{"title":"自由基SAM环烷合成酶催化在多个trp基序上形成均匀的环烷","authors":"Abujunaid Habib Khan , Jabal Rahmat Haedar , Anitra Zīle , Chin-Soon Phan","doi":"10.1016/j.tchem.2025.100128","DOIUrl":null,"url":null,"abstract":"<div><div>Cyclophane-containing products from ribosomally synthesized and post-translationally modified peptides (RiPPs) are generated by radical SAM cyclophane synthases (rSAM). In the past few years, rSAM enzymes that catalyze uniform cyclophanes at multiple Trp-motifs on the precursor peptides have been discovered more frequently. These enzymes install C–C or C–O cross-links at the three-residue motifs between Trp-C5/C6/C7 and an <em>sp</em><sup>3</sup> carbon side chain to generate strained macrocycles. This mini-review will focus on the rSAM enzymes, WprB, OscB, XncB, FwwB and RscB to summarize the biosynthesis and NMR characterization of Trp-containing cyclophane products, and promiscuity of these enzymes.</div></div>","PeriodicalId":74918,"journal":{"name":"Tetrahedron chem","volume":"14 ","pages":"Article 100128"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Radical SAM cyclophane synthase catalyzes uniform cyclophane formation at multiple Trp-motifs\",\"authors\":\"Abujunaid Habib Khan , Jabal Rahmat Haedar , Anitra Zīle , Chin-Soon Phan\",\"doi\":\"10.1016/j.tchem.2025.100128\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Cyclophane-containing products from ribosomally synthesized and post-translationally modified peptides (RiPPs) are generated by radical SAM cyclophane synthases (rSAM). In the past few years, rSAM enzymes that catalyze uniform cyclophanes at multiple Trp-motifs on the precursor peptides have been discovered more frequently. These enzymes install C–C or C–O cross-links at the three-residue motifs between Trp-C5/C6/C7 and an <em>sp</em><sup>3</sup> carbon side chain to generate strained macrocycles. This mini-review will focus on the rSAM enzymes, WprB, OscB, XncB, FwwB and RscB to summarize the biosynthesis and NMR characterization of Trp-containing cyclophane products, and promiscuity of these enzymes.</div></div>\",\"PeriodicalId\":74918,\"journal\":{\"name\":\"Tetrahedron chem\",\"volume\":\"14 \",\"pages\":\"Article 100128\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-03-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Tetrahedron chem\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2666951X25000105\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tetrahedron chem","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666951X25000105","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Radical SAM cyclophane synthase catalyzes uniform cyclophane formation at multiple Trp-motifs
Cyclophane-containing products from ribosomally synthesized and post-translationally modified peptides (RiPPs) are generated by radical SAM cyclophane synthases (rSAM). In the past few years, rSAM enzymes that catalyze uniform cyclophanes at multiple Trp-motifs on the precursor peptides have been discovered more frequently. These enzymes install C–C or C–O cross-links at the three-residue motifs between Trp-C5/C6/C7 and an sp3 carbon side chain to generate strained macrocycles. This mini-review will focus on the rSAM enzymes, WprB, OscB, XncB, FwwB and RscB to summarize the biosynthesis and NMR characterization of Trp-containing cyclophane products, and promiscuity of these enzymes.