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Difference between revisions of "Acetyl-CoA"

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{{MitoPedia
|description=[[File:Acetyl coenzyme A 700.png|left|100px|acetyl-CoA]]'''acetyl-CoA''', C<sub>23</sub>H<sub>38</sub>N<sub>7</sub>O<sub>17</sub>P<sub>3</sub>S, is a central piece in metabolism. It can be synthetized in many different ways: (i) in glycolysis from [[pyruvate]], by pyruvate dehydrogenase, which also forms NADH. (ii) from fatty acids Ξ²-oxidation, which releases one acetyl-CoA each round. (iii) catabolism of some aminoacids as leucine, lysine, phenylalanine, tyrosine and tryptophan.<br>
|description=[[File:Acetyl coenzyme A 700.png|left|100px|acetyl-CoA]]'''acetyl-CoA''', C<sub>23</sub>H<sub>38</sub>N<sub>7</sub>O<sub>17</sub>P<sub>3</sub>S, is a central piece in metabolism. It can be synthetized in different pathways: (i) in glycolysis from [[pyruvate]], by pyruvate dehydrogenase, which also forms NADH. (ii) from fatty acids Ξ²-oxidation, which releases one acetyl-CoA each round. (iii) catabolism of some aminoacids as leucine, lysine, phenylalanine, tyrosine and tryptophan.<br>
Inside the mitochondria, acetyl-CoA is condensed with [[oxaloacetate]] to form [[citrate]] through the action of [[citrate synthase]] in [[tricarboxylic acid cycle]]. Acetyl-CoA cannot cross the mitochondrial inner membrane but citrate can be transported out of the mitochondria. In the cytosol, citrate can be converted to acetyl-CoA and be used in fatty acid, cholesterol, ketone bodies, acetylcholine synthesis, and other processes.
Inside the mitochondria, acetyl-CoA is condensed with [[oxaloacetate]] to form [[citrate]] through the action of [[citrate synthase]] in [[tricarboxylic acid cycle]]. Acetyl-CoA cannot cross the mitochondrial inner membrane but citrate can be transported out of the mitochondria. In the cytosol, citrate can be converted to acetyl-CoA and be used in fatty acid, cholesterol, ketone bodies, acetylcholine synthesis, and other processes.



Revision as of 09:45, 14 October 2020


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Acetyl-CoA

Description

acetyl-CoA

acetyl-CoA, C23H38N7O17P3S, is a central piece in metabolism. It can be synthetized in different pathways: (i) in glycolysis from pyruvate, by pyruvate dehydrogenase, which also forms NADH. (ii) from fatty acids Ξ²-oxidation, which releases one acetyl-CoA each round. (iii) catabolism of some aminoacids as leucine, lysine, phenylalanine, tyrosine and tryptophan.

Inside the mitochondria, acetyl-CoA is condensed with oxaloacetate to form citrate through the action of citrate synthase in tricarboxylic acid cycle. Acetyl-CoA cannot cross the mitochondrial inner membrane but citrate can be transported out of the mitochondria. In the cytosol, citrate can be converted to acetyl-CoA and be used in fatty acid, cholesterol, ketone bodies, acetylcholine synthesis, and other processes.

Communicated by Cecatto Cristiane last update 2020-10-14






MitoPedia topics: Substrate and metabolite