首页> 外文OA文献 >Macromolecular interactions during gelatinisation and retrogradation in starch-whey systems as studied by rapid visco-analyser
【2h】

Macromolecular interactions during gelatinisation and retrogradation in starch-whey systems as studied by rapid visco-analyser

机译:快速粘度分析仪研究淀粉-乳清体系在糊化和回生过程中的大分子相互作用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Gelatinisation and retrogradation of starch-whey mixtures were studied in water (pH 7) using the Rapid Visco-Analyser (RVA). The starch:whey ratios ranged from 0:100 - 100:0. Wheat starch, and whey protein concentrate (about 80% solids basis) and isolate (about 96% solids basis) were used. Mixtures with whey isolates were generally more viscous than those with whey concentrates, and this was attributed to fewer non-protein milk components in the former. Whey protein concentrates and isolates reduced the peak, trough and final viscosities of the mixtures, but the breakdown and setback ratios of the mixtures were increased. The gelatinisation temperature increased with whey substitutions indicating that whey protein delayed starch gelatinisation. The temperature of fastest viscosity development decreased as the amount of whey was increased. Whey protein isolate generally exercised a lesser effect than the concentrate. At between 40 - 50% whey substitutions, the dominant phase changed from starch to protein irrespective of the source of the whey protein. An additive law poorly defined selected RVA parameters. Both macromolecules interacted to define the viscosity of the mixture, and an exponential model predicted the viscosity better than the additive law. The results obtained in this study are discussed to assist the understanding of extrusion processing of starch-whey systems as models for whey-fortified snack and ready-to-eat foods. Copyright ©2006 The Berkeley Electronic Press. All rights reserved.
机译:使用快速粘度分析仪(RVA)在水(pH 7)中研究了淀粉乳清混合物的糊化和回生。淀粉:乳清比例为0:100-100:0。使用小麦淀粉,乳清蛋白浓缩物(约80%固体含量)和分离物(约96%固体含量)。乳清分离物的混合物通常比乳清浓缩物的混合物更粘,这归因于前者中非蛋白质乳成分较少。乳清蛋白浓缩物和分离物降低了混合物的峰值,谷值和最终粘度,但混合物的分解率和挫折率却增加了。糊化温度随乳清取代而增加,表明乳清蛋白延迟了淀粉糊化。随着乳清量的增加,最快的粘度形成温度降低。乳清蛋白分离物通常比浓缩物具有较小的作用。在40-50%的乳清取代之间,无论乳清蛋白的来源如何,主导相都从淀粉变为蛋白质。加性法则定义的RVA参数选择不佳。两种大分子相互作用以定义混合物的粘度,并且指数模型比添加定律更好地预测了粘度。讨论了本研究中获得的结果,以帮助理解淀粉乳清体系的挤出加工作为乳清强化小吃和即食食品的模型。版权所有©2006伯克利电子出版社。版权所有。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号