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Peer-reviewedCC BY 4.0Metabolites

Untargeted Metabolomics Profiling of Growth-Year-Associated Changes in Relative Metabolite Abundance in Tetrastigma hemsleyanum Tuberous Roots

4 affiliations
  1. 1College of Biological and Environmental Engineering, Zhejiang Shuren University, Hangzhou 310015, China
  2. 2Zhejiang Key Laboratory of Environment and Health of New Pollutants, School of Environment, Hangzhou Institute for Advanced Study, University of Chinese Academy of Sciences, Hangzhou 310024, China
  3. 3State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China
  4. 4College of Life Sciences, Zhejiang University, Hangzhou 310058, China

Abstract

Background/Objectives:Tetrastigma hemsleyanum is a traditional medicinal plant whose tuberous roots are rich in flavonoids and phenolic acids, but how the relative abundance of these constituents changes across growth years remains poorly resolved. Methods: Tuberous roots from five growth years (S1–S5; three independently grown plants per year) were analyzed by UHPLC–Orbitrap-MS-based untargeted metabolomics. Annotations were graded using Metabolomics Standards Initiative (MSI) criteria: of 349 curated entries, 252 were Level 2 and 56 Level 3, and none reached Level 1 because authentic standards were not analyzed. Results: Principal component analysis showed non-linear differentiation, with first-year roots the most distinct. Combined VIP, fold-change, and t-test criteria identified 264 differential entries between adjacent growth years, all remaining significant after Benjamini–Hochberg correction (q < 0.01). Flavonol-related features (e.g., quercetin-related signals, myricetin, and rutin) were relatively abundant at S1; flavone C-glycoside, flavan-3-ol, and phenolic-acid features (e.g., vitexin, catechin, and ferulic acid) at S3; and amino-acid, organic-acid, and nucleotide features at S4. KEGG mapping of 46 differential annotations indicated flavonoid- and amino-acid-related pathways. Conclusions: Given the small sample size, relative peak-area data, and putative annotations, these results are hypothesis-generating; they identify candidate stages and constituents for targeted quantification rather than an optimal harvest year.

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BibTeX
@article{ye2026untargeted,
  title = {{Untargeted Metabolomics Profiling of Growth-Year-Associated Changes in Relative Metabolite Abundance in Tetrastigma hemsleyanum Tuberous Roots}},
  author = {Mingli Ye and Boya Liu and Xin Li and Haifeng Han and Yukai Ba and Zhengrui Chen and Yu Liu and Yonggang Zhao},
  journal = {Metabolites},
  year = {2026},
  month = oct,
  doi = {10.3390/metabo16110831},
  url = {https://www.mdpi.com/2218-1989/16/11/831},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Untargeted Metabolomics Profiling of Growth-Year-Associated Changes in Relative Metabolite Abundance in Tetrastigma hemsleyanum Tuberous Roots
AU  - Mingli Ye
AU  - Boya Liu
AU  - Xin Li
AU  - Haifeng Han
AU  - Yukai Ba
AU  - Zhengrui Chen
AU  - Yu Liu
AU  - Yonggang Zhao
PY  - 2026
DA  - 2026/10/30
JO  - Metabolites
DO  - 10.3390/metabo16110831
UR  - https://www.mdpi.com/2218-1989/16/11/831
AB  - Background/Objectives:Tetrastigma hemsleyanum is a traditional medicinal plant whose tuberous roots are rich in flavonoids and phenolic acids, but how the relative abundance of these constituents changes across growth years remains poorly resolved. Methods: Tuberous roots from five growth years (S1–S5; three independently grown plants per year) were analyzed by UHPLC–Orbitrap-MS-based untargeted metabolomics. Annotations were graded using Metabolomics Standards Initiative (MSI) criteria: of 349 curated entries, 252 were Level 2 and 56 Level 3, and none reached Level 1 because authentic standards were not analyzed. Results: Principal component analysis showed non-linear differentiation, with first-year roots the most distinct. Combined VIP, fold-change, and t-test criteria identified 264 differential entries between adjacent growth years, all remaining significant after Benjamini–Hochberg correction (q < 0.01). Flavonol-related features (e.g., quercetin-related signals, myricetin, and rutin) were relatively abundant at S1; flavone C-glycoside, flavan-3-ol, and phenolic-acid features (e.g., vitexin, catechin, and ferulic acid) at S3; and amino-acid, organic-acid, and nucleotide features at S4. KEGG mapping of 46 differential annotations indicated flavonoid- and amino-acid-related pathways. Conclusions: Given the small sample size, relative peak-area data, and putative annotations, these results are hypothesis-generating; they identify candidate stages and constituents for targeted quantification rather than an optimal harvest year.
SN  - 2218-1989
ER  -