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黄曲霉和卷枝毛霉共培养产生的细胞松弛素。

Cytochalasans Produced by the Coculture of Aspergillus flavipes and Chaetomium globosum.

机构信息

Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy , Tongji Medical College, Huazhong University of Science and Technology , Wuhan 430030 , People's Republic of China.

First College of Clinical Medical Science , China Three Gorges University & Yichang Central People's Hospital , Yichang 443003 , People's Republic of China.

出版信息

J Nat Prod. 2018 Jul 27;81(7):1578-1587. doi: 10.1021/acs.jnatprod.8b00110. Epub 2018 Jul 3.

Abstract

The cocultivation of Aspergillus flavipes and Chaetomium globosum, rich sources of cytochalasans, on solid rice medium, resulted in the production of 13 new, highly oxygenated cytochalasans, aspochalasinols A-D (1-4) and oxichaetoglobosins A-I (5-13), as well as seven known compounds (14-20). Of these compounds, 13 is a novel cytochalasan with an unexpected 2-norindole group. The isolated compounds were characterized by NMR spectroscopy, single-crystal X-ray crystallography, and ECD experiments. Compounds 1-4 represent the first examples of Asp-type cytochalasans with C-12 hydroxy groups, which may be a result of the coculture, as hydroxylated Me-12 groups are frequently found in Chae-type cytochalasans from C. globosum. In addition, 5-10 are unusual cytochalasans with an oxygenated C-10. Interestingly, 13 is the first example of a naturally occurring cytochalasan possessing a uniquely degraded indole ring that is derived from chaetoglobosin W, with 11 and 12 both serving as its biosynthetic intermediates. In the coculture of A. flavipes and C. globosum, most of these cytochalasans are more functionalized than normal cytochalasans, and the underlying causes may attract substantial attention from synthetic biologists. The cytotoxicities against five human cancer cell lines (SW480, HL-60, A549, MCF-7, and SMMC-7721) and the immunomodulatory activities of these new compounds were evaluated in vitro.

摘要

黄曲霉和卷枝毛霉在固体大米培养基中的共培养导致产生了 13 种新型高度氧化的细胞松弛素,分别为 aspochalasinols A-D(1-4)和 oxichaetoglobosins A-I(5-13),以及 7 种已知化合物(14-20)。在这些化合物中,13 是一种具有意外的 2-降吲哚基团的新型细胞松弛素。分离得到的化合物通过 NMR 光谱、单晶 X 射线晶体学和 ECD 实验进行了表征。化合物 1-4 代表了具有 C-12 羟基的 Asp 型细胞松弛素的第一个例子,这可能是共培养的结果,因为 C. globosum 中的 Chae 型细胞松弛素中经常存在羟基化的 Me-12 基团。此外,5-10 是具有含氧 C-10 的不寻常的细胞松弛素。有趣的是,13 是第一个具有独特降解吲哚环的天然存在的细胞松弛素的例子,该吲哚环源自 chaetoglobosin W,11 和 12 都是其生物合成中间体。在黄曲霉和卷枝毛霉的共培养中,这些细胞松弛素中的大多数比正常细胞松弛素具有更多的官能团,其潜在原因可能会引起合成生物学家的极大关注。对五种人癌细胞系(SW480、HL-60、A549、MCF-7 和 SMMC-7721)的体外细胞毒性以及这些新化合物的免疫调节活性进行了评估。

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