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凝胶化:糖类和多元醇对明胶和琼脂糖的作用

Gelation: the role of sugars and polyols on gelatin and agarose.

作者信息

Shimizu Seishi, Matubayasi Nobuyuki

机构信息

York Structural Biology Laboratory, Department of Chemistry, University of York , Heslington, York YO10 5YW, United Kingdom.

出版信息

J Phys Chem B. 2014 Nov 20;118(46):13210-6. doi: 10.1021/jp509099h. Epub 2014 Nov 6.

Abstract

Gelation is enhanced by the addition of sugars and polyols. How, at a microscopic level, do such cosolvents enhance gelation? The following two different hypotheses have been proposed so far to answer this question: (i) enhancement of water structure around the biopolymer induced by cosolvents; (ii) exclusion of cosolvents from biopolymer surfaces. To examine the validity of the above hypotheses, as well as to quantify the driving forces of cosolvent-induced gelation, we have constructed a statistical thermodynamic theory of gelation, by extending our Kirkwood-Buff theory of cosolvency; biopolymer-water and biopolymer-cosolvent interactions can both be determined from thermodynamic data. The exclusion of cosolvents is shown to be the dominant contribution, whereas the hydration change is a minor contribution, which may be important only so far as to mediate the exclusion of cosolvents.

摘要

添加糖和多元醇可增强凝胶化作用。在微观层面上,这些共溶剂是如何增强凝胶化作用的呢?迄今为止,人们提出了以下两种不同的假说来回答这个问题:(i)共溶剂诱导生物聚合物周围的水结构增强;(ii)共溶剂从生物聚合物表面被排斥。为了检验上述假说的有效性,以及量化共溶剂诱导凝胶化的驱动力,我们通过扩展我们的共溶柯克伍德-布夫理论,构建了一种凝胶化的统计热力学理论;生物聚合物-水和生物聚合物-共溶剂的相互作用都可以从热力学数据中确定。结果表明,共溶剂的排斥是主要贡献,而水合变化是次要贡献,仅在介导共溶剂的排斥方面可能很重要。

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