Mining the cryptic specialized metabolome of Streptomyces cyanogenus S136

I. Ostash, M. Deneka, M. Lopatniuk, T. Busche, J. Kalinowski, A. Luzhetskyy, V. Fedorenko, B. Ostash
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Abstract

Streptomyces cyanogenus S136 is known to produce landomycin family antibiotics, particularly its largest congener, landomycin A. Except for landomycins and polyene lucensomycin, no other specialized metabolites were sourced from S136. Nevertheless, S136 genome sequencing revealed over 40 biosynthetic gene clusters (BGCs), implying underappreciated potential of this strain for the production of novel bioactive natural compounds. We set out to gain deeper insight into the specialized metabolome of this strain. First, trans­criptomic analysis of S136 grown under landomycin production conditions has been carried out, revealing that most of them are expressed at a basal level. This, likely, leads to a phenotypic silence of most of the BGCs. Nevertheless, several notable exceptions have been spotted. First of all, landomycin BGC is expressed at high level (at least 100 Transcripts Per Million mapped reads (TPM); and around 1000 TPM for minimal polyketide synthase genes lanFABC). Similarly, high levels of expression showed BGCs # 2, 4, 7 and 33, of which #2, encoding unknown saccharide, is the most dissimilar to the described precedents. RNAseq data also allowed us to delineate better the borders of several presumed BGCs. In the next phase of the work we singled out a few BGCs within S136 that appeared to be promising. First, these BGCs exhibited low similarity to the other gene clusters directing the production of known natural products. Second, the BGCs harbored cluster-situated regulatory genes that can be employed in the attempts to activate the expression of cryptic pathways. For one such BGC we constructed two plasmids for expression of several such regulatory genes and introduced them into S136 and its derivative deficient in production of landomycin A. Bioassays showed no differences in bioactivity of the recombinant strains as compared to the initial strains. Liquid chromatography coupled to mass spectrometry (LC-MS) analysis of several S. cyanogenus samples revealed the effects of genotype, growth conditions and extraction on specialized metabolome of this species, setting reference point for further stu­dies.
挖掘氰基链霉 S136 的隐性特化代谢组
已知青色链霉菌 S136 可产生陆霉素家族抗生素,尤其是其最大的同系物陆霉素 A。然而,S136 基因组测序发现了 40 多个生物合成基因簇(BGC),这意味着该菌株生产新型生物活性天然化合物的潜力尚未得到充分重视。我们开始深入研究该菌株的特殊代谢组。首先,我们对在陆地霉素生产条件下生长的 S136 进行了转录组分析,结果表明它们中的大部分都在基础水平上表达。这很可能导致大多数 BGCs 的表型沉默。不过,也发现了几个明显的例外。首先,陆地霉素 BGC 的表达量很高(每百万映射读数至少有 100 个转录本(TPM);最小多酮合成酶基因 lanFABC 的表达量约为 1000 TPM)。同样,2 号、4 号、7 号和 33 号 BGC 也有高水平表达,其中 2 号编码未知糖,与所述先例最为相似。RNAseq 数据还使我们能够更好地划分几个假定的 BGCs 的边界。在下一阶段的工作中,我们在 S136 中挑出了几个看起来很有希望的 BGC。首先,这些 BGC 与其他指导生产已知天然产物的基因簇相似度较低。其次,这些 BGC 含有基因簇定位的调控基因,可用于激活隐性途径的表达。生物测定显示,重组菌株的生物活性与初始菌株相比没有差异。对几种蓝藻样本进行的液相色谱-质谱联用(LC-MS)分析表明了基因型、生长条件和提取对该物种特化代谢组的影响,为进一步研究提供了参考。
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