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Discovery of Novel Genes Encoding Antimicrobial Peptides from the Pedobacter silvilitoris Genome with Broad-Spectrum Antimicrobial Activity

Authors
Bang, Woo YoungHur, JinKim, Sam Woong
Issue Date
Jun-2025
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Keywords
antimicrobial peptide; AMP; cell-free supernatant; genome; transcriptome; Pedobacter silvilitoris
Citation
International Journal of Molecular Sciences, v.26, no.13
Indexed
SCIE
SCOPUS
Journal Title
International Journal of Molecular Sciences
Volume
26
Number
13
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/79493
DOI
10.3390/ijms26136176
ISSN
1661-6596
1422-0067
Abstract
The rising prevalence of antibiotic-resistant bacteria demands exploration of alternative antimicrobials. Antimicrobial peptides (AMPs) are a promising group of compounds naturally produced by microorganisms and could serve as potent agents against resistant pathogens. In this study, we evaluated the antimicrobial potential of the cell-free supernatant obtained from Pedobacter silvilitoris-a bacterium originally isolated from decomposing wood-and performed comprehensive genomic screening to uncover novel AMP-encoding genes. The supernatant showed strong inhibitory effects against a diverse selection of pathogens. Scanning electron microscopy (SEM) revealed extensive membrane damage, including pore formation in target bacterial cells, suggesting AMP-mediated activity. A genomic analysis identified 11 candidate AMP genes, named PS_AMP1 to PS_AMP11, based on the significant sequence similarity with known AMPs. Transcriptomic profiling further indicated that several candidates are expressed differentially between the logarithmic and stationary growth phases. Functional assays via gene cloning and peptide synthesis confirmed antimicrobial activity against both Gram-stain-negative and Gram-stain-positive bacteria, with PS_AMP11 emerging as the most effective candidate. Our findings demonstrate that AMPs derived from P. silvilitoris hold substantial promise as alternative antimicrobial agents. Nonetheless, additional structural optimizations may be necessary to fine-tune specificity and to reduce potential host toxicity before clinical deployment.
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