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首页> 外文期刊>Angewandte Chemie >Discovery of a Single Monooxygenase that Catalyzes Carbamate Formation and Ring Contraction in the Biosynthesis of the Legonmycins
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Discovery of a Single Monooxygenase that Catalyzes Carbamate Formation and Ring Contraction in the Biosynthesis of the Legonmycins

机译:一个单一的加氧酶的发现,催化氨基甲酸酯的生物合成中氨基甲酸酯的形成和环的收缩。

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摘要

Pyrrolizidine alkaloids (PAs) are a group of natural products with important biological activities. The discovery and characterization of the multifunctional FAD-dependent enzyme LgnC is now described. The enzyme is shown to convert indolizidine intermediates into pyrrolizidines through an unusual ring expansion/contraction mechanism, and catalyze the biosynthesis of new bacterial PAs, the so-called legonmycins. By genome-driven analysis, heterologous expression, and gene inactivation, the legonmycins were also shown to originate from non-ribosomal peptide synthetases (NRPSs). The biosynthetic origin of bacterial PAs has thus been disclosed for the first time.
机译:吡咯嗪核生物碱(PAs)是一组具有重要生物活性的天然产物。现在描述多功能FAD依赖性酶LgnC的发现和表征。已显示该酶通过异常的环扩展/收缩机制将吲哚并立定中间体转化为吡咯并立定,并催化新细菌PA(所谓的来古霉素)的生物合成。通过基因组驱动的分析,异源表达和基因失活,来霉素也显示出源自非核糖体肽合成酶(NRPS)。因此,首次公开了细菌PA的生物合成来源。

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