Kinetics of α‑dicarbonyl compounds formation in glucose‐glutamic acid model of Maillard reaction
Abstract As a potential health hazard, α‐dicarbonyl compounds have been detected in the thermally processed foods. In order to investigate the formation kinetics of α‐dicarbonyl compounds, liquid chromatography‐electrospray tandem mass spectrometry was employed to determine the content of α‐dicarbon...
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doaj-e09bcfd758134aab86633d4d93df5bda2021-03-19T11:50:38ZengWileyFood Science & Nutrition2048-71772021-01-019129030210.1002/fsn3.1995Kinetics of α‑dicarbonyl compounds formation in glucose‐glutamic acid model of Maillard reactionLili Zhang0Ying Sun1Dandan Pu2Yuyu Zhang3Baoguo Sun4Zhiyao Zhao5College of Food Science and Engineering Tianjin University of Science and Technology Tianjin ChinaBeijing Key Laboratory of Flavor Chemistry Beijing Technology and Business University Beijing ChinaBeijing Key Laboratory of Flavor Chemistry Beijing Technology and Business University Beijing ChinaBeijing Key Laboratory of Flavor Chemistry Beijing Technology and Business University Beijing ChinaCollege of Food Science and Engineering Tianjin University of Science and Technology Tianjin ChinaSchool of Artificial Intelligence Beijing Technology and Business University Beijing ChinaAbstract As a potential health hazard, α‐dicarbonyl compounds have been detected in the thermally processed foods. In order to investigate the formation kinetics of α‐dicarbonyl compounds, liquid chromatography‐electrospray tandem mass spectrometry was employed to determine the content of α‐dicarbonyl compounds in glucose‐only and glucose‐glutamic acid (glucose‐Glu) thermal reaction models. The 3‐deoxyglucosone content was significantly higher than 6 α‐dicarbonyl compounds at 90–110℃, 0–6 hr in the two tested systems. The glutamic acid promoted the content accumulation of 1‐deoxyglucosone, diacetyl, methylglyoxal, and glyoxal, whereas inhibited the content of 3‐deoxyglucosone and 3,4‐dideoxyglucosone. Three‐fifths of the tested compounds content increased linearly with time increasing, but in glucose‐only system, the 1‐deoxyglucosone content increased logarithmically at 95–110℃ over reaction time. The formation of glucose (100–110℃, glucose‐only and glucose‐Glu), 5‐hydroxymethylfurfural (100–110℃, glucose‐only), 1‐deoxyglucose (105–110℃, glucose‐Glu), 3,4‐dideoxyglucosone (110℃, glucose‐Glu), glyoxal (95–110℃, glucose‐Glu) and diacetyl (90–95℃, glucose‐Glu) could be well fitted by exponential equation. Shortening the heating time and reducing heating temperature (except glyoxal in glucose‐only system) were the effective methods to decrease α‐dicarbonyl compounds content in the two tested systems. Additionally, high temperature could also reduce α‐dicarbonyl compounds content, such as 3‐deoxyglucosone (≥110℃, glucose‐only), 1‐deoxyglucosone (≥110℃, glucose‐only), glucosone (≥110℃, glucose‐only; ≥100℃, glucose‐Glu), methyloxyl (≥110℃, glucose‐only; ≥100℃, glucose‐Glu), diacetyl (≥110℃, glucose‐only), and glyoxal (≥100℃, glucose‐Glu).https://doi.org/10.1002/fsn3.19955‐hydroxymethylfurfuralglucoseglutamic acidkineticsα‐dicarbonyl compounds |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Lili Zhang Ying Sun Dandan Pu Yuyu Zhang Baoguo Sun Zhiyao Zhao |
spellingShingle |
Lili Zhang Ying Sun Dandan Pu Yuyu Zhang Baoguo Sun Zhiyao Zhao Kinetics of α‑dicarbonyl compounds formation in glucose‐glutamic acid model of Maillard reaction Food Science & Nutrition 5‐hydroxymethylfurfural glucose glutamic acid kinetics α‐dicarbonyl compounds |
author_facet |
Lili Zhang Ying Sun Dandan Pu Yuyu Zhang Baoguo Sun Zhiyao Zhao |
author_sort |
Lili Zhang |
title |
Kinetics of α‑dicarbonyl compounds formation in glucose‐glutamic acid model of Maillard reaction |
title_short |
Kinetics of α‑dicarbonyl compounds formation in glucose‐glutamic acid model of Maillard reaction |
title_full |
Kinetics of α‑dicarbonyl compounds formation in glucose‐glutamic acid model of Maillard reaction |
title_fullStr |
Kinetics of α‑dicarbonyl compounds formation in glucose‐glutamic acid model of Maillard reaction |
title_full_unstemmed |
Kinetics of α‑dicarbonyl compounds formation in glucose‐glutamic acid model of Maillard reaction |
title_sort |
kinetics of α‑dicarbonyl compounds formation in glucose‐glutamic acid model of maillard reaction |
publisher |
Wiley |
series |
Food Science & Nutrition |
issn |
2048-7177 |
publishDate |
2021-01-01 |
description |
Abstract As a potential health hazard, α‐dicarbonyl compounds have been detected in the thermally processed foods. In order to investigate the formation kinetics of α‐dicarbonyl compounds, liquid chromatography‐electrospray tandem mass spectrometry was employed to determine the content of α‐dicarbonyl compounds in glucose‐only and glucose‐glutamic acid (glucose‐Glu) thermal reaction models. The 3‐deoxyglucosone content was significantly higher than 6 α‐dicarbonyl compounds at 90–110℃, 0–6 hr in the two tested systems. The glutamic acid promoted the content accumulation of 1‐deoxyglucosone, diacetyl, methylglyoxal, and glyoxal, whereas inhibited the content of 3‐deoxyglucosone and 3,4‐dideoxyglucosone. Three‐fifths of the tested compounds content increased linearly with time increasing, but in glucose‐only system, the 1‐deoxyglucosone content increased logarithmically at 95–110℃ over reaction time. The formation of glucose (100–110℃, glucose‐only and glucose‐Glu), 5‐hydroxymethylfurfural (100–110℃, glucose‐only), 1‐deoxyglucose (105–110℃, glucose‐Glu), 3,4‐dideoxyglucosone (110℃, glucose‐Glu), glyoxal (95–110℃, glucose‐Glu) and diacetyl (90–95℃, glucose‐Glu) could be well fitted by exponential equation. Shortening the heating time and reducing heating temperature (except glyoxal in glucose‐only system) were the effective methods to decrease α‐dicarbonyl compounds content in the two tested systems. Additionally, high temperature could also reduce α‐dicarbonyl compounds content, such as 3‐deoxyglucosone (≥110℃, glucose‐only), 1‐deoxyglucosone (≥110℃, glucose‐only), glucosone (≥110℃, glucose‐only; ≥100℃, glucose‐Glu), methyloxyl (≥110℃, glucose‐only; ≥100℃, glucose‐Glu), diacetyl (≥110℃, glucose‐only), and glyoxal (≥100℃, glucose‐Glu). |
topic |
5‐hydroxymethylfurfural glucose glutamic acid kinetics α‐dicarbonyl compounds |
url |
https://doi.org/10.1002/fsn3.1995 |
work_keys_str_mv |
AT lilizhang kineticsofadicarbonylcompoundsformationinglucoseglutamicacidmodelofmaillardreaction AT yingsun kineticsofadicarbonylcompoundsformationinglucoseglutamicacidmodelofmaillardreaction AT dandanpu kineticsofadicarbonylcompoundsformationinglucoseglutamicacidmodelofmaillardreaction AT yuyuzhang kineticsofadicarbonylcompoundsformationinglucoseglutamicacidmodelofmaillardreaction AT baoguosun kineticsofadicarbonylcompoundsformationinglucoseglutamicacidmodelofmaillardreaction AT zhiyaozhao kineticsofadicarbonylcompoundsformationinglucoseglutamicacidmodelofmaillardreaction |
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1724213144464654336 |