References
- Wijewickreme AN, Kitts DD, Durance TD. 1997. Reaction conditions influence the elementary composition and metal chelating affinity of nondialyzable model Maillard reaction products. J Agric Food Chem 45: 4577-4583. https://doi.org/10.1021/jf970041n
- Baxter JH. 1995. Free amino acid stability in reducing sugar systems. J Food Sci 60: 405-407. https://doi.org/10.1111/j.1365-2621.1995.tb05682.x
- Ashoor SH, Zent JB. 1984. Maillard browning of common amino acids and sugars. J Food Sci 49: 1206-1207. https://doi.org/10.1111/j.1365-2621.1984.tb10432.x
- Naranjo GB, Malec LS, Vigo MS. 1998. Reducing sugars effect on available lysine loss of casein by moderate heat treatment. Food Chem 62: 309-313. https://doi.org/10.1016/S0308-8146(97)00176-3
- Tanaka M, Chiba N, Ishizaki S, Takai R, Taguchi T. 1994. Influence of water activity and Maillard reaction on the polymerization of myosin heavy chain in freeze-dried squid meat. Fisheries Sci 60: 607-611. https://doi.org/10.2331/fishsci.60.607
- Yoshimura Y, Ujima T, Watanabe T, Nakazawa H. 1997. Antioxidative effect of Maillard reaction products using glucose-glycine model system. J Agric Food Chem 45: 4106-4109. https://doi.org/10.1021/jf9609845
- Yen GC, Hsieh PP. 1995. Antioxidative activity and scavenging effects on xylose-lysine Maillard reaction products. J Sci Food Agr 67: 415-420. https://doi.org/10.1002/jsfa.2740670320
- Friedman M. 1999. Chemistry, nutrition, and microbiology of D-amino acids. J Agric Food Chem 47: 3457-3479. https://doi.org/10.1021/jf990080u
- Bruckner H, Justus J, Kirschbaum J. 2001. Saccharide induced racemization of amino acids in the course of the Maillard reaction. Amino Acids 21: 429-433. https://doi.org/10.1007/s007260170007
- Ledl F, Schleicher E. 1990. New aspects of the Maillard reaction in foods and in the human body. Angew Chem Int Ed 29: 565-594. https://doi.org/10.1002/anie.199005653
- Patzold R, Bruckner H. 2005. Mass spectrometric detection and formation of D-amino acids in processed plant saps, syrups, and fruit juice concentrates. J Agric Food Chem 53: 9722-9729. https://doi.org/10.1021/jf051433u
- Patzold R, Bruckner H. 2006a. Gas chromatographic detection of D-amino acids in natural and thermally treated bee honeys and studies on the mechanism of their formation as result of the Maillard reaction. Eur Food Res Technol 223: 347-354. https://doi.org/10.1007/s00217-005-0211-y
- Patzold R, Bruckner H. 2006b. Gas chromatographic determination and mechanism of formation of D-amino acids occurring in fermented and roasted cocoa beans, cocoa powder, chocolate and other cocoa products. Amino Acids 31: 63-72. https://doi.org/10.1007/s00726-006-0330-1
- Bada JL. 1972. Kinetics of racemization of amino acids as a function of pH. J Am Chem Soc 94: 1371-1373. https://doi.org/10.1021/ja00759a064
- Bailey JR, Ames JM, Monti SM. 1996. An analysis of the non-volatile reaction products of aqueous Maillard model system at pH 5, using reversed-phase HPLC with diode-array detection. J Sci Food Agr 72: 97-103. https://doi.org/10.1002/(SICI)1097-0010(199609)72:1<97::AID-JSFA626>3.0.CO;2-Q
- Marfey P. 1984. Determination of D-amino acids. II. Use of a bifunctional reagent, 1,5-difluoro-2,4-dinitrobenzene. Carlsberg Res Commun 49: 591-596. https://doi.org/10.1007/BF02908688
- Dinis TCP, Madeira VMC, Almerida LM. 1994. Action of phenolic derivatives (acetoaminophen, salycilate and 5-aminosalycilate) as inhibitors of membrane lipid peroxidation and as peroxyl radical scavenges. Arch Biochem Biophys 315: 161-169. https://doi.org/10.1006/abbi.1994.1485
- Benzie IFF, Strain JJ. 1996. The ferric reducing ability of plasma (FRAP) as a measure of antioxidant power the FRAP assay. Anal Biochem 239: 70-76. https://doi.org/10.1006/abio.1996.0292
- Re R, Pellegrini N, Proteggente A, Pannala A, Yang M, Rice-Evans C. 1999. Antioxidant activity applying an improved ABTS radical cation decolorization assay. Free Radic Biol Med 26: 1231-1237. https://doi.org/10.1016/S0891-5849(98)00315-3
- Speck JCJ. 1958. The Lobry de Bruyn-Alberda van Ekenstein transformation. Adv Carbohydr Chem 13: 63-103.
- Ajandouz EH, Puigserver A. 1999. Nonenzymatic browning reaction of essential amino acids: Effect of pH on caramelization and Maillard reaction kinetics. J Agric Food Chem 47: 1786-1793. https://doi.org/10.1021/jf980928z
- Ajandouz EH, Tchiakpe LS, DalleOre F, Benajiba A, Puigserver A. 2001. Effect of pH on caramelization and Maillard reaction kinetics in fructose-lysine model systems. J Food Sci 66: 926-931. https://doi.org/10.1111/j.1365-2621.2001.tb08213.x
- Benjakul S, Visessanguan W, Phongkanpai V, Tanaka M. 2005. Antioxidative activity of caramelisation products and their preventive effect on lipid oxidation in fish mince. Food Chem 90: 231-239. https://doi.org/10.1016/j.foodchem.2004.03.045
- Van Boekel MAJS. 1996. Kinetic modelling of sugar reactions in heated milk-like systems. Neth Milk Dairy J 50: 245-266.
- Friedman M. 1996. Food browning and its prevention: an overview. J Agric Food Chem 44: 631-653. https://doi.org/10.1021/jf950394r
- Patzold R, Bruckner H. 2004. Mechanistische aspekte und konsequenzen der bildung von D-aminosauren im laufe der Maillardreaktion. Lebensmittelchemie 58: 100.
- Casal S, Mendes E, Oliveira MBPP, Ferreira MA. 2005. Roast effects on coffee amino acid enantiomers. Food Chem 89: 333-340. https://doi.org/10.1016/j.foodchem.2004.02.039
- Kutz N, Patzold R, Bruckner H. 2004. Bestimmung von Aminosaureenantiomeren in Kakao und Kakaoprodukten. Lebensmittelchemie 58: 106-107.
- Morales FJ, Jimenez-Perez S. 2001. Free radical scavenging capacity of Maillard reaction products as related to colour and fluorescence. Food Chem 72: 119-125. https://doi.org/10.1016/S0308-8146(00)00239-9
- Hofmann T. 1998. Studies on the relationship between molecular weight and the color potency of fractions obtained by thermal treatment of glucose/amino acid and glucose/protein solutions by using ultracentifugation and color dilution techniques. J Agric Food Chem 46: 3891-3895. https://doi.org/10.1021/jf980397e
- Brands C, Wedzicha B, Van Boekel MAJS. 2002. Quantification of melanoidin concentration in sugar-casein systems. J Agric Food Chem 50: 1178-1183. https://doi.org/10.1021/jf010789c
- Guimaraes C, Bento LSM, Mota M. 1996. A study of sugar colourants through ion exchange and salt regeneration. Int Sugar J 98: 584-587.
- Rafik M, Mas A, Elharfi A, Schue F. 1997. Decoloration de solutions sucrees par ultrafiltration sur une membrane a base de poly(organocyclophosphazene). Eur Polymer J 33: 679-690. https://doi.org/10.1016/S0014-3057(96)00232-7
- Delgado-Andrade C, Seiquer I, Navarro P. 2004. Bioavailability of iron from a heat treated glucose-lysine model food system: assays in rats and in Caco-2 cells. J Sci Food Agr 84: 1507-1513. https://doi.org/10.1002/jsfa.1839
- Jing H, Kitts DD. 2004. Antioxidant activity of sugarlysine Maillard reaction products in cell free and cell culture systems. Arch Biochem Biophys 429: 154-163. https://doi.org/10.1016/j.abb.2004.06.019
- O'Brien JO, Morrissey PA. 1997. Metal ion complexation by products of the Maillard reaction. Food Chem 58: 17-27. https://doi.org/10.1016/S0308-8146(96)00162-8
- Morales FJ, Fernandez-Fraguas C, Jimenez-Perez S. 2005. Iron binding ability of melanoidins from food and model systems. Food Chem 90: 821-827. https://doi.org/10.1016/j.foodchem.2004.05.030
- Delgado-Andrade C, Seiquer I, Nieto R, Navarro P. 2004. Effects of heated glucose-lysine and glucose-methionine model-systems on mineral solubility. Food Chem 87: 329-337. https://doi.org/10.1016/j.foodchem.2003.12.002
- Shon MY, Kim TH, Sung NJ. 2003. Antioxidants and free radical scavenging activity of Phellinus baumii extracts. Food Chem 82: 593-597. https://doi.org/10.1016/S0308-8146(03)00015-3
- Shih PW, Lai PL, Jen HWK. 2006. Antioxidant activities of aqueous extracts of selected plants. Food Chem 99: 775-783. https://doi.org/10.1016/j.foodchem.2005.07.058
- Benjakul S, Lertittikul W, Bauer F. 2005. Antioxidant activity of Maillard reaction products from a porcine plasma protein-sugar model system. Food Chem 93: 189-196. https://doi.org/10.1016/j.foodchem.2004.10.019
- Bersuder P, Hole M. 2003. Melanoidins in food and health. Office for Official Publications of the European Communities, Luxemburg. Chapter 4, p 158-166.
- Gao X, Bjork L, Trajkovski V, Uggla M. 2000. Evaluation of antioxidant activities of rosehip ethanol extracts in different test systems. J Sci Food Agr 80: 2021-2027. https://doi.org/10.1002/1097-0010(200011)80:14<2021::AID-JSFA745>3.0.CO;2-2
- Rufian-Henares JA, Morales FJ. 2007. Functional properties of melanoidins: In vitro antioxidant, antimicrobial and antihypertensive activities. Food Res Int 40: 995-1002. https://doi.org/10.1016/j.foodres.2007.05.002
- Hwang JY, Shue YS, Chang HM. 2001. Antioxidative activity of roasted and defatted peanut kernels. Food Res Int 34: 639-647. https://doi.org/10.1016/S0963-9969(01)00083-7
- Charurin P, Ames JM, Castiello MD. 2002. Antioxidant activity of coffee model systems. J Agric Food Chem 50: 3751-3756. https://doi.org/10.1021/jf011703i
- Eichner K. 1981. Antioxidant effect of Maillard reaction intermediates. Prog Food Nutr Sci 5: 441-451.
- Miller DD. 1996. Mineral. In Food Chemistry. Fennema OR, ed. Marcel Dekker, New York, USA. p 618-649.
- Prior RL, Wu X, Schaich K. 2005. Standardized method for the determination of antioxidant capacity and phenolics in foods and dietary supplements. J Agric Food Chem 53: 4290-4302. https://doi.org/10.1021/jf0502698
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