Seyedsayamdost Mohammad R, Traxler Matthew F, Clardy Jon, Kolter Roberto
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts, USA.
Department of Microbiology and Immunobiology, Harvard Medical School, Boston, Massachusetts, USA.
Methods Enzymol. 2012;517:89-109. doi: 10.1016/B978-0-12-404634-4.00005-X.
Actinomycetes, a group of filamentous, Gram-positive bacteria, have long been a remarkable source of useful therapeutics. Recent genome sequencing and transcriptomic studies have shown that these bacteria, responsible for half of the clinically used antibiotics, also harbor a large reservoir of gene clusters, which have the potential to produce novel secreted small molecules. Yet, many of these clusters are not expressed under common culture conditions. One reason why these clusters have not been linked to a secreted small molecule lies in the way that actinomycetes have typically been studied: as pure cultures in nutrient-rich media that do not mimic the complex environments in which these bacteria evolved. New methods based on multispecies culture conditions provide an alternative approach to investigating the products of these gene clusters. We have recently implemented binary interspecies interaction assays to mine for new secondary metabolites and to study the underlying biology of interactinomycete interactions. Here, we describe the detailed biological and chemical methods comprising these studies.
放线菌是一类丝状革兰氏阳性细菌,长期以来一直是有用治疗药物的重要来源。最近的基因组测序和转录组学研究表明,这些产生了一半临床所用抗生素的细菌还拥有大量基因簇,这些基因簇有可能产生新的分泌型小分子。然而,许多这些基因簇在常见培养条件下并不表达。这些基因簇尚未与分泌型小分子联系起来的一个原因在于研究放线菌的典型方式:即在营养丰富的培养基中进行纯培养,而这种培养基并不能模拟这些细菌进化所处的复杂环境。基于多物种培养条件的新方法为研究这些基因簇的产物提供了一种替代方法。我们最近实施了二元种间相互作用测定,以挖掘新的次生代谢产物并研究种间相互作用的潜在生物学机制。在此,我们描述了构成这些研究的详细生物学和化学方法。