The electron transport chain (ETC) is a series of protein complexes located in the inner mitochondrial membrane that transfers electrons from electron carriers to oxygen. This establishes an electrochemical gradient that drives ATP synthesis. Electrons are passed through complexes I-IV via redox reactions, pumping protons out of the membrane and creating a proton gradient. Complex V uses this gradient to synthesize ATP from ADP and phosphate through oxidative phosphorylation. The ETC and oxidative phosphorylation are essential for aerobic respiration in eukaryotic cells.
The electron transport chain (ETC) is a series of protein complexes located in the inner mitochondrial membrane that transfers electrons from electron carriers to oxygen. This establishes an electrochemical gradient that drives ATP synthesis. Electrons are passed through complexes I-IV via redox reactions, pumping protons out of the membrane and creating a proton gradient. Complex V uses this gradient to synthesize ATP from ADP and phosphate through oxidative phosphorylation. The ETC and oxidative phosphorylation are essential for aerobic respiration in eukaryotic cells.
The electron transport chain (ETC) is a series of protein complexes located in the inner mitochondrial membrane that transfers electrons from electron carriers to oxygen. This establishes an electrochemical gradient that drives ATP synthesis. Electrons are passed through complexes I-IV via redox reactions, pumping protons out of the membrane and creating a proton gradient. Complex V uses this gradient to synthesize ATP from ADP and phosphate through oxidative phosphorylation. The ETC and oxidative phosphorylation are essential for aerobic respiration in eukaryotic cells.
The Electron Transport Chain (ETC) is a series of protein complexes located in the inner mitochondrial membrane in eukaryotic cells or the plasma membrane in prokaryotic cells. These complexes work together to transfer electrons and create an electrochemical gradient that drives the synthesis of ATP. The ETC is located in the inner mitochondrial membrane in eukaryotic cells. In prokaryotes, it is embedded in the plasma membrane. The ETC consists of a series of protein complexes, including Complex I (NADH dehydrogenase), Complex II (Succinate dehydrogenase), Complex III (Cytochrome bc1 complex), and Complex IV (Cytochrome c oxidase). Electrons from electron donors (NADH and FADH 2) are sequentially transferred through the protein complexes. The electrons move through redox reactions, leading to the reduction of molecular oxygen (O2) at the end of the chain. The ETC involves a series of redox reactions where electrons are transferred between protein complexes, which contain various electron carriers, including flavins, iron- sulfur clusters, and heme groups. Protons (H+) are actively pumped across the inner mitochondrial membrane during the transfer of electrons through Complexes I, III, and IV. This creates a proton gradient or proton motive force (PMF). The proton gradient generated across the inner mitochondrial membrane is a form of potential energy. The proton motive force is utilized in oxidative phosphorylation for the synthesis of ATP. The final electron acceptor in the ETC is molecular oxygen (O 2), which is reduced to water (H2O). Oxygen consumption is a crucial indicator of ETC activity. The ETC is coupled with oxidative phosphorylation, leading to the synthesis of ATP. ATP synthase utilizes the proton motive force to generate ATP from ADP and inorganic phosphate (Pi). Complexes of ETC: Complex I - NADH Dehydrogenase (NADH-CoQ Reductase): Complex I is responsible for the transfer of electrons from NADH to coenzyme Q (CoQ) and is the entry point for electrons into the ETC. NADH is oxidized, and electrons are transferred to a series of iron-sulfur clusters within Complex I. Simultaneously, protons (H+) are pumped across the inner mitochondrial membrane from the matrix to the intermembrane space. Complex I contributes to the proton motive force by pumping protons across the inner mitochondrial membrane.
Complex II - Succinate Dehydrogenase:
Complex II participates in both the TCA cycle and the ETC. It transfers electrons from succinate to CoQ. Succinate is oxidized to fumarate in the TCA cycle, and electrons are transferred to flavin adenine dinucleotide (FAD) within Complex II. Then, electrons are transferred to CoQ. Unlike Complex I, Complex II does not actively pump protons. However, it contributes to the overall electron flow and proton gradient.
Complex III - Cytochrome bc1 Complex (CoQH2-Cytochrome c Reductase):
Complex III transfers electrons from CoQ to cytochrome c and is a crucial site for preventing the leakage of electrons. Electrons from CoQ are transferred through cytochrome b and c1 to cytochrome c. Complex III actively pumps protons across the inner mitochondrial membrane into the intermembrane space.
Complex IV - Cytochrome c Oxidase:
Complex IV is the terminal complex that transfers electrons from cytochrome c to molecular oxygen (O2), forming water. Electrons from cytochrome c are transferred through cytochrome a and a3 to oxygen, which is reduced to water. Complex IV actively pumps protons, contributing to the establishment of the proton motive force.
Complex V - ATP Synthase (F1Fo ATPase):
Complex V synthesizes ATP using the energy stored in the proton motive force generated by the previous complexes. Protons flow back into the mitochondrial matrix through ATP synthase, driving the rotation of the enzyme"s components and allowing the synthesis of ATP from ADP and inorganic phosphate (Pi). Complex V does not actively pump protons; instead, it utilizes the proton motive force generated by the other complexes.
Mechanism of Electron Transport Chain:
Electrons from NADH, generated during glycolysis and the TCA cycle, are donated to Complex I (NADH dehydrogenase), leading to the oxidation of NADH and the transfer of electrons to the flavin mononucleotide (FMN) within Complex I. As electrons move through Complex I, protons are actively pumped from the mitochondrial matrix to the intermembrane space. Electrons are transferred from Complex I to Coenzyme Q (CoQ), leading to the reduction of CoQ to CoQH2. Electrons from FADH2, produced in the TCA cycle, enter Complex II (Succinate dehydrogenase), resulting in the oxidation of FADH2 and the transfer of electrons through iron-sulfur clusters within Complex II. Electrons from Complex II are transferred to CoQ, forming CoQH2. CoQH2 transfers electrons to Complex III (cytochrome bc1 complex), leading to the active pumping of protons across the inner mitochondrial membrane. Electrons move through cytochrome b and c1, ultimately reaching cytochrome c. Cytochrome c transfers electrons to Complex IV (cytochrome c oxidase), leading to the reduction of oxygen (O2) to water (H2O). This step completes the electron transport chain. Protons pumped across the inner mitochondrial membrane during the previous steps flow back into the mitochondrial matrix through Complex V (ATP synthase). The flow of protons through ATP synthase powers the rotation of its components. Oxidative phosphorylation: Oxidative phosphorylation is the process by which ATP is synthesized using the energy released during the transfer of electrons in the ETC. It occurs in the inner mitochondrial membrane and involves the enzyme ATP synthase. ATP synthase is a molecular machine embedded in the inner mitochondrial membrane. It consists of a rotor (Fo) and a catalytic knob (F1). Protons flow back into the mitochondrial matrix through ATP synthase, driven by the proton motive force. The flow of protons causes the rotor to spin within ATP synthase, inducing conformational changes in the catalytic knob. As the rotor turns, the conformational changes in the catalytic knob enable the synthesis of ATP from ADP and inorganic phosphate (Pi). This process is known as chemiosmotic coupling, as it couples the flow of protons (chemiosmosis) with ATP synthesis. Oxidative phosphorylation is tightly coupled with the ETC. The energy released during the transfer of electrons down the ETC establishes the proton motive force necessary for ATP synthesis.