Department of Pharmaceutical Microbiology at the Hans-Knöll-Institute, Friedrich-Schiller-University Jena , Winzerlaer Strasse 2, 07745 Jena, Germany.
Department of Biochemical and Chemical Engineering, Technical University Dortmund , Emil-Figge-Strasse 66, 44227 Dortmund, Germany.
Org Lett. 2017 Sep 15;19(18):4868-4871. doi: 10.1021/acs.orglett.7b02329. Epub 2017 Aug 28.
Ralsolamycin, an inducer of chlamydospore formation in fungi, was recently reported from the plant pathogenic bacterium Ralstonia solanacearum. Although interpretation of tandem mass data and bioinformatics enabled a preliminary chemical characterization, the full structure of ralsolamycin was not resolved. We now report the recovery of this secondary metabolite from an engineered R. solanacearum strain. The structure of ralsolamycin was elucidated by extensive spectroscopic analyses. Chemical derivatization as well as bioinformatics were used to assign the absolute stereochemistry. Our results identified an erroneous genome sequence, thereby emphasizing the value of chemical methods to complement bioinformatics-based procedures in natural product research.
拉尔索霉素是一种诱导真菌产生厚垣孢子的物质,最近从植物病原菌罗尔斯通氏菌中被发现。尽管串联质谱数据和生物信息学的解释能够初步进行化学表征,但拉尔索霉素的完整结构仍未得到解析。我们现在报告从工程化的罗尔斯通氏菌菌株中回收这种次级代谢产物。通过广泛的光谱分析阐明了拉尔索霉素的结构。化学衍生化以及生物信息学被用于确定绝对立体化学。我们的结果确定了一个错误的基因组序列,从而强调了化学方法在天然产物研究中补充基于生物信息学的程序的价值。