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采用OSMAC策略从北极海洋来源菌株sp. MNP-1中获得的生物活性次生代谢产物

Bioactive Secondary Metabolites from an Arctic Marine-Derived Strain, sp. MNP-1, Using the OSMAC Strategy.

作者信息

Wu Mengna, Liu Zijun, Wang Jiahui, Hu Wentao, Zhang Huawei

机构信息

School of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou 310014, China.

College of Pharmaceutical Science & Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, Zhejiang University of Technology, Hangzhou 310014, China.

出版信息

Molecules. 2025 Apr 8;30(8):1657. doi: 10.3390/molecules30081657.

DOI:10.3390/molecules30081657
PMID:40333590
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12029766/
Abstract

An Arctic marine-derived strain, MNP-1, was characterized by a combined methodological approach, incorporating a variety of analytical techniques including morphological features, biochemical characteristics, and 16S ribosomal RNA (rRNA) sequence analysis. The chemical investigation of sp. MNP-1 using the OSMAC (one strain many compounds) strategy yielded the isolation of twenty known compounds (), which were unambiguously identified by various spectroscopic approaches including H and C NMR and ESI-MS (previously reported data). Bioassay results indicated that compounds , , , , , , and had antimicrobial activity against human pathogenic strains including , , and with MIC values ranging from 4 to 32 μg/mL, and compounds and exhibited moderate inhibitory activity on A549, MCF-7, and HepG2 tumor lines showing IC values within the range of 19.88 to 35.82 µM. These findings suggest that sp. MNP-1 is one of the prolific manufacturers of bioactive secondary metabolites with therapeutic potential.

摘要

一株源自北极海洋的菌株MNP - 1通过综合方法进行了表征,该方法结合了多种分析技术,包括形态特征、生化特性和16S核糖体RNA(rRNA)序列分析。使用OSMAC(一种菌株多种化合物)策略对MNP - 1菌株进行化学研究,分离出了20种已知化合物(),通过包括氢谱和碳谱核磁共振以及电喷雾电离质谱(先前报道的数据)在内的各种光谱方法对其进行了明确鉴定。生物测定结果表明,化合物,,,,,,和对包括,和在内的人类致病菌株具有抗菌活性,最低抑菌浓度值范围为4至32μg/mL,化合物和对A549、MCF - 7和HepG2肿瘤细胞系表现出中等抑制活性,半数抑制浓度值在19.88至35.82μM范围内。这些发现表明,MNP - 1菌株是具有治疗潜力的生物活性次级代谢产物的多产制造商之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4cc/12029766/78c2e5f1529a/molecules-30-01657-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4cc/12029766/fb03677bd6af/molecules-30-01657-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4cc/12029766/d3f3df46d44a/molecules-30-01657-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4cc/12029766/dd029837cb90/molecules-30-01657-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4cc/12029766/78c2e5f1529a/molecules-30-01657-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4cc/12029766/fb03677bd6af/molecules-30-01657-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4cc/12029766/d3f3df46d44a/molecules-30-01657-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4cc/12029766/dd029837cb90/molecules-30-01657-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4cc/12029766/78c2e5f1529a/molecules-30-01657-g004.jpg

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