Evidence map›Paper›PMID 38286754›Full record

ArticleAngewandte Chemie (International ed. in English)2024

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

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

Open access · hybridAbstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Huanrong OuyangDepartment of Chemical Engineering, Texas A&M University, College Station, 77843, United States.
Zhao XuDepartment of Computer Science & Engineering, Texas A&M University, College Station, 77843, United States.
Joshua HongDepartment of Chemical Engineering, Texas A&M University, College Station, 77843, United States.
Jeshua MalroyDepartment of Chemical Engineering, Texas A&M University, College Station, 77843, United States.
Liangyu QianDepartment of Chemical Engineering, Texas A&M University, College Station, 77843, United States.
Shuiwang JiDepartment of Computer Science & Engineering, Texas A&M University, College Station, 77843, United States.
Xuejun ZhuDepartment of Chemical Engineering, Texas A&M University, College Station, 77843, United States.ORCID 0000-0002-9839-2924
Texas A&M University · US

Funding

Genetics of deep-learning-derived neuroimaging endophenotypes for Alzheimer's Disease (Parent grant)U01AG070112 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FORNAGE, MYRIAM, JI, SHUIWANG · 2021 to 2025
$7.2M
Discovery and development of drug cocktails evolved by NatureR35GM146984 · NIGMS · TEXAS ENGINEERING EXPERIMENT STATION · PI Xuejun Zhu · 2022 to 2026
$1.7M
NIA NIH HHS U01 AG070112NIA NIH HHS U01AG070112NIGMS NIH HHS R35 GM146984NIGMS NIH HHS R35GM146984
6 · The paper itself

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.

Indexed as

ClostridiumEverolimusBacteria, AnaerobicHumansEverolimusAnaerobesenzyme identificationmachine learningmetabolic capacitysmall molecules

Identifiers

PMID38286754
PMCPMC10986427
OpenAlexW4391329789

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.