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借助机器学习挖掘产孢梭菌的代谢能力

Mining the Metabolic Capacity of Clostridium sporogenes Aided by Machine Learning.

作者信息

Ouyang Huanrong, Xu Zhao, Hong Joshua, Malroy Jeshua, Qian Liangyu, Ji Shuiwang, Zhu Xuejun

机构信息

Department of Chemical Engineering, Texas A&M University, College Station, 77843, United States.

Department of Computer Science & Engineering, Texas A&M University, College Station, 77843, United States.

出版信息

Angew Chem Int Ed Engl. 2024 Mar 18;63(12):e202319925. doi: 10.1002/anie.202319925. Epub 2024 Feb 15.

DOI:10.1002/anie.202319925
PMID:38286754
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10986427/
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.

摘要

厌氧菌在胃肠道微生物群中占主导地位,在胃肠道中,很大一部分小分子会被降解或修饰。然而,与需氧菌相比,肠道厌氧菌巨大的代谢能力在很大程度上仍不为人所知,这主要是由于需要复杂的实验室环境。在本研究中,我们采用了一个计算机机器学习平台MoleculeX来预测肠道厌氧菌产孢梭菌对小分子的代谢能力。实验表明,在预测为不稳定的前七个候选物中,有六个在产孢梭菌培养物中确实表现出不稳定性。我们还首次在细菌培养物中补充依维莫司后鉴定出了几种代谢产物。通过利用生物信息学和体外生化分析,我们成功鉴定出了产孢梭菌基因组中负责依维莫司转化的一种酶。因此,我们的框架有可能促进未来对肠道小分子代谢的理解,通过个性化医疗进一步改善患者护理,并指导新的小分子药物和治疗方法的开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cb9/10986427/c6c525aa84c1/nihms-1975649-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cb9/10986427/6959565c037a/nihms-1975649-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cb9/10986427/7783b028da33/nihms-1975649-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cb9/10986427/c6c525aa84c1/nihms-1975649-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cb9/10986427/6959565c037a/nihms-1975649-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cb9/10986427/7783b028da33/nihms-1975649-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cb9/10986427/c6c525aa84c1/nihms-1975649-f0003.jpg

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