Gluten Structural Evolution During Pasta Processing of Refined and Whole Wheat Pasta from Hard White Winter Wheat: The Influence of Mixing, Drying, and Cooking

被引:29
作者
Bock, Jayne E. [1 ]
West, Ryan [1 ]
Iametti, Stefania [2 ]
Bonomi, Francesco [2 ]
Marengo, Mauro [2 ]
Seetharaman, Koushik [3 ]
机构
[1] Univ Guelph, Dept Food Sci, Guelph, ON N1G 2W1, Canada
[2] Univ Milan, Dipartimento Sci Alimenti Nutr & Ambiente DeFENS, I-20122 Milan, Italy
[3] Univ Minnesota, Dept Food Sci & Nutr, St Paul, MN 55108 USA
关键词
TRANSFORM INFRARED-SPECTROSCOPY; PROTEIN SECONDARY STRUCTURES; RICE PASTA; QUALITY; DURUM; WATER; BRAN; SPAGHETTI; FOOD; CONFORMATION;
D O I
10.1094/CCHEM-07-14-0152-R
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
An attempt was made to evaluate gluten structural changes in refined and whole wheat pasta from hard white winter wheat to elucidate the impact of whole wheat components on the formation and structure of the gluten network in pasta. Attenuated total reflectance-FTIR spectroscopy was used to track gluten secondary structure through most of the major steps in pasta processing: raw material, mixing, drying, and cooking. Protein solubility, accessible thiols, and SDS-PAGE data were also collected to provide additional information on the nature of protein interactions and network composition. Few secondary structural differences were observed between refined and whole wheat flours from hard white wheat. However, mixing induced a significant shift to b-sheet structures in refined dough that was not equally matched by whole wheat dough. Drying under both high temperature, short time (HT) and low temperature, long time (LT) conditions resulted in a reversion to structural distributions similar to those for flour in both pastas. However, greater protein denaturation in HT samples was indicated by lower protein solubility also in the presence of denaturants and disulfide reducing agents. Cooking generated a substantial increase in b-sheet structures for both pasta systems. This structure was greatest in refined and LT samples. Thiol accessibility data indicate the presence of a highly aggregated, compact gluten network in refined pasta, mostly driven by hydrophobic association. Conversely, the network in whole wheat pasta was more loosely associated and dependent on disulfide bonding, both of which fit well with the secondary structural data.
引用
收藏
页码:460 / 465
页数:6
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