{"title":"在Kinamycin生物合成中催化氮-氮键形成的血红素依赖酶的发现。","authors":"Yuchun Zhao,Zhihong Xiao,Xiangyang Liu,Chenxi Zhu,Xingcan Liang,Xinyi He,Shuangjun Lin,Zixin Deng,Ming Jiang","doi":"10.1002/anie.202513778","DOIUrl":null,"url":null,"abstract":"A nitrogen-nitrogen (N─N) bond is a core feature of diverse natural products with interesting structural and biological properties. Kinamycin and lomaiviticin, featuring a diazobenzo[b]fluorene core, exhibit exceptional potency as chemotherapeutic agents. However, the N─N bond forming step in their biosynthesis has remained elusive. Through extensive mutagenesis and biochemical studies, we herein report that Alp1J, belonging to a new family of heme-dependent enzymes, catalyzes the N─N bond formation in kinamycin biosynthesis. Interestingly, Alp1J forms a stable complex with its partner ferredoxin Alp1I, which can protect the cofactors and is critical for the N─N bond formation activity. With its partner ferredoxin, Alp1J catalyzes formation of the hydrazine intermediate directly from l-aspartate and nitrite by a pathway involving four-electron reduction. Our findings expand the knowledge of enzymatic N─N bond formation and show the potential for the discovery and development of novel N─N bond containing natural products through genome mining and synthetic biology.","PeriodicalId":125,"journal":{"name":"Angewandte Chemie International Edition","volume":"101 1","pages":"e202513778"},"PeriodicalIF":16.9000,"publicationDate":"2025-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Discovery of a Heme-Dependent Enzyme Catalyzing Nitrogen-Nitrogen Bond Formation in Kinamycin Biosynthesis.\",\"authors\":\"Yuchun Zhao,Zhihong Xiao,Xiangyang Liu,Chenxi Zhu,Xingcan Liang,Xinyi He,Shuangjun Lin,Zixin Deng,Ming Jiang\",\"doi\":\"10.1002/anie.202513778\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A nitrogen-nitrogen (N─N) bond is a core feature of diverse natural products with interesting structural and biological properties. Kinamycin and lomaiviticin, featuring a diazobenzo[b]fluorene core, exhibit exceptional potency as chemotherapeutic agents. However, the N─N bond forming step in their biosynthesis has remained elusive. Through extensive mutagenesis and biochemical studies, we herein report that Alp1J, belonging to a new family of heme-dependent enzymes, catalyzes the N─N bond formation in kinamycin biosynthesis. Interestingly, Alp1J forms a stable complex with its partner ferredoxin Alp1I, which can protect the cofactors and is critical for the N─N bond formation activity. With its partner ferredoxin, Alp1J catalyzes formation of the hydrazine intermediate directly from l-aspartate and nitrite by a pathway involving four-electron reduction. Our findings expand the knowledge of enzymatic N─N bond formation and show the potential for the discovery and development of novel N─N bond containing natural products through genome mining and synthetic biology.\",\"PeriodicalId\":125,\"journal\":{\"name\":\"Angewandte Chemie International Edition\",\"volume\":\"101 1\",\"pages\":\"e202513778\"},\"PeriodicalIF\":16.9000,\"publicationDate\":\"2025-10-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Angewandte Chemie International Edition\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1002/anie.202513778\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Angewandte Chemie International Edition","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/anie.202513778","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Discovery of a Heme-Dependent Enzyme Catalyzing Nitrogen-Nitrogen Bond Formation in Kinamycin Biosynthesis.
A nitrogen-nitrogen (N─N) bond is a core feature of diverse natural products with interesting structural and biological properties. Kinamycin and lomaiviticin, featuring a diazobenzo[b]fluorene core, exhibit exceptional potency as chemotherapeutic agents. However, the N─N bond forming step in their biosynthesis has remained elusive. Through extensive mutagenesis and biochemical studies, we herein report that Alp1J, belonging to a new family of heme-dependent enzymes, catalyzes the N─N bond formation in kinamycin biosynthesis. Interestingly, Alp1J forms a stable complex with its partner ferredoxin Alp1I, which can protect the cofactors and is critical for the N─N bond formation activity. With its partner ferredoxin, Alp1J catalyzes formation of the hydrazine intermediate directly from l-aspartate and nitrite by a pathway involving four-electron reduction. Our findings expand the knowledge of enzymatic N─N bond formation and show the potential for the discovery and development of novel N─N bond containing natural products through genome mining and synthetic biology.
期刊介绍:
Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.