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| Names | |
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| Preferred IUPAC name
(1s,4s)-1-(2-Carboxy-2-oxoethyl)-4-hydroxycyclohexa-2,5-diene-1-carboxylic acid | |
| Other names
Prephenate; cis-1-Carboxy-4-hydroxy-α-oxo-2,5-cyclohexadiene-1-propanoic acid
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| Identifiers | |
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3D model (JSmol)
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| ChEBI | |
| ChemSpider | |
| MeSH | Prephenic+acid |
PubChem CID
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| UNII |
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CompTox Dashboard (EPA)
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| Properties | |
| C10H10O6 | |
| Molar mass | 226.184 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Prephenic acid, commonly also known by its anionic form prephenate, is an intermediate in the biosynthesis of the aromatic amino acids phenylalanine and tyrosine, as well as of a large number of secondary metabolites of the shikimate pathway.
Occurrence and biological significance
Prephenic acid occurs naturally as an intermediate in the biosynthesis of phenylalanine and tyrosine via the shikimic acid pathway.[1][2] It is formed from chorismic acid by chorismate mutase. It can be dehydrated by prephenate dehydratase to phenylpyruvic acid, which is a precursor of phenylalanine. Alternatively, it can be dehydrated by prephenate dehydrogenase to 4-hydroxyphenylpyruvic acid, which is a precursor of tyrosine.[1]
It is biosynthesized by a [3,3]-sigmatropic Claisen rearrangement of chorismate.[3][4]
Synthesis
Prephenic acid is unstable; as a 1,4-cyclohexadiene, it is easily aromatized, for example, under the influence of acids or bases. This instability makes both isolation and synthesis difficult. Prephenic acid was first isolated from mutants of Escherichia coli that were unable to convert prephenic acid to phenylpyruvic acid. During this process, the barium salt was obtained.[2]
Stereochemistry
Prephenic acid is an example of achiral (optically inactive) molecule which has two pseudoasymmetric atoms (i.e. stereogenic but not chirotopic centers), the C1 and the C4 cyclohexadiene ring atoms. It has been shown[5] that of the two possible diastereoisomers, the natural prephenic acid is one that has both substituents at higher priority (according to CIP rules) on the two pseudoasymmetric carbons, i.e. the carboxyl and the hydroxyl groups, in the cis configuration, or (1s,4s) according to the new IUPAC stereochemistry rules (2013).[6]
The other stereoisomer, i.e. trans or, better, (1r,4r), is called epiprephenic.
See also
References
- ^ a b Richard G.H. Cotton, Frank Gibson (April 1965), "The biosynthesis of phenylalanine and tyrosine; enzymes converting chorismic acid into prephenic acid and their relationships to prephenate dehydratase and prephenate dehydrogenase", Biochimica et Biophysica Acta (BBA) - General Subjects, vol. 100, no. 1, pp. 76–88, doi:10.1016/0304-4165(65)90429-0
- ^ a b H. Plieninger (July 1962), "Prephenic Acid: Properties and the Present Status of its Synthesis", Angewandte Chemie International Edition in English, vol. 1, no. 7, pp. 367–372, doi:10.1002/anie.196203671
- ^ Helmut Goerisch (1978). "On the mechanism of the chorismate mutase reaction". Biochemistry. 17 (18): 3700–3705. doi:10.1021/bi00611a004. PMID 100134.
- ^ Peter Kast, Yadu B. Tewari, Olaf Wiest, Donald Hilvert, Kendall N. Houk, and Robert N. Goldberg (1997). "Thermodynamics of the Conversion of Chorismate to Prephenate: Experimental Results and Theoretical Predictions". J. Phys. Chem. B. 101 (50): 10976–10982. doi:10.1021/jp972501l.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Danishefsky, Samuel; Hirama, Masahiro; Fritsch, Nancy; Clardy, Jon (1979-11-01). "Synthesis of disodium prephenate and disodium epiprephenate. Stereochemistry of prephenic acid and an observation on the base-catalyzed rearrangement of prephenic acid to p-hydroxyphenyllactic acid". Journal of the American Chemical Society. 101 (23): 7013–7018. doi:10.1021/ja00517a039. ISSN 0002-7863.
- ^ Favre, Henri A; Powell, Warren H (2013-12-17). Nomenclature of Organic Chemistry. doi:10.1039/9781849733069. ISBN 9780854041824.
This page was last edited on 25 July 2024, at 00:34