Biosystems Chemistry, Department of Chemistry and Center for Integrated Protein Science Munich (CIPSM), Lichtenbergstrasse 4, 85748, Garching, Germany.
Angew Chem Int Ed Engl. 2017 Apr 3;56(15):4351-4355. doi: 10.1002/anie.201611063. Epub 2017 Jan 27.
Nature provides an inexhaustible diversity of small organic molecules with beautiful molecular architectures that have strong and selective inhibitory activities. However, this tremendous biomedical potential often remains inaccessible, as the structural complexity of natural products can render their synthetic preparation extremely challenging. This problem is addressable by harnessing the biocatalytic procedures evolved by nature. In this work, we present an enzymatic total synthesis of ikarugamycin. The use of an iterative PKS/NRPS machinery and two reductases has allowed the construction of 15 carbon-carbon and 2 carbon-nitrogen bonds in a biocatalytic one-pot reaction. By scaling-up this method we demonstrate the applicability of biocatalytic approaches for the ex vivo synthesis of complex natural products.
大自然提供了无穷无尽的具有美丽分子结构的小分子有机化合物,它们具有强大而选择性的抑制活性。然而,这种巨大的生物医药潜力往往难以实现,因为天然产物的结构复杂性可能使其合成制备极具挑战性。通过利用自然界进化而来的生物催化程序,可以解决这个问题。在这项工作中,我们展示了伊卡鲁霉素的酶法全合成。使用迭代的 PKS/NRPS 机械和两个还原酶,在生物催化一锅反应中构建了 15 个碳-碳和 2 个碳-氮键。通过扩大这种方法,我们证明了生物催化方法在复杂天然产物的体外合成中的适用性。