Department of Biochemistry, Duke University School of Medicine, 307 Research Drive, Durham, NC 27710, USA.
Department of Chemistry, Duke University, 307 Research Drive, Durham, NC 27710, USA.
Chembiochem. 2023 Sep 1;24(17):e202300342. doi: 10.1002/cbic.202300342. Epub 2023 Jul 26.
Nucleoside natural products show diverse biological activities and serve as leads for various application purposes, including human and veterinary medicine and agriculture. Studies in the past decade revealed that these nucleosides are biosynthesized through divergent mechanisms, in which early steps of the pathways can be classified into two types (C5' oxidation and C5' radical extension), while the structural diversity is created by downstream tailoring enzymes. Based on this biosynthetic logic, we investigated the genome mining discovery potentials of these nucleosides using the two enzymes representing the two types of C5' modifications: LipL-type α-ketoglutarate (α-KG) and Fe-dependent oxygenases and NikJ-type radical S-adenosyl-L-methionine (SAM) enzymes. The results suggest that this approach allows discovery of putative nucleoside biosynthetic gene clusters (BGCs) and the prediction of the core nucleoside structures. The results also revealed the distribution of these pathways in nature and implied the possibility of future genome mining discovery of novel nucleoside natural products.
核苷天然产物具有多样的生物活性,可作为人类和兽医医学以及农业等各种应用的先导化合物。过去十年的研究表明,这些核苷是通过不同的机制生物合成的,其中途径的早期步骤可分为两类(C5'氧化和 C5'自由基延伸),而结构多样性则由下游修饰酶创造。基于这一生物合成逻辑,我们使用代表两种 C5'修饰类型的两种酶(LipL 型 α-酮戊二酸(α-KG)和 Fe 依赖性氧合酶以及 NikJ 型自由基 S-腺苷-L-甲硫氨酸(SAM)酶),研究了这些核苷的基因组挖掘发现潜力。结果表明,这种方法可以发现潜在的核苷生物合成基因簇(BGC),并预测核心核苷结构。结果还揭示了这些途径在自然界中的分布,并暗示了未来通过基因组挖掘发现新型核苷天然产物的可能性。