Krug Daniel, Zurek Gabriela, Schneider Birgit, Garcia Ronald, Müller Rolf
Institute for Pharmaceutical Biotechnology, Universität des Saarlandes, Saarbrücken, Germany.
Anal Chim Acta. 2008 Aug 22;624(1):97-106. doi: 10.1016/j.aca.2008.06.036. Epub 2008 Jun 28.
Bacteria producing secondary metabolites are an important source of natural products with highly diverse structures and biological activities. Developing methods to efficiently mine procaryotic secondary metabolomes for the presence of potentially novel natural products is therefore of considerable interest. Modern mass spectrometry-coupled liquid chromatography can effectively capture microbial metabolic diversity with ever improving sensitivity and accuracy. In addition, computational and statistical tools increasingly enable the targeted analysis and exploration of information-rich LC-MS datasets. In this article, we describe the use of such techniques for the characterization of myxobacterial secondary metabolomes. Using accurate mass data from high-resolution ESI-TOF measurements, target screening has facilitated the rapid identification of known myxobacterial metabolites in extracts from nine Myxococcus species. Furthermore, principal component analysis (PCA), implementing an advanced compound-based bucketing approach, readily revealed the presence of further compounds which contribute to variation among the metabolite profiles under investigation. The generation of molecular formulae for putative novel compounds with high confidence due to evaluation of both exact mass position and isotopic pattern, is exemplified as an important key for de-replication and prioritization of candidates for further characterization.
产生次级代谢产物的细菌是具有高度多样结构和生物活性的天然产物的重要来源。因此,开发有效挖掘原核生物次级代谢组以寻找潜在新型天然产物的方法备受关注。现代质谱联用液相色谱能够以不断提高的灵敏度和准确性有效捕捉微生物代谢多样性。此外,计算和统计工具越来越有助于对富含信息的液相色谱 - 质谱数据集进行靶向分析和探索。在本文中,我们描述了使用此类技术来表征粘细菌次级代谢组。利用高分辨率电喷雾电离飞行时间(ESI - TOF)测量获得的精确质量数据,目标筛选有助于快速鉴定来自九种粘球菌物种提取物中的已知粘细菌代谢产物。此外,主成分分析(PCA)采用先进的基于化合物的分桶方法,很容易揭示出导致所研究代谢物谱之间差异的其他化合物的存在。由于对精确质量位置和同位素模式进行了评估,从而能够高置信度地生成推定新型化合物的分子式,这被视为去重复和确定进一步表征候选物优先级的重要关键。