Edna Bode, Daniela Assmann, Petra Happel, Elmar Meyer, Karin Münch, Nicole Rössel, Helge B Bode
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引用次数: 0
摘要
easyacid (easy Promoter Activation and Compound Identification)方法专注于靶向激活编码非核糖体肽合成酶(NRPS)、聚酮合成酶(PKS)、NRPS-PKS杂交或其他BGC类的天然产物生物合成基因簇(BGC)。将该方法应用于Xenorhabdus属和photohabdus属昆虫病原细菌,将所需BGCs的天然启动子与各自菌株的∆hfq突变体中的l -阿拉伯糖诱导的PBAD启动子交换。培养的easyacid突变体的粗(培养)提取物富含单一化合物或化合物类别,可以直接针对各种目标生物进行测试,而无需进一步纯化所产生的天然产物。此外,由于∆hfq菌株的背景降低,从这些突变体中分离和鉴定化合物也简化了。该方法避免了在异源表达宿主、化学合成或从野生型粗提取物中提取所需化合物时经常遇到的问题。该方案描述了用于Xenorhabdus和photohabdus的easyPACId,但它也成功地适用于嗜虫假单胞菌,可能适用于其他携带hfq的变形菌。
easyPACId, a Simple Method for Induced Production, Isolation, Identification, and Testing of Natural Products from Proteobacteria.
The easyPACId (easy Promoter Activation and Compound Identification) approach is focused on the targeted activation of natural product biosynthetic gene clusters (BGCs) encoding non-ribosomal peptide synthetases (NRPS), polyketide synthases (PKS), NRPS-PKS hybrids, or other BGC classes. It was applied to entomopathogenic bacteria of the genera Xenorhabdus and Photorhabdus by exchanging the natural promoter of desired BGCs against the L-arabinose inducible PBAD promoter in ∆hfq mutants of the respective strains. The crude (culture) extracts of the cultivated easyPACId mutants are enriched with the single compound or compound class and can be tested directly against various target organisms without further purification of the produced natural products. Furthermore, isolation and identification of compounds from these mutants is simplified due to the reduced background in the ∆hfq strains. The approach avoids problems often encountered in heterologous expression hosts, chemical synthesis, or tedious extraction of desired compounds from wild-type crude extracts. This protocol describes easyPACId for Xenorhabdus and Photorhabdus, but it was also successfully adapted to Pseudomonas entomophila and might be suitable for other proteobacteria that carry hfq.