The electron transport chain's main function is to transfer electrons from NADH and FADH2, generated during glycolysis and the Krebs cycle, to oxygen, the final electron acceptor.

The electron transport chain is located on the inner mitochondrial membrane, which is folded into cristae to increase the surface area for efficient electron transfer.

Complex I, also known as NADH dehydrogenase, is the first enzyme complex in the electron transport chain that receives electrons from NADH generated during glycolysis and the Krebs cycle.

Coenzyme Q and cytochrome c are mobile electron carriers that transfer electrons between the different complexes of the electron transport chain.

Complex III, also known as cytochrome c reductase, pumps protons across the inner mitochondrial membrane, contributing to the proton gradient necessary for ATP synthesis.

Oxygen is the final electron acceptor in the electron transport chain, receiving electrons from cytochrome c oxidase and combining with protons to form water.

Oxidative phosphorylation is the process by which ATP is synthesized in the mitochondria using the energy released from the electron transport chain.

ATP synthase is an enzyme complex located in the inner mitochondrial membrane that uses the energy from the proton gradient to synthesize ATP from ADP and inorganic phosphate.

During oxidative phosphorylation, approximately 32 ATP molecules are produced per glucose molecule, representing the majority of ATP generated during cellular respiration.

The electron transport chain is crucial in cellular respiration as it generates most of the ATP, produces NADH and FADH2, and creates a proton gradient, which are all essential for energy production.

Complex I, also known as NADH dehydrogenase, contains iron-sulfur proteins that participate in the transfer of electrons from NADH to coenzyme Q.

Cytochrome c oxidase is the final enzyme complex in the electron transport chain that transfers electrons from cytochrome c to oxygen, the final electron acceptor.

Oxidative phosphorylation is a highly efficient process, with an overall efficiency of approximately 40%, meaning that around 40% of the energy stored in glucose is converted into ATP.

Complex I, also known as NADH dehydrogenase, is also referred to as the rotenone-sensitive complex because it is inhibited by the chemical rotenone.

The proton gradient across the inner mitochondrial membrane drives the synthesis of ATP by ATP synthase through a process called chemiosmosis.