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来源于链霉菌属的环状脂肽蛋白酶抑制剂 cystargamide B

Cystargamide B, a cyclic lipodepsipeptide with protease inhibitory activity from Streptomyces sp.

机构信息

International Center for Biotechnology, Osaka University, Osaka, Japan.

Department of Biotechnology, Faculty of Science, Mahidol University, Bangkok, Thailand.

出版信息

J Antibiot (Tokyo). 2018 Jul;71(7):662-666. doi: 10.1038/s41429-018-0044-0. Epub 2018 Mar 22.

Abstract

We identified a new cyclic lipodepsipeptide, cystargamide B (1), from the mycelial extract of a Kaempferia galanga rhizome-derived actinomycete strain, Streptomyces sp. PB013. The planar structure was elucidated based on high resolution fast-atom bombardment mass spectrometry (HRFABMS) spectroscopy and one-dimensional (1D) and two-dimensional (2D) nuclear magnetic resonance (NMR) spectroscopic data. The absolute configurations of the constituent amino acids were determined using advanced Marfey's method. Cystargamide B (1) includes rare structural units: a 5-hydroxytryptophan residue and a 2,3-epoxy fatty acid side chain. Notably, cystargamide B (1) inhibited the protease activity of the NS2B/NS3 complex from dengue virus.

摘要

我们从姜黄根内生放线菌菌株 Streptomyces sp. PB013 的菌丝体提取物中鉴定出一种新型环状脂肽,cystargamide B(1)。基于高分辨快原子轰击质谱(HRFABMS)光谱和一维(1D)和二维(2D)核磁共振(NMR)光谱数据,阐明了其平面结构。使用先进的 Marfey 法确定了组成氨基酸的绝对构型。cystargamide B(1)包含罕见的结构单元:5-羟色氨酸残基和 2,3-环氧脂肪酸侧链。值得注意的是,cystargamide B(1)抑制了登革热病毒 NS2B/NS3 复合物的蛋白酶活性。

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