.
Total ATP synthesis from complete breakdown of glucose (glycolysis + PDH + CAC + ETC) can reach up to 30-38 ATP, depending on reducing agents used and cellular conditions.
Certain poisons can inhibit electron transport:
Rotenone: Blocks electron flow from iron-sulfur clusters to ubiquinone in Complex I.
Cyanide: Blocks Complex IV, preventing oxygen reduction.
Carbon monoxide: Inhibits electron transport; may be lethal in high concentrations.
Importance of monitoring environmental conditions to prevent poisoning.
The mitochondria play a critical role in cellular respiration and energy production through electron transport and ATP synthesis.
Understanding the function and mechanism of the ETC and how energy is harvested from electrons is key for comprehending cellular metabolism.