{"title":"利用化学酶法全合成茜草霉素 A","authors":"","doi":"10.1038/s44160-024-00580-y","DOIUrl":null,"url":null,"abstract":"Owing to its structural complexity, the total synthesis of alchivemycin A has proved challenging. Now, the total synthesis of alchivemycin A is achieved using a chemoenzymatic approach that combines de novo skeleton construction with a late-stage enzymatic oxidation cascade. Following rational protein engineering of a key enzyme, the final product is obtained in high yield.","PeriodicalId":74251,"journal":{"name":"Nature synthesis","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-06-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Total synthesis of alchivemycin A using a chemoenzymatic strategy\",\"authors\":\"\",\"doi\":\"10.1038/s44160-024-00580-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Owing to its structural complexity, the total synthesis of alchivemycin A has proved challenging. Now, the total synthesis of alchivemycin A is achieved using a chemoenzymatic approach that combines de novo skeleton construction with a late-stage enzymatic oxidation cascade. Following rational protein engineering of a key enzyme, the final product is obtained in high yield.\",\"PeriodicalId\":74251,\"journal\":{\"name\":\"Nature synthesis\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-06-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature synthesis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.nature.com/articles/s44160-024-00580-y\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"0\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature synthesis","FirstCategoryId":"1085","ListUrlMain":"https://www.nature.com/articles/s44160-024-00580-y","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"0","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
由于茜草霉素 A 结构复杂,全合成茜草霉素 A 具有挑战性。现在,我们采用化学酶法实现了茜草霉素 A 的全合成,该方法结合了从头构建骨架和后期酶促氧化级联反应。在对一种关键酶进行合理的蛋白质工程设计后,最终产品以高产率获得。
Total synthesis of alchivemycin A using a chemoenzymatic strategy
Owing to its structural complexity, the total synthesis of alchivemycin A has proved challenging. Now, the total synthesis of alchivemycin A is achieved using a chemoenzymatic approach that combines de novo skeleton construction with a late-stage enzymatic oxidation cascade. Following rational protein engineering of a key enzyme, the final product is obtained in high yield.