Department of Medicinal Chemistry and Pharmacognosy and Center for Biomolecular Sciences, College of Pharmacy , University of Illinois at Chicago , Chicago , Illinois 60607 , United States.
CAPES Foundation, Ministry of Education of Brazil , Brasília , Federal District 70040-020 , Brazil.
J Nat Prod. 2018 Sep 28;81(9):2057-2068. doi: 10.1021/acs.jnatprod.8b00394. Epub 2018 Aug 15.
Actinomycete bacteria isolated from freshwater environments are an unexplored source of natural products. Here we report the complete genome of the Great Lakes-derived Micromonospora sp. strain B006, revealing its potential for natural product biosynthesis. The 7-megabase pair chromosome of strain B006 was sequenced using Illumina and Oxford Nanopore technologies followed by Sanger sequencing to close remaining gaps. All identified biosynthetic gene clusters (BGCs) were manually curated. Five known BGCs were identified encoding desferrioxamine, alkyl- O-dihydrogeranylmethoxyhydroquinone, a spore pigment, sioxanthin, and diazepinomicin, which is currently in phase II clinical trials to treat Phelan-McDermid syndrome and co-morbid epilepsy. We report here that strain B006 is indeed a producer of diazepinomicin and at yields higher than previously reported. Moreover, 11 of the 16 identified BGCs are orphan, eight of which were transcriptionally active under the culture condition tested. Orphan BGCs include an enediyne polyketide synthase and an uncharacteristically large, 36-module polyketide synthase-nonribosomal peptide synthetase BGC. We developed a genetics system for Micromonospora sp. B006 that will contribute to deorphaning BGCs in the future. This study is one of the few attempts to report the biosynthetic capacity of a freshwater-derived actinomycete and highlights this resource as a potential reservoir for new natural products.
从淡水环境中分离出的放线菌是天然产物的未开发来源。在这里,我们报告了源自大湖的 Micromonospora sp. 菌株 B006 的完整基因组,揭示了其天然产物生物合成的潜力。使用 Illumina 和 Oxford Nanopore 技术对 B006 菌株的 700 兆碱基对染色体进行测序,然后进行 Sanger 测序以闭合其余的缺口。所有鉴定的生物合成基因簇 (BGC) 均经过手动整理。鉴定出五个已知的 BGC,分别编码去铁胺、烷基-O-二氢香叶基甲氧基对苯二酚、孢子色素、硅氧黄素和 diazepinomicin,后者目前正在进行治疗 Phelan-McDermid 综合征和合并癫痫的 II 期临床试验。我们在这里报告,B006 菌株确实是 diazepinomicin 的产生者,其产量高于之前报道的水平。此外,在测试的培养条件下,16 个鉴定的 BGC 中有 11 个是孤儿 BGC,其中 8 个转录活跃。孤儿 BGC 包括一个烯二炔聚酮合酶和一个异常大的 36 模块聚酮合酶-非核糖体肽合酶 BGC。我们为 Micromonospora sp. B006 开发了一种遗传学系统,这将有助于未来对 BGC 的去孤儿化。这项研究是为数不多的尝试报告淡水来源的放线菌生物合成能力的研究之一,突出了这一资源作为新天然产物的潜在来源。