Cellular respiration is the process by which cells, mainly on glucose, convert the nutrients to adenosine triphosphate energy. This is a multi-step process involving glycolysis, the Krebs cycle, and the electron transport chain. At the end, there is oxidative phosphorylation and chemiosmosis, which are both vital for energy production.
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Oxidative phosphorylation occurs when there is electron transport via protein complexes in the inner mitochondrial membrane, ultimately reducing the oxygen to water. This electron transfer at each step forms a proton gradient across the membrane. Such gradient flow drives the making of ATP through chemiosmosis. The duo is extremely effective in the production of ATP energy currency necessary for driving a variety of cellular functions and the survival of the organism as a whole.
Cellular respiration is described below-
Glycolysis
This is the first step in cellular respiration and happens in the cytoplasm. It is the pathway by which one molecule of glucose is broken down to become two molecules of pyruvate, for a net gain of two ATP molecules and two NADH molecules.
Krebs Cycle (Citric Acid Cycle)
This entire process occurs in the mitochondrial matrix, where each pyruvate is converted to acetyl-CoA and then enters into the cycle. Further, with many catalyzed enzyme reactions, it undergoes reduction into carbon dioxide, ATP, NADH, FADH2, and other activated high-energy electron carriers ready for the next process.
Oxidative Phosphorylation
This is the step of the electron transport chain and chemiosmosis and takes place in the inner mitochondrial membrane, where most of the ATP is synthesized.
Explanation of oxidative phosphorylation.
Oxidative phosphorylation is the final phase of cellular respiration whereby the high-energy electrons from NADH and FADH2 pass to the oxygen through the ETC, forming water.
Role in ATP production.
This is the major way of synthesizing ATP. In this context, electron transfer provides energy used in the pumping of protons across the mitochondrial inner membrane to generate a gradient of protons which then drives the process of ATP synthesis.
Components of the ETC.
ETC includes four main protein complexes, I-IV, and mobile electron carriers like ubiquinone, Q, or CoQ, and the cytochrome c.
Oxidative Phosphorylation and Chemiosmosis: Definition, Topics, Steps
Step by Step electron carriers pass their electrons as donated from NADH and FADH2 through the complexes, moving protons into the intermembrane space. Electron transport is coupled to the reduction of oxygen into water.
NADH and FADH2
NADH and FADH2: They are byproducts of the glycolysis and Kreb cycle. They are electron donors for the Electron Transport Chain that then drives the oxidative phosphorylation.
Transfer of electrons to the ETC.
NADH gives its electrons to Complex I and those from FADH2 to Complex II. The transfer hence occurs down the chain transport till the reduction of oxygen at the last of the transport chain.
Protons move across the inner mitochondrial membrane through the action of the enzyme ATP synthase. This process is powered by the gradient that is built during the ETC.
Proton gradient and its significance.
It is this gradient that generates an electrochemical potential or, across the membrane, which drives the synthesis of ATP.
Generation of proton gradient.
As electrons flow through the ETC, protons get pumped into the intermembrane space, thus developing a proton gradient, otherwise known as proton motive force.
Movement of protons across the inner mitochondrial membrane.
The protons then flow back into the mitochondrial matrix through the enzyme ATP synthase and drive the synthesis of ATP from ADP and inorganic phosphate.
Structure and function of ATP synthase.
The ATP synthase enzyme is multimeric, multi-subunit, and traverses the inner mitochondrial membrane with a rotor component and a stator component. The movement of protons through the rotor causes it to spin, which drives the production of ATP.
Mechanism of ATP production.
The flow of protons through ATP synthase applies released energy to ADP and inorganic phosphate to form ATP.
Oxidative phosphorylation and chemiosmosis are integrated processes; together they provide most of the ATP produced in the process of cellular respiration.
How the ETC and chemiosmosis work together.
During oxidative phosphorylation, the electron transport chain includes four protein complexes, namely Complexes I-IV, situated in the inner mitochondrial membrane. These protein complexes, in effect, transfer electrons from NADH and FADH2 through them, which provokes the pumping of protons—or H⁺ ions—from the mitochondrial matrix to the intermembrane space.
This electron transport, exactly like what happened during photosynthesis, is also coupled to the reduction of oxygen as the final electron acceptor to water.
Proton gradient formation: Due to the pumping action, an ETC induces a large concentration of protons within the intermembrane space relative to that within the mitochondrial matrix, thereby forming the gradient of protons. The gradient formed across in inner mitochondrial creates an electrochemical potential.
Overall production of ATP.
Chemiosmosis exploits the proton gradient developed by the Electron Transfer Chain. The protons diffuse back into the mitochondrial matrix; as they do so, they pass through a protein complex called ATP synthase, functioning like a molecular turbine. Energy is provided for the conversion of ADP and inorganic phosphate to ATP as protons move through it.
Coupling: The energy from this proton motive force, because of ETC itself, is used to power the synthesis of ATP via chemiosmosis. Electron transport and proton gradient are thus coupled to the synthesis of ATP in driving ATP production efficiently. Again, this plays a vital role in several cellular activities.
The process by which ATP is made on the inner mitochondrial membrane is referred to as oxidative phosphorylation.
Chemiosmosis is responsible for the transfer of protons across the membrane, the formation of a proton motive force, and powering the synthesis of ATP with the aid of ATP synthase.
The ETC includes complex I (NADH dehydrogenase), complex II (succinate dehydrogenase), complex III (cytochrome bc1 complex), complex IV (cytochrome c oxidase), and cytochrome c.
The inhibitors can inhibit electron flow through the ETC, which will decrease the amount of produced ATP and affect the cellular energy levels.
Other examples include mitochondrial myopathy, Leigh syndrome, and MELAS.
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