This document summarizes information about the enzyme urease. It discusses that urease is a nickel-containing metalloenzyme found in many organisms that catalyzes the hydrolysis of urea to produce ammonia and carbon dioxide. The active site contains two nickel ions that are bridged by ligands. Urease plays important roles in nitrogen cycling in soils and the digestive systems of ruminants and humans. Deficiencies in urease or related enzymes can cause health issues if not properly treated.
3. 1. Ureases functionally belong to superfamily of amidohydrolases and
phosphotriesterases.
2. Found in numerous bacteria, fungi, algae, plants, and some
invertebrates, as well as in soils as soil enzyme.
3. Nickel containing metalloenzyme.
4. Not synthesized by animals.
5. Jack bean urease was the first enzyme to be crystallized.
6. By James. B. Sumner in 1926, Nobel Prize in chemistry in 1946.
7. Urease catalyzes the hydrolysis of urea to form ammonia and CO2.
5. The active site of all known ureases is located in the α
(alpha) subunits. It is a bis-μ-hydroxo dimeric nickel center, with an
interatomic distance of ~3.5 Å,magnetic susceptibility experiments
have indicated that, in jack bean urease, high spin octahedrally
coordinated Ni(II) ions are weakly antiferromagnetically coupled.[
The Ni ions are bridged by a carbamylated lysine and an oxygen
donor.
The active site contains two nickel ions with an interatomic distance
of about 3.5 A.
In addition to the bridges, one of the nickel ions (Ni1) is coordinated
by two histidine and a water molecule.
The coordination of Ni2 is similar to the one of Ni1 and includes two
histidine residues, a water molecule and a terminally bound
aspartate.
6. In vitro activation also has been achieved
with manganese and cobalt in place of nickel .Lead salts
are inhibiting.
Molecular weight:- 480 manganese and cobalt in place of nickelIn
.[12] Lead salts arekDa or 545 kDa for Jack Bean Urease (Hexamer).
Optimum pH:- 7.4
Optimum Temperature:- 60 degrees Celsius.
Enzymatic Specificity:- Urea and Hydroxyurea.
Inhibitors:- Heavy Metals (Pb- & Pb2+), Fluorine (F).
Catalysis hydrolysis of urea to CO2 and NH3.
7. The hydrolysis of urea occurs in two stages.
In the first stage, ammonia and carbamate are produced.
The carbamate spontaneously and rapidly hydrolyzes to
ammonia and carbonic acid.
Urease activity increase the pH of its environment as it produces
ammonia, which is basic
8. • Urea binds in a bidentate
manner with its carbonyl
oxygen bound to Ni(1) and
one of the amino group
bound to Ni(2).
• Thus replacing two water
moieties, leaving only the
bridging hydroxide.
• This hydroxide attacks
urea to give the tetrahedral
transition state leading to
formation of ammonia and
carbamate.
9.
10.
11. [Ni2(µ-OH)(µ-urea)(bdptz)(urea)(CH3CN)](ClO4)3
[Ni2(µ-OH)(µ-H2O)(bdptz)(µ-OCN)]2(OTs)4
[Ni2(µ-OH)(µ-H2O)(bdptz)(urea)2](ClO4)3
The fact that no dinuclear nickel complex reported thus far has proved capable of hydrolyzing urea to ammonia
and carbon dioxide provides an intriguing challenge to the synthetic bioinorganic chemist. The design of a
complex that can produce a sufficiently nucleophilic hydroxide ion and at the same time activate a urea molecule
by coordination to one or both metal ions should facilitate the successful hydrolysis of urea under the right
conditions. So, a dinuclear nickel complex, [Ni2(µ-OH)(µ-H2O)(bdptz)(H2O)2](OTs)3 (where bdptz is the
dinucleating ligand 1,4-bis(2,2′-dipyridylmethyl)- phthalazine), that is capable of hydrolyzing a bound amide
substrate by intramolecular attack of a coordinated hydroxide ion.
Upon heating, this complex effects the hydrolysis of urea by a pathway involving cyanate ion that is distinct
from that previously proposed for the enzyme. These results provide the first direct evidence for a mechanism
long considered as an alternative for the enzymatic hydrolysis of urea.
12. Ammonia is the preferred nitrogen source among enteric bacteria and the
ureolytic activity of the human gut microbiota hydrolyzes about 15%-30%
of the urea synthesized by the human body.(Aoyagi et al.,1966;Walser and Bodenlos,1959)
Microbial ureases are an important factor to be considered in dental
health.(Burne et al., 2012).
Bacterial ureases in the forestomach of ruminants cleave animal-derived
urea allowing the released ammonia to be used as major nitrogen source
for the rumen microbiota.(Laukova and Koniarova, 1995; Pearson and Smith, 1943)
13. Urea hydrolysis to release ammonia and carbon dioxide is the main
physiological role attributed to ureases in plants.(Witte, 2011)
Worldwide used as a soil fertilizer, urea can only be assimilated after
hydrolysis by urease.(Sirko and Brodzik,2000)
However, the efficiency of urea fertilization can be decreased by higher
levels of this soil urease, which can cause massive release of ammonia into
the atmosphere, further inducing plant damage by ammonia toxicity and
soil pH increase.(Watson et al., 1994)
14. People with genetic defects in any enzyme involved in urea formation cannot tolerate
protein-rich diets. Amino acids ingested in excess of the minimum daily requirements for
protein synthesis are deaminated in the liver, producing free ammonia that cannot be
converted to urea and exported into the bloodstream, as ammonia is highly toxic. The
absence of urea cycle enzyme can result in hyperammonemia.
Although the breakdown of amino acids can have serious health consequences in individuals
with urea cycle deficiencies, a protein-free diet is not a treatment option.
The absent enzyme activity can often be identified by determining which cycle intermediate
is present in especially elevated concentration in the blood and/or urine.
A variety of treatments are available for individuals with urea cycle defects. Careful
administration of the aromatic acids benzoate or phenyl butyrate in the diet can help lower
the level of ammonia in the blood.