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Acetyl-CoA (acetyl coenzyme A) is a molecule that participates in many biochemical reactions in protein, carbohydrate and lipid metabolism. [2] Its main function is to deliver the acetyl group to the citric acid cycle (Krebs cycle) to be oxidized for energy production.
Its acetyl-coenzyme A form is the primary input in the citric acid cycle and is obtained from glycolysis, amino acid metabolism, and fatty acid beta oxidation. This process is the body's primary catabolic pathway and is essential in breaking down the building blocks of the cell such as carbohydrates , amino acids , and lipids .
Acetyl Co-A can also be used in fatty acid synthesis, and a common function of the synthetase is to produce acetyl Co-A for this purpose. [3] The reaction catalyzed by acetyl-CoA synthetase takes place in two steps. First, AMP must be bound by the enzyme to cause a conformational change in the active site, which allows the reaction to take place.
Acetyl-CoA is an intermediate in the biological synthesis and in the breakdown of many organic molecules. Acetyl-CoA is also created during the second stage of cellular respiration (pyruvate decarboxylation) by the action of pyruvate dehydrogenase on pyruvic acid. [8] Proteins are often modified via acetylation, for various purposes.
Acetyl-CoA is formed into malonyl-CoA by acetyl-CoA carboxylase, at which point malonyl-CoA is destined to feed into the fatty acid synthesis pathway. Acetyl-CoA carboxylase is the point of regulation in saturated straight-chain fatty acid synthesis, and is subject to both phosphorylation and allosteric regulation. Regulation by phosphorylation ...
A proposed mechanism is the release of CO 2 from biotin, which subsequently abstracts a proton from the methyl group from acetyl-CoA carboxylase. The resulting enolate attacks CO 2 to form malonyl-CoA. In a competing mechanism, proton abstraction is concerted with the attack of acetyl-CoA.
Two specific enzymes participate on the carbon monoxide side of the pathway: CO dehydrogenase and acetyl-CoA synthase. The former catalyzes the reduction of the CO 2 and the latter combines the resulting CO with a methyl group to give acetyl-CoA. [1] [2] Some anaerobic bacteria use the Wood–Ljungdahl pathway in reverse to break down acetate.
The 4 substrates of this enzyme are acetyl-CoA, malonyl-CoA, NADPH, and H +, whereas its 4 products are acyl-CoA, CoA, CO 2, and NADP +. More specifically, the FAS catalysis mechanism consumes an acetyl coenzyme A ( acetyl-CoA ) and seven malonyl-CoA molecules to produce a palmitoyl-CoA .