Abstract
Anaerobes dominate the microbiota of the gastrointestinal (GI) tract, where a significant portion of small molecules can be degraded or modified. However, the enormous metabolic capacity of gut anaerobes remains largely elusive in contrast to aerobic bacteria, mainly due to the requirement of sophisticated laboratory settings. In this study, we employed an in silico machine learning platform, MoleculeX, to predict the metabolic capacity of a gut anaerobe, Clostridium sporogenes, against small molecules. Experiments revealed that among the top seven candidates predicted as unstable, six indeed exhibited instability in C. sporogenes culture. We further identified several metabolites resulting from the supplementation of everolimus in the bacterial culture for the first time. By utilizing bioinformatics and in vitro biochemical assays, we successfully identified an enzyme encoded in the genome of C. sporogenes responsible for everolimus transformation. Our framework thus can potentially facilitate future understanding of small molecules metabolism in the gut, further improve patient care through personalized medicine, and guide the development of new small molecule drugs and therapeutic approaches.
Original language | English |
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Article number | e202319925 |
Journal | Angewandte Chemie - International Edition |
Volume | 63 |
Issue number | 12 |
DOIs | |
State | Published - Mar 18 2024 |
Funding
This research was supported by Texas A&M Engineering Experiment Station (TEES) and Chemical Engineering Department (TAMU) start‐up funds, NIH grant (Award No. R35GM146984), and a Robert A. Welch Foundation Grant (Grant No. A‐2129‐20220331) to X. Z.; Texas A&M Engineering Experiment Station (TEES) and Computer Science and Engineering Department (TAMU) start‐up funds, NIH grant (Award No. U01AG070112) to S. J.
Keywords
- Anaerobes
- enzyme identification
- machine learning
- metabolic capacity
- small molecules