This means that, when there is abundant acetyl-CoA in the cell cytoplasm for fat synthesis, it proceeds at an appropriate rate.

Unable to be used in the citric acid cycle, the excess acetyl-CoA is therefore rerouted to ketogenesis.

However, the excess acetyl-CoA in the liver is converted to ketones (ketone bodies), that are transported to other tissues.

The carbon backbone of these amino acids can become a source of energy by being converted to acetyl-coA and entering into the citric acid cycle.

The -carnitine is cycled back into the mitochondria with acyl groups to facilitate fatty acid utilization, but excess acetyl-CoA may block it.

Acetoacetate and D-β-hydroxybutyrate are exported to non-hepatic tissues, where they are converted back into acetyl-coA and used for fuel.

In biological organisms, acetyl groups are commonly transferred from acetyl-CoA to coenzyme A (CoA).

In plants and animals, cytosolic acetyl-CoA is synthesized by ATP citrate lyase.

ATP citrate lyase is the primary enzyme responsible for the synthesis of cytosolic acetyl-CoA in many tissues.

This enzyme covalently attaches an acetyl group from acetyl-CoA to chloramphenicol, which prevents chloramphenicol from binding to ribosomes.

This results in shunting of excess acetyl-CoA into the ketone synthesis pathway via HMG-CoA, leading to the development of diabetic ketoacidosis.

Despite these findings, it is considered unlikely that the 2-carbon acetyl-CoA derived from the oxidation of fatty acids would produce a net yield of glucose via the citric acid cycle.

In eukaryotes, ATP citrate synthase is a homotetramer of a single large polypeptide, and is used to produce cytosolic acetyl-CoA from mitochondrial produced citrate.

The complex acts to convert pyruvate (a product of glycolysis in the cytosol) to acetyl-coA, which is then oxidized in the mitochondria to produce energy, in the citric acid cycle.

It is suggested that AANAT catalyzes the transfer of an acetyl group from acetyl-CoA to serotonin, with the involvement of an intermediate ternary complex, to produce N-acetylserotonin.

This is energetically unfavourable, and evidence suggests that the process requires ATP, GTP and acetyl-coA, fusion is also linked to budding, which is why the term budding and fusing arises.

Beta-oxidation is the process by which fatty acid molecules are broken down in the mitochondria to generate acetyl-coA, which enters the citric acid cycle, and NADH and FADH2, which are used by the electron transport chain.

Citrate is a positive modulator of this conversion and allosterically regulates the enzyme acetyl-coa carboxylase, which is the regulating enzyme in the conversion of Acetyl CoA into malonyl CoA (the commitment step in fatty acid synthesis).