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Skeletocutins A-L:来自肯尼亚木栖担子菌, sp. 的抗菌剂

Skeletocutins A-L: Antibacterial Agents from the Kenyan Wood-Inhabiting Basidiomycete, sp.

机构信息

Department of Microbial Drugs , Helmholtz Centre for Infection Research (HZI), German Centre for Infection Research (DZIF) , Partner Site Hannover/Braunschweig, Inhoffenstrasse 7 , 38124 Braunschweig , Germany.

Department of Biochemistry , Egerton University , P.O. BOX 536, 20115 Njoro , Kenya.

出版信息

J Agric Food Chem. 2019 Aug 7;67(31):8468-8475. doi: 10.1021/acs.jafc.9b02598. Epub 2019 Jul 29.

Abstract

Fermentation of the fungal strain sp. originating from Mount Elgon Natural Reserve in Kenya, followed by bioassay guided fractionation led to the isolation of 12 previously undescribed metabolites named skeletocutins A-L (- and -) together with the known tyromycin A (). Their structures were assigned by NMR spectroscopy complemented by HR-ESIMS. Compounds - and - exhibited selective activities against Gram-positive bacteria, while compound weakly inhibited the formation of biofilm of . The isolated metabolites were also evaluated for inhibition of -leucine aminopeptidase, since tyromycin A had previously been reported to possess such activities but only showed weak effects. Furthermore, all compounds were tested for antiviral activity against Hepatitis C virus (HCV), and compound moderately inhibited HCV infectivity with an IC of 6.6 μM.

摘要

对源自肯尼亚埃尔冈山自然保护区的真菌菌株 sp. 进行发酵,然后进行生物测定导向的分段分离,得到了 12 种以前未描述的代谢物,命名为骨架菌素 A-L(-和-)以及已知的酪氨酸霉素 A()。通过 NMR 光谱学辅以高分辨率 ESIMS 确定了它们的结构。化合物 - 和 - 对革兰氏阳性菌表现出选择性活性,而化合物 则弱抑制 的生物膜形成。还评估了分离出的代谢物对 - 亮氨酸氨肽酶的抑制作用,因为酪氨酸霉素 A 先前已被报道具有这种活性,但仅显示出微弱的效果。此外,所有化合物都针对丙型肝炎病毒 (HCV) 的抗病毒活性进行了测试,化合物 对 HCV 感染具有中等抑制作用,IC 为 6.6 μM。

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