Glycinocins E–H, Antimicrobial Lipopeptides Produced by a Streptomyces Strain

IF 3.6 2区 生物学 Q2 CHEMISTRY, MEDICINAL
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*, 
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Abstract

In an antifungal screening of extracts from microbial strains isolated from gypsum outcrops in Granada, Spain, four new cyclic lipopeptides, glycinocins E–H (14), 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.

Abstract Image

链霉菌菌株产生的抗菌脂肽甘氨酸E-H。
通过对西班牙格莱纳达地区石膏露头微生物菌株提取物的抗真菌筛选,从Streptomyces sp. CA-297274中鉴定出4个新的环状脂肽glycinocins E-H(1-4),它们对小麦小麦黑斑病的病原菌——小麦酵母菌(Zymoseptoria小麦黑斑病)具有较强的抗真菌活性。利用HR-MS/MS、1D和2D NMR以及Marfey的分析进行分离和结构解析,发现肽支架中含有一个Asp-Gly-Asp-Gly基序,这是典型的钙依赖性抗生素。该菌株的基因组测序和生物信息学分析揭示了与这些化合物的产生一致的生物合成基因簇,并有助于纠正Marfey对一些氨基酸残基的分析所确定的绝对构型。化合物4和化合物9.5 μM的最小抑菌浓度均在微摩尔范围内,对耐甲氧西林金黄色葡萄球菌(5.2 μM)和耐万古霉素屎肠球菌(3.0 μM)的钙依赖性抑菌活性与结构分析一致。甘草酸E-H对人肝癌细胞株HepG2无细胞毒性。这些发现扩大了钙依赖性抗生素的化学多样性,并突出了极端微生物衍生的放线菌作为新型生物活性化合物来源的生态和治疗潜力。
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来源期刊
CiteScore
9.10
自引率
5.90%
发文量
294
审稿时长
2.3 months
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.
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