Influence of alkylation and esterification of 2-(4-methoxyphenoxy) propionic acid on sweet inhibition property and its manipulating mechanism

ABSTRACTThe current study applied 2-(4-methoxyphenoxy) propionic acid (HPMP) to prepare its alkylated and esterified derivatives and then investigated their corresponding sweetness inhibitory effect. The structure of these substituted derivatives were characterized by NMR and IR for ensuring their i...

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Main Authors: Dan Zhou, Wenting Deng, Junhan Zhou, Hongying Deng, Jianxian Zheng, Zhongkai Zhou
Format: Article
Language:English
Published: Taylor & Francis Group 2023-09-01
Series:International Journal of Food Properties
Subjects:
Online Access:https://www.tandfonline.com/doi/10.1080/10942912.2022.2154610
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author Dan Zhou
Wenting Deng
Junhan Zhou
Hongying Deng
Jianxian Zheng
Zhongkai Zhou
author_facet Dan Zhou
Wenting Deng
Junhan Zhou
Hongying Deng
Jianxian Zheng
Zhongkai Zhou
author_sort Dan Zhou
collection DOAJ
description ABSTRACTThe current study applied 2-(4-methoxyphenoxy) propionic acid (HPMP) to prepare its alkylated and esterified derivatives and then investigated their corresponding sweetness inhibitory effect. The structure of these substituted derivatives were characterized by NMR and IR for ensuring their individual modification. The electronic tongue was used to predict the sweetness inhibitory effect of the derivatives, and a sweet prediction model was established via a three-dimensional measurement in term of sweetener type, sweetener and derivative concentrations. Furthermore, the interaction of sweetness inhibition with other taste properties was also studied. The current results indicated that, for alkylated derivatives, the sweetness inhibition rate of methyl-modified derivatives was higher than that of ethyl and propyl derivatives, and the inhibition rate of para-substituted derivatives was greater than that of ortho- and meta-positions. Interestingly, this study revealed that the esterification led to a minor sweetness inhibitory effect. Based on the current results, it is proposed that the ratio of hydrophobic and hydrophilic groups on the HPMP molecules plays the key role in regulating their corresponding sweetness inhibition via a binding capacity with the active site of sweet taste receptors.
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spelling doaj.art-dfbac8976bf849529b83f11f73ef04812024-04-17T13:20:13ZengTaylor & Francis GroupInternational Journal of Food Properties1094-29121532-23862023-09-0126110812110.1080/10942912.2022.2154610Influence of alkylation and esterification of 2-(4-methoxyphenoxy) propionic acid on sweet inhibition property and its manipulating mechanismDan Zhou0Wenting Deng1Junhan Zhou2Hongying Deng3Jianxian Zheng4Zhongkai Zhou5College of Food Science and Engineering, South China University of Technology, Guangzhou, ChinaCollege of Food Science and Engineering, South China University of Technology, Guangzhou, ChinaCollege of Food Science and Engineering, South China University of Technology, Guangzhou, ChinaCollege of Food Science and Engineering, South China University of Technology, Guangzhou, ChinaCollege of Food Science and Engineering, South China University of Technology, Guangzhou, ChinaCollege of Food Science and Engineering, Tianjin University of Science and Technology, Tianjin, ChinaABSTRACTThe current study applied 2-(4-methoxyphenoxy) propionic acid (HPMP) to prepare its alkylated and esterified derivatives and then investigated their corresponding sweetness inhibitory effect. The structure of these substituted derivatives were characterized by NMR and IR for ensuring their individual modification. The electronic tongue was used to predict the sweetness inhibitory effect of the derivatives, and a sweet prediction model was established via a three-dimensional measurement in term of sweetener type, sweetener and derivative concentrations. Furthermore, the interaction of sweetness inhibition with other taste properties was also studied. The current results indicated that, for alkylated derivatives, the sweetness inhibition rate of methyl-modified derivatives was higher than that of ethyl and propyl derivatives, and the inhibition rate of para-substituted derivatives was greater than that of ortho- and meta-positions. Interestingly, this study revealed that the esterification led to a minor sweetness inhibitory effect. Based on the current results, it is proposed that the ratio of hydrophobic and hydrophilic groups on the HPMP molecules plays the key role in regulating their corresponding sweetness inhibition via a binding capacity with the active site of sweet taste receptors.https://www.tandfonline.com/doi/10.1080/10942912.2022.2154610HPMPSweetness inhibitionAlkylationEsterificationRegulation mechanism
spellingShingle Dan Zhou
Wenting Deng
Junhan Zhou
Hongying Deng
Jianxian Zheng
Zhongkai Zhou
Influence of alkylation and esterification of 2-(4-methoxyphenoxy) propionic acid on sweet inhibition property and its manipulating mechanism
International Journal of Food Properties
HPMP
Sweetness inhibition
Alkylation
Esterification
Regulation mechanism
title Influence of alkylation and esterification of 2-(4-methoxyphenoxy) propionic acid on sweet inhibition property and its manipulating mechanism
title_full Influence of alkylation and esterification of 2-(4-methoxyphenoxy) propionic acid on sweet inhibition property and its manipulating mechanism
title_fullStr Influence of alkylation and esterification of 2-(4-methoxyphenoxy) propionic acid on sweet inhibition property and its manipulating mechanism
title_full_unstemmed Influence of alkylation and esterification of 2-(4-methoxyphenoxy) propionic acid on sweet inhibition property and its manipulating mechanism
title_short Influence of alkylation and esterification of 2-(4-methoxyphenoxy) propionic acid on sweet inhibition property and its manipulating mechanism
title_sort influence of alkylation and esterification of 2 4 methoxyphenoxy propionic acid on sweet inhibition property and its manipulating mechanism
topic HPMP
Sweetness inhibition
Alkylation
Esterification
Regulation mechanism
url https://www.tandfonline.com/doi/10.1080/10942912.2022.2154610
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