Urea cycle

The urea cycle (also known as the ornithine cycle) is a cycle of biochemical reactions occurring in many animals that produces urea ((NH₂)₂CO) from ammonia (NH₃). This cycle was the first metabolic cycle discovered (Hans Krebs and Kurt Henseleit, 1932), five years before the discovery of the TCA cycle. In mammals, the urea cycle takes place primarily in the liver, and to a lesser extent in the kidney.

Function

Organisms that cannot easily and quickly remove ammonia usually have to convert it to some other substance, like urea or uric acid, which are much less toxic. Insufficiency of the urea cycle occurs in some genetic disorders (inborn errors of metabolism), and in liver failure. The result of liver failure is accumulation of nitrogenous waste, mainly ammonia, which leads to hepatic encephalopathy.

Reactions

The urea cycle consists of five reactions: two mitochondrial and three cytosolic. The cycle converts two amino groups, one from NH₄⁺ and one from Asp, and a carbon atom from HCO₃⁻, to the relatively nontoxic excretion product urea at the cost of four "high-energy" phosphate bonds (3 ATP hydrolyzed to 2 ADP and one AMP). Ornithine is the carrier of these carbon and nitrogen atoms.

Reactions of the urea cycle

Step	Reactants	Products	Catalyzed by	Location
1	NH4+ + HCO3− + 2ATP	carbamoyl phosphate + 2ADP + Pi	CPS1	mitochondria
2	carbamoyl phosphate + ornithine	citrulline + Pi	OTC	mitochondria
3	citrulline + aspartate + ATP	argininosuccinate + AMP + PPi	ASS	cytosol
4	argininosuccinate	Arg + fumarate	ASL	cytosol
5	Arg + H2O	ornithine + urea	ARG1	cytosol

The reactions of the urea cycle

1 L-ornithine
2 carbamoyl phosphate
3 L-citrulline
4 argininosuccinate
5 fumarate
6 L-arginine
7 urea
L-Asp L-aspartate
CPS-1 carbamoyl phosphate synthetase I
OTC Ornithine transcarbamoylase
ASS argininosuccinate synthetase
ASL argininosuccinate lyase
ARG1 arginase 1

In the first reaction, NH₄⁺ + HCO₃⁻ is equivalent to NH₃ + CO₂ + H₂O.

Thus, the overall equation of the urea cycle is:

• NH₃ + CO₂ + aspartate + 3 ATP + 2 H₂O → urea + fumarate + 2 ADP + 2 P_i + AMP + PP_i

Since fumarate is obtained by removing NH₃ from aspartate (by means of reactions 3 and 4), and PP_i + H₂O → 2 P_i, the equation can be simplified as follows:

• 2 NH₃ + CO₂ + 3 ATP + H₂O → urea + 2 ADP + 4 P_i + AMP

Note that reactions related to the urea cycle also cause the oxidation of 2 NADH, so the urea cycle releases slightly more energy than it consumes. These NADH are produced in two ways:

• One NADH molecule is reduced by the enzyme glutamate dehydrogenase in the conversion of glutamate to ammonium and α-ketoglutarate. Glutamate is the non-toxic carrier of amine groups. This provides the ammonium ion used in the initial synthesis of carbamoyl phosphate.
• The fumarate released in the cytosol is converted to malate by cytosolic fumarase. This malate is then converted to oxaloacetate by cytosolic malate dehydrogenase, generating a reduced NADH in the cytosol. Oxaloacetate is one of the keto acids preferred by transaminases, and so will be recycled to aspartate, maintained the flow of nitrogen into the urea cycle.

The two NADH produced can provide energy for the formation of 5 ATP, a net production of one high-energy phosphate bond for the urea cycle. However, if gluconeogenesis is underway in the cytosol, the latter reducing equivalent is used to drive the reversal of the GAPDH step instead of generating ATP.

The fate of oxaloacetate is either to produce aspartate via transamination or to be converted to phosphoenol pyruvate, which is a substrate to glucose.

Regulation

N-Acetylglutamic acid

The synthesis of carbamoyl phosphate and the urea cycle are dependent on the presence of NAcGlu, which allosterically activates CPS1. Synthesis of NAcGlu by NAGS, is stimulated by both Arg, allosteric stimulator of NAGS, and Glu, a product in the transamination reactions and one of NAGS's substrates, both of which are elevated when free amino acids are elevated. So, Arg is not only a substrate for the urea cycle reactions but also serves as an activator for the urea cycle.

Substrate concentrations

The remaining enzymes of the cycle are controlled by the concentrations of their substrates. Thus, inherited deficiencies in the cycle enzymes other than ARG1 do not result in significant decrease in urea production (the total lack of any cycle enzyme results in death shortly after birth). Rather, the deficient enzyme's substrate builds up, increasing the rate of the deficient reaction to normal.

The anomalous substrate buildup is not without cost, however. The substrate concentrations become elevated all the way back up the cycle to NH₄⁺, resulting in hyperammonemia (elevated [NH₄⁺]_P).

Although the root cause of NH₄⁺ toxicity is not completely understood, a high [NH₄⁺] puts an enormous strain on the NH₄⁺-clearing system, especially in the brain (symptoms of urea cycle enzyme deficiencies include mental retardation and lethargy). This clearing system involves GLUD1 and GLUL, which decrease the 2-oxoglutarate (2OG) and Glu pools. The brain is most sensitive to the depletion of these pools. Depletion of 2OG decreases the rate of TCAC, whereas Glu is both a neurotransmitter and a precursor to GABA, another neurotransmitter. [1](p.734)

Pathology

Anomalies of the urea cycle cause urea cycle disorders:

• ornithine transcarbamoylase deficiency
• Carbamoyl phosphate synthetase deficiency (Ornithine translocase deficiency)
• Argininosuccinic aciduria
• Argininemia
• Hyperornithinemia, hyperammonemia, homocitrullinuria syndrome (HHH syndrome)
• Lysinuric protein intolerance
• Citrullinemia
• N-Acetylglutamate synthase deficiency

Most of them are associated with hyperammonemia.

Additional images

• 

  Urea cycle.

• 

  Urea cycle colored.

External links

• The chemical logic behind the urea cycle
• Basic Neurochemistry - amino acid disorders