Kostenko Anastasiia, Lien Yi, Mendauletova Aigera, Ngendahimana Thacien, Novitskiy Ivan M, Eaton Sandra S, Latham John A
Department of Chemistry and Biochemistry, University of Denver, Denver, Colorado, USA.
Department of Chemistry and Biochemistry, University of Denver, Denver, Colorado, USA.
J Biol Chem. 2022 May;298(5):101881. doi: 10.1016/j.jbc.2022.101881. Epub 2022 Mar 31.
Peptide-derived natural products are a large class of bioactive molecules that often contain chemically challenging modifications. In the biosynthesis of ribosomally synthesized and posttranslationally modified peptides (RiPPs), radical-SAM (rSAM) enzymes have been shown to catalyze the formation of ether, thioether, and carbon-carbon bonds on the precursor peptide. The installation of these bonds typically establishes the skeleton of the mature RiPP. To facilitate the search for unexplored rSAM-dependent RiPPs for the community, we employed a bioinformatic strategy to screen a subfamily of peptide-modifying rSAM enzymes which are known to bind up to three [4Fe-4S] clusters. A sequence similarity network was used to partition related families of rSAM enzymes into >250 clusters. Using representative sequences, genome neighborhood diagrams were generated using the Genome Neighborhood Tool. Manual inspection of bacterial genomes yielded numerous putative rSAM-dependent RiPP pathways with unique features. From this analysis, we identified and experimentally characterized the rSAM enzyme, TvgB, from the tvg gene cluster from Halomonas anticariensis. In the tvg gene cluster, the precursor peptide, TvgA, is comprised of a repeating TVGG motif. Structural characterization of the TvgB product revealed the repeated formation of cyclopropylglycine, where a new bond is formed between the γ-carbons on the precursor valine. This novel RiPP modification broadens the functional potential of rSAM enzymes and validates the proposed bioinformatic approach as a practical broad search tool for the discovery of new RiPP topologies.
肽衍生的天然产物是一大类生物活性分子,通常含有具有化学挑战性的修饰。在核糖体合成和翻译后修饰肽(RiPPs)的生物合成中,自由基-SAM(rSAM)酶已被证明可催化前体肽上醚键、硫醚键和碳-碳键的形成。这些键的形成通常构建了成熟RiPP的骨架。为了便于该领域寻找未被探索的依赖rSAM的RiPPs,我们采用了一种生物信息学策略来筛选已知可结合多达三个[4Fe-4S]簇的肽修饰rSAM酶亚家族。利用序列相似性网络将rSAM酶的相关家族划分为250多个簇。使用代表性序列,通过基因组邻域工具生成基因组邻域图。对细菌基因组的人工检查产生了许多具有独特特征的假定的依赖rSAM的RiPP途径。通过该分析,我们从抗龋嗜盐单胞菌的tvg基因簇中鉴定并通过实验表征了rSAM酶TvgB。在tvg基因簇中,前体肽TvgA由重复的TVGG基序组成。TvgB产物的结构表征揭示了环丙基甘氨酸的重复形成,其中在前体缬氨酸的γ-碳之间形成了新的键。这种新型的RiPP修饰拓宽了rSAM酶的功能潜力,并验证了所提出的生物信息学方法作为发现新RiPP拓扑结构的实用广泛搜索工具的有效性。