从城市土壤样本中分离出的贵州毛霉中提取的具有细胞毒性的肽类化合物。

IF 3.3 2区 生物学 Q2 CHEMISTRY, MEDICINAL
Journal of Natural Products Pub Date : 2024-08-23 Epub Date: 2024-08-05 DOI:10.1021/acs.jnatprod.4c00438
Jae Sang Han, Eun-Sook Kim, Yong Beom Cho, Sun Young Kim, Mi Kyeong Lee, Bang Yeon Hwang, Jin Woo Lee
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引用次数: 0

摘要

土壤通过滋养农作物、储存食物来源和容纳微生物来维持人类的生活,而微生物可能会影响次生代谢物的营养和生物合成,其中一些次生代谢物可用作药物。为了确定一类新药的先导化合物,我们从包括城市地区在内的各种环境中收集了源自土壤的真菌菌株。由于假定各种人类病原体会影响土壤真菌中代谢物的生物合成途径,从而导致新型支架的产生,因此我们将工作重点放在了人口稠密的城市地区和旅游景点。我们针对 MDA-MB-231 细胞筛选了源自土壤的真菌提取物库,以获得其细胞毒性活性。值得注意的是,10 μg/mL 的贵州毛霉(DS9-1)提取物显示出 71% 的抑制作用。通过分馏、分离和结构阐明工作,鉴定出了九种新的庚二酚,即由 14 个氨基酸残基(14-AA 庚二酚)组成的 trichoguizaibols A-I(1-9),以及由 18 个氨基酸残基(18-AA 庚二酚)组成的三种新的庚二酚,即 trichoguizaibols J-L(10-12)。根据 1D 和 2D NMR 光谱、HRESIMS、电子圆二色性数据以及先进的 Marfey 方法的结果,确定了 1-12 的化学结构。研究发现,18-AA 七叶烷醇对 MDA-MB-231、SK-Hep1、SKOV3、DU145 和 HCT116 细胞的细胞毒性高于 14-AA 七叶烷醇。在这些化合物中,10-12 个化合物表现出了强效的亚微摩 IC50 值。这些结果有望为开发新型抗癌剂支架指明新的方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cytotoxic Peptaibols from <i>Trichoderma guizhouense</i>, a Fungus Isolated from an Urban Soil Sample.

Cytotoxic Peptaibols from Trichoderma guizhouense, a Fungus Isolated from an Urban Soil Sample.

Soil sustains human life by nourishing crops, storing food sources, and housing microbes, which may affect the nutrition and biosynthesis of secondary metabolites, some of which are used as drugs. To identify lead compounds for a new class of drugs, we collected soil-derived fungal strains from various environments, including urban areas. As various human pathogens are assumed to influence the biosynthetic pathways of metabolites in soil fungi, leading to the production of novel scaffolds, we focused our work on densely populated urban areas and tourist attractions. A soil-derived fungal extract library was screened against MDA-MB-231 cells to derive their cytotoxic activity. Notably, 10 μg/mL of the extract of Trichoderma guizhouense (DS9-1) was found to exhibit an inhibitory effect of 71%. Fractionation, isolation, and structure elucidation efforts led to the identification of nine new peptaibols, trichoguizaibols A-I (1-9), comprising 14 amino acid residues (14-AA peptaibols), and three new peptaibols, trichoguizaibols J-L (10-12), comprising 18 amino acid residues (18-AA peptaibols). The chemical structures of 1-12 were determined based on their 1D and 2D NMR spectra, HRESIMS, electronic circular dichroism data, and results of the advanced Marfey's method. The 18-AA peptaibols were found to exhibit cytotoxicity against MDA-MB-231, SK-Hep1, SKOV3, DU145, and HCT116 cells greater than that of the 14-AA peptaibols. Among these compounds, 10-12 exhibited potent sub-micromolar IC50 values. These results are expected to shed light on a new direction for developing novel scaffolds as anticancer agents.

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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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