Evidence map›Paper›PMID 41025244›Full record

ArticleJournal of microbiology (Seoul, Korea)2025

Exploring the biosynthetic potential of Korean Actinobacteria for antibacterial metabolite discovery.

Sehong Park, Hyun-Woo Je, Yujin Cha, Boncheol Gu, Yeojeong Cho, Jin-Il Kim, Ji Won Seo, Seung Bum Kim, Jino Son, Moonsuk Hur and 3 more

Abstract read
In one paragraph

Article in Journal of microbiology (Seoul, Korea), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Sehong ParkDepartment of Biomedical Science and Engineering, Konkuk University, Seoul 05029, Republic of Korea.
Hyun-Woo JeDepartment of Biomedical Science and Engineering, Konkuk University, Seoul 05029, Republic of Korea.
Yujin ChaDepartment of Chemical and Biological Engineering, Korea University, Seoul 02841, Republic of Korea.
Boncheol GuDepartment of Chemical and Biological Engineering, Korea University, Seoul 02841, Republic of Korea.
Yeojeong ChoDoping Control Center, Korea Institute of Science and Technology, Seoul 02792, Republic of Korea.
Jin-Il KimDepartment of Microbiology and Molecular Biology, Chungnam National University, Daejeon 34134, Republic of Korea.
Ji Won SeoDepartment of Microbiology and Molecular Biology, Chungnam National University, Daejeon 34134, Republic of Korea.
Seung Bum KimDepartment of Microbiology and Molecular Biology, Chungnam National University, Daejeon 34134, Republic of Korea.
Jino SonBiological Resources Assessment Division, National Institute of Biological Resources, Incheon 22689, Republic of Korea.
Moonsuk HurBiological Resources Assessment Division, National Institute of Biological Resources, Incheon 22689, Republic of Korea.
Changmin SungDoping Control Center, Korea Institute of Science and Technology, Seoul 02792, Republic of Korea.
Min-Kyu OhDepartment of Chemical and Biological Engineering, Korea University, Seoul 02841, Republic of Korea.
Hahk-Soo KangDepartment of Biomedical Science and Engineering, Konkuk University, Seoul 05029, Republic of Korea.

Funding

Ministry of EnvironmentNational Institute of Biological Resources NIBR202420201National Research Foundation of Korea NRF-2022R1A2C4001258National Research Foundation of Korea RS-2024-00509338
6 · The paper itself

Abstract

Actinobacteria, a phylum of Gram-positive bacteria, are renowned for their remarkable ability to produce antibacterial natural products. The National Institute of Biological Resources (NIBR) of Korea maintains a collection of Korean native actinobacteria. In this study, we explored the phylogenetic and biosynthetic diversity of the NIBR actinobacteria collection to assess its potential as a source of new antibacterial natural products. A 16S rDNA-based phylogenetic analysis revealed a high level of genetic diversity within the collection, with a predominance of Streptomyces, along with rare actinobacterial genera such as Kitasatospora and Micromonospora. Additionally, genetic network analysis of biosynthetic gene clusters (BGCs) from 15 sequenced NIBR actinobacterial strains demonstrated extensive BGC diversity, with many clusters identified as cryptic. Screening of culture extracts for antibacterial activity, followed by dereplication of active extracts, suggested the presence of potentially novel antibacterial natural products. Activity-guided isolation and whole-genome sequencing of the active strain KU57 led to the isolation of one new and three known svetamycin congeners along with their BGC. Overall, our findings highlight the NIBR actinobacteria collection as a valuable source for the discovery of new antibacterial natural products.

Indexed as

ActinobacteriaAnti-Bacterial AgentsBiological ProductsBiosynthetic PathwaysDNA, BacterialGenetic VariationGenome, BacterialMicrobial Sensitivity TestsMultigene FamilyPhylogenyRepublic of KoreaRNA, Ribosomal, 16SStreptomycesAnti-Bacterial AgentsBiological ProductsDNA, BacterialRNA, Ribosomal, 16Sactinobacteriaantibacterial activitybiosynthetic gene clusterssvetamycins

Identifiers

PMID41025244
PMCPMC13577020

What OpenQuestion holds

Textmetadata
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.