Evidence map›Paper›PMID 40890732›Full record

ArticleMicrobial cell factories2025

Identification of novel Gramicidin S analogs from Aneurinibacillus aneurinilyticus isolated from corn steep liquor with potential antifungal activity.

Ksenia Lvova, Manuel Marcos, Benita Pérez-Cid, Xanel Vecino, José Manuel Cruz, Ana Belén Moldes

Abstract read
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Article in Microbial cell factories, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Ksenia LvovaChemical Engineering Department, School of Industrial Engineering, University of Vigo, Campus As Lagoas-Marcosende, 36310, Vigo, Spain.
Manuel MarcosStructural Determination and Proteomics Service, CACTI, University of Vigo, 36310, Vigo, Spain.
Benita Pérez-CidEQ10, CINTECX, University of Vigo, Campus As Lagoas-Marcosende, 36310, Vigo, Spain.
Xanel VecinoChemical Engineering Department, School of Industrial Engineering, University of Vigo, Campus As Lagoas-Marcosende, 36310, Vigo, Spain.
José Manuel CruzChemical Engineering Department, School of Industrial Engineering, University of Vigo, Campus As Lagoas-Marcosende, 36310, Vigo, Spain.
Ana Belén MoldesChemical Engineering Department, School of Industrial Engineering, University of Vigo, Campus As Lagoas-Marcosende, 36310, Vigo, Spain. amoldes@uvigo.es.

Funding

Spanish Ministry of Science and Innovation (MICINN) PID2021-122221OB-I00
6 · The paper itself

Abstract

In the existing literature, there is ample information available concerning the analogs constituting linear Gramicidin (Gramicidin A). However, the literature lacks information regarding the microbial production of cyclic Gramicidin S (GR-S) and the study of its analogs' amino acid composition. Thus, in this study, GR-S was produced by Aneurinibacillus aneurinilyticus, isolated from corn steep liquor (CSL) and grown in synthetic or CSL-based medium. The extract was obtained from microbial biomass and underwent analysis with ultra performance liquid chromatography coupled with electrospray ionization tandem mass spectrometry (UPLC-ESI-MS/MS) to ascertain the presence and abundance of GR-S clusters, identifying five GR S analogs. Hence, when using a synthetic medium, the dominant cluster compromised the sequence Val-Orn-Leu-Phe-Pro-Val-Orn-Leu-Phe-Pro. Contrarily, when using CSL-based medium, the main analog was composed of Val-Orn-Leu-Phe-Pro-Val-Lys-Leu-Phe-Pro. In the remaining analogs, one or both Ornithine (Orn) residues were replaced by Lysine (Lys) or diaminobutyric acid (D-Dab). Microscopy images revealed that the use of CSL-based medium resulted in a lower yield of GR-S and a higher accumulation of vacuoles compatible with the presence of intracellular polyhydroxyalkanoates (PHA) when comparing with TSB medium. The antifungal assay revealed a superior conidial inhibition activity of GR-S extract under evaluation against Aspergillus brasiliensis in comparison to the commercial GR-S. Consequently, it can be concluded that this novel microbial GR-S extract exhibits favorable antifungal activity, positioning it as a promising candidate for antimicrobial treatments. However, further research is necessary to address the global challenge of antibiotic-resistant pathogens.

Indexed as

Antifungal AgentsBacillaceaeBacillalesGramicidinZea maysMicrobial Sensitivity TestsTandem Mass SpectrometryAntifungal AgentsGramicidinAntibioticAntifungalFermentationNew Gramicidin SSporulated Bacillus

Identifiers

PMID40890732
PMCPMC12403468

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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.