AI Chat Paper
Note: Please note that the following content is generated by AMiner AI. SciOpen does not take any responsibility related to this content.
{{lang === 'zh_CN' ? '文章概述' : 'Summary'}}
{{lang === 'en_US' ? '中' : 'Eng'}}
Chat more with AI
PDF (891.1 KB)
Collect
Submit Manuscript AI Chat Paper
Show Outline
Outline
Show full outline
Hide outline
Outline
Show full outline
Hide outline
Research Article | Open Access

Comprehensive comparison on the chemical metabolites and taste evaluation of tea after roasting using untargeted and pseudotargeted metabolomics

Zongde Jianga,bZisheng HancMingchun Wena,bChi-Tang Hob,cYou Wua,bYijun Wanga,bNa Xua,bZhongwen Xiea,bJinsong Zhanga,bLiang Zhanga,b( )Xiaochun Wana,b( )
State Key Laboratory of Tea Plant Biology and Utilization, Anhui Agricultural University, Hefei 230036, China
International Joint Laboratory on Tea Chemistry and Health Effects of Ministry of Education, Anhui Agricultural University, Hefei 230036, China
Department of Food Science, Rutgers University, New Brunswick, NJ 08901, USA

Peer review under responsibility of KeAi Communications Co., Ltd.

Show Author Information

Abstract

Roasting is a common manufacture technology for processing various teas. It is not only used in decreasing the water content of finished tea, but also improving the flavor of teas. In the present study, the roasted and non-roasted teas were compared by liquid-chromatography mass spectrometry and sensory evaluation. The roasted tea tasted less bitter and astringent. The content of main galloylated and simple catechins, caffeine and theobromine in roasted were significantly lower than non-roasted teas. Targeted taste-compounds metabolomics revealed that (–)-epigallocatechin gallate, kaempferol-glucose-rhamnose-glucose and (–)-epicatechin gallate were main contributors tightly correlated to astringent intensity. Flavonol glycosides including kaempferol-glucose, quercetin-glucose, kaempferol-glucose-rhamnose-glucose, and quercetin-glucose-rhamnose-glucose in roasted teas were also significantly less than non-roasted teas. To study the chemical changes during roasting, tea with a strong astringency was roasted under 80, 100, 120, 140, and 160 ℃. With the increase of roasting temperature, the bitter and astringent intensity of tea was gradually decreased, but the main astringent compounds including (–)-epigallocatechin, (–)-epigallocatechin gallate and kaempferol/quercetin glycosides were irregularly varied with temperature. The Pearson correlation coefficient analysis suggested procyanidin B2, coumaroylquinic acids and gallotannins were tightly correlated to the astringent and bitter perceptions, while N-ethyl-2-pyrrolidone-substituted flavan-3-ols were negatively correlated.

References

[1]

M.D. Castillo, J.M. Ames, M.H. Gordon, Effect of roasting on the antioxidant activity of coffee brews, J. Agric. Food Chem. 50(13) (2002) 3698-3703. https://doi.org/10.1021/jf011702q.

[2]

E. Satoh, N. Tohyama, M. Nishimura, Comparison of the antioxidant activity of roasted tea with green, oolong, and black teas, Food Sci. Nutr. 56(8) (2005) 551-559. https://doi.org/10.1080/09637480500398835.

[3]

X. Guo, C. Song, C. Ho, et al., Contribution of L-theanine to the formation of 2, 5-dimethylpyrazine, a key roasted peanutty flavor in Oolong tea during manufacturing processes, Food Chem. 263(15) (2018) 18-28. https://doi.org/10.1016/j.foodchem.2018.04.117.

[4]

X. Guo, W. Schwab, C. Ho, et al., Aroma compositions of large-leaf yellow tea and potential effect of theanine on volatile formation in tea, Food Chem. 280 (2019) 73-82. https://doi.org/10.1016/j.foodchem.2018.12.066.

[5]

J. Zhou, Y. Wu, P. Long, et al., LC-MS-based metabolomics reveals the chemical changes of polyphenols during high-temperature roasting of large-leaf yellow tea, J. Agric. Food Chem. 67(19) (2019) 5405-5412. https://doi.org/10.1021/acs.jafc.8b05062.

[6]

J. Zhou, L. Zhang, Q. Meng, et al., Roasting improves the hypoglycemic effects of a large-leaf yellow tea infusion by enhancing the levels of epimerized catechins that inhibit α-glucosidase, Food Funct. 9(10) (2018) 5162-5168. https://doi.org/10.1039/C8FO01429A.

[7]

C.T. Ho, X. Zheng, S. Li, Tea aroma formation, Food Sci. Hum. Well. 4(1) (2015) 9-27. https://doi.org/10.1016/j.fshw.2015.04.001.

[8]

W. Wang, L. Zhang, S. Wang, et al., 8-C N-ethyl-2-pyrrolidinone substituted flavan-3-ols as the marker compounds of Chinese dark teas formed in the post-fermentation process provide significant antioxidative activity, Food Chem. 152 (2014) 539-545. https://doi.org/10.1016/j.foodchem.2013.10.117.

[9]

L. Chen, W. Wang, J. Zhang, et al., Dual effects of ascorbic acid on the stability of EGCG by the oxidation product dehydroascorbic acid promoting the oxidation and inhibiting the hydrolysis pathway, Food Chem. 337 (2020) 127639. https://doi.org/10.1016/j.foodchem.2020.127639.

[10]

S. LÓpez, A. BarcelÓ, Reversed-phase and size-exclusion chromatography as useful tools in the resolution of peroxidase-mediated (+)-catechin oxidation products, J. Chromatogr. A. 919(2) (2001) 267-273. https://doi.org/10.1016/s0021-9673(01)00817-2.

[11]

L. Zhang, Q.Q. Cao, D. Granato, et al., Association between chemistry and taste of tea: a review, Trends Food Sci. Technol. 101 (2020) 139-149. https://doi.org/10.1016/j.tifs.2020.05.015.

[12]

D. Xie, W. Dai, M. Lu, et al., Nontargeted metabolomics predicts the storage duration of white teas with 8-C N-ethyl-2-pyrrolidinone-substituted flavan-3-ols as marker compounds, Food Res. Int. 125 (2019) 108635. https://doi.org/10.1016/j.foodres.2019.108635.

[13]

J. Cheng, F. Wu, P. Wang, et al., Flavoalkaloids with a pyrrolidinone ring from Chinese ancient cultivated tea Xi-Gui, J. Agric. Food Chem. 66(30) (2018) 7948-7957. https://doi.org/10.1021/acs.jafc.8b02266.

[14]

W. Dai, N. Lou, D. Xie, et al., N-ethyl-2-pyrrolidinone-substituted flavan-3-ols with anti-inflammatory activity in lipopolysaccharide-stimulated macrophages are storage-related marker compounds for green tea, J. Agric. Food Chem. 68(43) (2020) 12164-12172. https://doi.org/10.1021/acs.jafc.0c03952.

[15]

Y.Q. Xu, C. Zou, Y. Gao, et al., Effect of the type of brewing water on the chemical composition, sensory quality and antioxidant capacity of Chinese teas, Food Chem. 236 (2017) 142. https://doi.org/10.1016/j.foodchem.2016.11.110.

[16]

Y.Q. Xu, Y.N. Zhang, J.X. Chen, et al., Quantitative analyses of the bitterness and astringency of catechins from green tea, Food Chem. 258 (2018) 16-24. https://doi.org/10.1016/j.foodchem.2018.03.042.

[17]

Y.N. Zhang, J.F. Yin, J.X. Chen, et al., Improving the sweet aftertaste of green tea infusion with tannase, Food Chem. 192 (2016) 470-476. https://doi.org/10.1016/j.foodchem.2015.07.046.

[18]

J. Zhang, X. Wu, J. Qiu, et al., Comprehensive comparison on the chemical profile of guang chen pi at different ripeness stages using untargeted and pseudotargeted metabolomics, J. Agric. Food Chem. 68(31) (2020) 8483-8495. https://doi.org/10.1021/acs.jafc.0c02904.

[19]

A. Mao, H. Su, S. Fang, et al., Effects of roasting treatment on non-volatile compounds and taste of green tea, Int. J. Food Sci. Tech. (2018). https://doi.org/10.1111/ijfs.13853.

[21]

J. Zhuang, X. Dai, M. Zhu, et al., Evaluation of astringent taste of green tea through mass spectrometry-based targeted metabolic profiling of polyphenols, Food Chem. 305 (2020) 125507.1-125507.8. https://doi.org/10.1039/c8fo01429a.

[22]

L. Zhang, Y. Xia, D. Peterson. Identification of bitter modulating Maillard-catechin reaction products, J. Agric. Food Chem. 62(33) (2014) 8470-8477. https://doi.org/10.1021/jf502040e.

[23]

X. Guo, P. Long, Q. Meng, et al., An emerging strategy for evaluating the grades of Keemun black tea by combinatory liquid chromatography-Orbitrap mass spectrometry-based untargeted metabolomics and inhibition effects on α-glucosidase and α-amylase, Food Chem. 246 (2018) 74-81. https://doi.org/10.1016/j.foodchem.2017.10.148.

[24]

S. Scharbert, T. Hofmann, Molecular definition of black tea taste by means of quantitative studies, taste reconstitution, and omission experiments, J. Agric. Food Chem. 53(13) (2005) 5377-5384. https://doi.org/10.1021/jf050294d.

[25]

R. Mateos, G. Baeza, B. Sarriá, et al., Improved LC-MSn characterization of hydroxycinnamic acid derivatives and flavonols in different commercial mate (Ilex paraguariensis) brands. Quantification of polyphenols, methylxanthines, and antioxidant activity, Food Chem. 241 (2017) 232-241. https://doi.org/10.1016/j.foodchem.2017.08.085.

[26]

N. Berardini, R. Carle, A. Schieber, Characterization of gallotannins and benzophenone derivatives from mango (Mangifera indica L. cv. 'Tommy Atkins') peels, pulp and kernels by high-performance liquid chromatography/electrospray ionization mass spectrometry, Rapid. Commun. Mass. Spectrom. 18(19) (2004) 2208-2216. https://doi.org/10.1002/rcm.1611.

[27]

L. Zhang, N. Li, Z.Z. Ma, et al., Comparison of the chemical constituents of aged pu-erh tea, ripened pu-erh tea, and other teas using HPLC-DAD-ESI-MSn, J. Agric. Food Chem. 59(16) (2011) 8754-8760. https://doi.org/10.1021/jf2015733.

[28]

H. Kelebek, LC-DAD-ESI-MS/MS characterization of phenolic constituents in Turkish black tea: effect of infusion time and temperature. Food Chem. 204 (2016) 227-238. https://doi.org/10.1016/j.foodchem.2016.02.132.

[29]

S. Scharbert, N. Holzmann, T. Hofmann, Identification of the astringent taste compounds in black tea infusions by combining instrumental analysis and human bioresponse, J. Agric. Food Chem. 52(11) (2004) 3498-3508. https://doi.org/10.1021/jf049802u.

Food Science and Human Wellness
Pages 606-617
Cite this article:
Jiang Z, Han Z, Wen M, et al. Comprehensive comparison on the chemical metabolites and taste evaluation of tea after roasting using untargeted and pseudotargeted metabolomics. Food Science and Human Wellness, 2022, 11(3): 606-617. https://doi.org/10.1016/j.fshw.2021.12.017

584

Views

79

Downloads

35

Crossref

31

Web of Science

34

Scopus

3

CSCD

Altmetrics

Received: 11 December 2020
Revised: 25 January 2021
Accepted: 25 January 2021
Published: 04 February 2022
© 2022 Beijing Academy of Food Sciences.

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

Return