Benjdia Alhosna, Balty Clémence, Berteau Olivier
Micalis Institute, ChemSyBio, INRA, AgroParisTech, Université Paris-Saclay, Jouy-en-Josas, France.
Front Chem. 2017 Nov 8;5:87. doi: 10.3389/fchem.2017.00087. eCollection 2017.
Ribosomally-synthesized and post-translationally modified peptides (RiPPs) are a large and diverse family of natural products. They possess interesting biological properties such as antibiotic or anticancer activities, making them attractive for therapeutic applications. In contrast to polyketides and non-ribosomal peptides, RiPPs derive from ribosomal peptides and are post-translationally modified by diverse enzyme families. Among them, the emerging superfamily of radical SAM enzymes has been shown to play a major role. These enzymes catalyze the formation of a wide range of post-translational modifications some of them having no counterparts in living systems or synthetic chemistry. The investigation of radical SAM enzymes has not only illuminated unprecedented strategies used by living systems to tailor peptides into complex natural products but has also allowed to uncover novel RiPP families. In this review, we summarize the current knowledge on radical SAM enzymes catalyzing RiPP post-translational modifications and discuss their mechanisms and growing importance notably in the context of the human microbiota.
核糖体合成及翻译后修饰肽(RiPPs)是一类庞大且多样的天然产物家族。它们具有诸如抗生素或抗癌活性等有趣的生物学特性,这使得它们在治疗应用方面颇具吸引力。与聚酮化合物和非核糖体肽不同,RiPPs源自核糖体肽,并由多种酶家族进行翻译后修饰。其中,新兴的自由基S-腺苷甲硫氨酸(radical SAM)酶超家族已被证明发挥着主要作用。这些酶催化形成多种翻译后修饰,其中一些在生命系统或合成化学中并无对应物。对自由基SAM酶的研究不仅揭示了生命系统将肽加工成复杂天然产物所采用的前所未有的策略,还使得发现新的RiPP家族成为可能。在本综述中,我们总结了目前关于催化RiPP翻译后修饰的自由基SAM酶的知识,并讨论了它们的作用机制以及日益增长的重要性,特别是在人类微生物群的背景下。