A Chemical Reaction Similarity-Based Prediction Algorithm Identifies the Multiple Taxa Required to Catalyze an Entire Metabolic Pathway of Dietary Flavonoids
E. E. Gulsan, F. Nowshad, P. Yamaguchi, X. Dong, A. Jayaraman, K. Lee
Abstract
Flavonoids are polyphenolic phytochemicals abundant in plant-based, health-promoting foods. They are only partially absorbed in the small intestine, and gut microbiota plays a significant role in their metabolism. As flavonoids are not natural substrates of gut bacterial enzymes, reactions of flavonoid metabolism have been attributed to the ability of general classes of enzymes to metabolize non-natural substrates. To systematically characterize this promiscuous enzyme activity, we developed a prediction tool that is based on chemical reaction similarity. The tool takes a list of enzymes or organisms to match microbial enzymes with their non-native flavonoid substrates and orphan reactions. We successfully predicted the promiscuous activity of known flavonoid-metabolizing bacterial and plant enzymes. Next, we used this tool to identify the multiple taxa required to catalyze an entire metabolic pathway of dietary flavonoids. Tilianin is a flavonoid-O-glycoside having biological and pharmacological activities, including neuroprotection. Using our prediction tool, we defined a novel bacterial pathway of tilianin metabolism that includes O-deglycosylation to acacetin, demethylation of acacetin to apigenin, and hydrogenation of apigenin to naringenin. We predicted and confirmed using in vitro experiments and LC-MS techniques that Bifidobacterium longum subsp. animalis, Blautia coccoides and Flavonifractor plautii can catalyze this pathway. Prospectively, the prediction-validation methodology developed in this work could be used to systematically characterize gut microbial metabolism of dietary flavonoids and other phytochemicals. The bioactivities of flavonoids and their metabolic products can vary widely. We used an in vitro rat neuronal model to show that tilianin metabolites exhibit protective effect against H2O2 through reactive oxygen species (Delepine et al.) scavenging activity and thus, improve cell viability, while the parent compound, tilianin, was ineffective. These results are important to understand the gut microbiota-dependent physiological effects of dietary flavonoids.
02 /Specification & Classification
Click any tag to browse matching papers- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- A Chalcone Synthase-Like Bacterial Protein Catalyzes Heterocyclic C-Ring Cleavage of Naringenin to Alter Bioactivity Against Nuclear Receptors in Colonic Epithelial Cells
E. E. Gulsan, F. Nowshad, … K. Lee·bioRxiv·Apr 22, 2022
- Assessment of inter-individual variation in metabolism of flavonoids from bilberry and grape seed extracts using an in vitro digestion and faecal fermentation model
Teresa Grohmann, Paul Antony Kroon, … Baukje de Roos·bioRxiv·Mar 3, 2026
- Automatic identification of players in the flavonoid biosynthesis with application on the biomedicinal plant Croton tiglium
B. Pucker, F. Reiher, H. M. Schilbert·bioRxiv·Jun 27, 2020
- Extending PROXIMAL to predict degradation pathways of phenolic compounds in the human gut microbiota
F. Balzerani, T. Blasco, … S. Hassoun·bioRxiv·May 17, 2023
- A gut microbial metabolite of dietary polyphenols reverses obesity-driven hepatic steatosis
L. J. Osborn, K. Schultz, … J. Claesen·bioRxiv·Sep 16, 2021
- Enzymatic carbon-fluorine bond cleavage by human gut microbes
Silke I. Probst, Florian D. Felder, … Serina L. Robinson·Proceedings of the National Academy of SciencesPeer-reviewed·Jun 13, 2025