Evidence map›Paper›PMID 38717668›Full record

ArticleApplied microbiology and biotechnology2024

Biosynthetic gene clusters with biotechnological applications in novel Antarctic isolates from Actinomycetota.

Pablo Bruna, Kattia Núñez-Montero, María José Contreras, Karla Leal, Matías García, Michel Abanto, Leticia Barrientos

Abstract read
In one paragraph

Article in Applied microbiology and biotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. International journal of systematic and evolutionary microbiology · 2026
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  6. Draft genome sequences ofMicrobiology resource announcements · 2026
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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.

Pablo BrunaPrograma de Doctorado en Ciencias mención Biología Celular y Molecular Aplicada, Universidad de La Frontera, Temuco, Chile.
Kattia Núñez-MonteroFacultad de Ciencias de la Salud, Instituto de Ciencias Aplicadas, Universidad Autónoma de Chile, Avenida Alemania 1090, Temuco, Chile.
María José ContrerasFacultad de Ingeniería, Instituto de Ciencias Aplicadas, Universidad Autónoma de Chile, Avenida Alemania 1090, Temuco, Chile.
Karla LealFacultad de Ingeniería, Instituto de Ciencias Aplicadas, Universidad Autónoma de Chile, Avenida Alemania 1090, Temuco, Chile.
Matías GarcíaPrograma de Doctorado en Ciencias mención Biología Celular y Molecular Aplicada, Universidad de La Frontera, Temuco, Chile.
Michel AbantoNúcleo Científico y Tecnológico en Biorecursos (BIOREN), Universidad de La Frontera, Avenida Francisco Salazar, 01145, Temuco, Chile. mfabanto@gmail.com.ORCID http://orcid.org/0000-0001-9136-0041
Leticia BarrientosFacultad de Ciencias de la Salud, Instituto de Ciencias Aplicadas, Universidad Autónoma de Chile, Avenida Alemania 1090, Temuco, Chile. leticia.barrientos@uautonoma.cl.

Funding

Agencia Nacional de Investigación y Desarrollo 1210563Agencia Nacional de Investigación y Desarrollo 2023-21230832Agencia Nacional de Investigación y Desarrollo 2023-21231681
6 · The paper itself

Abstract

Actinomycetota have been widely described as valuable sources for the acquisition of secondary metabolites. Most microbial metabolites are produced via metabolic pathways encoded by biosynthetic gene clusters (BGCs). Although many secondary metabolites are not essential for the survival of bacteria, they play an important role in their adaptation and interactions within microbial communities. This is how bacteria isolated from extreme environments such as Antarctica could facilitate the discovery of new BGCs with biotechnological potential. This study aimed to isolate rare Actinomycetota strains from Antarctic soil and sediment samples and identify their metabolic potential based on genome mining and exploration of biosynthetic gene clusters. To this end, the strains were sequenced using Illumina and Oxford Nanopore Technologies platforms. The assemblies were annotated and subjected to phylogenetic analysis. Finally, the BGCs present in each genome were identified using the antiSMASH tool, and the biosynthetic diversity of the Micrococcaceae family was evaluated. Taxonomic annotation revealed that seven strains were new and two were previously reported in the NCBI database. Additionally, BGCs encoding type III polyketide synthases (T3PKS), beta-lactones, siderophores, and non-ribosomal peptide synthetases (NRPS) have been identified, among others. In addition, the sequence similarity network showed a predominant type of BGCs in the family Micrococcaceae, and some genera were distinctly grouped. The BGCs identified in the isolated strains could be associated with applications such as antimicrobials, anticancer agents, and plant growth promoters, among others, positioning them as excellent candidates for future biotechnological applications and innovations. KEY POINTS: • Novel Antarctic rare Actinomycetota strains were isolated from soil and sediments • Genome-based taxonomic affiliation revealed seven potentially novel species • Genome mining showed metabolic potential for novel natural products.

Indexed as

Geologic SedimentsMultigene FamilyPhylogenySoil MicrobiologyActinobacteriaAntarctic RegionsBiosynthetic PathwaysBiotechnologyGenome, BacterialPeptide SynthasesPolyketide SynthasesSecondary Metabolismnon-ribosomal peptide synthasePeptide SynthasesPolyketide SynthasesActinomycetotaAntarcticBiosynthetic gene clustersMicrococcaceaeSecondary metabolites

Identifiers

PMID38717668
PMCPMC11078813

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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.