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基于分子网络策略从海洋附生真菌哈茨木霉NTU2180中发现的新菖蒲烷倍半萜和抗视网膜母细胞瘤成分。

New acorane-sesequiterpenes and anti-retinoblastoma constituents from the marine algicolous fungus Trichoderma harzianum NTU2180 guided by molecular networking strategy.

作者信息

Gu Andrea, Lin Fan-Li, Lu Chung-Kuang, Yeh Tz-Wei, Chen Yih-Fung, Wu Ho-Cheng, Lee Tzong-Huei

机构信息

Institute of Fisheries Science, College of Life Science, National Taiwan University, No. 1, Sec. 4, Roosevelt Rd., Da'an Dist, Taipei, 106319, Taiwan (R.O.C.).

School of Pharmacy, College of Pharmacy, Kaohsiung Medical University, No. 100, Shiquan 1st Rd., Sanmin Dist., Kaohsiung, 807378, Taiwan.

出版信息

Bot Stud. 2025 Jan 14;66(1):2. doi: 10.1186/s40529-024-00449-5.

Abstract

BACKGROUND

Trichoderma species, known as biocontrol agents against plant diseases, contain diverse compounds, especially terpenoids, with various bioactivities. To facilitate the exploration of bioactive secondary metabolites of Trichoderma harzianum NTU2180, the OSMAC approach MS/MS molecular networking was applied in the current study.

RESULTS

The feature-based molecular networking (FBMN) analysis showed that T. harzianum NTU2180 fermented on germinated brown rice (GBR) produced more terpenoids. Here, two new acorane-sesequiterpenes, trichospirols A (1) and B (2), and 12 known compounds (3 - 14) were isolated from the EtOAc layer of T. harzianum NTU2180 fermentation on GBR. Structures of these compounds were determined through NMR, UV, IR, and MS analyses. The absolute configuration of trichospirols A (1) was also elucidated by x-ray with Cu K-α radiation. Among them, six compounds (1, 2, 3, 4, 5, and 11) were annotated as terpenoids by the NPClassifier on FBMN. 5-Hydroxy-3-hydroxmethyl-2-methyl-7-methoxychromone (7) and ergosterol peroxide (11) showed significant anti-angiogenic activity in ex vivo experiments with respective 0.57 ± 0.12- and 0.20 ± 0.12-fold changes. In addition, compound 11 displayed cytotoxicity against Y79 retinoblastoma cells with IC value of 35.3 ± 6.9 µM.

CONCLUSIONS

The current study utilizes FBMN concept with OSMAC approach to accelerate the exploration of potential metabolites of the fungus Trichoderma harzianum NTU2180. Through a series of FBMN-guided isolation and purification, two new acorane-sesequiterpenes and 12 known compounds were obtained. The ex vivo and in vitro experiments were evaluated to assess anticancer isolates. It is worth noting that compound 11 was identified as a dual inhibitor targeting both angiogenesis and proliferation of retinoblastomas. Altogether, the results revealed the novel potential of T. harzianum for developing natural therapeutics against retinoblastomas.

摘要

背景

木霉属物种作为植物病害的生物防治剂,含有多种具有不同生物活性的化合物,尤其是萜类化合物。为了便于探索哈茨木霉NTU2180的生物活性次生代谢产物,本研究采用了OSMAC方法和MS/MS分子网络技术。

结果

基于特征的分子网络(FBMN)分析表明,在发芽糙米(GBR)上发酵的哈茨木霉NTU2180产生了更多的萜类化合物。在此,从哈茨木霉NTU2180在GBR上发酵的乙酸乙酯层中分离出两种新的菖蒲烷倍半萜,即哈茨螺旋醇A(1)和B(2),以及12种已知化合物(3 - 14)。通过核磁共振、紫外、红外和质谱分析确定了这些化合物的结构。哈茨螺旋醇A(1)的绝对构型也通过铜K-α辐射的X射线晶体学得以阐明。其中,6种化合物(1、2、3、4、5和11)在FBMN上被NPClassifier注释为萜类化合物。5-羟基-3-羟甲基-2-甲基-7-甲氧基色酮(7)和过氧化麦角甾醇(11)在体外实验中显示出显著的抗血管生成活性,变化倍数分别为0.57±0.12和0.20±0.12。此外,化合物11对Y79视网膜母细胞瘤细胞具有细胞毒性,IC值为35.3±6.9μM。

结论

本研究利用FBMN概念结合OSMAC方法,加速了对哈茨木霉NTU2180潜在代谢产物的探索。通过一系列FBMN指导的分离和纯化,获得了两种新的菖蒲烷倍半萜和12种已知化合物。通过体外和体内实验对抗癌分离物进行了评估。值得注意的是,化合物11被鉴定为一种双重抑制剂,可同时靶向视网膜母细胞瘤的血管生成和增殖。总之,这些结果揭示了哈茨木霉在开发针对视网膜母细胞瘤的天然疗法方面的新潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/499c/11732828/7acbae09c0d7/40529_2024_449_Fig1_HTML.jpg

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