Literature DB >> 29920095

Hydrogen Bond Length as a Key To Understanding Sweetness.

F Bruni1, C Di Mino1, S Imberti2, S E McLain3, N H Rhys3, M A Ricci1.   

Abstract

Neutron diffraction experiments have been performed to investigate and compare the structure of the hydration shell of three monosaccharides, namely, fructose, glucose, and mannose. It is found that despite their differences with respect to many thermodynamical quantities, bioprotective properties against environmental stresses, and taste, the influence of these monosaccharides on the bulk water solvent structure is virtually identical. Conversely, these sugars interact with the neighboring water molecules by forming H bonds of different length and strength. Interestingly, the sweetness of these monosaccharides, along with that of the disaccharide trehalose, is correlated with the length of these H bonds. This suggests that the small differences in stereochemistry between the different sugars determine a relevant change in polarity, which has a fundamental impact on the behavior of these molecules in vivo.

Entities:  

Year:  2018        PMID: 29920095     DOI: 10.1021/acs.jpclett.8b01280

Source DB:  PubMed          Journal:  J Phys Chem Lett        ISSN: 1948-7185            Impact factor:   6.475


  6 in total

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2.  Short-Distance Intermolecular Correlations of Mono- and Disaccharides in Condensed Solutions: Bulky Character of Trehalose.

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6.  Role of Water in Sucrose, Lactose, and Sucralose Taste: The Sweeter, The Wetter?

Authors:  Silvia Imberti; Sylvia E McLain; Natasha H Rhys; Fabio Bruni; Maria Antonietta Ricci
Journal:  ACS Omega       Date:  2019-12-18
  6 in total

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