2006
DOI: 10.1016/j.foodchem.2005.01.033
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Chemical properties and antioxidative activity of glycated α-lactalbumin with a rare sugar, d-allose, by Maillard reaction

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Cited by 91 publications
(67 citation statements)
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“…The MRPs of WPI conjugated to rare sugars show enhanced binding of free radicals. These data agree with those of Sun et al (2006b) who found that the antioxidant activity of α-lactalbumin glycated with All was higher than that glycated with Glc or Fru. The configuration of the sugar is expected to have a greater effect on antioxidant activity than the number of sugar molecules attached to glycated proteins.…”
Section: Resultssupporting
confidence: 92%
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“…The MRPs of WPI conjugated to rare sugars show enhanced binding of free radicals. These data agree with those of Sun et al (2006b) who found that the antioxidant activity of α-lactalbumin glycated with All was higher than that glycated with Glc or Fru. The configuration of the sugar is expected to have a greater effect on antioxidant activity than the number of sugar molecules attached to glycated proteins.…”
Section: Resultssupporting
confidence: 92%
“…Thus among ice cream extracts containing 17.5 mg/ml of added WPI, those extracted from WPI glycated with the rare sugars All and Psi had the highest antioxidant activity of all of the glycated WPI samples. MRPs have been found to have a higher radical scavenging activity compared to the native protein (Chevalier et al, 2001) and MRPs of protein conjugated to All were shown to have the highest antioxidant activity of all MRPs conjugated with D-aldohexoses (Sun et al, 2006a;Sun et al, 2006b). …”
Section: Resultsmentioning
confidence: 99%
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“…To improve functional properties of proteins including their emulsifying ability, chemical modifications have often been made. Over the past few years, there has been growing interest in the modification of proteins with sugars through the Maillard reaction [4][5][6][7][8][9][10][11][12][13][14] ; a complex network of non-enzymatic reactions between reducing sugars and protein amino groups (see ). At an early stage of the Maillard reaction, amino groups in proteins react with carbonyl groups of sugars to give 1-amino-1-deoxy-ketose, known as the Amadori compound 15) .…”
Section: Introductionmentioning
confidence: 99%
“…The set of reactions that occurs thereafter results in the formation of both large protein aggregates and low molecular weight products that are believed to confer flavor, aroma, color, texture, and antioxidant characteristics to various foods. The reactivity of reducing sugars in the Maillard reaction was reported to decrease in the following order: aldopentoses > aldohexoses > aldoketoses > disaccharides 8,9,16) , but little information is available on comparisons among the sugar isomers 10) . It has been reported that products of the Maillard reaction exhibit improved emulsifying and foaming ability in some cases.…”
Section: Introductionmentioning
confidence: 99%