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A Regulator Based Semi-Targeted Approach to Activate Silent Biosynthetic Gene Clusters

机译:基于稳压器的半靶向方法来激活无声生物合成基因集群

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摘要

By culturing microorganisms under standard laboratory conditions, most biosynthetic gene clusters (BGCs) are not expressed, and thus, the products are not produced. To explore this biosynthetic potential, we developed a novel “semi-targeted” approach focusing on activating “silent” BGCs by concurrently introducing a group of regulator genes into streptomycetes of the Tübingen strain collection. We constructed integrative plasmids containing two classes of regulatory genes under the control of the constitutive promoter ermE*p (cluster situated regulators (CSR) and Streptomyces antibiotic regulatory proteins (SARPs)). These plasmids were introduced into Streptomyces sp. TÜ17, Streptomyces sp. TÜ10 and Streptomyces sp. TÜ102. Introduction of the CSRs-plasmid into strain S. sp. TÜ17 activated the production of mayamycin A. By using the individual regulator genes, we proved that Aur1P, was responsible for the activation. In strain S. sp. TÜ102, the introduction of the SARP-plasmid triggered the production of a chartreusin-like compound. Insertion of the CSRs-plasmid into strain S. sp. TÜ10 resulted in activating the warkmycin-BGC. In both recombinants, activation of the BGCs was only possible through the simultaneous expression of aur1PR3 and griR in S. sp. TÜ102 and aur1P and pntR in of S. sp. TÜ10.
机译:通过在标准实验室条件下培养微生物,未表达大多数生物合成基因簇(BGC),因此不产生产品。为了探索这种生物合成潜力,我们开发了一种小说“半靶向”方法,重点是通过同时将一组调节基因与杜宾菌菌素收集的链霉菌引入“静音”BGCS。我们在组成促进剂ERME * P的控制下构建了含有两类调节基因的一体化质粒(簇定位调节剂(CSR)和链霉菌抗生素调节蛋白(SARPS))。将这些质粒引入链霉菌SP中。 TÜ17,Streptomyces sp。 TÜ10和Streptomyces sp。 TÜ102。将CSRS-质粒引入菌株S. SP中。 TÜ17激活了MASAMICIN A.通过使用个体调节基因,我们证明AUR1P负责激活。在菌株S. SP。 TÜ102,引入SARP-polasmid引发了鲜光素样化合物的生产。将CSRS质粒插入菌株S. SP。 TÜ10导致激活Warkmycin-BGC。在两种重组中,通过在S.SP中同时表达Aur1pr3和Grir,才能激活BGC。 TÜ102和AUR1P和S. SP的PNTR。 TÜ10。

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