Korean Journal of Agricultural Science (농업과학연구)

Institute of Agricultural Science, CNU (충남대학교 농업과학연구소)
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Physicochemical effects of different processing temperatures on 5-hydroxymethyl-2-furaldehyde and the volatile flavor of domestic honey

  • Suk-Ho, Choi (Department of Animal Biotechnology, Sangji University) ;
  • Myoung Soo, Nam (Division of Animal and Dairy Science, Chungnam National University)
  • Received : 2021.09.15
  • Accepted : 2021.11.11
  • Published : 2021.12.01
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Abstract

This study was performed to suggest concentration methods leading to the production ofhoney with an excellent flavor by examining the effects of the concentration temperature and method on changes in 5-hydroxymethyl-2-furaldehyde (5-HMF) levels and the flavor components of honey. The 5-HMF contents of honey samples concentrated in a tray concentrator at 45, 50, 60, and 70℃ were 2.1, 2.3, 2.5, and 3.1 mg·kg-1, respectively, demonstrating that the 5-HMF contents increased as the concentration temperatures were increased. The honey vacuum-concentrated at 70℃ showed a higher 5-HMF content than that at 60℃, similar to the tray-concentrated honey at different temperatures. The main and other minor flavor components of the honey were volatilized and significantly reduced after vacuum concentration. In the tray concentration, all of the honey samples concentrated at 40, 50, 60, and 70℃ showed flavor component patterns similar to each other, and most of the main and other minor flavor components in the honey were volatilized and significantly reduced after tray concentration. As such, most of the main and other minor flavor components of the honey were mostly removed at 70℃ after both the vacuum concentration and tray concentration processes. The effects of the concentration method and temperature on the viscosity, 5-HMF level, and flavor components of the honey were found to be significant in this study. Given that the components of honey were shown to undergo significant physicochemical changes depending on the concentration method used and temperature during laboratory-scale production, the concentration methods devised in this study can be applied industrially.

Keywords

Acknowledgement

본 연구는 한국양봉농협의 지원으로 수행되었으며 이에 감사드립니다.

References

  1. Alimentarius C. 2001. Revised codex standard for honey. Codex Standard 12:1982.
  2. Aslanova D, Bakkalbasi E, Artik N. 2010. Effect of storage on 5-hydroxymethylfurfural (HMF) formation and color change in jams. International Journal of Food Properties 13:904-912. https://doi.org/10.1080/10942910902908896
  3. Ball DW. 2007. The chemical composition of honey. Journal of Chemistry Education 84:1643-1646. https://doi.org/10.1021/ed084p1643
  4. Bogdanov S, Lullmann C, Martin P, von der Ohe W, Russmann H, Vorwohl G, Oddo LP, Sabatini AG, Marcazzan GL, Piro R, et al. 1999. Honey quality and international regulatory standards: Review by International Honey Commission. Bee World 80:61-69. https://doi.org/10.1080/0005772X.1999.11099428
  5. Bouseta A, Collins S, Dufour JP. 1992. Characteristic aroma profiles of unifloral honeys obtained with a dynamic headspace GC-MS system. Journal of Apicultural Research 31:96-109. https://doi.org/10.1080/00218839.1992.11101268
  6. Capuano E, Fogliano V. 2011. Acrylamide and 5-hydroxymethylfurfural (HMF): A review on metabolism, toxicity, occurrence in food and mitigation strategies. LWT- Food Science Technology 44:793-810. https://doi.org/10.1016/j.lwt.2010.11.002
  7. Castro-Vazquez L, Perez-Coello MS, Cabezudo MD. 2003. Analysis of volatile compounds of rosemary honey. Comparison of different extraction techniques. Chromatographia 57:227-233. https://doi.org/10.1007/bf02491721
  8. Choi SH, Nam MS. 2019. Classification of honeydew and blossom honeys by principal component analysis of physicochemical parameters. Korean Journal of Agricultural Science 47:67-81. https://doi.org/10.7744/KJOAS.20190088
  9. Crane E. 2020. Honey, a comprehensive survey; illustrated edition. IBRA & NBB, Montagomery, IL, USA.
  10. Dogan M, Sienkiewicz T, Oral RA. 2005. Hydroxymethylfurfural content of some commercial whey protein concentrates. Milchwissenschaft 60:309-311.
  11. Eshete Y, Eshete T. 2019. A review on the effect of processing temperature and time duration on commercial honey quality. Madridge Journal of Food Technology 4:158-162. doi: 10.18689/mjft-1000124
  12. Fallico B, Zappala M, Arena E, Verzera A. 2004. Effects of conditioning on HMF content in unifloral honeys. Food Chemistry 85:305-313.
  13. Fukuda M, Kobayashi K, Hirono Y, Miyagawa M, Ishida T, Ejiogu EC, Sawai M, Pinkerton KE, Takeuchi M. 2010. Jungle honey enhances immune function and antitumor activity. Evidence Based Complementary Alternative Medicine 2011:1-8. doi. org/10.1093/ ecam/nen086
  14. Glatt H, Schneider H, Liu Y. 2005. V79-hCYP2E1-hSULT1A1, a cell line for the sensitive detection of genotoxic effects induced by carbohydrate pyrolysis products and other food-borne chemicals. Mutation Research/Genetic Toxicology and Environmental Mutagenesis 580:41-52. https://doi.org/10.1016/j.mrgentox.2004.11.005
  15. Gupta JK, Kaushik R, Joshi V. 1992. Influence of different treatments, storage temperature and period on some physicochemical characteristics and sensory qualities of indian honey. Journal of Food Science and Technology 29:84-87.
  16. Islam N, Khalil I, Islam A, Gan SH. 2014. Toxic compounds in honey. Journal of Applied Toxicology 34:733-742. https://doi.org/10.1002/jat.2952
  17. Khalil MI, Sulaiman SA, Gan SH. 2010. High 5-hydroxymethylfurfural concentrations are found in Malaysian honey samples stored for more than 1 year. Food Chemical Toxicology 48:2388-2392. https://doi.org/10.1016/j.fct.2010.05.076
  18. Kitts DD, Chen XM, Jing H. 2012. Demonstration of antioxidant and anti-inflammatory bioactivities from sugar-amino acid Maillard reaction products. Journal of Agricultural and Food Chemistry 60:6718-6727. https://doi.org/10.1021/jf2044636
  19. Kowalski S, Lukasiewicz M, Duda-Chodak A, Ziec G. 2013. 5-hydroxymethyl-2-furfural (HMF)-heat-induced formation, occurrence in food and biotransformation-a review. Polish Journal of Food and Nutrition Sciences 63:207-225. doi:10.2478/v10222-012-0082-4
  20. Kuster BFM. 1990. 5-Hydroxymethylfurfural (HMF). A review focusing on its manufacture. Starch 42:314-321. doi.org/10.1002/star.19900420808
  21. LeBlanc BW, Eggleston G, Sammataro D, Cornett C, Dufault R, Deeby T, Cyr ES. 2009. Formation of hydroxymethylfurfural in domestic high-fructose corn syrup and its toxicity to the honey bee (Apis mellifera). Journal of Agricultural and Food Chemistry 57:7369-7376. https://doi.org/10.1021/jf9014526
  22. Li MM, Wu LY, Zhao T, Xiong L, Huang X, Liu ZH, Fan XL, Xiao CR, Gao Y, Ma YB, et al. 2011. The protective role of 5-HMF against hypoxic injury. Cell Stress Chaperones 16:267-273. https://doi.org/10.1007/s12192-010-0238-2
  23. Lin SM, Wu JY, Su C, Ferng S, Lo CY, Chiou RYY. 2012. Identification and mode of action of 5-hydroxymethyl-2-furfural (5-HMF) and 1-methyl-1,2,3,4-tetrahydro-β-carboline-3-carboxylic acid (MTCA) as potent xanthine oxidase inhibitors in vinegars. Journal of Agricultural and Food Chemistry 60:9856-9862. https://doi.org/10.1021/jf302711e
  24. Majtan J. 2014. Honey: An immunomodulator in wound healing. Wound Repair and Regeneration 22:187-192. https://doi.org/10.1111/wrr.12117
  25. Markowicz DB, Monaro E, Siguemoto E, Sefora M, Valdez B. 2012. Maillard reaction products in processed foods: Pros and cons. In Food industrial processes-methods and equipment edited by Valdez B. pp. 281-300. InTech, Rijeka, Croatia.
  26. Michail K, Matzi V, Maier A, Herwig R, Greilberger J, Juan H, Kunert O, Wintersteiger R. 2007. Hydroxymethylfurfural: An enemy or a friendly xenobiotic? A bioanalytical approach. Analytical and Bioanalytical Chemistry 387:2801-2814. https://doi.org/10.1007/s00216-007-1121-6
  27. Monien BH, Engst W, Barknowitz G, Seidel A, Glatt H. 2012. Mutagenicity of 5-hydroxymethylfurfural in V79 cells expressing human SULT1A1: Identifcation and mass spectrometric quantification of DNA adducts formed. Chemical Research in Toxicology 25:1484-1492. https://doi.org/10.1021/tx300150n
  28. Murkovic M, Pichler N. 2006. Analysis of 5-hydroxymethylfurfual in coffee, dried fruits and urine. Molecular Nutrition Food Research 50:842-846. https://doi.org/10.1002/mnfr.200500262
  29. Overton SV, Manura JJ. 1999. Note 25: Flavor and aroma in natural bee honey. Scientific Instrument Services, CA, USA.
  30. Ruckriemen J, Schwarzenbolz U, Adam S, Henle T. 2015. Identification and quantitation of 2-Acetyl-1-pyrroline in Manuka Honey (Leptospermum scoparium). Journal of Agricultural and Food Chemistry 63:8488-8492. https://doi.org/10.1021/acs.jafc.5b03042
  31. Shapla UM, Solayman MD, Alam N, Khalil I, Gan SH. 2018. 5-Hydroxymethylfurfural (HMF) levels in honey and other food products: Effects on bees and human health. Chemistry Central Journal 12:35. doi.org/10.1186/s13065-018-0408-3
  32. Subramanian R, Hebbar HU, Rastogi NK. 2007. Processing of honey: A review. International Journal of Food Properties 10:127-143. doi: 10.1080/10942910600981708
  33. Tan ST, Wilkins AL, Molan PC, Holland PT, Reid M. 1989. A chemical approach to the determination of floral sources of New Zealand honeys. Journal of Apicultural Research 28:212-222. https://doi.org/10.1080/00218839.1989.11101187
  34. Teixido E, Santos F, Puignou L, Galceran MT. 2006. Analysis of 5-hydroxymethylfurfural in foods by gas chromatography-mass spectrometry. Journal of Chromatography A 1135:85-90. https://doi.org/10.1016/j.chroma.2006.09.023
  35. Yamada P, Nemoto M, Shigemori H, Yokota S, Isoda H. 2011. Isolation of 5-(hydroxymethyl) furfural from lycium chinense and its inhibitory effect on the chemical mediator release by basophilic cells. Planta Medica 77:434-440. https://doi.org/10.1055/s-0030-1250402
  36. Zhao L, Chen J, Su J, Li L, Hu S, Li B, Zhang X, Xu Z, Chen T. 2013. In vitro antioxidant and antiproliferative activities of 5-hydroxymethylfurfural. Journal of Agricultural and Food Chemistry 61:10604-10611. https://doi.org/10.1021/jf403098y