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How is acetyl CoA produced?

Acetyl CoA is produced from the metabolism of carbohydrates, proteins, and fats in a process called cellular respiration. During the first step of cellular respiration, known as glycolysis, the six-carbon glucose molecule is broken down into two three-carbon molecules.

These three-carbon molecules are transported into the mitochondria, where they enter the Kreb’s cycle (or tricarboxylic acid cycle). During the Kreb’s cycle, the three-carbon molecules are processed and broken down further.

Two molecules of acetyl CoA are produced from each glucose molecule, and these molecules of acetyl coA are then passed into the electron transport chain. In the electron transport chain, acetyl coA is combined with oxygen to form two molecules of water and the energy-carrying molecule called ATP.

This ATP then serves as the energy resource used by cells. Additionally, acetyl CoA is also produced when fats are metabolized. During this process, enzymes known as lipases break down lipids into fatty acids, which then enter the mitochondria and are processed through beta-oxidation.

During beta-oxidation, two-carbon molecules are removed from the fatty acids, and these two-carbon molecules are combined to form one molecule of Acetyl CoA. This acetyl CoA then enters the Kreb’s cycle and the product of ATP is the same as when Acetyl coA is produced from carbohydrates.

How is CoA synthesized?

Coenzyme A (CoA) is synthesized in a two-step process, beginning with the synthesis of pantethine from cysteine. This is catalyzed by the enzyme pantetheine synthase and occurs in the mitochondria. Pantethine then reacts with ATP and the enzyme pantetheine kinase to form CoA, which is the end product.

CoA is a coenzyme of acyltransferase reactions and is important in the formation of acyl-CoA compounds. It is also important for fatty acid oxidation, the citric acid cycle, and the generation of energy in mitochondria.

CoA is also involved in acyl group transfers, and these reactions are important in many metabolic processes, including the synthesis of ketones, amino acids and neurotransmitters. In particular, CoA is used in the oxidation of fatty acids and in the production of acetyl-CoA, which can then be used in the citric acid cycle to generate energy.

As such, CoA is essential for many cellular processes, including energy production.

How is acetyl CoA formed after glycolysis?

Acetyl-CoA is formed after glycolysis when pyruvate from the glycolytic pathway is transported into the mitochondria and converted into acetyl CoA. It is the first step in the citric acid cycle and occurs through a reaction driven by the enzyme pyruvate dehydrogenase (PDH).

The process involves the oxidation of pyruvate and the cleavage of its leaving group as CO2. The product of this reaction is acetyl CoA, which is then used to enter the citric acid cycle, where energy is ultimately produced.

The acetyl CoA molecule also carries a two carbon acetyl group, which it donates to oxaloacetate, the first substrate of the citric acid cycle. This acetyl group is made up of a carbon (C) and two hydrogen (H) atoms, which have been taken from pyruvate.

During the conversion of pyruvate to acetyl CoA, electrons are also transferred to the electron transport chain, which is responsible for generating the majority of the energy in cells.

How does pyruvate become acetyl-CoA?

Pyruvate, the end-product of glycolysis, is transformed into acetyl-CoA through a three-step metabolic process known as the Pyruvate-Dehydrogenase (PDH) pathway. This pathway involves the following steps:

Step 1: Oxidation of Pyruvate – In this step, pyruvate is oxidized and a carbon dioxide molecule is released, while the remaining two-carbon molecule is converted into Acetyl-CoA. This reaction is catalyzed by an enzyme known as the pyruvate dehydrogenase complex (PDC).

The PDC is composed of three enzymes: pyruvate dehydrogenase, dihydrolipoyl transacetylase, and dihydrolipoyl dehydrogenase. PDC also requires the aid of thiamine pyrophosphate and other co-factors for this reaction to take place.

Step 2: Conversion of Acetyl-CoA to CoA – In this step, the acetyl-CoA formed in the previous step is converted into an active form of CoA by the enzyme known as Acetyl-CoA synthetase.

Step 3: Conversion of CoA to Acetyl-CoA – In this final step, the CoA that was previously generated is converted back into the active form of Acetyl-CoA. This reaction is catalyzed by an enzyme known as Thiolase.

Once these three steps have been completed, pyruvate is successfully converted into Acetyl-CoA, which can then be used in the Citric Acid Cycle to produce energy.

Is acetyl-CoA formed in the mitochondria?

Yes, acetyl-CoA is formed in the mitochondria. Acetyl-CoA is a key molecule involved in the metabolism of carbohydrates, fats, and proteins. Its formation is the result of the breakdown of glucose, fatty acids, and certain amino acids.

This occurs in the mitochondria, the organelles responsible for energy production in the cell. During the process of aerobic respiration, the chemical energy stored in carbohydrates, fats, and proteins is converted into a form the cell can use – ATP.

Acetyl-CoA is an intermediate in this process. It is generated from pyruvate, the end product of glycolysis, the initial step of the breakdown of glucose. The formation of acetyl-CoA also occurs during the oxidation of fatty acids and the catabolism of certain amino acids.

Acetyl-CoA plays a major role in the citric acid cycle, which is the second main step in aerobic respiration. During the citric acid cycle, acetyl-CoA is combined with oxaloacetate to produce citrate, a process that releases high-energy electrons.

These electrons are used to produce ATP in the electron transport chain.

What is the role of acetyl coenzyme A?

Acetyl coenzyme A (also known as CoA or acetyl-CoA) is a key metabolite in the metabolism of all organisms – from bacteria to humans. It is an important link in the energy-producing pathways of the Krebs cycle and fatty acid synthesis and can be involved in the synthesis of acetylcholine and other neurotransmitters.

Acetyl CoA is generated when carbohydrates, proteins and fats are broken down in the cells by the process of glycolysis. It is then used in a number of metabolic pathways, such as the Citric Acid Cycle (Krebs Cycle), fatty acid synthesis and the production of ketones.

In the Krebs cycle, Acetyl CoA combines with oxaloacetate (OAA) to form citrate, which is then broken down to produce energy in the form of ATP molecules. Acetyl CoA is also essential for the production of ketones, which are produced as a by-product of fatty acid breakdown in the liver.

Acetyl CoA is also required for the synthesis of cholesterol in the body, as well as for the synthesis of certain amino acids, such as Phenylalanine, Tyrosine and Valine. In other words, Acetyl CoA is an important coenzyme required for the synthesis of many important metabolites, including lipids, proteins and neurotransmitters.

Consequently, it plays a major role in all metabolic processes, ensuring the body’s efficient functioning.

Which can produce Acetyl-CoA quizlet?

Acetyl-CoA is produced primarily by the breakdown of carbohydrates, fatty acids, and ketone bodies. When carbohydrates such as glucose are broken down during the process of glycolysis, the energy-storage molecule known as pyruvate is produced.

Pyruvate then enters the mitochondria and is further processed during the citric acid cycle. As this process continues, the citric acid cycle produces an intermediate molecule known as acetyl-CoA. Acetyl-CoA is also produced during the break down of fatty acids in a process called beta oxidation.

In this process, fatty acids are broken down into smaller units called acyl-CoA, which are then converted into acetyl-CoA molecules. Lastly, acetyl-CoA is produced by the metabolism of ketone bodies.

This is the process by which the body breaks down its own fat stores in the absence of carbohydrates. All three of these processes ultimately lead to the formation of acetyl-CoA, which is then used in the next stage of metabolism.

What vitamin is coenzyme A derived from?

Coenzyme A is derived from vitamin B5, also known as pantothenic acid. Vitamin B5 is a water-soluble vitamin found in some foods, including eggs, legumes, meat, whole-grain cereals, and mushrooms. It is also part of most multivitamin and B-complex supplements.

Vitamin B5 plays an essential role in the production of energy, so it’s important for a proper metabolism. Additionally, it is involved in the synthesis of fatty acids, cholesterol, and steroid hormones, as well as in the activation and maintenance of coenzyme A, which is essential for aerobic cell respiration.

What is Acetyl-CoA how is it made?

Acetyl-CoA is a molecule that exists in cells. It is a derivative of pyruvate and it is used to produce energy in the form of ATP, as well as to form fatty acids and cholesterol. During the process of respiration, sugar and other compounds are broken down by cells to form energy-rich molecules such as ATP.

One byproduct of this process is pyruvate, which is then converted into Acetyl-CoA by the enzyme pyruvate dehydrogenase. Acetyl-CoA is then used to begin the Kreb’s cycle, a metabolic pathway that produces more ATP and other molecules.

Acetyl-CoA is also involved in the synthesis of fatty acids and cholesterol. In the process of fatty acid synthesis, Acetyl-CoA is used to form fatty acids, which can then be stored by the cell to be used later as energy, or to form other molecules such as steroids and hormones.

Similarly, cholesterol is produced by the body when Acetyl-CoA combines with a molecule known as HMG-CoA. These molecules are used by cells for important biological functions such as cell membrane formation, hormone production, and energy storage.

What Acetyl-CoA means?

Acetyl-CoA (acetyl coenzyme A) is an intermediate molecule that is involved in many biochemical pathways, including the metabolism of proteins, fats, and carbohydrates. Acetyl-CoA is formed by oxidation of organic compounds in the Krebs cycle in which energy is released.

It is made up of two molecules – acetate and coenzyme A – and is a carrier of carbon atoms between metabolic pathways. It acts as an energy currency, transferring the energy released in the breakdown of carbohydrates, proteins, and fats to the cells where it can be used to generate ATP (adenosine triphosphate), the body’s main energy source.

Acetyl-CoA is also involved in the process of fatty acid synthesis, cholesterol synthesis, and the production of ketone bodies. In addition, it can be further processed to make glucose or used for the synthesis of fatty acids and cholesterol.

Overall, acetyl-CoA has an important role in regulating the metabolic process in the body and is crucial for proper functioning of the body’s systems.

Where does Acetyl-CoA formation?

Acetyl-CoA formation is a reaction that takes place in the mitochondria, the organelle responsible for cellular respiration. It begins with the condensation of a two-carbon acetyl molecule with a four-carbon molecule called coenzyme A (CoA).

The two molecules then undergo a series of chemical modifications and react with each other to form acetyl-CoA.

The reaction is driven by the hydrolysis of a single high-energy phosphate bond from adenosine triphosphate (ATP). During the reaction, the acetyl group transfers its energy to the CoA molecule, allowing the resting energy from ATP to be utilized to help drive the reaction.

The ATP-dependent reaction is called the citric acid cycle (AKA the Krebs cycle) as it is the first step in a series of metabolic reactions that ultimately produce energy in the form of adenosine diphosphate (ADP) and inorganic phosphate.

The resulting acetyl-CoA molecule is then used to produce fatty acids, Cholesterol, or enter the citric acid cycle and produce aerobic respiration. Thus, Acetyl-CoA formation occurs in the mitochondria and is the beginning of cellular respiration.

How is acetyl-CoA formed what is its role in citric acid cycle?

Acetyl-CoA is a key molecule formed in many metabolic pathways, and its most crucial role is in the citric acid cycle (CAC) or Krebs Cycle. In the CAC, acetyl-CoA is formed by the transfer of a coenzyme A (CoASH) molecule to the acetyl group of an activated two-carbon molecule, creating a molecule known as acetyl-CoA.

Before being incorporated into the CAC, acetyl-CoA is produced by the oxidation of energy-rich nutrients such as carbohydrates, proteins, and fats. The acetyl-CoA joins with oxaloacetate – another four-carbon molecule – to form citrate.

The citrate molecule is then broken down further in a series of eight enzymatic reactions to form intermediates, some of which are recycled and others of which are used to form other energy-containing molecules like ATP, FADH and NADH.

These molecules then pass electrons onto the electron transport chain, which produces ATP for cell energy and also provides energy for the synthesis of cellular components. The overall result of the CAC is the generation of high-energy compounds and a decrease in carbon skeletons.

Ultimately, the CAC is crucial for producing the ATP necessary for cellular processes and harvests the energy released from the breakdown of the raw materials.

What happens when pyruvate is converted to Acetyl-CoA quizlet?

When pyruvate is converted to acetyl-CoA, a two-step process of oxidative decarboxylation and transfer of coenzyme A occurs. In the first step of this process, pyruvate is oxidized by the enzyme pyruvate dehydrogenase.

This results in the release of a molecule of carbon dioxide. In the second step, the reduced cofactor NADH donates its electrons to the enzyme acyl-CoA synthetase, forming acetyl-CoA and also regenerating NAD+.

Acetyl-CoA is a molecule that can be further oxidized for the generation of energy via the citric acid cycle or the fatty acid oxidation pathway. Acetyl-CoA is an important molecule in the metabolism of sugar, amino acids, and fatty acids.

It is an energy rich three-carbon molecule that is used to synthesize fatty acids and cholesterol, produce important molecules called ketone bodies, and is a key intermediate in the citric acid cycle.

What are the 4 steps of fatty acid synthesis?

The four steps of fatty acid synthesis are known as the Acetyl-CoA pathway, and they are as follows:

1. Activation: Acetyl-CoA is activated by the enzyme acetyl-CoA carboxylase, which produces a derivative of Acetyl-CoA known as acetyl-CoA carboxylase (ACC). This activates the Acetyl-CoA by attaching a carboxyl group to it, forming malonyl-CoA.

2. Condensation: Malonyl-CoA reacts with acetyl-CoA to form a 6-carboxyhexanoyl-CoA molecule. This step is catalyzed by the enzyme acetyl-CoA synthetase.

3. Reduction: Enoyl-CoA reductase reduces the 6-carboxyhexanoyl-CoA molecule to form a 6-oxohexanoyl-CoA. This step is necessary for the absorption of fatty acids into the cell membrane.

4. Acyl-Group Migration: The final step in fatty acid synthesis is the migration of the acyl group from the 6-oxohexanoyl-CoA to the sulfur atom of a molecule of Coenzyme A. This process is catalyzed by the enzyme acyl-CoA transferase.

The resulting molecule is an acetyl-CoA molecule, ready to start the cycle again.

How are fatty acids synthesized?

Fatty acids are synthesized in an energy-requiring process that takes place in the endoplasmic reticulum of cells. This process is known as fatty acid synthesis, or FAS for short. It begins with the conversion of acetyl-CoA, a byproduct of metabolic processes, into malonyl-CoA.

This is done via the enzyme acetyl-CoA carboxylase, which uses biotin as a coenzyme and ATP as an energy source. Acetyl-CoA carboxylase is a rate-limiting enzyme in fatty acid synthesis, meaning that it is the step at which FAS is most sluggish and can be rate-limited if the cell has an inadequate supply of biotin.

Once the malonyl-CoA is formed, the enzyme fatty acid synthase (FAS) steps in. FAS is composed of several subunits and can synthesize multiple forms of fatty acids. It works by adding two carbon molecules at a time by a process known as condensation.

Each condensation reaction requires one molecule of malonyl-CoA and one molecule of acyl carrier protein, which carries the fatty acid through the process of FAS. Each round of condensation reduces the number of malonyl-CoA molecules present, until the desired number of carbons is reached.

When the desired length of the fatty acid is obtained, the reaction is finished and the fatty acid is released from the acyl carrier protein.

Overall, fatty acid synthesis is an energy-intensive process that relies on a variety of enzymes and cofactors in order to build up a fatty acid. It begins with the conversion of acetyl-CoA into malonyl-CoA, followed by the release of fatty acids from the enzyme FAS, which work by adding two carbon molecules at a time.

Once the desired length of the fatty acid is obtained, it is then released from the acyl-carrier protein and the reaction is complete.

How is acetyl-CoA transported into the cytosol for fatty acid synthesis to begin?

Acetyl-CoA is transported into the cytosol through a membrane protein complex called the carnitine-acylcarnitine translocase (CACT). CACT consists of two subunits, an inward-facing catalytic subunit and an outward-facing membrane subunit.

The catalytic subunit contains the enzyme carnitine acyltransferase, which transfers acyl groups from acetyl-CoA to carnitine. The membrane subunit contains a channel that allows carnitine and acylcarnitines to pass through the membrane.

The transport of acetyl-CoA into the cytosol is driven by the gradient of carnitine and acylcarnitines across the inner mitochondrial membrane.

Carnitine acyltransferase is reversibly inhibited by palmitoylcarnitine and long-chain acylcarnitines. These acylcarnitines bind to the active site of carnitine acyltransferase and prevent the transfer of acyl groups from acetyl-CoA to carnitine.

The accumulation of long-chain acylcarnitines in the inner mitochondrial membrane inhibits the transport of acetyl-CoA into the cytosol and thus limits the rate of fatty acid synthesis.