Non-targeted Metabolomics Reveals the Unique Chemical Composition of Green Tea and Black Tea from Camellia ptilophylla

Abstract

To reveal the chemical composition profile of Camellia ptilophylla, a rare natural low-caffeine tea variety, non-targeted metabolomics based on high-resolution mass spectrometry (HR-MS) was employed to identify the metabolite composition of green tea and black tea from C. ptilophylla and C. sinensis var. assamica. Additionally, the metabolomic differences between the two types of tea and between the two tea varieties were analyzed using principal component analysis (PCA), cluster analysis (CA), and orthogonal partial least squares-discriminant analysis (OPLS-DA). Differential metabolites were identified using standards and database. A total of 152 metabolites were identified in the four tea samples, the major ones being flavonoids (42%). These metabolites were categorized into four clusters. The metabolomic difference between C. ptilophylla and C. sinensis var. assamica was more pronounced than that between green and black teas. Notably, 24 metabolites including theasinensin B isomers, theobromine and 14 flavonoids such as tetrahydroxyxanthone and epitheaflagallin 3-O-gallate, which were more abundant in C. ptilophylla green tea than in C. sinensis green tea, were considered as the characteristic metabolites of C. ptilophylla green tea. In black tea from C. ptilophylla, 40 characteristic metabolites were identified including 25 flavonoids such as gallocatechin-3,5-digallate, tetrahydroxyxanthone and dihydromyricetin; 4 tannins such as theaflavin 3-gallate, theasinensin A isomers and theaflavin 3,3’-digallate; and theobromine. This study provides a reference for further exploration of bioactive compounds in C. ptilophylla.

Keywords

• camellia ptilophylla; green tea; black tea; non-targeted metabolomics; chemical composition