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海洋来源真菌土曲霉 NTU243 中的生物活性菌核酮。

Bioactive pulvinones from a marine algicolous fungus Aspergillus terreus NTU243.

机构信息

Graduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, 11031, Taiwan; Department of Pharmacology, School of Medicine, College of Medicine, Taipei Medical University, Taipei, 11031, Taiwan.

Department of Food Science, National Quemoy University, Kinmen, 89250, Taiwan.

出版信息

Phytochemistry. 2022 Aug;200:113229. doi: 10.1016/j.phytochem.2022.113229. Epub 2022 May 11.

Abstract

Marine fungi are regarded as an under-explored source of structurally interesting and bioactive natural products with the potential to provide attractive lead compounds for drug discovery. In this study, several fungal strains were isolated from marine algae collected from the northeastern coast of Taiwan. In the preliminary antimicrobial screening against bacteria and fungi, the ethyl acetate extract of the fermented products of Aspergillus terreus NTU243 derived from a green alga Ulva lactuca was found to exhibit significant antimicrobial activities. Therefore, bioassay-guided separations of the active principle from liquid and solid fermented products of A. terreus NTU243 were undertaken, which resulted in the isolation and purification of 16 compounds. Their structures were elucidated by spectroscopic analysis to be four previously undescribed aspulvinones S-V as well as twelve known compounds. All the isolates were assessed for anti-inflammatory activity by measuring the amount of nitric oxide (NO) production in lipopolysaccharide (LPS)-induced BV-2 cells, and aspulvinone V, butyrolactone I, and (+)-terrein inhibited 45.0%, 34.5%, and 49.2% of NO production, respectively, at 10 μM concentration. Additionally, zymography showed that the conditioned medium of THP-1 cells post-LPS challenged significantly enhanced matrix metalloproteinase (MMP)-9-mediated gelatinolysis, and pretreatment with aspulvinones U and V significantly attenuated MMP-9-mediated gelatinolysis by 56.0% and 67.8%, separately.

摘要

海洋真菌被认为是结构有趣且具有生物活性的天然产物的未充分探索来源,具有为药物发现提供有吸引力的先导化合物的潜力。在这项研究中,从台湾东北海岸采集的海洋藻类中分离出了几种真菌菌株。在针对细菌和真菌的初步抗菌筛选中,从绿藻浒苔中分离出的土曲霉 NTU243 的发酵产物的乙酸乙酯提取物显示出显著的抗菌活性。因此,从土曲霉 NTU243 的液体和固体发酵产物中进行了生物活性导向分离,分离并纯化了 16 种化合物。通过光谱分析阐明了它们的结构,它们是四个以前未描述的 aspulvinones S-V 以及十二个已知化合物。所有分离物均通过测量脂多糖 (LPS) 诱导的 BV-2 细胞中一氧化氮 (NO) 产生的量来评估其抗炎活性,aspulvinone V、丁内酯 I 和 (+)-terrein 分别在 10 μM 浓度下抑制了 45.0%、34.5%和 49.2%的 NO 产生。此外,凝胶电泳显示,经 LPS 刺激后的 THP-1 细胞的条件培养基显著增强了基质金属蛋白酶 (MMP)-9 介导的明胶水解,而预处理用 aspulvinones U 和 V 则分别显著抑制了 56.0%和 67.8%的 MMP-9 介导的明胶水解。

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