Ergothioneine

Ergothioneine
Names
IUPAC name
3-(2-Sulfanylidene-1,3-dihydroimidazol-4-yl)-2-(trimethylazaniumyl)propanoate
Other names
L-Ergothioneine; (+)-Ergothioneine; Thiasine; Sympectothion; Ergothionine; Erythrothioneine; Thiolhistidinebetaine
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.007.131
KEGG
UNII
Properties
C9H15N3O2S
Molar mass 229.30 g/mol
Appearance white solid
Melting point 275 to 277 °C (527 to 531 °F; 548 to 550 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Ergothioneine is a naturally occurring amino acid and is a thiourea derivative of histidine, containing a sulfur atom on the imidazole ring. This compound is made in relatively few organisms, notably Actinobacteria, Cyanobacteria, and certain fungi.[1][2] Ergothioneine was discovered in 1909 and named after the ergot fungus from which it was first purified, with its structure being determined in 1911.[3]

In vitro assays, as well as in vivo animal models, are used in basic research to identify its potential biological properties.[4][5][6]

In humans, ergothioneine is acquired exclusively through the diet and accumulates in erythrocytes, bone marrow, liver, kidney, seminal fluid and eyes.[4] Ergothioneine requires a specific transporter, ETT, also known as OCTN1 (gene symbol SLC22A4), to enter cells.[4][7] ETT expression has been confirmed in human and animal cell lines and its functional transport of ergothioneine has been observed in preliminary studies in vivo.[4][8][9] Although the effect of ergothioneine in vivo is an active area of research, its physiological role in humans is undetermined.[4]

Metabolism and sources

Ergothioneine has been found in bacteria, plants and animals, sometimes at millimolar levels.[10] Foods found to contain ergothioneine include liver, kidney, black beans, kidney bean and oat bran, with the highest levels in bolete and oyster mushrooms.[10] Levels can be variable, even within species and some tissues can contain much more than others. In the human body, the largest amounts of ergothioneine are found in erythrocytes, eye lens and semen,[3] and it is also present in the skin.[11]

Although many species contain ergothioneine, only a few make it, the others absorbing it from their diet or, in the case of plants, from their environment.[12] Biosynthesis has been detected in Actinobacteria, such as Mycobacterium smegmatis and certain fungi, such as Neurospora crassa.[1]

The metabolic pathway to produce ergothioneine starts with the methylation of histidine to produce histidine betaine (hercynine). The sulfur atom is then incorporated from cysteine.[10][13] The biosynthetic genes of ergothioneine have been described in Mycobacterium smegmatis,[14] Neurospora crassa,[15] and Schizosaccharomyces pombe.[16]

Other species of bacteria, such as Bacillus subtilis, Escherichia coli, Proteus vulgaris and Streptococcus, as well as fungi in the Saccharomycotina cannot make ergothioneine.[17][18]

Chemistry

Ergothioneine is a thiourea derivative of the betaine of histidine and contains a sulfur atom bonded to the 2-position of the imidazole ring. This compound is unusual since the sulfur atom is most stable in solution in the thione form, rather than the sulfhydryl, in contrast to the structurally related ovothiol.[6] This makes ergothioneine much less reactive than thiols such as glutathione towards alkylating agents like maleimides, and also prevents the compound from oxidizing in air.[10] However, ergothioneine can be slowly oxidized over several days to the disulfide form in acidic solutions.[19] If ergothioneine does become oxidized, the disulfide is a very strong oxidizing agent, so this will in turn rapidly oxidize other thiols in the cell such as glutathione.[20]

Ergothioneine derivatives

Various derivatives of ergothioneine have been reported in the literature, such as S-methyl-ergothioneine[21] or selenium-containing selenoneine.[22]

Preliminary research

Ergothioneine has antioxidant properties in vitro.[1][23] Under laboratory conditions, it scavenges hydroxyl radicals and hypochlorous acid, inhibits production of oxidants by metal ions,[24][25] and may participate in metal ion transport and regulation of metalloenzymes.[25]

Although potential effects of ergothioneine are under preliminary research, its physiological role in vivo is unknown.[4]

See also

References

  1. 1 2 3 Fahey RC (2001). "Novel thiols of prokaryotes". Annu. Rev. Microbiol. 55: 333–56. PMID 11544359. doi:10.1146/annurev.micro.55.1.333.
  2. ↑ Pfeiffer, C; Bauer, T; Surek, B; Schömig, E; Gründemann, D (2011). "Cyanobacteria produce high levels of ergothioneine". Food Chemistry. Elsevier. 129 (4): 1766–1769. doi:10.1016/j.foodchem.2011.06.047.
  3. 1 2 Mann T, Leone E (January 1953). "Studies on the metabolism of semen. 8. Ergothioneine as a normal constituent of boar seminal plasma. Purification and crystallization. Site of formation and function". Biochem. J. 53 (1): 140–8. PMC 1198115 Freely accessible. PMID 13032046.
  4. 1 2 3 4 5 6 Cheah, Irwin K.; Halliwell, Barry (2012-05-01). "Ergothioneine; antioxidant potential, physiological function and role in disease". Biochimica et Biophysica Acta. 1822 (5): 784–793. ISSN 0006-3002. PMID 22001064. doi:10.1016/j.bbadis.2011.09.017.
  5. ↑ Gründemann, Dirk. "The ergothioneine transporter controls and indicates ergothioneine activity — A review". Preventive Medicine. 54: S71–S74. doi:10.1016/j.ypmed.2011.12.001.
  6. 1 2 Hartman PE (1990). "Ergothioneine as antioxidant". Meth. Enzymol. Methods in Enzymology. 186: 310–8. ISBN 978-0-12-182087-9. PMID 2172707. doi:10.1016/0076-6879(90)86124-E.
  7. ↑ Markova, Nelli G.; Karaman-Jurukovska, Nevena; Dong, Kelly K.; Damaghi, Niusha; Smiles, Kenneth A.; Yarosh, Daniel B. (2009-04-15). "Skin cells and tissue are capable of using L-ergothioneine as an integral component of their antioxidant defense system". Free Radical Biology & Medicine. 46 (8): 1168–1176. ISSN 1873-4596. PMID 19439218. doi:10.1016/j.freeradbiomed.2009.01.021.
  8. ↑ Koepsell (2014). Drug Transporters: Molecular Characterization and Role in Drug Disposition, Second Edition - Wiley Online Library. pp. 7–24. doi:10.1002/9781118705308.
  9. ↑ Aruoma, Okezie I.; Coles, L. Stephen; Landes, Bernie; Repine, John E. "Functional benefits of ergothioneine and fruit- and vegetable-derived nutraceuticals: Overview of the supplemental issue contents". Preventive Medicine. 54: S4–S8. doi:10.1016/j.ypmed.2012.04.001.
  10. 1 2 3 4 Ey J, Schömig E, Taubert D (August 2007). "Dietary sources and antioxidant effects of ergothioneine". J. Agric. Food Chem. 55 (16): 6466–74. PMID 17616140. doi:10.1021/jf071328f.
  11. ↑ Markova NG, Karaman-Jurukovska N, Dong KK, Damaghi N, Smiles KA, Yarosh DB (April 2009). "Skin cells and tissue are capable of using l-ergothioneine as an integral component of their antioxidant defense system". Free Radic Biol Med. 46 (8): 1168–76. PMID 19439218. doi:10.1016/j.freeradbiomed.2009.01.021.
  12. ↑ Audley, B.S.; Tan, C.H. (1968). "The uptake of ergothioneine from the soil into the latex of Hevea brasiliensis". Phytochemistry. 7 (11): 1999–2000. doi:10.1016/S0031-9422(00)90759-3.
  13. ↑ Melville DB, Ludwig ML, Inamine E, Rachele JR (May 1959). "Transmethylation in the biosynthesis of ergothioneine". J. Biol. Chem. 234 (5): 1195–8. PMID 13654346.
  14. ↑ Seebeck, F. P. (2010). "In vitro reconstitution of Mycobacterial ergothioneine biosynthesis". Journal of the American Chemical Society. 132 (19): 6632–3. PMID 20420449. doi:10.1021/ja101721e.
  15. ↑ Bello, M. H.; Barrera-Perez, V; Morin, D; Epstein, L (2012). "The Neurospora crassa mutant NcΔEgt-1 identifies an ergothioneine biosynthetic gene and demonstrates that ergothioneine enhances conidial survival and protects against peroxide toxicity during conidial germination". Fungal Genetics and Biology. 49 (2): 160–72. PMID 22209968. doi:10.1016/j.fgb.2011.12.007.
  16. ↑ Pluskal, T; Ueno, M; Yanagida, M (2014). "Genetic and metabolomic dissection of the ergothioneine and selenoneine biosynthetic pathway in the fission yeast, S. Pombe, and construction of an overproduction system". PLoS ONE. 9 (5): e97774. PMC 4020840 Freely accessible. PMID 24828577. doi:10.1371/journal.pone.0097774.
  17. ↑ Genghof DS (1 August 1970). "Biosynthesis of Ergothioneine and Hercynine by Fungi and Actinomycetales". J. Bacteriol. 103 (2): 475–8. PMC 248105 Freely accessible. PMID 5432011.
  18. ↑ Genghof DS, Inamine E, Kovalenko V, Melville DB (November 1956). "Ergothioneine in microorganisms". J. Biol. Chem. 223 (1): 9–17. PMID 13376573.
  19. ↑ Heath H, Toennies G (February 1958). "The preparation and properties of ergothioneine disulphide" (PDF). Biochem. J. 68 (2): 204–10. PMC 1200325 Freely accessible. PMID 13522601.
  20. ↑ Hand CE, Taylor NJ, Honek JF (March 2005). "Ab initio studies of the properties of intracellular thiols ergothioneine and ovothiol". Bioorg. Med. Chem. Lett. 15 (5): 1357–60. PMID 15713386. doi:10.1016/j.bmcl.2005.01.014.
  21. ↑ Asmus, K. D.; Bensasson, R. V.; Bernier, J. L.; Houssin, R; Land, E. J. (1996). "One-electron oxidation of ergothioneine and analogues investigated by pulse radiolysis: Redox reaction involving ergothioneine and vitamin C". The Biochemical Journal. 315 (2): 625–9. PMC 1217242 Freely accessible. PMID 8615839. doi:10.1042/bj3150625.
  22. ↑ Yamashita, Y; Yamashita, M (2010). "Identification of a novel selenium-containing compound, selenoneine, as the predominant chemical form of organic selenium in the blood of bluefin tuna". Journal of Biological Chemistry. 285 (24): 18134–8. PMC 2881734 Freely accessible. PMID 20388714. doi:10.1074/jbc.C110.106377.
  23. ↑ Hand CE, Honek JF (February 2005). "Biological chemistry of naturally occurring thiols of microbial and marine origin". J. Nat. Prod. 68 (2): 293–308. PMID 15730267. doi:10.1021/np049685x.
  24. ↑ Akanmu D, Cecchini R, Aruoma OI, Halliwell B (July 1991). "The antioxidant action of ergothioneine". Arch Biochem Biophys. 288 (1): 10–6. PMID 1654816. doi:10.1016/0003-9861(91)90158-F.
  25. 1 2 Misiti F, Castagnola M, Zuppi C, Giardina B, Messana I (June 2001). "Role of ergothioneine on S-nitrosoglutathione catabolism". Biochem J. 356 (Pt 3): 799–804. PMC 1221906 Freely accessible. PMID 11389687. doi:10.1042/0264-6021:3560799.
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