The impact of bifunctional molecules on the gluten network during mixing

被引:7
作者
Auvergne, Remi [1 ]
Morel, Marie-Helene [2 ]
Menut, Paul [2 ]
Guilbert, Stephane [2 ]
Robin, Jean-Jacques [1 ]
机构
[1] ENSCM, Inst Charles Gerhardt Montpellier, Equipe IAM SOM, CNRS,UMR 5253,UM2,UM1, F-34296 Montpellier 5, France
[2] Univ Montpellier 2, INRA, CIRAD, UMR Ingn Agropolymeres & Technol Emergentes 1208, F-34000 Montpellier, France
关键词
Renewable resources; Proteins; Reactivity; Functionalization; Crosslinking; POLY(VINYL ALCOHOL) BLENDS; PLASTICIZED WHEAT GLUTEN; CHEMICAL-MODIFICATION; NATURAL POLYMERS; PROTEIN; AGGREGATION; GLYCEROL; HEAT;
D O I
10.1016/j.reactfunctpolym.2010.11.008
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The protein network in gluten was either cross-linked or functionalized by using chain extenders to afford novel bio-based materials. These chain extenders consist on di- or tri- ethylene glycol oligomers functionalized at both end with maleimide or maleate groups and also with commercially available vinyl ether. These bi-functional additives are incorporated into standard gluten/glycerol blends during batch mixing. The gluten polymerization proceeds by thiol/disulfide exchanges during mixing and was assessed by the loss of the soluble fraction of protein in SDS. Modifications of protein size distribution revealed a cross-linking between chain extender and gluten, depending on the reactivity of the terminal functions of the used extender. Maleimide end-groups induced a high gluten polymerization whereas maleate ones lead to a complete depolymerization. Depending on their reactivity, bi-functional additives can thus act either as non-reducible chain extender or, thanks to the grafting of one of the additives-end onto the gluten thiol groups, as functionalizing agent: in this last case, one of the end-groups remained free and thus available for further reaction. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:70 / 79
页数:10
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