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组蛋白去乙酰化酶抑制剂伏立诺他的意外生物转化产生含苯胺的真菌代谢产物。

Unexpected Biotransformation of the HDAC Inhibitor Vorinostat Yields Aniline-Containing Fungal Metabolites.

作者信息

Adpressa Donovon A, Stalheim Kayla J, Proteau Philip J, Loesgen Sandra

机构信息

Department of Chemistry, College of Science, and ‡ Department of Pharmaceutical Sciences, College of Pharmacy, Oregon State University , Corvallis, Oregon 97331, United States.

出版信息

ACS Chem Biol. 2017 Jul 21;12(7):1842-1847. doi: 10.1021/acschembio.7b00268. Epub 2017 May 31.

Abstract

The diversity of genetically encoded small molecules produced by filamentous fungi remains largely unexplored, which makes these fungi an attractive source for the discovery of new compounds. However, accessing their full chemical repertoire under common laboratory culture conditions is a challenge. Epigenetic manipulation of gene expression has become a well-established tool for overcoming this obstacle. Here, we report that perturbation of the endophytic ascomycete Chalara sp. 6661, producer of the isofusidienol class of antibiotics, with the HDAC inhibitor vorinostat resulted in the production of four new modified xanthones. The structures of chalanilines A (1) and B (2) and adenosine-coupled xanthones A (3) and B (4) were determined by extensive NMR spectroscopic analyses, and the bioactivities of 1-4 were tested in antibiotic and cytotoxicity assays. Incorporation studies with deuterium-labeled vorinostat indicate that the aniline moiety in chalalanine A is derived from vorinostat itself. Our study shows that Chalara sp. is able to metabolize the HDAC inhibitor vorinostat to release aniline. This is a rare report of fungal biotransformation of the popular epigenetic modifier vorinostat into aniline-containing polyketides.

摘要

丝状真菌产生的基因编码小分子的多样性在很大程度上仍未被探索,这使得这些真菌成为发现新化合物的有吸引力的来源。然而,在普通实验室培养条件下获取它们完整的化学组成是一项挑战。基因表达的表观遗传操作已成为克服这一障碍的成熟工具。在这里,我们报告说,用组蛋白去乙酰化酶(HDAC)抑制剂伏立诺他对内生子囊菌Chalara sp. 6661(异呋甾烯醇类抗生素的生产者)进行扰动,导致产生了四种新的修饰呫吨酮。通过广泛的核磁共振光谱分析确定了查拉尼林A(1)和B(2)以及腺苷偶联呫吨酮A(3)和B(4)的结构,并在抗生素和细胞毒性试验中测试了1-4的生物活性。用氘标记的伏立诺他进行的掺入研究表明,查拉尼林A中的苯胺部分源自伏立诺他本身。我们的研究表明,Chalara sp.能够代谢HDAC抑制剂伏立诺他以释放苯胺。这是一份将流行的表观遗传修饰剂伏立诺他真菌生物转化为含苯胺聚酮化合物的罕见报告。

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