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Investigating 5-hydroxymethylfurfural formation kinetic and antioxidant activity in heat treated honey from different floral sources

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Abstract

The quality and biochemical properties of honey are affected by heating or during storage period. The most important biochemical reaction that occurs in this process is the Maillard reaction. HMF (5-hydroxymethylfurfural) is one of the major intermediate products in the Maillard reaction that can lead to quality reduction in heated honey. In this study, the effect of heating on the antioxidant activity, and colour values as Maillard reaction indicators of three different botanical honeys were investigated; the HMF formation was also determined. Temperatures of 50, 70 and 80 °C were applied on the honeys between 0 and 48 h. Total phenolic content, ferric reducing/antioxidant power and scavenging of 2,2-diphenyl-1-picrylhydrazyl free radical assays are used to determine the antioxidant capacity. Results showed that the formation of HMF and the antioxidant properties of honeys were significantly increased during the heating process. Pure HMF compound also showed lower antioxidant activity. The formation of HMF has higher degree of linearity in the fit of the zero order reaction and also it was the highest in the chestnut honey. Furthermore, it was found that as the biochemical value of the honeys increased, the HMF formation decelerated.

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Abbreviations

MRP:

Maillard reaction product

HMF:

5-hydroxymethylfurfural

TPC:

Total phenolic content

FRAP:

Ferric reducing/antioxidant power

Trolox®:

6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid

TPTZ:

2,4,6-tripyridyl-s-triazine

DPPH 2:

2-diphenyl-1-picrylhydrazyl

GAE:

Gallic acid equivalent

RP-HPLC:

Reverse phase high performance liquid chromatography

Ea:

Activation energy

KT :

Reaction rate constant

KR :

Pre-exponential factor

References

  1. S. Soares, J.S. Amaral, M.B.P. Oliveira, I. Mafra, Compr. Rev. Food Sci. Food Saf. 16(5), 1072–1100 (2017)

    Article  CAS  Google Scholar 

  2. K. Pyrzynska, M. Biesaga, TrAC Trends Anal. Chem. 28(7), 893–902 (2009)

    Article  CAS  Google Scholar 

  3. M. Kucuk, S. Kolayli, Ş Karaoglu, E. Ulusoy, C. Baltaci, F. Candan, Food Chem. 100, 526–534 (2007)

    Article  Google Scholar 

  4. J.M. Alvarez-Suarez, M. Gasparrini, T.Y. Forbes-Hernández, L. Mazzoni, F. Giampieri, Foods 3(3), 420–432 (2014)

    Article  Google Scholar 

  5. F. Tezcan, S. Kolayli, H. Sahin, E. Ulusoy, B.F. Erim, J. Food Nutr. Res. 50, 33–40 (2011)

    CAS  Google Scholar 

  6. J. Bertoncelj, U. DobersˇEk, M. Jamnık, T. Golob, Food Chem. 105, 822–828 (2007)

    Article  CAS  Google Scholar 

  7. O. Escuredo, I. Dobre, M. Fernández-González, M.C. Seijo, Food Chem. 149, 84–90 (2014)

    Article  CAS  Google Scholar 

  8. F. Tornuk, S. Karaman, I. Ozturk, O.S. Toker, B. Tastemur, O. Sagdic, A. Kayacier, Ind. Crops Prod. 46, 124–131 (2013)

    Article  CAS  Google Scholar 

  9. E. Tosi, M. Ciappini, H. Lucero, Food Chem. 77(1), 71–74 (2002)

    Article  CAS  Google Scholar 

  10. B. Fallico, M. Zappala, E. Arena, A. Verzera, Food Chem. 85, 305–313 (2004)

    Article  CAS  Google Scholar 

  11. D.A.C. Yáñez, M. Gagneten, G.E. Leiva, L.S. Malec, LWT-Food Sci. Technol. 89, 344–349 (2018)

    Article  Google Scholar 

  12. T. Nagai, N. Kai, Y. Tanoue, N. Suzuki, J Food Sci. Technol. 55(2), 586–597 (2018)

    Article  CAS  Google Scholar 

  13. L. Manzocco, S. Calligaris, D. Mastrocola, M.C. Nicoli, C.R. Lerici, Trends Food Sci. Technol. 11, 340–346 (2001)

    Article  Google Scholar 

  14. J.M. Silván, J. van de Lagemaat, A. Olano, M.D. Del Castillo, J. Pharm. Biomed. Anal. 41, 1543–1551 (2006)

    Article  Google Scholar 

  15. O. Yıldız, H. Şahın, M. Kara, R. Alıyazıcıoglu, Ö Tarhan, S. Kolaylı, Acad. Food J. 8, 44–51 (2010)

    Google Scholar 

  16. P. Vagnarelli, A.D. Sario, M.T. Cuzzoni, P. Mazza, L.D. Carli, J. Agric. Food Chem. 39, 2237–2239 (1991)

    Article  CAS  Google Scholar 

  17. G.C. Yen, C.F. Chau, D.J. Lii, J. Agric. Food Chem. 41, 771–776 (1993)

    Article  CAS  Google Scholar 

  18. G.C. Yen, L.C. Tsai, Food Chem. 47, 11–15 (1993)

    Article  CAS  Google Scholar 

  19. N. Turkmen, F. Sarı, E.S. Poyrazoglu, Y.S. Velioglu, Food Chem. 95, 653–657 (2006)

    Article  CAS  Google Scholar 

  20. F. Chevalier, J.M. Chobert, C. Genot, T. Haertle, J. Agric. Food Chem. 49, 5031–5038 (2001)

    Article  CAS  Google Scholar 

  21. A. Kato, Food Sci. Technol. Res. 8, 193–199 (2002)

    Article  CAS  Google Scholar 

  22. R.C. Borrelli, C. Mennella, F. Barba, M. Russo, G.L. Russo, K. Krome, H.F. Erbersdobler, V. Faist, V. Fogliano, Food Chem. Toxicol. 41, 1367–1374 (2003)

    Article  CAS  Google Scholar 

  23. M. Lindermeier, T. Hofmann, J. Agric. Food Chem. 52, 350–354 (2004)

    Article  Google Scholar 

  24. Y. Yilmaz, R. Toledo, Food Chem. 93, 273–278 (2005)

    Article  CAS  Google Scholar 

  25. J.M. Ames, The Maillard reaction. (B. J. F. Hudson Ed., 1992) pp. 150–154

    Chapter  Google Scholar 

  26. L.W. Kroh, Food Chem. 51, 373–379 (1994)

    Article  CAS  Google Scholar 

  27. J.A. Rufıán-Henares, C. Delgado-Andrade, F.J. Morales, Non-enzymatic browning:the case of the Maillard reaction. (C. Delgado-Andrade, J. A. Rufıán-Henares, eds. 2009), pp. 9–19

  28. D.M. Bastos, E. Monaro, E. Siguemoto, M. Séfora, Food Industrial Processes-Methods and Equipment. (InTech, Rijeka, 2012)

    Google Scholar 

  29. E. Guerra-Hernandez, B. Garcıa-Vılanova, J. Montılla-Gomez, J. Liq. Chromatogr. 15, 2551–2559 (1992)

    Article  CAS  Google Scholar 

  30. S. Albala´-Hurtado, M.T. Veciana-Nogue´S, A. Marine´-Font, M.C. Vidal-Carou, J. Agric. Food Chem. 46, 2998 (1998)

    Article  Google Scholar 

  31. Codex Alimentarius Commission, 1st edn. Revised (Rev. 2001) p. 2

  32. S. Ajlouni, P. Sujirapınyokul, Food Chem. 119, 1000–1005 (2010)

    Article  CAS  Google Scholar 

  33. J. Loveaux, J. Pourtallıe, G. Vorwohl, Bull. Apic. Inf. Doc. Sci. Technol. 16, 7 (1973)

    Google Scholar 

  34. W. Von Der Ohe, L. Persano-Oddo, M.L. Piana, M. Morlot, P. Martin, Apidologie 35, 18–25 (2004)

    Article  Google Scholar 

  35. K. Slinkard, V.L. Singleton, Am. J. Enol. Vitic. 28, 49–55 (1977)

    CAS  Google Scholar 

  36. A. Meda, C.E. Lamıen, M. Romıto, J. Mıllogo, O.G. Nacoulma, Food Chem. 91, 571–577 (2005)

    Article  CAS  Google Scholar 

  37. L.A. Chen, M. Mehta, A.R. Berenbaum, I. Zanger, N.J. Engeseth, J. Agric. Food Chem. 48, 4997–5000 (2000)

    Article  CAS  Google Scholar 

  38. T.P. Labuza, D. Riboh, Food Technol. 36, 55–74 (1982)

    Google Scholar 

  39. D. Aslanova, E. Bakkalbası, N. Artık, Int. J. Food Prop. 13, 904–912 (2010)

    Article  CAS  Google Scholar 

  40. O. Yildiz, M. Alpaslan, Food Technol. Biotechnol. 50, 98–106 (2012)

    CAS  Google Scholar 

  41. S. Boonchiangma, S. Chanthai, S. Srijaranai, S. Srijaranai, J. Food Process Eng. 34(5), 1584–1596 (2011)

    Article  CAS  Google Scholar 

  42. B. Fallico, M. Zappala, E. Arena, A. Verzera, Food Chem. 85(2), 305–313 (2004)

    Article  CAS  Google Scholar 

  43. L. Bulut, M. Kilic, J. Food Process. Preserv. 33(1), 22–32 (2009)

    Article  CAS  Google Scholar 

  44. N. Turhan, M. Tetik, F. Karhan, H.R. Gurel, Tavukcuoglu, LWT Food Sci. Technol. 41, 1396–1399 (2008)

    Article  CAS  Google Scholar 

  45. A.O. Sarıkaya, E. Ulusoy, N. Öztürk, M. Tuncel, S. Kolayli, J. Food Biochem. 33, 470–481 (2009)

    Article  Google Scholar 

  46. D. Mastrocola, M. Munari, J. Agric. Food Chem. 48, 3555–3559 (2000)

    Article  CAS  Google Scholar 

  47. T. Kahraman, S.K. Buyukunal, A. Vural, S.S. Altunatmaz, Food Chem. 123, 41–44 (2010)

    Article  CAS  Google Scholar 

  48. E. Nebesny, G. Budryn, Eur. Food Res. Technol. 217(2), 157–163 (2003)

    Article  CAS  Google Scholar 

  49. D. Mastrocola, M. Munari, M. Cioroi, C.R. Lerici, J. Sci. Food Agric. 80, 684–690 (2000)

    Article  CAS  Google Scholar 

Download references

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Correspondence to Atiye Degirmenci.

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Turkut, G.M., Degirmenci, A., Yildiz, O. et al. Investigating 5-hydroxymethylfurfural formation kinetic and antioxidant activity in heat treated honey from different floral sources. Food Measure 12, 2358–2365 (2018). https://doi.org/10.1007/s11694-018-9852-y

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  • DOI: https://doi.org/10.1007/s11694-018-9852-y

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