Chair of Technical Biochemistry, Technical University of Dresden, Bergstraße 66, 01069, Dresden, Germany.
Biosystems Chemistry, Technical University of Munich, Lichtenbergstraße 4, 85748, Garching bei München, Germany.
Chemistry. 2022 Jun 7;28(32):e202200394. doi: 10.1002/chem.202200394. Epub 2022 Apr 26.
The increasing emergence of resistances against established antibiotics is a substantial threat to human health. The discovery of new compounds with potent antibiotic activity is thus of utmost importance. Within this work, we identify strong antibiotic activity of the natural product myxocoumarin B from Stigmatella aurantiaca MYX-030 against a range of clinically relevant bacterial pathogens, including clinical isolates of MRSA. A focused library of structural analogs was synthesized to explore initial structure-activity relationships and to identify equipotent myxocoumarin derivatives devoid of the natural nitro substituent to significantly streamline synthetic access. The cytotoxicity of the myxocoumarins as well as their potential to cure bacterial infections in vivo was established using a zebrafish model system. Our results reveal the exceptional antibiotic activity of the myxocoumarin scaffold and hence its potential for the development of novel antibiotics.
日益出现的对抗生素的耐药性对人类健康构成了重大威胁。因此,发现具有强大抗生素活性的新化合物至关重要。在这项工作中,我们发现来自橙色游动放线菌 MYX-030 的天然产物粘菌素 B 对一系列临床相关的细菌病原体具有很强的抗生素活性,包括耐甲氧西林金黄色葡萄球菌 (MRSA) 的临床分离株。合成了一个结构类似物的聚焦文库,以探索初始的结构-活性关系,并确定具有等效活性且不含天然硝基取代基的粘菌素衍生物,以显著简化合成途径。使用斑马鱼模型系统确定了粘菌素的细胞毒性及其在体内治愈细菌感染的潜力。我们的结果揭示了粘菌素骨架的特殊抗生素活性,因此它有可能开发出新型抗生素。