Introduction.
Metabolism produces a number of toxic by-products, particularly the nitrogenous wastes that result from the breakdown of proteins and nucleic acids. Amino (NH2) groups are the result of such metabolic reactions and can be toxic if ammonia (NH3) is formed from them. Ammonia tends to raise the pH of bodily fluids and interfere with membrane transport functions. To avoid this the amino groups are converted into urea, which is less toxic and can be transported and stored to be released by the excretory system.
Urea is the result of two amino groups being joined to a carbonyl (C=O) to form CO(NH2)2, the process of which is called the ornithine cycle and takes place in the liver. The ornithine cycle was developed by Hans Krebs in 1932 and is similar to the Krebs cycle through the use of oxaloacetate. One of the steps in the cycle the breakdown of arginine into ornithine and urea, a reaction catalysed by the enzyme arginase. (See below) (Fig 1.0)
Arginine Orthinine Urea
Urease is the enzyme which catalyses the hydrolysis of urea according to the following equation:
(NH2)2CO(aq) + 3H2O(l) CO2(g) + 2NH3(g)
The acidic ammonium carbonate is formed because the carbon dioxide dissolves in water to produce carbonic acid (H2CO3), which immediately reacts with ammonia to form the ammonium carbonate. This is shown by the following equation:
2NH3(g) + H2CO3(aq) (NH4+)2CO3(aq)
The resulting solution can then be titrated against hydrochloric acid with methyl orange as the indicator in order to determine how much urea was present initially. The point of neutralisation using a methyl orange indicator is determined using the following colour changes.
Acid Red.
Neutral Yellow.
Alkali Orange.
Enzymes are nearly all made up of globular proteins. The structure