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The cytosolic acetyl-CoA can also condense with acetoacetyl-CoA to form 3-hydroxy-3-methylglutaryl-CoA which is the rate-limiting step controlling the synthesis of cholesterol. [16] Cholesterol can be used as is, as a structural component of cellular membranes, or it can be used to synthesize steroid hormones , bile salts , and vitamin D .
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.
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 .
The starting material is acetyl-CoA. It is a molecule that is involved in ATP synthesis, protein metabolism, and lipid metabolism. [6] As the inner membrane is not permeable to this molecule, acetyl-CoA needs to be converted into other products for effective transport. [7] It is also the first step of the reaction.
The regioselectivity of this step is essential for the subsequent hydration and oxidation reactions. acyl CoA dehydrogenase: trans-Δ 2-enoyl-CoA Hydration: The next step is the hydration of the bond between C-2 and C-3. The reaction is stereospecific, forming only the L isomer. Hydroxyl group is positioned suitable for the subsequent oxidation ...
Glyoxylate condenses with acetyl-CoA (a step catalyzed by malate synthase), yielding malate. Both malate and oxaloacetate can be converted into phosphoenolpyruvate , which is the product of phosphoenolpyruvate carboxykinase , the first enzyme in gluconeogenesis .
It begins with acetyl-CoA and involves the stepwise condensation of two-carbon units, typically derived from malonyl-CoA, to form increasingly longer carbon chains. In fatty acid synthesis, these chains are fully reduced after each elongation step, while in polyketide synthesis, the reduction steps may be partially or completely omitted ...
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 .