Cuervo Lorena, Malmierca Mónica G, García-Salcedo Raúl, Méndez Carmen, Salas José A, Olano Carlos, Ceniceros Ana
Functional Biology Department, University of Oviedo, 33006 Oviedo, Spain.
University Institute of Oncology of Asturias (I.U.O.P.A.), University of Oviedo, 33006 Oviedo, Spain.
Microorganisms. 2023 Jun 15;11(6):1585. doi: 10.3390/microorganisms11061585.
The search for novel bioactive compounds to overcome resistance to current therapeutics has become of utmost importance. spp. are one of the main sources of bioactive compounds currently used in medicine. In this work, five different global transcriptional regulators and five housekeeping genes, known to induce the activation or overproduction of secondary metabolites in , were cloned in two separated constructs and expressed in 12 different strains of spp. from the in-house CS collection. These recombinant plasmids were also inserted into streptomycin and rifampicin resistant strains (mutations known to enhance secondary metabolism in ). Different media with diverse carbon and nitrogen sources were selected to assess the strains' metabolite production. Cultures were then extracted with different organic solvents and analysed to search for changes in their production profiles. An overproduction of metabolites already known to be produced by the biosynthesis wild-type strains was observed such as germicidin by CS113, collismycins by CS149 and CS014, or colibrimycins by CS147. Additionally, the activation of some compounds such as alteramides in CS090a pSETxkBMRRH and CS065a pSETxkDCABA or inhibition of the biosynthesis of chromomycins in CS065a in pSETxkDCABA when grown in SM10 was demonstrated. Therefore, these genetic constructs are a relatively simple tool to manipulate metabolism and explore their wide secondary metabolites production potential.
寻找新型生物活性化合物以克服对当前治疗方法的耐药性已变得至关重要。 属是目前医学中使用的生物活性化合物的主要来源之一。在这项工作中,已知能诱导 中次生代谢产物激活或过量产生的五种不同的全局转录调节因子和五个管家基因,被克隆到两个单独的构建体中,并在来自内部CS collection的12种不同的 菌株中表达。这些重组质粒也被插入到对链霉素和利福平耐药的 菌株中(已知这些突变会增强 中的次生代谢)。选择了含有不同碳源和氮源的不同培养基来评估菌株的代谢产物产生情况。然后用不同的有机溶剂对培养物进行提取并分析,以寻找其生产谱的变化。观察到生物合成野生型菌株已产生的代谢产物过量产生,例如CS113产生的杀菌素、CS149和CS014产生的碰撞霉素,或CS147产生的共栖霉素。此外,还证明了在SM10中生长时,CS090a pSETxkBMRRH和CS065a pSETxkDCABA中某些化合物如交替酰胺的激活,或pSETxkDCABA中CS065a中色霉素生物合成的抑制。因此,这些基因构建体是操纵 代谢并探索其广泛的次生代谢产物生产潜力的相对简单的工具。