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合成甜味剂中不良余味的起源:一种假说。

The Origin of Unpleasant Aftertastes in Synthetic Sweeteners: A Hypothesis.

作者信息

Acevedo Waldo, Temussi Piero A

机构信息

Institute of Chemistry, Pontificia Universidad Católica de Valparaíso, Valparaíso, Chile.

Dipartimento di Chimica, Universita' di Napoli Federico II, Napoli, Italy.

出版信息

Front Mol Biosci. 2019 Jan 18;5:119. doi: 10.3389/fmolb.2018.00119. eCollection 2018.

Abstract

Most sweeteners are plagued with unwanted unpleasant aftertastes. Here we examined the possibility that one of the main reasons for this is the similarity of sweet and umami receptors. We performed docking calculations on models of sweet and umami receptors using as template the recently determined solid state structure of the first taste receptor, the medaka fish T1R2-T1R3 receptor. Our results show convincingly that sweeteners can be recognized also by the T1R1-T1R3 umami receptor, owing to the similarity of its architecture to that of the sweet receptor. We hypothesize that the T1R1-T1R3 receptor plays a key role in modulating the quality of sweet tastants, hinting at a simple explanation of their aftertaste. The prevailing ideas on taste coding favor strict labeling of taste cells, which would exclude that umami receptors can recognize other taste sensations. If some cross-talk based on the combinatorial model of taste is accepted, some sweet ligands can exert a bitter sensation. However, even if cross-talk is not admitted, direct stimulation of the umami receptor is bound to cause an aftertaste incompatible with good sweet quality.

摘要

大多数甜味剂都存在令人不悦的余味问题。在此,我们研究了造成这种情况的一个主要原因可能是甜味受体和鲜味受体存在相似性。我们以首个味觉受体——青鳉鱼T1R2-T1R3受体最近确定的固态结构为模板,对甜味和鲜味受体模型进行了对接计算。我们的结果令人信服地表明,由于T1R1-T1R3鲜味受体的结构与甜味受体相似,甜味剂也能被该受体识别。我们推测,T1R1-T1R3受体在调节甜味剂的品质方面起着关键作用,这为甜味剂的余味提供了一个简单的解释。关于味觉编码的主流观点倾向于味觉细胞的严格标记,这将排除鲜味受体能识别其他味觉的可能性。如果基于味觉组合模型的某种相互作用被认可,一些甜味配体可能会产生苦味。然而,即使不承认存在相互作用,直接刺激鲜味受体也必然会导致与优质甜味不相容的余味。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6276/6345712/d9698513e611/fmolb-05-00119-g0001.jpg

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