Literature DB >> 33199121

Enzymatic hydrolysis and auto-isomerization during β-glucosidase treatment improve the aroma of instant white tea infusion.

Hui Ni1, Qingxiang Jiang2, Qi Lin3, Qiongqing Ma4, Lu Wang5, Shuyi Weng6, Gaoling Huang7, Lijun Li8, Feng Chen9.   

Abstract

The aroma changes in instant white tea resulting from β-glucosidase treatment was investigated by quantitative descriptive analysis (QDA), gas chromatography-mass spectrometry (GC-MS), odour activity value analysis (OAV), aroma reconstruction and omission tests. The grassy, floral and sweet notes increased significantly (P < 0.05), and the roasted note decreased significantly (P < 0.05) upon β-glucosidase treatment. Quantitative analysis showed that the concentrations of benzaldehyde, benzeneacetaldehyde, (Z)-3-hexen-1-ol, linalool, phenylethyl alcohol, cis-linalool oxide, trans-linalool oxide, hexanol, hotrienol and (E)-2-hexen-1-ol increased significantly (P < 0.05) after treatment; however, (Z)-3-hexen-1-ol isomerized to (E)-2-hexen-1-ol. OAV analysis, aroma reconstruction and the omission test showed that the grassy, floral and sweet notes increased as the (Z)-3-hexen-1-ol, cis/trans-linalool oxide and benzeneacetaldehyde increased, whereas the roasted note declined under the same conditions. The enzymatic hydrolysis of glycosidic precursors and the auto-isomerization of volatile compounds provide new information for understanding how β-glucosidase treatment improves the aroma of tea products.
Copyright © 2020 Elsevier Ltd. All rights reserved.

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Keywords:  (E)-2-(2-Pentenyl)-furan (PubChem CID: 5369957); (E)-2-Hexen-1-ol (PubChem CID: 5318042); (E)-β-Ionone (PubChem CID: 638014); (Z)-3-Hexen-1-ol (PubChem CID: 5281167); 1-Ethyl-1H-pyrrole (PubChem CID: 185226); 1-Ethyl-1H-pyrrole-2-carboxaldehyde (PubChem CID: 579338); 2,4-Ditert-butylphenol (PubChem CID: 6911); 2-Ethyl-furan (PubChem CID: 18554); 2-Methyl-butanal (PubChem CID: 7284); 2-Methyl-furan (PubChem CID: 10797); 2-Methyl-propanal (PubChem CID: 6561); 2-Pentyl-furan (PubChem CID: 19602); 3-Methyl-butanal (PubChem CID: 11552); Aroma reconstruction and omission test; Benzaldehyde (PubChem CID: 240); Benzeneacetaldehyde (PubChem CID: 998); Cis-limonene oxide (PubChem CID: 6452061); Cis-linalool oxide (PubChem CID: 6428573); Dihydroactinidiolide (PubChem CID: 6432173); Dimethyl sulphide (PubChem CID: 1068); GC–MS; Hexanol (PubChem CID: 8103); Hotrienol (PubChem CID: 5366264); Instant white tea; Limonene (PubChem CID: 440917); Linalool (PubChem CID: 6549); OAV; Phenylethyl alcohol (PubChem CID: 6054); Safranal (PubChem CID: 61041); Trans-linalool oxide (PubChem CID: 6432254); Volatile compounds; β-Glucosidase

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Year:  2020        PMID: 33199121     DOI: 10.1016/j.foodchem.2020.128565

Source DB:  PubMed          Journal:  Food Chem        ISSN: 0308-8146            Impact factor:   7.514


  2 in total

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Authors:  Dea Risfika Faustina; Rachmad Gunadi; Aprilia Fitriani; Supriyadi Supriyadi
Journal:  Int J Food Sci       Date:  2022-03-01

2.  Characterisation of the volatile compounds profile of Chinese pan-fried green tea in comparison with baked green tea, steamed green tea, and sun-dried green tea using approaches of molecular sensory science.

Authors:  Yali Shi; Yin Zhu; Wanjun Ma; Zhi Lin; Haipeng Lv
Journal:  Curr Res Food Sci       Date:  2022-07-08
  2 in total

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