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利用金黄色葡萄球菌适应度测试的全基因组筛选方法分离、结构鉴定和研究 Altersolanol P 的生物活性。

Isolation, structure elucidation, and biological activity of altersolanol P using Staphylococcus aureus fitness test based genome-wide screening.

机构信息

Merck Research Laboratories , Rahway, New Jersey 07065 and Kenilworth, New Jersey 07033, United States.

出版信息

J Nat Prod. 2014 Mar 28;77(3):497-502. doi: 10.1021/np400759f. Epub 2014 Jan 15.

Abstract

Bacteria continue to evade existing antibiotics by acquiring resistance by various mechanisms, leading to loss of antibiotic effectiveness. To avoid an epidemic from infections of incurable drug-resistant bacteria, new antibiotics with new modes of action are desperately needed. Using a genome-wide mechanism of action-guided whole cell screening approach based on antisense Staphylococcus aureus fitness test technology, we report herein the discovery of altersolanol P (1), a new tetrahydroanthraquinone from an unknown fungus from the Hypocreales isolated from forest litter collected in Puerto Rico. The structure was elucidated by high-resolution mass spectrometry and 2D NMR spectroscopy. Relative stereochemistry was established by NOESY correlations, and absolute configuration was deduced by the application of MPA ester-based methodology. Observed (1)H and (13)C NMR shifts were well aligned with the corresponding chemical shifts predicted by DFT calculations. Altersolanol P exhibited Gram-positive antibacterial activity (MIC range 1-8 μg/mL) and inhibited the growth of Gram-negative Haemophilus influenzae (MIC 2 μg/mL). The isolation, structure elucidation, and antibacterial activity of altersolanol P are described.

摘要

细菌通过各种机制获得耐药性以继续逃避现有抗生素,导致抗生素有效性丧失。为了避免因无法治愈的耐药菌感染而爆发疫情,急需具有新作用模式的新型抗生素。本研究采用基于反义金黄色葡萄球菌适合度测试技术的全细胞筛选方法,对作用机制进行了全基因组指导,报道了一种新的四氢蒽醌化合物 altersolanol P(1),它来自于从波多黎各森林落叶中分离出的未知 Hypocreales 真菌。通过高分辨质谱和二维 NMR 光谱确定了其结构。通过 NOESY 相关确定了相对立体化学,通过 MPA 酯基方法学确定了绝对构型。观察到的 1H 和 13C NMR 位移与 DFT 计算预测的相应化学位移很好地吻合。Altersolanol P 表现出革兰氏阳性抗菌活性(MIC 范围为 1-8 μg/mL),并抑制革兰氏阴性流感嗜血杆菌的生长(MIC 2 μg/mL)。描述了 altersolanol P 的分离、结构阐明和抗菌活性。

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