Ignacio Fernández-Pastor*, , , Victor González-Menéndez, , , Ignacio González, , , Pilar Sanchez, , , Rachel Serrano, , , Thomas A Mackenzie, , , Daniel Oves-Costales, , , Manuel Casares Porcel, , , Olga Genilloud, , and , Fernando Reyes*,
{"title":"链霉菌菌株产生的抗菌脂肽甘氨酸E-H。","authors":"Ignacio Fernández-Pastor*, , , Victor González-Menéndez, , , Ignacio González, , , Pilar Sanchez, , , Rachel Serrano, , , Thomas A Mackenzie, , , Daniel Oves-Costales, , , Manuel Casares Porcel, , , Olga Genilloud, , and , Fernando Reyes*, ","doi":"10.1021/acs.jnatprod.5c00740","DOIUrl":null,"url":null,"abstract":"<p >In an antifungal screening of extracts from microbial strains isolated from gypsum outcrops in Granada, Spain, four new cyclic lipopeptides, glycinocins E–H (<b>1</b>–<b>4</b>), were identified from <i>Streptomyces</i> sp. CA-297274 and exhibited potent activity against <i>Zymoseptoria tritici</i>, the causal agent of septoria tritici blotch of wheat. Isolation and structure elucidation performed using HR-MS/MS, 1D and 2D NMR, and Marfey’s analyses, revealed that structures contained an Asp-Gly-Asp-Gly motif in the peptide scaffold, typical of calcium-dependent antibiotics. Genome sequencing and bioinformatic analysis of the strain uncovered a biosynthetic gene cluster consistent with the production of these compounds and helped to correct the absolute configuration determined by Marfey’s analysis of some amino acid residues. The isolated metabolites displayed notable antifungal activity against <i>Z. tritici</i>, with minimum inhibitory concentration values in the micromolar range (Compound <b>4</b>, 9.5 μM), and calcium-dependent antibacterial activity against methicillin-resistant <i>Staphylococcus aureus</i> (5.2 μM for <b>4</b>) and vancomycin-resistant <i>Enterococcus faecium</i> (3.0 μM for <b>4</b>), as anticipated by their structural analysis. Glycinocins E–H displayed no cytotoxicity against the human liver cancer cell line HepG2. These findings expand the chemical diversity of calcium-dependent antibiotics and highlight the ecological and therapeutic potential of extremophile-derived actinomycetes as a source of novel bioactive compounds.</p>","PeriodicalId":47,"journal":{"name":"Journal of Natural Products ","volume":"88 9","pages":"2127–2137"},"PeriodicalIF":3.6000,"publicationDate":"2025-08-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Glycinocins E–H, Antimicrobial Lipopeptides Produced by a Streptomyces Strain\",\"authors\":\"Ignacio Fernández-Pastor*, , , Victor González-Menéndez, , , Ignacio González, , , Pilar Sanchez, , , Rachel Serrano, , , Thomas A Mackenzie, , , Daniel Oves-Costales, , , Manuel Casares Porcel, , , Olga Genilloud, , and , Fernando Reyes*, \",\"doi\":\"10.1021/acs.jnatprod.5c00740\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >In an antifungal screening of extracts from microbial strains isolated from gypsum outcrops in Granada, Spain, four new cyclic lipopeptides, glycinocins E–H (<b>1</b>–<b>4</b>), were identified from <i>Streptomyces</i> sp. CA-297274 and exhibited potent activity against <i>Zymoseptoria tritici</i>, the causal agent of septoria tritici blotch of wheat. Isolation and structure elucidation performed using HR-MS/MS, 1D and 2D NMR, and Marfey’s analyses, revealed that structures contained an Asp-Gly-Asp-Gly motif in the peptide scaffold, typical of calcium-dependent antibiotics. Genome sequencing and bioinformatic analysis of the strain uncovered a biosynthetic gene cluster consistent with the production of these compounds and helped to correct the absolute configuration determined by Marfey’s analysis of some amino acid residues. The isolated metabolites displayed notable antifungal activity against <i>Z. tritici</i>, with minimum inhibitory concentration values in the micromolar range (Compound <b>4</b>, 9.5 μM), and calcium-dependent antibacterial activity against methicillin-resistant <i>Staphylococcus aureus</i> (5.2 μM for <b>4</b>) and vancomycin-resistant <i>Enterococcus faecium</i> (3.0 μM for <b>4</b>), as anticipated by their structural analysis. Glycinocins E–H displayed no cytotoxicity against the human liver cancer cell line HepG2. 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Glycinocins E–H, Antimicrobial Lipopeptides Produced by a Streptomyces Strain
In an antifungal screening of extracts from microbial strains isolated from gypsum outcrops in Granada, Spain, four new cyclic lipopeptides, glycinocins E–H (1–4), were identified from Streptomyces sp. CA-297274 and exhibited potent activity against Zymoseptoria tritici, the causal agent of septoria tritici blotch of wheat. Isolation and structure elucidation performed using HR-MS/MS, 1D and 2D NMR, and Marfey’s analyses, revealed that structures contained an Asp-Gly-Asp-Gly motif in the peptide scaffold, typical of calcium-dependent antibiotics. Genome sequencing and bioinformatic analysis of the strain uncovered a biosynthetic gene cluster consistent with the production of these compounds and helped to correct the absolute configuration determined by Marfey’s analysis of some amino acid residues. The isolated metabolites displayed notable antifungal activity against Z. tritici, with minimum inhibitory concentration values in the micromolar range (Compound 4, 9.5 μM), and calcium-dependent antibacterial activity against methicillin-resistant Staphylococcus aureus (5.2 μM for 4) and vancomycin-resistant Enterococcus faecium (3.0 μM for 4), as anticipated by their structural analysis. Glycinocins E–H displayed no cytotoxicity against the human liver cancer cell line HepG2. These findings expand the chemical diversity of calcium-dependent antibiotics and highlight the ecological and therapeutic potential of extremophile-derived actinomycetes as a source of novel bioactive compounds.
期刊介绍:
The Journal of Natural Products invites and publishes papers that make substantial and scholarly contributions to the area of natural products research. Contributions may relate to the chemistry and/or biochemistry of naturally occurring compounds or the biology of living systems from which they are obtained.
Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.
When new compounds are reported, manuscripts describing their biological activity are much preferred.
Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.