Phenylalanine
From Free net encyclopedia
| Phenylalanine | |
|---|---|
| Systematic_name | 2-Amino-3-phenyl- propanoic acid |
| Abbreviations | Phe F |
| Chemical formula | C9H11NO2 |
| Molecular mass | 165.19 g mol-1 |
| Melting point | 283 °C |
| Density | 1.29 g cm-3 |
| Isoelectric point | 5.5 |
| pKa | 2.20 9.09 |
| CAS number | 63-91-2 Template:Ref N |
| SMILES | C1=CC=C(C=C1)CC(C(=O)O)N |
| Image:L-phenylalanine-skeletal.pngImage:L-phenylalanine-3D-sticks.png | |
| Disclaimer and references | |
- Phe redirects here. For the BitTorrent feature, see PHE.
The alpha-amino acid Phenylalanine exists in two forms, the D- and L- forms, which are enantiomers (mirror-image molecules) of each other. It has a benzyl side chain. Its name comes from its chemical structure's consisting of a phenyl group substituted for one of the hydrogens in the side chain of alanine. Because of its phenyl group, phenylalanine is an aromatic compound. At room temperature, it is a white, powdery solid.
L-Phenylalanine (LPA) is an electrically-neutral amino acid, one of the twenty common amino acids used to biochemically form proteins, coded for by DNA. Its enantiomer, D-phenylalanine (DPA), can be synthesized artificially.
L-phenylalanine is used in living organisms, including the human body, where it is an essential amino acid. L-phenylalanine can also be converted into L-tyrosine, another one of the twenty protein-forming amino acids. L-tyrosine is converted into L-DOPA, which is further converted into dopamine, norepinephrine, and epinephrine (latter three are known as the catecholamines). D-phenylalanine can be converted only into phenylethylamine.
The genetic disorder phenylketonuria is an inability to metabolize phenylalanine. Individuals with this disorder are known as "phenylketonurics", and must abstain from consumption of phenylalanine. It is present in many sugarless gums and other food products, which are labeled: "Phenylketonurics: Contains phenylalanine." The reason is not that phenylalanine is in the food per se. Aspartame (NutraSweet) is an ester that is hydrolyzed in the body to form phenylalanine, aspartic acid and methanol (wood alcohol), and it is the phenylalanine portion of aspartame which then builds up in the person with PKU.
The synthesized mix DL-Phenylalanine (DLPA), which is a combination of the D- and L- forms (e.g. a racemate: a racemic compound or mixture), is used as a nutritional supplement. Research indicates that DLPA can be an effective part of an overall program to fight chronic pain and depression in some cases, including the mood swings of premenstrual syndrome (PMS). Some sources contend that DPLA can increase energy and mental alertness, as well as heighten the ability to focus in individuals with attention deficit hyperactivity disorder (ADHD).
The genetic codon for phenylalanine was the first to be discovered. Marshall W. Nirenberg discovered that, when he inserted m-RNA made up of multiple uracil repeats into E. coli, the bacterium produced a new protein, made up solely of repeated phenylalanine amino acids.
Phenylalanine uses the same active transport channel as tryptophan to cross the blood-brain barrier, and, in large quantities, interferes with the production of serotonin.
| Forms of Phenylalanine | |||||
|---|---|---|---|---|---|
| Common name | phenylalanine | D-phenylalanine | L-phenylalanine | DL-phenylalanine | |
| Synonyms | alpha-Amino-beta- phenylpropionic acid | (2R)-2-amino-3- phenylpropanoic acid | (2S)-2-amino-3- phenylpropanoic acid | ||
| PubChem | Template:PubChemCID | Template:PubChemCID | Template:PubChemCID | ||
| EINECS number | Template:EINECS | Template:EINECS | Template:EINECS | ||
| CAS number | 673-06-3 | 63-91-2 | 150-30-1 | ||
Biosynthesis
Phenylalanine cannot be made by animals, which have to obtain it from their diet. It is produced by plants and most microorganisms from prephenate, an intermediate on the shikimate pathway.
Image:Phenylalanine biosynthesis.png
Prephenate is decarboxylated with loss of the hydroxyl group to give phenylpyruvate. This is transaminated using glutamate as the nitrogen source to give phenylalanine and α-ketoglutarate.
References
External links
- Phenylalanine and tyrosine biosynthesis
- Computational Chemistry Wiki
- Molecule of the Week
- DL-phenylalanine versus imipramine in depression
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