Study of the Metabolites and Flavor Characteristics in Different Subtypes of White Tea by Metabolomics Profiling
Applications | 2019 | Agilent TechnologiesInstrumentation
White tea is valued for its delicate aroma, minimal processing and potential health benefits. Understanding its nonvolatile metabolite profile is essential for quality control, flavor evaluation and the detection of adulteration or mislabeling in commercial products.
This study applied a nontargeted metabolomics approach to characterize and compare three subtypes of white tea—Silver Needle (SN), White Peony (WP) and Shoumei (SM). The aims were to extract the tea metabolome, identify differential compounds and correlate them with sensory attributes such as umami, bitterness and astringency.
• Sample preparation involved suspending 0.10 g of powdered tea in 10 mL boiling water, vortexing, sonication, centrifugation and filtration through a 0.22 µm membrane.
• Quality control pooled aliquots of all samples to monitor analytical consistency.
• Metabolite features were extracted, aligned and filtered using MassHunter Profinder and Mass Profiler Professional software.
• Chemometric analyses included principal component analysis (PCA), partial least squares discriminant analysis (PLS-DA), hierarchical clustering and Pearson correlation with sensory data.
• Agilent 1290 Infinity II UHPLC system with built-in degasser and column thermostat
• Agilent ZORBAX Eclipse Plus C18 column (150 × 3.0 mm, 1.8 µm)
• Agilent 6540/6545 Q-TOF mass spectrometer with dual Jet Stream ESI source
• Agilent MassHunter Profinder 8.0 and Mass Profiler Professional 14.8 software
• A total of 1,915 metabolite features were detected and aligned across samples.
• PCA and PLS-DA achieved clear separation of SN, WP and SM subtypes, with 100 % classification accuracy.
• Ninety-nine compounds were identified by database matching and authentic standards; 64 showed significant abundance differences among subtypes.
• Forty-one metabolites demonstrated strong correlation (R² ≥ 0.90, p ≤ 0.01) with taste attributes. Theanine, asparagine, aspartic acid and AMP correlated positively with umami, while flavan-3-ols, theasinensins, procyanidin B3 and theobromine correlated with bitterness and astringency.
• Hierarchical clustering revealed distinct compound groups such as catechins, phenolic acids, flavonol glycosides and alkaloids, each varying by tea subtype.
• Provides a robust chemical fingerprinting tool for differentiating white tea varieties.
• Identifies potential marker compounds for detecting adulteration or mislabeling.
• Supports quality assurance efforts in tea production and trade.
• Integration of targeted and nontargeted metabolomics for deeper compound quantitation.
• Use of expanded spectral libraries and machine learning for automated tea classification.
• Correlation of metabolite markers with consumer preference and health bioactivity.
• Application to other tea types and processing variations for broader quality assessment.
Nontargeted UHPLC-Q-TOF/MS metabolomic profiling, combined with multivariate statistics, effectively differentiated three white tea subtypes and identified key metabolites linked to flavor attributes. These results pave the way for improved quality control, authentication and understanding of tea flavor chemistry.
LC/TOF, LC/HRMS, LC/MS, LC/MS/MS
IndustriesFood & Agriculture, Metabolomics
ManufacturerAgilent Technologies
Summary
Importance of the Topic
White tea is valued for its delicate aroma, minimal processing and potential health benefits. Understanding its nonvolatile metabolite profile is essential for quality control, flavor evaluation and the detection of adulteration or mislabeling in commercial products.
Objectives and Overview of the Study
This study applied a nontargeted metabolomics approach to characterize and compare three subtypes of white tea—Silver Needle (SN), White Peony (WP) and Shoumei (SM). The aims were to extract the tea metabolome, identify differential compounds and correlate them with sensory attributes such as umami, bitterness and astringency.
Methodology
• Sample preparation involved suspending 0.10 g of powdered tea in 10 mL boiling water, vortexing, sonication, centrifugation and filtration through a 0.22 µm membrane.
• Quality control pooled aliquots of all samples to monitor analytical consistency.
• Metabolite features were extracted, aligned and filtered using MassHunter Profinder and Mass Profiler Professional software.
• Chemometric analyses included principal component analysis (PCA), partial least squares discriminant analysis (PLS-DA), hierarchical clustering and Pearson correlation with sensory data.
Used Instrumentation
• Agilent 1290 Infinity II UHPLC system with built-in degasser and column thermostat
• Agilent ZORBAX Eclipse Plus C18 column (150 × 3.0 mm, 1.8 µm)
• Agilent 6540/6545 Q-TOF mass spectrometer with dual Jet Stream ESI source
• Agilent MassHunter Profinder 8.0 and Mass Profiler Professional 14.8 software
Main Results and Discussion
• A total of 1,915 metabolite features were detected and aligned across samples.
• PCA and PLS-DA achieved clear separation of SN, WP and SM subtypes, with 100 % classification accuracy.
• Ninety-nine compounds were identified by database matching and authentic standards; 64 showed significant abundance differences among subtypes.
• Forty-one metabolites demonstrated strong correlation (R² ≥ 0.90, p ≤ 0.01) with taste attributes. Theanine, asparagine, aspartic acid and AMP correlated positively with umami, while flavan-3-ols, theasinensins, procyanidin B3 and theobromine correlated with bitterness and astringency.
• Hierarchical clustering revealed distinct compound groups such as catechins, phenolic acids, flavonol glycosides and alkaloids, each varying by tea subtype.
Benefits and Practical Applications of the Method
• Provides a robust chemical fingerprinting tool for differentiating white tea varieties.
• Identifies potential marker compounds for detecting adulteration or mislabeling.
• Supports quality assurance efforts in tea production and trade.
Future Trends and Applications
• Integration of targeted and nontargeted metabolomics for deeper compound quantitation.
• Use of expanded spectral libraries and machine learning for automated tea classification.
• Correlation of metabolite markers with consumer preference and health bioactivity.
• Application to other tea types and processing variations for broader quality assessment.
Conclusion
Nontargeted UHPLC-Q-TOF/MS metabolomic profiling, combined with multivariate statistics, effectively differentiated three white tea subtypes and identified key metabolites linked to flavor attributes. These results pave the way for improved quality control, authentication and understanding of tea flavor chemistry.
Reference
- Mao J.T.; et al. White Tea Extract Induces Apoptosis in Non–Small Cell Lung Cancer Cells: the Role of Peroxisome Proliferator-Activated Receptor-γ and 15-Lipoxygenases. Cancer Prev. Res. 2010, 3(9), 1132–1140.
- Ning J.-M.; et al. Chemical Constituents Analysis of White Tea of Different Qualities and Different Storage Times. Eur. Food Res. Technol. 2016, 242(12), 2093–2104.
- Tan J.; et al. Flavonoids, Phenolic Acids, Alkaloids and Theanine in Different Types of Authentic Chinese White Tea Samples. J. Food Compos. Anal. 2017, 57, 8–15.
- Dai W.; et al. Nontargeted Analysis Using UPLC-Q-TOF/MS Uncovers the Effects of Harvest Season on the Metabolites and Taste Quality of Tea (Camellia sinensis L.). J. Agric. Food Chem. 2015, 63, 9869–9878.
- Tan J.; et al. Study of the Dynamic Changes in the Non-Volatile Chemical Constituents of Black Tea During Fermentation Processing by a Nontargeted Metabolomics Approach. Food Res. Int. 2016, 79, 106–113.
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