Czech J. Food Sci., 2016, 34(6):503-510 | DOI: 10.17221/86/2016-CJFS

Kinetics of non-enzymatic browning reaction from the l-ascorbic acid/l-cysteine model systemFood Chemistry and Safety

Ai-Nong YU1, 2, Le-Pan TANG2
1 Key Laboratory of Biologic Resources Protection and Utilization of Hubei Province, Enshi, Hubei, P.R. China
2 School of Chemistry &
Environmental Engineering, Hubei University for Nationalities, Enshi, Hubei, P.R. China

The kinetics of the non-enzymatic browning reaction from l-ascorbic acid/l-cysteine model systems was investigated at 125-155°C for 10-120 min by measuring the loss of reactants and monitoring the brown colour development. The result showed that the browning products were produced at the first order reaction kinetics requirement, with the Ea being 114.33 kJ/mol. The mechanism for the browning development was proposed. The correlation coefficient between browning products and uncoloured intermediate products increased with the rising temperature. At temperatures below 110°C, the non-enzymatic browning reaction did not occur at all or the reaction was slow. Browning products could not be produced solely by self-degradation of l-cysteine. The amount of browning products negatively correlated with the l-ascorbic acid concentration.

Keywords: Maillard; mechanism; amino acid; first order reaction; activation energy

Published: December 31, 2016  Show citation

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Ai-Nong Y, TANG L. Kinetics of non-enzymatic browning reaction from the l-ascorbic acid/l-cysteine model system. Czech J. Food Sci. 2016;34(6):503-510. doi: 10.17221/86/2016-CJFS.
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References

  1. Adams A., De Kimpe N. (2009): Formation of pyrazines from ascorbic acid and amino acids under dry-roasting conditions. Food Chemistry, 115: 1417-1423. Go to original source...
  2. Ajandouz E.H., Tchiakpe L.S., Ore F.D., Benajiba A., Puigserver A. (2001): Effects of pH on caramelization and Maillard reaction kinetics in fructose-lysine model systems. Journal of Food Science, 66: 926-931. Go to original source...
  3. Benjakul S., Lertittikul W., Bauer F. (2005a): Antioxidant activity of Maillard reaction products from a porcine plasma protein-sugar model system. Food Chemistry, 93: 189-196. Go to original source...
  4. Benjakul S., Visessanguan W., Phongkanpai V., Tanaka M. (2005b): Antioxidative activity of caramelisation products and their preventive effect on lipid oxidation in fish mince. Food Chemistry, 90: 231-239. Go to original source...
  5. Burdurlu H.S., Karadeniz F. (2003): Effect of storage on nonenzymatic browning of apple juice concentrates. Food Chemistry, 80: 91-97. Go to original source...
  6. Corzo-Martínez M., Corzo N., Villamiel M., del Castillo M.D. (2012): Food Biochemistry and Food Processing. 2nd Ed. Ames, Wiley & Sons: 56-71. Go to original source...
  7. Davies C.G.A., Wezicha B.L. (1994): Ascorbic acid browning; the incorporation of C1 from ascorbic acid into melanoidins. Food Chemistry, 49: 165-167. Go to original source...
  8. Ding F.C., Jiang Y.H., Zhang J. (2003): Study on the thermal decomposition kinetic and thermalstability of five common amino acids. Chemistry and Bioengineering, 18: 156-158.
  9. Hong X., Meng J., Lu R.R. (2015): Improvement of ACE inhibitory activity of casein hydrolysate by Maillard reaction with xylose. Journal of the Science of Food and Agriculture, 95: 66-71. Go to original source... Go to PubMed...
  10. Kitrytė V., Adams A., Venskutonis P.R., De Kimpe N. (2012): Impact of lipid oxidation-derived aldehydes and ascorbic acid on the antioxidant activity of model melanoidins. Food Chemistry, 135: 1273-1283. Go to original source... Go to PubMed...
  11. Lertittikul W., Benjakul S., Tanaka M. (2007): Characteristics and antioxidative activity of Maillard reaction products from a porcine plasma protein-glucose model system as influenced by pH. Food Chemistry, 100: 669- 677. Go to original source...
  12. Li Y., Yang Y., Yu A.N., Wang K. (2016): Effects of reaction parameters on self-degradation of l-ascorbic acid and self-degradation kinetics. Food Science and Biotechnology, 25: 97-104. Go to original source... Go to PubMed...
  13. Liang C., Yuan F., Liu F., Wang Y., Gao Y. (2014): Structure and antimicrobial mechanism of ε-polylysine-chitosan conjugates through Maillard reaction. International Journal of Biological Macromolecules, 70: 427-434. Go to original source... Go to PubMed...
  14. Ling B., Tang J., Kong F., Mitcham E.J., Wang S. (2015): Kinetics of food quality changes during thermal processing: a review. Food and Bioprocess Technology, 8: 343-358. Go to original source...
  15. Liu S.C., Yang D.J., Chen H.Y., Chen S.L., Chen M.L. (2011): Kinetics of fructose on the Maillard brown colour development, pH change and antioxidative activity development in model fructose/glycine systems. International Journal of Food Science and Technology, 46: 1768-1774. Go to original source...
  16. Lü Y.G., Zhang H., Meng X.Y., Wang L., Guo X.N., Tao G.J. (2009): Determination of glutamate decarboxylase activity in plant by pre-column derivatization with 2,4-dinitrofluorobenzene. Chinese Journal of Analytical Chemistry, 37: 347-350.
  17. Martins S.I.F.S., Jongen W.M.F., van Boekel M.A.J.S. (2001): A review of Maillard reaction in food and implications to kinetic modelling. Trends in Food Science and Technology, 11: 364-373. Go to original source...
  18. Obretenov C., Demyttenaere J., Tehrani K.A., Adams A., Keršiene M., De Kimpe N. (2002): Flavor release in the presence of melanoidins prepared from l-(+)-ascorbic acid and amino acids. Journal of Agricultural and Food Chemistry, 50: 4244-4250. Go to original source... Go to PubMed...
  19. O'Charoen S., Hayakawa S., Ogawa M. (2015): Food properties of egg white protein modified by rare ketohexoses through Maillard reaction. International Journal of Food Science and Technology, 50: 194-202. Go to original source...
  20. Rogacheva S.M., Kuntcheva M.J., Panchev I.N., Obretenov T.D. (1999): Melanoidin formation in l-ascorbic acidamino acids interaction. A comparative study. Nahrung, 43: 105-108. Go to original source...
  21. Rozycki S.D., Buera M.P., Piagentini A.M., Costa S.C., Pauletti M.S. (2010): Advances in the study of the kinetics of color and fluorescence development in concentrated milk systems. Journal of Food Engineering, 101: 59-66. Go to original source...
  22. Tang L.P., Zhou Y.Y., Yu A.N. (2014): Comparison of UV spectrophotometry and HPLC in determination of ascorbic acid in Maillard reaction. Science and Technology of Food Industry, 35: 79-82.
  23. Tang L.P., Yang X.H., Yu A.N. (2015): Kinetics of forming volatiles in Maillard reaction from ascorbic acid/cysteine system. Food Science, 36: 63-68.
  24. Taylor J.L.S., Demyttenaere J.C.R., Tehrani K.A., Olave C.A., Regniers L., Verschaeve L., Maes A., Elgorashi E.E., van Staden J., De Kimpe N. (2004): Genotoxicity of melanoidin fractions derived from a standard glucose/ glycine model. Journal of Agricultural and Food Chemistry, 52: 318-323. Go to original source... Go to PubMed...
  25. Wrolstad R.E. (2012): Food Carbohydrate Chemistry. USA, Wiley & Sons: 50-72. Go to original source...
  26. Yu A.N., Zhang A.D. (2010): Aroma compounds generated from thermal reaction of l-ascorbic acid with l-cysteine. Food Chemistry, 121: 1060-1065. Go to original source...
  27. Yu M.H., Wu M.T., Wang D.J., Salunkhe D.K. (1974): Nonenzymatic browning in synthetic systems containing ascorbic acid, amino acids, organic acids, and inorganic salts. Canadian Institute of Food Science and Technology Journal, 7: 279-282. Go to original source...
  28. Yu A.N., Tan Z.W., Wang F.S. (2012a): Mechanism of formation of sulphur aroma compounds from l-ascorbic acid and l-cysteine during the Maillard reaction. Food Chemistry, 132: 1316-1323. Go to original source... Go to PubMed...
  29. Yu X., Zhao M., Hu J., Zeng S., Bai X. (2012b): Correspondence analysis of antioxidant activity and UV-Vis absorbance of Maillard reaction products as related to reactants. LWT-Food Science and Technology, 46: 1-9. Go to original source...

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