Aspartic acid
Aspartate is formed, along with glutamate and alanine, by adding an amino acid to an alpha-ketoacid [3]. In the aspartic acid formation the amino group from glutamate is added to oxaloacetate to create aspartate and alpha-ketoglutarate. This reaction is driven by pyridoxal phoshate-dependent transaminases. Aspartate can also be used to create asparagine (another amino acid). It is a transformation driven by the hydrolysis of ATP and is an amidation. In bacteria, the reaction is: [4]
Aspartate + NH4 + ATP → asparagine + AMP + PPi+ H+
In mammals the nitrogen used in the reactions comes from glutamine rather than ammonia, which has the advantage that the cell does not come in direct contact with ammmonia which can be toxic to the cells in high doses.
Aspartate is one of the two amino acids that triggers a taste response in the body. The receptors that are used to detect sweetness are also amino acid receptors and so the flavour is called Umami from the japanese word meaning deliciousness. However, the umami taste is on a different subunit of the receptor to the normal sweetness receptor which is T1T3. The additional subunit is the T1R1 [5].
References:
- ↑ pg33, Biochemistry 6th edition, Stryer,Lubert, Tymoczko,John.L, Berg,Jeremy, published by W.H.Freeman and Company
- ↑ 3D structure - accessed on 14/11/2011 WolframAlpha http://www.wolframalpha.com/input/?i=aspartate
- ↑ pg.686, Biochemistry edition 6, Stryer,Lubert, Tymoczko,John.L, Berg,Jeremy M., published by W.H.Freeman and company
- ↑ pg 687, Biochemistry edition 6, Stryer,Lubert, Tymoczko,John.L, Berg,Jeremy M., published by W.H.Freeman and company
- ↑ pg.930, Biochemistry edition 6, Stryer,Lubert, Tymoczko,John.L, Berg,Jeremy M., published by W.H.Freeman and company