Dehydroalanine

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Dehydroalanine
Structural formula Dehydroalanin.svg
Structural formula
Ball-and-stick model of the zwitterion Dehydroalanine-zwitterion-3D-balls.png
Ball-and-stick model of the zwitterion
Names
Preferred IUPAC name
2-Aminoprop-2-enoic acid
Other names
Cα,β-didehydroalanine, α,β-didehydroalanine, 2-aminoacrylate, 2,3-didehydroalanine
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
DrugBank
KEGG
PubChem CID
UNII
  • InChI=1S/C3H5NO2/c1-2(4)3(5)6/h1,4H2,(H,5,6) Yes check.svgY
    Key: UQBOJOOOTLPNST-UHFFFAOYSA-N Yes check.svgY
  • InChI=1/C3H5NO2/c1-2(4)3(5)6/h1,4H2,(H,5,6)
    Key: UQBOJOOOTLPNST-UHFFFAOYAW
  • C=C(C(=O)O)N
  • O=C(O)C(=C)N
Properties
C3H5NO2
Molar mass 87.08 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Yes check.svgY  verify  (what is  Yes check.svgYX mark.svgN ?)

Dehydroalanine is an organic compound with the formula CH2=CH(NH2)CO2H. It does not exist in its free form, but it occurs naturally as a residue found in peptides of microbial origin. Unlike most amino acid residues, it has an unsaturated backbone. [1]

Contents

Structure and reactivity

Like most primary enamines, dehydroalanine is unstable. It would hydrolyze to pyruvate: [2]

CH2=CH(NH2)CO2H + H2O → CH3−C(O)CO2H + NH3

N-Acylated derivatives of dehydroalanine, such as are found peptides and related compounds, are stable. One such example is methyl 2-acetamidoacrylate. [3] As a residue in a peptide, dehydroalanine is generated by a post translational modification. The required precursors are serine or cysteine residues, which undergo enzyme-mediated loss of water and hydrogen sulfide, respectively.

Most amino acid residues are unreactive toward nucleophiles, but those containing dehydroalanine or some other dehydroamino acids are exceptions. These residues are electrophilic due to the α,β-unsaturated carbonyl, [1] and can, for example, alkylate other amino acids. This activity has made DHA useful synthetically to prepare lanthionine.

Occurrence

Dehydroalanine had been proposed as early as 1937, but it was established by analysis of the reactions of base with glutathione. [2] Alkaline degradation of cystine-containing peptides and proteins was shown to give derivatives containing lanthionine and lysinoalanine. N-acetyldehydroglycine was also shown to add amines. [3]

The dehydroalanine residue was first detected in nisin, a cyclic peptide with antimicrobial activity. [1] Dehydroalanine is also present in some lantibiotics and microcystins.

DHA can be formed from cysteine or serine by simple base catalysis without the need for an enzyme, which can happen during cooking and alkaline food preparation processes. It can then alkylate other amino acid residues, such as lysine, forming lysinoalanine cross-links and racemization of the original alanine. The resulting proteins have lower nutritional quality for some species but higher nutritional quality for others. Some lysinoalanines may also cause kidney enlargement in rats. [4]

Many dehydroalanine-containing peptides are toxic. [1]

The antimicrobial bacteriocin nisin contains three dehydro amino acid residues, two of which are dehydroalanine residues. Nisin.png
The antimicrobial bacteriocin nisin contains three dehydro amino acid residues, two of which are dehydroalanine residues.

A dehydroalanine residue was long thought to be an important electrophilic catalytic residue in histidine ammonia-lyase and phenylalanine ammonia-lyase enzymes, but the active residue was later found instead to be a different unsaturated alanine derivative — 3,5-dihydro-5-methyldiene-4H-imidazol-4-one — that is even more electrophilic. [5] [6]

Chemical synthesis

N-Acyl dehydroalanine derivatives have been synthesized by dehydration of serines using a tert-butoxycarbonate leaving group, [7] or by conversion of Cysteine derivatives using various reagents for the elimination of the Thiol-group. [8] Various protected dehydroamino acids can be produced by electrochemical oxidation of the respective amino acid derivative in methanol. [9]

Dehydroalanine derivatives are useful precursors to other amino acids. [10]

References

  1. 1 2 3 4 Siodłak, Dawid (2015). "α,β-Dehydroamino Acids in Naturally Occurring Peptides". Amino Acids. 47 (1): 1–17. doi:10.1007/s00726-014-1846-4. PMC   4282715 . PMID   25323736.
  2. 1 2 Asquith, R.S.; Carthew, P. (1972). "The preparation and subsequent identification of a dehydroalanyl peptide from alkali-treated oxidised glutathione". Biochimica et Biophysica Acta (BBA) - Protein Structure. 285 (2): 346–351. doi:10.1016/0005-2795(72)90319-4. PMID   4659645.
  3. 1 2 Asquith, R.S.; Carthew, P. (1972). "Synthesis and PMR properties of some dehydroalanine derivatives". Tetrahedron. 28 (18): 4769–4773. doi:10.1016/0040-4020(72)88085-2.
  4. ↑ Friedman, Mendel (1999). "Lysinoalanine in food and in antimicrobial proteins". In Jackson, Lauren S.; Knize, Mark G.; Morgan, Jeffrey N. (eds.). Impact of Processing on Food Safety. Advances in Experimental Medicine and Biology. Vol. 459. Springer. pp. 145–159. doi:10.1007/978-1-4615-4853-9_10. ISBN   978-1-4615-4853-9. PMID   10335374.
  5. ↑ Rétey, János (2003). "Discovery and role of methylidene imidazolone, a highly electrophilic prosthetic group". Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1647 (1–2): 179–184. doi:10.1016/S1570-9639(03)00091-8. PMID   12686130.
  6. ↑ Calabrese JC, Jordan DB, Boodhoo A, Sariaslani S, Vannelli T (September 2004). "Crystal structure of phenylalanine ammonia lyase: multiple helix dipoles implicated in catalysis". Biochemistry. 43 (36): 11403–16. Bibcode:2004Bioc...4311403C. doi:10.1021/bi049053+. PMID   15350127.
  7. ↑ Ferreira, Paula M. T.; Maia, Hernâni L. S.; Monteiro, Luís S.; Sacramento, Joana (1999). "High yielding synthesis of dehydroamino acid and dehydropeptide derivatives". Journal of the Chemical Society, Perkin Transactions 1 (24): 3697–3703. doi:10.1039/a904730a. hdl: 1822/2188 .
  8. ↑ Chalker, Justin M.; Bernardes, Gonçalo J. L.; Davis, Benjamin G. (2011). "A "Tag-and-Modify" Approach to Site-Selective Protein Modification". Accounts of Chemical Research. 44 (9): 730–741. doi:10.1021/ar200056q. PMID   21563755.
  9. ↑ Gausmann, Marcel; Kreidt, Nadine; Christmann, Mathias (2023-04-07). "Electrosynthesis of Protected Dehydroamino Acids" . Organic Letters. 25 (13): 2228–2232. doi:10.1021/acs.orglett.3c00403. ISSN   1523-7060. PMID   36952622. S2CID   257716096.
  10. ↑ Dadová, Jitka; Galan, Sébastien RG; Davis, Benjamin G. (2018). "Synthesis of modified proteins via functionalization of dehydroalanine". Current Opinion in Chemical Biology. 46: 71–81. doi:10.1016/j.cbpa.2018.05.022. PMID   29913421.
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