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Heterologous expression reveals the biosynthesis of the antibiotic pleuromutilin and generates bioactive semi-synthetic derivatives

机译:异源表达揭示了抗生素截短侧耳素的生物合成并产生具有生物活性的半合成衍生物

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摘要

The rise in antibiotic resistance is a major threat for human health. Basidiomycete fungi represent an untapped source of underexploited antimicrobials, with pleuromutilin—a diterpene produced by Clitopilus passeckerianus—being the only antibiotic from these fungi leading to commercial derivatives. Here we report genetic characterisation of the steps involved in pleuromutilin biosynthesis, through rational heterologous expression in Aspergillus oryzae coupled with isolation and detailed structural elucidation of the pathway intermediates by spectroscopic methods and comparison with synthetic standards. A. oryzae was further established as a platform for bio-conversion of chemically modified analogues of pleuromutilin intermediates, and was employed to generate a semi-synthetic pleuromutilin derivative with enhanced antibiotic activity. These studies pave the way for future characterisation of biosynthetic pathways of other basidiomycete natural products in ascomycete heterologous hosts, and open up new possibilities of further chemical modification for the growing class of potent pleuromutilin antibiotics.
机译:抗生素耐药性的上升是对人类健康的主要威胁。担子菌真菌是未开发的抗菌药物的未开发来源,截短侧耳素(一种由Clitopilus passeckerianus生产的二萜)是这些真菌中唯一可商业化的抗生素。在这里,我们报道了米色曲霉生物合成中涉及的步骤的遗传特征,通过米曲霉中合理的异源表达,再加上通过光谱学方法分离和详细分析途径中间体的结构,并与合成标准品进行了比较。米曲霉被进一步建立为生物转化截短侧耳素中间体的化学修饰类似物的平台,并被用于产生具有增强的抗生素活性的半合成截短侧耳素衍生物。这些研究为子囊菌异源宿主中其他担子菌天然产物的生物合成途径的未来表征铺平了道路,并为日益增长的有效截短侧耳素抗生素类打开了进一步化学修饰的新可能性。

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