Literature DB >> 21272567

Evaluation of the bitterness of green tea catechins by a cell-based assay with the human bitter taste receptor hTAS2R39.

Masataka Narukawa1, Chiaki Noga, Yohei Ueno, Tsutomu Sato, Takumi Misaka, Tatsuo Watanabe.   

Abstract

Catechins have a broad range of physiological functions and act as the main taste ingredient of green tea. Although catechins show a strong bitterness, the bitter taste receptor for catechins has not been fully understood. The objective of this study was to identify the receptor for the major green tea catechins such as (-)-epicatechin (EC), (-)-epicatechin gallate (ECg), (-)-epigallocatechin (EGC), and (-)-epigallocatechin gallate (EGCg). By the cell-based assay using cultured cells expressing human bitter taste receptor, a clear response of hTAS2R39-expressing cells was observed to 300μM of either ECg or EGCg, which elicit a strong bitterness in humans. The response of hTAS2R39-expressing cells to ECg was the strongest among the tested catechins, followed by EGCg. Because the cellular response to EC and EGC is much weaker than those of ECg and EGCg, galloyl groups was strongly supposed to be involved in the bitter intensity. This finding is similar to the observations of taste intensity obtained from a human sensory study. Our results suggest the participation of hTAS2R39 in the detection of catechins in humans, indicating the possibility that bitterness of tea catechins can be evaluated by using cells expressing hTAS2R39.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21272567     DOI: 10.1016/j.bbrc.2011.01.079

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  16 in total

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2.  Repeated exposure to epigallocatechin gallate solution or water alters bitterness intensity and salivary protein profile.

Authors:  Lissa A Davis; Cordelia A Running
Journal:  Physiol Behav       Date:  2021-10-14

3.  In vitro effects of anthocyanidins on sinonasal epithelial nitric oxide production and bacterial physiology.

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Journal:  Am J Rhinol Allergy       Date:  2016-07       Impact factor: 2.467

4.  Establishment of a new cell-based assay to measure the activity of sweeteners in fluorescent food extracts.

Authors:  Yasuka Toda; Shinji Okada; Takumi Misaka
Journal:  J Agric Food Chem       Date:  2011-10-20       Impact factor: 5.279

5.  Snooker structure-based pharmacophore model explains differences in agonist and blocker binding to bitter receptor hTAS2R39.

Authors:  Wibke S U Roland; Marijn P A Sanders; Leo van Buren; Robin J Gouka; Harry Gruppen; Jean-Paul Vincken; Tina Ritschel
Journal:  PLoS One       Date:  2015-03-02       Impact factor: 3.240

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Authors:  Chen Wang; Shidong Lv; Yuanshuang Wu; Xuemei Gao; Jiangbing Li; Wenrui Zhang; Qingxiong Meng
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Review 7.  Tannins in Food: Insights into the Molecular Perception of Astringency and Bitter Taste.

Authors:  Susana Soares; Elsa Brandão; Carlos Guerreiro; Sónia Soares; Nuno Mateus; Victor de Freitas
Journal:  Molecules       Date:  2020-06-02       Impact factor: 4.411

8.  (-)-Epigallocatechin-3-gallate induces secretion of anorexigenic gut hormones.

Authors:  Won-Young Song; Yoshiko Aihara; Takashi Hashimoto; Kazuki Kanazawa; Masashi Mizuno
Journal:  J Clin Biochem Nutr       Date:  2015-09-01       Impact factor: 3.114

9.  6-methoxyflavanones as bitter taste receptor blockers for hTAS2R39.

Authors:  Wibke S U Roland; Robin J Gouka; Harry Gruppen; Marianne Driesse; Leo van Buren; Gerrit Smit; Jean-Paul Vincken
Journal:  PLoS One       Date:  2014-04-10       Impact factor: 3.240

10.  Overcoming chemoresistance in pancreatic cancer cells: role of the bitter taste receptor T2R10.

Authors:  Louisa Stern; Nathalia Giese; Thilo Hackert; Oliver Strobel; Peter Schirmacher; Klaus Felix; Matthias M Gaida
Journal:  J Cancer       Date:  2018-02-01       Impact factor: 4.207

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