Miraculin

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Miraculin glycoprotein
Miraculin.png
Crystallographic structure of a dimeric miraculin-like protein from seeds of Murraya koenigii . [1]
Identifiers
Organism Synsepalum dulcificu
SymbolMIRA_RICDU
PDB 3IIR
UniProt P13087
Search for
Structures Swiss-model
Domains InterPro

Miraculin is a taste modifier, a glycoprotein extracted from the fruit of Synsepalum dulcificum . [2] The berry, also known as the miracle fruit, was documented by explorer Chevalier des Marchais, who searched for many different fruits during a 1725 excursion to its native West Africa.

Contents

Miraculin itself does not taste sweet. When taste buds are exposed to miraculin, the protein binds to the sweetness receptors. This causes normally sour-tasting acidic foods, such as citrus, to be perceived as sweet. [2] [3] The effect can last for one or two hours. [4] [5]

History

The sweetening properties of Synsepalum dulcificum berries were first noted by des Marchais during expeditions to West Africa in the 18th century. [6] The term miraculin derived from experiments to isolate and purify the active glycoprotein that gave the berries their sweetening effects, results that were published simultaneously by Japanese and Dutch scientists working independently in the 1960s (the Dutch team called the glycoprotein mieraculin). [7] [8] The word miraculin was in common use by the mid-1970s. [9] [10] [11]

Glycoprotein structure

Miraculin was first sequenced in 1989 and was found to be a 24.6  kilodalton [2] glycoprotein consisting of 191 amino acids [12] and 13.9% by weight of various sugars. [2]

SIGNAL (29) M K E L TMLSLS FFFVSALLAA AAN PLLSAA
1–50 DSAPNPVLDI DGEKLRTGTN YYIVPVLRDH GGGLTVSATT PNGTFVCPPR
51–100VVQTRKEVDH DRPLAFFPEN PKEDVVRVST DLNINFSAFM PNPGPETISS
101–150 WCRWTSSTVW RLDKYDESTG QYFVTIGGVK FKIEEFCGSG FYKLVFCPTV
151–191CGSCKVKCGD VGIYIDQKGR GRRLALSDKP FAFEFNKTVY F
Amino acids sequence of glycoprotein miraculin unit adapted from Swiss-Prot biological database of protein sequences. [13]

The sugars consist of a total of 3.4 kDa, composed of a molar ratio of glucosamine (31%), mannose (30%), fucose (22%), xylose (10%), and galactose (7%). [2]

The native state of miraculin is a tetramer consisting of two dimers, each held together by a disulfide bridge. [14] Both tetramer miraculin and native dimer miraculin in its crude state have the taste-modifying activity of turning sour tastes into sweet tastes. [15] Miraculin belongs to the Kunitz STI protease inhibitor family.

Sweetness properties

Miraculin, unlike curculin (another taste-modifying agent), [16] is not sweet by itself, but it can change the perception of sourness to sweetness, even for a long period after consumption. [4] The duration and intensity of the sweetness-modifying effect depends on various factors, such as miraculin concentration, duration of contact of the miraculin with the tongue, and acid concentration. [3] [4] Miraculin reaches its maximum sweetness with a solution containing at least 4*10−7  mol/L miraculin, which is held in the mouth for about 3 minutes. Maximum is equivalent in sweetness to a 0.4 mol/L solution of sucrose. [17] Miraculin degrades permanently via denaturation at high temperatures and at pH below 3 or above 12. [18]

Although the detailed mechanism of the taste-inducing behavior is unknown, it appears the sweet receptors are activated by acids which are related to sourness, an effect remaining until the taste buds perceive a neutral pH. [3] [4] Sweeteners are perceived by the human sweet taste receptor, hT1R2-hT1R3, which belongs to G protein-coupled receptors, [4] modified by the two histidine residues (i.e. His30 and His60) which participate in the taste-modifying behavior. [19] One site maintains the attachment of the protein to the membranes while the other (with attached xylose or arabinose) activates the sweet receptor membrane in acid solutions. [14]

As a sweetener

As miraculin is a readily soluble protein and relatively heat stable, it is a potential sweetener in acidic food, such as soft drinks. While attempts to express it in yeast and tobacco plants have failed, researchers have succeeded in preparing genetically modified E. coli bacteria that express miraculin. [20] Lettuce and tomato have also been used for mass production of miraculin. [21] [22]

The use of miraculin as a food additive was denied in 1974 by the United States Food and Drug Administration. [23] However, it can still be sold in the form of whole berries or tablets (as "dietary supplements"). [24] [25] In 2011 the FDA banned a certain brand of miraculin tablets imported from Taiwan as it was thought to be "hard candy" with non-approved sweeteners. [26] Miraculin has a novel food status in the European Union. [27] It is approved in Japan as a safe food additive, according to the List of Existing Food Additives published by the Ministry of Health and Welfare (published by the Japan External Trade Organization).

See also

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References

  1. PDB: 3IIR ; Gahloth D, Selvakumar P, Shee C, Kumar P, Sharma AK (February 2010). "Cloning, sequence analysis and crystal structure determination of a miraculin-like protein from Murraya koenigii". Archives of Biochemistry and Biophysics. 494 (1): 15–22. doi:10.1016/j.abb.2009.11.008. PMID   19914199.
  2. 1 2 3 4 5 Theerasilp S, Kurihara Y (August 1988). "Complete purification and characterization of the taste-modifying protein, miraculin, from miracle fruit". The Journal of Biological Chemistry. 263 (23): 11536–9. doi: 10.1016/S0021-9258(18)37991-2 . PMID   3403544. Archived from the original on 2005-08-27. Retrieved 2009-04-09.
  3. 1 2 3 Sanematsu K, Kitagawa M, Yoshida R, Nirasawa S, Shigemura N, Ninomiya Y (March 2016). "Intracellular acidification is required for full activation of the sweet taste receptor by miraculin". Scientific Reports. 6: 22807. Bibcode:2016NatSR...622807S. doi:10.1038/srep22807. PMC   4785348 . PMID   26960429.
  4. 1 2 3 4 5 Koizumi A, Tsuchiya A, Nakajima K, Ito K, Terada T, Shimizu-Ibuka A, Briand L, Asakura T, Misaka T, Abe K (October 2011). "Human sweet taste receptor mediates acid-induced sweetness of miraculin". Proceedings of the National Academy of Sciences of the United States of America. 108 (40): 16819–24. Bibcode:2011PNAS..10816819K. doi: 10.1073/pnas.1016644108 . PMC   3189030 . PMID   21949380.
  5. Swamy KB, Hadi SA, Sekaran M, Pichika MR (November 2014). "The clinical effects of Synsepalum dulcificum: a review". Journal of Medicinal Food. 17 (11): 1165–9. doi:10.1089/jmf.2013.3084. PMID   25314134.
  6. Cudnik DR (27 July 2014). "The miracle berry and miraculin: A review". WordPress. Retrieved 21 September 2019.
  7. Kurihara K, Beidler LM (September 1968). "Taste-modifying protein from miracle fruit". Science. 161 (3847): 1241–3. Bibcode:1968Sci...161.1241K. doi:10.1126/science.161.3847.1241. PMID   5673432. S2CID   24451890.
  8. Brouwer JN, van der Wel H, Francke A, Henning GJ (October 1968). "Mieraculin, the sweetness-inducing protein from miracle fruit". Nature. 220 (5165): 373–4. Bibcode:1968Natur.220..373B. doi:10.1038/220373a0. PMID   5684879. S2CID   4146207.
  9. Cagan RH (July 1973). "Chemostimulatory protein: a new type of taste stimulus". Science. 181 (4094): 32–5. Bibcode:1973Sci...181...32C. doi:10.1126/science.181.4094.32. PMID   4714290. S2CID   23665011.
  10. Giroux EL, Henkin RI (1974). "Purification and some properties of miraculin, a glycoprotein from Synsepalum dulcificum which provokes sweetness and blocks sourness". Journal of Agricultural and Food Chemistry. 22 (4): 595–601. doi:10.1021/jf60194a033. PMID   4840911.
  11. von Baumgarten R (1975). "[Physiology of smell and taste]". Archives of Oto-Rhino-Laryngology. 210 (1): 43–65. doi:10.1007/bf00453707. PMID   233846. S2CID   40054832.
  12. Theerasilp S, Hitotsuya H, Nakajo S, Nakaya K, Nakamura Y, Kurihara Y (April 1989). "Complete amino acid sequence and structure characterization of the taste-modifying protein, miraculin". The Journal of Biological Chemistry. 264 (12): 6655–9. doi: 10.1016/S0021-9258(18)83477-9 . PMID   2708331. Archived from the original on 2020-06-09. Retrieved 2009-04-09.
  13. UniProtKB/Swiss-Prot database entry P13087
  14. 1 2 Kurihara Y (1992). "Characteristics of antisweet substances, sweet proteins, and sweetness-inducing proteins". Critical Reviews in Food Science and Nutrition. 32 (3): 231–52. doi:10.1080/10408399209527598. PMID   1418601.
  15. Igeta H, Tamura Y, Nakaya K, Nakamura Y, Kurihara Y (September 1991). "Determination of disulfide array and subunit structure of taste-modifying protein, miraculin". Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology. 1079 (3): 303–7. doi:10.1016/0167-4838(91)90073-9. PMID   1911854.
  16. Kurimoto E, Suzuki M, Amemiya E, Yamaguchi Y, Nirasawa S, Shimba N, Xu N, Kashiwagi T, Kawai M, Suzuki E, Kato K (November 2007). "Curculin exhibits sweet-tasting and taste-modifying activities through its distinct molecular surfaces". The Journal of Biological Chemistry. 282 (46): 33252–6. doi: 10.1074/jbc.C700174200 . PMID   17895249.
  17. Mérillon J, et al. (2018). Sweeteners: pharmacology, biotechnology, and applications. p. 169. doi:10.1007/978-3-319-27027-2_17. ISBN   9783319270272. OCLC   1019806685.
  18. Mangla, B; Kohli, K (2018). "Pharmaceutical and therapeutic potential of miraculin and miracle berry". Tropical Journal of Natural Product Research. 2 (1): 12–17. doi: 10.26538/tjnpr/v2i1.3 . ISSN   2616-0684.
  19. Ito K, Asakura T, Morita Y, Nakajima K, Koizumi A, Shimizu-Ibuka A, Masuda K, Ishiguro M, Terada T, Maruyama J, Kitamoto K, Misaka T, Abe K (August 2007). "Microbial production of sensory-active miraculin". Biochemical and Biophysical Research Communications. 360 (2): 407–11. doi:10.1016/j.bbrc.2007.06.064. PMID   17592723.
  20. Matsuyama T, Satoh M, Nakata R, Aoyama T, Inoue H (April 2009). "Functional expression of miraculin, a taste-modifying protein in Escherichia coli". Journal of Biochemistry. 145 (4): 445–50. doi:10.1093/jb/mvn184. PMID   19122203.
  21. Sun HJ, Cui ML, Ma B, Ezura H (January 2006). "Functional expression of the taste-modifying protein, miraculin, in transgenic lettuce". FEBS Letters. 580 (2): 620–6. doi: 10.1016/j.febslet.2005.12.080 . PMID   16406368. S2CID   9524453.
  22. Kato K, Yoshida R, Kikuzaki A, Hirai T, Kuroda H, Hiwasa-Tanase K, Takane K, Ezura H, Mizoguchi T (September 2010). "Molecular breeding of tomato lines for mass production of miraculin in a plant factory". Journal of Agricultural and Food Chemistry. 58 (17): 9505–10. doi:10.1021/jf101874b. PMID   20695489.
  23. Gollner AL (31 March 2009). The Fruit Hunters: A Story of Nature, Adventure, Commerce and Obsession. Anchor Canada. ISBN   978-0385662680.
  24. Hieggelke B (2013-04-18). "Sugar Freedom: Chef Homaro Cantu and his Magnificent Miracle Berry Obsession". NewCity Communications Inc. Retrieved 2018-02-25.
  25. Cox D (2014-05-29). "The 'Miracle' Berry That Could Replace Sugar". The Atlantic Monthly Group . Retrieved 2018-02-25.
  26. "Import Alert 45-07". www.accessdata.fda.gov. Retrieved 2024-09-06.
  27. "Novel Food Catalogue" . Retrieved 21 August 2021.