State Key Laboratory of Bioactive Substance and Function of Natural Medicines, NHC Key Laboratory of Biosynthesis of Natural Products, CAMS Key Laboratory of Enzyme and Catalysis of Natural Drugs, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100050, P. R. China.
Angew Chem Int Ed Engl. 2021 Mar 15;60(12):6639-6645. doi: 10.1002/anie.202015442. Epub 2021 Feb 2.
Self-resistance genes are employed by many microbial producers of bioactive natural products to avoid self-harm. Herein, we describe a unique strategy for self-resistance toward a macrolide antibiotic, A26771B (1), identified by elucidating its biosynthetic pathway in the fungus Penicillium egyptiacum. A highly reducing polyketide synthase and a trans-acting thioesterase generate the macrolide backbone, and a cytochrome P450 and an acyltransferase, respectively catalyze hydroxylation and succinylation to form the prodrug berkeleylactone E (2). Then, extracellular oxidative activation by a secreted flavin-dependent oxidase forms 1, while intracellular reductive inactivation by a short-chain reductase reforms 2, forming a redox cycle. Our work illustrates a unique redox-mediated resistance mechanism for fungal antibiotics and contributes to the understanding of antibiotic biosynthesis and resistance.
自我抵抗基因被许多产生生物活性天然产物的微生物生产者用来避免自我伤害。在此,我们描述了一种针对大环内酯抗生素 A26771B(1)的独特自我抵抗策略,该抗生素是通过阐明其在真菌 Penicillium egyptiacum 中的生物合成途径而发现的。一个高度还原的聚酮合酶和一个反式作用硫酯酶生成大环内酯骨架,而一个细胞色素 P450 和一个酰基转移酶分别催化羟化和琥珀酰化形成前药伯克利内酯 E(2)。然后,由分泌的黄素依赖氧化酶进行细胞外氧化激活形成 1,而由短链还原酶进行细胞内还原失活形成 2,形成一个氧化还原循环。我们的工作说明了真菌抗生素的一种独特的氧化还原介导的抵抗机制,并有助于理解抗生素的生物合成和抵抗。