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The electrochemical connection in Phosphorylation and respiration is described with chemiosmatic theory.
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The chemi-osmatic theory is about an electrochemical link between respiration and phosphorylation. It was proposed by Peter Mitchell in 1961. He was awarded a Nobel prize in 1978 for his work..
Chemi – osmosis refers to the movement of chemical ions across a semi – permeable membrane down their electrochemical gradient (from an area of higher to lower concentration) similar to movement of water molecules by osmosis. An example of this is the generation of ATP by the movement of hydrogen ions across a membrane during cellular respiration or photosynthesis.
The chemi-osmotic theory deals with the generation of ATP by ATP synthase. Chemi-osmosis involves the pumping of protons through special channels in the membranes of mitochondria from the inner to the outer compartment.
The protons originating from the electron transport chain are translocated by the respiratory chain across the membrane from the M – side to the C – side of mitochondrial inner membrane. According to this theory, this translocation creates a pH change and a membrane potential.
Since the inner mitochondrial membrane is highly impermeable to protons (H+), these can reach the M-side only through the Proton channel of the ATPase.
When H+ moves from the C-side to M-side, the F 1 - ATPase operating in reverse, catalyzes the ATP synthesis. Conversely, when the F 1 -ATPase hydrolyzes ATP, it functions as a “proton pump” and ejects H+ from the M - side to C-side. For each NADH that is oxidized, 6 protons are translocated through the inner membrane, these 6 H+, when returning to the M-side through the F 1 -ATPase, gives rise to 3 ATP molecules.
According to this theory, the inner membrane of the mitochondria acts as a transducer, converting the energy, provided by the electrochemical gradient, into the chemical energy of ATP. The inner mitochondrial membrane is impermeable to both H+ and OH-. Therefore if pH differences are established across the membrane, they act as energy rich gradients.
When protons (H+) are ejected towards the cytoplasmic side (C side ) and OH- remain on the matrix side , that creates a difference in pH ( lower pH on C side and higher pH on M side) which results in an electrical potential.
The enzyme ATPase synthesizes ATP under the influence of the vectorial field of protein motive force generated by the transfer of the electrons through the respiratory chain and the release of protons on the C-side.
ATP is synthesized by its precursor ADP, by the enzyme ATP synthase also called complex V. This enzyme is found in the cristae and inner mitochondrial membrane. The ATP synthase has two parts F 0 and F 1. The part embedded within the membrane of mitochondria is called F 0. F 0 is made of c-ring and subunits a, two band F 1. This is a motor that is powered by H+ ions flowing across the membrane. The part within the mitochondria is called F 1. It is made up of subunits alpha, beta, gamma and delta. F 1 has a water soluble part which can hydrolyze ATP. This is another motor that is used to generate ATP. The F 0 region is similar to DNA helicase (enzyme which unzips DNA so that it can be used as a template for replication) while the F 1 -ATPase region is similar to the H+ motors that allows it to move.