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Glycolysis of 1 glucose molecule
(transferred to electron transport system; in cardiac muscle and liver cells, it is first accepted by the the electron acceptor , NAD+ when it enters the ETS and in 3 points of the ETS, energy released by oxidation is sufficient to create ATP molecule from oxidative phosphorylation. This explains why in cardiac muscle and liver cells, only 36 ATP are produced instead of 38 ; in skeletal muscle and nervous tissues, it is first accepted electron acceptor in ETS, Coenzmye Q and only in 2 points where the energy released by oxidation is sufficient to create ATP molecule from oxidative phosphorylation. This explains why in skeletal muscle and nervous tissue, 38 ATP are produced). NADH + H+ produced in glycolysis has to be transferred to the mitochondrion to enter ETS from cytoplasm. This is where it differs from the NADH + H+ produced in Link's reaction and Kreb's cycle where they directly enter the ETS with each producing 3 ATPs.
Link Reaction Pyruvate Oxidation
In the process a molecule of CO2 and 2H are removed. The hydrogen atoms are transferred to the Electron Transport System. The 2C acetyl coenzyme A disassociates forming coenzyme A acetate which enters the Krebs Cycle.
Krebs CycleAcetyl coenzyme A from Link Reaction is used to make:
The most important part of the Krebs Cycle is the release of hydrogen ions to be used in the Electron Transport System for generation of ATP. Electron Transport System
The hydrogen ions received from the Krebs Cycle are attached to hydrogen carriers (NAD and FAD) which are reduced. As reduced NAD and FAD are passed along the electron transport chain, the hydrogens are removed and the hydrogen atoms split into:
At the end of the system the hydrogen ions and electrons recombine and are then used to reduce oxygen to form water. The formation of ATP through the oxidation of hydrogen atoms is called Oxidative Phosphorylation (formation of ATP that uses energy released from oxidation of NADH + H+ and FADH2.
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