4.7 Article

Aromatic Profiles and Enantiomeric Distributions of Chiral Volatile Compounds in Pu-Erh Tea

Journal

JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
Volume 70, Issue 27, Pages 8395-8408

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jafc.2c03264

Keywords

Pu-Erh tea; RAPT; RIPT; chiral compounds; enantiomeric

Funding

  1. Shuguang Program - Shanghai Education Development Foundation [20SG55]
  2. Shanghai Municipal Education Commission [20SG55]
  3. Collaborative Innovation Center of Fragrance Flavor and Cosmetics [1021ZK215003009-A06]
  4. Capacity building project of local universities Science and Technology Commission of Shanghai Municipality [21010503900]
  5. Program of Shanghai Academic Research Leader [21XD1423800]

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This study aims to explore the aroma characteristics of Pu-Erh tea from the perspective of enantiomers of chiral compounds. A total of 15 enantiomers were determined, among which 7 were identified as important compounds contributing to the aroma of Pu-Erh tea. Different enantiomeric compounds have different contributions to the aroma characteristics of Pu-Erh tea.
Pu-Erh tea, as a typical post-fermented tea, can be divided into raw Pu-Erh tea (RAPT) and ripened Pu-Erh tea (RIPT) according to the processing technology. It is famous for its unique aroma after aging. Although previous research on the aroma characteristics of Pu-Erh tea mostly focused on the aroma compounds, little research on chiral compounds in RAPT and RIPT has been performed. Therefore, the current work aims to explore the aroma characteristics of Pu-Erh tea from the perspective of enantiomers of chiral compounds. A total of 15 enantiomers were determined in this study, among which (R)-(-)-2,2,6-trimethylcyclohexanone, (R)-(-)-linalool, (S)-(+)-linalool, (R)-(+)-delta-octanolactone, (R)-(+)-gamma-nonanolactone, (2R,5R)-(+)-the-aspirone A, and (R)-(-)-dihydroactinidiolide were identified as enantiomeric compounds that play an important role in the aroma of RAPT and RIPT. Furthermore, (2S,5R)-trans-linalool oxide and (R)-(+)-alpha-terpineol were important contributors to the aroma profile of RAPT, while (S)-(+)-2-methylbutanal, (S)-(-)-limonene, S-(-)-alpha-terpineol, and (1R,2R)-(-)-methyl jasmonate contributed to the characteristic aroma of RIPT. The addition of these enantiomeric compounds brings the aroma closer to that of the original tea sample. In addition, the analysis of chiral enantiomers of linalool, limonene, theaspirone A, and gamma-nonanolactone can provide guidance for the quality and flavor control of Pu-Erh tea aroma.

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