Evidence map›Paper›PMID 42702668›Full record

ArticleProbiotics and antimicrobial proteins2026

Integrated Genome Mining and Bioactivity-Guided Isolation of Antimicrobial Peptides from Bacillus amyloliquefaciens BS4.

Ana Paula Palacios-Rodriguez, Abraham Espinoza-Culupú, Joel Torres Villena, Pablo Ramirez, Tito Sánchez-Rojas, Pedro Ismael Silva Junior

Abstract read
PubMed Publisher
In one paragraph

Article in Probiotics and antimicrobial proteins, 2026. 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

6 authors.

Ana Paula Palacios-RodriguezLaboratory for Applied Toxinology (LETA) - Center of Toxins, Immune- Response and Cell Signaling - CeTICS/CEPID, Butantan Institute, São Paulo, 05503-900, Brazil.ORCID http://orcid.org/0000-0003-2687-3208
Abraham Espinoza-CulupúLaboratory of Molecular Microbiology and Biotechnology, Faculty of Biological Sciences, Universidad Nacional Mayor de San Marcos, Lima, 15081, Peru.
Joel Torres VillenaLaboratory of Environmental Biotechnology and Industrial Bioprocess, Faculty of Biological Sciences, Universidad Nacional Mayor de San Marcos, Lima, 15081, Peru.
Pablo RamirezLaboratory of Molecular Microbiology and Biotechnology, Faculty of Biological Sciences, Universidad Nacional Mayor de San Marcos, Lima, 15081, Peru.
Tito Sánchez-RojasLaboratory of Environmental Biotechnology and Industrial Bioprocess, Faculty of Biological Sciences, Universidad Nacional Mayor de San Marcos, Lima, 15081, Peru.
Pedro Ismael Silva JuniorLaboratory for Applied Toxinology (LETA) - Center of Toxins, Immune- Response and Cell Signaling - CeTICS/CEPID, Butantan Institute, São Paulo, 05503-900, Brazil. pisjr@butantan.gov.br.ORCID http://orcid.org/0000-0001-6619-6489

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacterial resistance remains a critical global health challenge, driving the continuous search for novel antimicrobial agents. Bacillus amyloliquefaciens is a recognized repository of bioactive metabolites; however, its full biosynthetic potential requires integrated genomic and experimental validation. This study characterized the antimicrobial profile of B. amyloliquefaciens BS4 through a hybrid pipeline. Genome sequencing and de novo assembly revealed a 3.9 Mb chromosome with a G + C content of 46.14%. Functional annotation identified 3,887 coding sequences, including pathways for siderophore biosynthesis and a complete bacilysin biosynthetic cluster. BGC analysis using antiSMASH v7.1.0 and BAGEL4 identified 18 biosynthetic gene clusters, while similarity network analysis via BiG-SCAPE highlighted unique singleton BGCs, indicating untapped biosynthetic diversity. Although in silico screening via Macrel predicted two putative cationic antimicrobial peptides (AMPs), bioactivity-guided purification utilizing sequential RP-HPLC, and de novo sequencing revealed a distinct set of four active peptides. Notably, three of these sequences were identified as fragments derived from the BclA exosporium protein family, highlighting the structural proteome as a non-canonical source of antimicrobials. The purified fractions exhibited activity against M. luteus and E. coli, while displaying no significant hemolytic activity or cytotoxicity, even above the MIC values. Molecular docking further supported the interaction of these candidates with bacterial targets. Overall, this hybrid strategy effectively uncovers the antimicrobial complexity of BS4, revealing 'cryptic' peptide candidates with therapeutic potential.

Indexed as

Antimicrobial PeptidesBacillus amyloliquefaciens BS4De novo SequencingGenome MiningMolecular DockingWhole Genome Sequencing

Identifiers

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.