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 ultracentrifugation and color dilution techniques

被引:146
作者
Hofmann, T [1 ]
机构
[1] Deutsch Forsch Anstalt Lebensmittelchem, D-85748 Garching, Germany
关键词
melanoidins; Maillard reaction; protein oligomerization; nonenzymatic browning; protein cross-linking; color dilution factor;
D O I
10.1021/jf980397e
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
In heated aqueous solutions of glucose and alanine or glycine, respectively, the majority of colored compounds formed were shown to have molecular weights <1000 Da. Compounds with molecular weights >3000 Da were found in only trace amounts, whereas high molecular colorants could not be observed under the conditions applied, which are typical for cooking processes of foods. In contrast, the reaction between casein and glucose leads to a drastic increase in the molecular weights by a carbohydrate-induced oligomerization of the protein. More than 43% of the reaction mixture was shown to be pentamers or even higher oligomers of casein exhibiting molecular weights of >100000 Da. This cross-linking of casein was found to run in parallel with the color intensity of the products formed, indicating that chromophoric substructures, derived from carbohydrates, are incorporated into these oligomers. The data indicate that the formation of melanoidins during cooking of foods by polymerization of reactive low molecular weight compounds should be very unlikely in the Maillard reaction between carbohydrates and amino acids.
引用
收藏
页码:3891 / 3895
页数:5
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[1]   New colored compounds from the Maillard reaction between xylose and lysine [J].
Arnoldi, A ;
Corain, EA ;
Scaglioni, L ;
Ames, JM .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1997, 45 (03) :650-655
[2]  
AURICH H., 1967, Z LEBENSMITTEL UNTERS FORSCH, V135, P59, DOI 10.1007/BF01713066
[3]   ELUCIDATION OF THE NITROGEN FORMS IN MELANOIDINS AND HUMIC-ACID BY N-15 CROSS POLARIZATION MAGIC ANGLE SPINNING NUCLEAR MAGNETIC-RESONANCE SPECTROSCOPY [J].
BENZINGPURDIE, L ;
RIPMEESTER, JA ;
PRESTON, CM .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1983, 31 (04) :913-915
[4]   INVESTIGATION OF THE INFLUENCE OF REACTION CONDITIONS ON THE ELEMENTARY COMPOSITION OF MELANOIDINS [J].
CAMMERER, B ;
KROH, LW .
FOOD CHEMISTRY, 1995, 53 (01) :55-59
[5]  
CHO RK, 1984, AGR BIOL CHEM TOKYO, V48, P3081
[6]   ISOLATION AND CHARACTERIZATION OF PIGMENTS FROM PROTEIN-CARBONYL BROWNING SYSTEMS - ISOLATION, PURIFICATION, AND PROPERTIES [J].
CLARK, AV ;
TANNENBAUM, SR .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1970, 18 (05) :891-+
[7]   ISOLATION AND CHARACTERIZATION OF PIGMENTS FROM PROTEIN-CARBONYL BROWNING SYSTEMS - MODELS FOR 2 INSULIN-GLUCOSE PIGMENTS [J].
CLARK, AV ;
TANNENBA.SR .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1974, 22 (06) :1089-1093
[8]   MAILLARD POLYMERS DERIVED FROM D-GLUCOSE, D-FRUCTOSE, 5-(HYDROXYMETHYL)-2-FURALDEHYDE, AND GLYCINE AND METHIONINE [J].
FEATHER, MS ;
NELSON, D .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1984, 32 (06) :1428-1432
[9]   CHEMICAL STUDIES ON MELANOIDINS .3. EFFECTS OF HEATING ON CHEMICAL PROPERTIES OF MELANOIDIN PREPARED FROM GLYCINE-XYLOSE SYSTEM [J].
GOMYO, T ;
UDAKA, K ;
HORIKOSH.M ;
KATO, H ;
FUJIMAKI, M .
AGRICULTURAL AND BIOLOGICAL CHEMISTRY, 1972, 36 (01) :125-&
[10]   STUDIES OF THE REACTION BETWEEN PROTEINS AND REDUCING SUGARS IN THE DRY STATE .6. THE REACTIVITY OF THE TERMINAL AMINO GROUPS OF LYSINE IN MODEL SYSTEMS [J].
HANNAN, RS ;
LEA, CH .
BIOCHIMICA ET BIOPHYSICA ACTA, 1952, 9 (03) :293-305