Evidence map›Paper›PMID 37653463›Full record

ArticleJournal of industrial microbiology & biotechnology2023

Diversity and taxonomic distribution of bacterial biosynthetic gene clusters predicted to produce compounds with therapeutically relevant bioactivities.

Max L Beck, Siyeon Song, Isra E Shuster, Aarzu Miharia, Allison S Walker

Abstract read
In one paragraph

Article in Journal of industrial microbiology & biotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. AI-Assisted Isolation of Bioactive Dipyrimicins fromJournal of natural products · 2026
    Article
  4. Review
  5. Review
  6. Why Do FilamentousAnnual review of microbiology · 2025
    Review
  7. Article
  8. AI-assisted isolation of bioactive Dipyrimicins frombioRxiv : the preprint server for biology · 2025
    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

5 authors.

Max L BeckDepartment of Chemistry, Vanderbilt University. 1234 Stevenson Center Lane, Nashville, TN 37240, Untited States.
Siyeon SongDepartment of Chemistry, Vanderbilt University. 1234 Stevenson Center Lane, Nashville, TN 37240, Untited States.
Isra E ShusterDepartment of Chemistry, Vanderbilt University. 1234 Stevenson Center Lane, Nashville, TN 37240, Untited States.
Aarzu MihariaDepartment of Chemistry, Vanderbilt University. 1234 Stevenson Center Lane, Nashville, TN 37240, Untited States.
Allison S WalkerDepartment of Chemistry, Vanderbilt University. 1234 Stevenson Center Lane, Nashville, TN 37240, Untited States.ORCID 0000-0001-5666-7232

Funding

Machine learning approaches for the discovery, repurposing, and optimization of natural products with therapeutic potential - Supplement to support grad training of Adrian RussR35GM146987 · NIGMS · VANDERBILT UNIVERSITY · PI Allison Sara Walker · 2022 to 2026
$2.4M
NIGMS NIH HHS R35 GM146987NIH HHS
6 · The paper itself

Abstract

Bacteria have long been a source of natural products with diverse bioactivities that have been developed into therapeutics to treat human disease. Historically, researchers have focused on a few taxa of bacteria, mainly Streptomyces and other actinomycetes. This strategy was initially highly successful and resulted in the golden era of antibiotic discovery. The golden era ended when the most common antibiotics from Streptomyces had been discovered. Rediscovery of known compounds has plagued natural product discovery ever since. Recently, there has been increasing interest in identifying other taxa that produce bioactive natural products. Several bioinformatics studies have identified promising taxa with high biosynthetic capacity. However, these studies do not address the question of whether any of the products produced by these taxa are likely to have activities that will make them useful as human therapeutics. We address this gap by applying a recently developed machine learning tool that predicts natural product activity from biosynthetic gene cluster (BGC) sequences to determine which taxa are likely to produce compounds that are not only novel but also bioactive. This machine learning tool is trained on a dataset of BGC-natural product activity pairs and relies on counts of different protein domains and resistance genes in the BGC to make its predictions. We find that rare and understudied actinomycetes are the most promising sources for novel active compounds. There are also several taxa outside of actinomycetes that are likely to produce novel active compounds. We also find that most strains of Streptomyces likely produce both characterized and uncharacterized bioactive natural products. The results of this study provide guidelines to increase the efficiency of future bioprospecting efforts. ONE-SENTENCE SUMMARY: This paper combines several bioinformatics workflows to identify which genera of bacteria are most likely to produce novel natural products with useful bioactivities such as antibacterial, antitumor, or antifungal activity.

Indexed as

ActinobacteriaBiological ProductsActinomycesComputational BiologyHumansMultigene FamilyBiological ProductsGenome miningMachine learningNatural products

Identifiers

PMID37653463
PMCPMC10548851

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.