Department of Biochemistry and Biomedical Sciences, MG DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, Ontario, Canada.
Bioorg Med Chem Lett. 2013 Sep 15;23(18):5123-7. doi: 10.1016/j.bmcl.2013.07.031. Epub 2013 Jul 24.
Here we report the biosynthetic pathway for the neoantimycin and present three novel neoantimycin analogues, neoantimycin D (1), E (2) and F (3), from this assembly system from Streptoverticillium orinoci. Identification of these novel neoantimycin variants was achieved by selective MS/MS interrogation of natural product extracts using diagnostic fragments of the known neoantimycins. Their structures, including the absolute configurations, were elucidated using a combination of NMR experiments, detailed MS/MS experiments and the advanced Marfey's method. The biosynthetic pathway of neoantimycin was dissected by genome sequencing data analysis for the first time, which includes a hybrid nonribosomal peptide synthetase (NRPS) and polyketide synthetase (PKS) assembly lines.
在这里,我们报告了新型氨基慈霉素的生物合成途径,并从Orinoci 链霉菌的这个组装系统中呈现了三种新型氨基慈霉素类似物,即新型氨基慈霉素 D(1)、E(2)和 F(3)。通过使用已知新型氨基慈霉素的诊断片段对天然产物提取物进行选择性 MS/MS 询问,鉴定了这些新型氨基慈霉素变体。通过 NMR 实验、详细的 MS/MS 实验和先进的 Marfey 方法的组合,阐明了它们的结构,包括绝对构型。首次通过基因组测序数据分析剖析了新型氨基慈霉素的生物合成途径,其中包括一个杂合非核糖体肽合成酶(NRPS)和聚酮合酶(PKS)组装线。