Affiliation:
1. Department of Chemical Engineering Texas A&M University College Station 77843 United States
2. Department of Computer Science & Engineering Texas A&M University College Station 77843 United States
3. Interdisciplinary Graduate Program in Genetics and Genomics Texas A&M University College Station 77843 United States
Abstract
AbstractAnaerobes 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.
Funder
Artie McFerrin Department of Chemical Engineering, Texas A and M University
Texas A and M Engineering Experiment Station, Texas A and M University
National Institute of General Medical Sciences
Welch Foundation
Texas A and M University
National Institute on Aging