| Literature DB >> 28128495 |
Christian Greunke1, Anna Glöckle1, Janine Antosch1, Tobias A M Gulder1.
Abstract
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.Entities:
Keywords: biocatalysis; enzyme catalysis; ikarugamycin; natural products; total synthesis
Year: 2017 PMID: 28128495 DOI: 10.1002/anie.201611063
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336