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Urea cycle
The urea cycle (ornithine cycle) is a cycle
of biochemical reactions that produces urea (NH2)2CO
from ammonia (NH3). This cycle occurs
in ureotelic organisms. The urea cycle converts highly
toxic ammonia to urea for excretion. This cycle was the
first metabolic cycle to be discovered (Hans
Krebs and Kurt Henseleit, 1932.The urea cycle takes place
primarily in the liver and, to a lesser extent, in
the kidneys.
Function
Amino acid catabolism results in waste ammonia. All animals need a way
to excrete this product. Most aquatic organisms, or ammoniotelic
organisms, excrete ammonia without converting it. Organisms that cannot
easily and safely remove nitrogen as ammonia convert it to a less toxic
substance such as urea via the urea cycle, which occurs mainly in the liver.
Urea produced by the liver is then released into the bloodstream where it
travels to the kidneys and is ultimately excreted in urine. The urea cycle is
essential to these organisms, because if the nitrogen or ammonia are not
eliminated from the organism it can be very detrimental. In species
including birds and most insects, the ammonia is converted into uric acid
or its urate salt, which is excreted in solid form.
Reactions
The entire process converts two amino groups, one from NH+
4 and one
from Aspartate, and a carbon atom from HCO−
3, to the relatively
nontoxic excretion product urea at the cost of four "high-energy"
phosphate bonds (3 ATP hydrolysed to 2 ADP and one AMP). The
conversion from ammonia to urea happens in five main steps. The first
is needed for ammonia to enter the cycle and the following four are all
a part of the cycle itself. To enter the cycle, ammonia is converted to
carbamoyl phosphate. The urea cycle consists of four enzymatic
reactions: one mitochondrial and three cytosolic.
Step Reactants Products Catalyzed by Location
1
NH3 + HCO−
3 + 2ATP
carbamoyl
phosphate +
2ADP + Pi
CPS1 mitochondria
2
carbamoyl
phosphate + orni
thine
citrulline + Pi OTC, zinc, biotin mitochondria
3
citrulline + aspart
ate + ATP
argininosuccinate
+ AMP + PPi
ASS cytosol
4 argininosuccinate
arginine + fumar
ate
ASL cytosol
5 arginine + H2O ornithine + urea
ARG1,
manganese
cytosol
Reactions of the urea cycle
1. L-ornithine
2. carbamoyl phosphate
3. L-citrulline
4. arginosuccinate
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
Steps of the urea cycle
1. Carbamoyl phosphate is converted to citrulline. With catalysis
by ornithine transcarbamoylase, the carbamoyl phosphate group is
donated to ornithine and releases a phosphate group.
2. A condensation reaction occurs between the amino group of aspartate
and the carbonyl group of citrulline to form argininosuccinate. This
reaction is ATP dependent and is catalysed by argininosuccinate
synthetase.
3. Argininosuccinate undergoes cleavage by argininosuccinase to
form arginine and fumarate.
4. Arginine is cleaved by arginase to form urea and ornithine. The
ornithine is then transported back to the mitochondria to begin the urea
Overall reaction equation
In the first reaction, NH+
4 + HCO−
3 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 Pi + AMP + Ppi
Since fumarate is obtained by removing NH3 from aspartate (by
means of reactions 3 and 4), and PPi + H2O → 2 Pi, the
equation can be simplified as follows:
2 NH3 + CO2 + 3 ATP + H2O → urea + 2 ADP + 4 Pi + AMP
CO2 + glutamate + aspartate + 3 ATP + 2 NAD++ 3 H2O → urea + α-
ketoglutarate + oxaloacetate + 2 ADP + 2 Pi + AMP + PPi + 2 NADH.
The two NADH produced can provide energy for the
formation of 5 ATP.
Urea cycle disorders
1. coma or death
2. delirium episodes, lethargy, and stroke.
3. Cirrhosis
4. sarcopenia

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Urea cycle

  • 2. The urea cycle (ornithine cycle) is a cycle of biochemical reactions that produces urea (NH2)2CO from ammonia (NH3). This cycle occurs in ureotelic organisms. The urea cycle converts highly toxic ammonia to urea for excretion. This cycle was the first metabolic cycle to be discovered (Hans Krebs and Kurt Henseleit, 1932.The urea cycle takes place primarily in the liver and, to a lesser extent, in the kidneys.
  • 3.
  • 4. Function Amino acid catabolism results in waste ammonia. All animals need a way to excrete this product. Most aquatic organisms, or ammoniotelic organisms, excrete ammonia without converting it. Organisms that cannot easily and safely remove nitrogen as ammonia convert it to a less toxic substance such as urea via the urea cycle, which occurs mainly in the liver. Urea produced by the liver is then released into the bloodstream where it travels to the kidneys and is ultimately excreted in urine. The urea cycle is essential to these organisms, because if the nitrogen or ammonia are not eliminated from the organism it can be very detrimental. In species including birds and most insects, the ammonia is converted into uric acid or its urate salt, which is excreted in solid form.
  • 5. Reactions The entire process converts two amino groups, one from NH+ 4 and one from Aspartate, and a carbon atom from HCO− 3, to the relatively nontoxic excretion product urea at the cost of four "high-energy" phosphate bonds (3 ATP hydrolysed to 2 ADP and one AMP). The conversion from ammonia to urea happens in five main steps. The first is needed for ammonia to enter the cycle and the following four are all a part of the cycle itself. To enter the cycle, ammonia is converted to carbamoyl phosphate. The urea cycle consists of four enzymatic reactions: one mitochondrial and three cytosolic.
  • 6. Step Reactants Products Catalyzed by Location 1 NH3 + HCO− 3 + 2ATP carbamoyl phosphate + 2ADP + Pi CPS1 mitochondria 2 carbamoyl phosphate + orni thine citrulline + Pi OTC, zinc, biotin mitochondria 3 citrulline + aspart ate + ATP argininosuccinate + AMP + PPi ASS cytosol 4 argininosuccinate arginine + fumar ate ASL cytosol 5 arginine + H2O ornithine + urea ARG1, manganese cytosol Reactions of the urea cycle
  • 7. 1. L-ornithine 2. carbamoyl phosphate 3. L-citrulline 4. arginosuccinate 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
  • 8. Steps of the urea cycle 1. Carbamoyl phosphate is converted to citrulline. With catalysis by ornithine transcarbamoylase, the carbamoyl phosphate group is donated to ornithine and releases a phosphate group. 2. A condensation reaction occurs between the amino group of aspartate and the carbonyl group of citrulline to form argininosuccinate. This reaction is ATP dependent and is catalysed by argininosuccinate synthetase. 3. Argininosuccinate undergoes cleavage by argininosuccinase to form arginine and fumarate. 4. Arginine is cleaved by arginase to form urea and ornithine. The ornithine is then transported back to the mitochondria to begin the urea
  • 9. Overall reaction equation In the first reaction, NH+ 4 + HCO− 3 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 Pi + AMP + Ppi Since fumarate is obtained by removing NH3 from aspartate (by means of reactions 3 and 4), and PPi + H2O → 2 Pi, the equation can be simplified as follows: 2 NH3 + CO2 + 3 ATP + H2O → urea + 2 ADP + 4 Pi + AMP
  • 10. CO2 + glutamate + aspartate + 3 ATP + 2 NAD++ 3 H2O → urea + α- ketoglutarate + oxaloacetate + 2 ADP + 2 Pi + AMP + PPi + 2 NADH. The two NADH produced can provide energy for the formation of 5 ATP.
  • 11. Urea cycle disorders 1. coma or death 2. delirium episodes, lethargy, and stroke. 3. Cirrhosis 4. sarcopenia