Pascal Püllmann, Dominik Homann, Lewis Thomas-Hargreaves
{"title":"探索非特异性过氧酶在非天然亚硝基化学中的作用。","authors":"Pascal Püllmann, Dominik Homann, Lewis Thomas-Hargreaves","doi":"10.1002/cbic.202500332","DOIUrl":null,"url":null,"abstract":"<p><p>Unspecific peroxygenases (UPOs) perform challenging oxyfunctionalization chemistry with high catalytic efficiency and reaction stability.[1-5] In this report, we add nitrene chemistry to the current repertoire of UPO chemistry, utilizing the inexpensive commodity chemical hydroxylamine as co-substrate. 1,2,3,4-tetrahydronaphthalene was investigated as model substrate employing a diverse panel of UPOs, reaching turnover numbers up to 745 and enantiomeric excess values up to 62 %. Overall, we report the first account of UPO activity regarding non-natural reactivities.</p>","PeriodicalId":140,"journal":{"name":"ChemBioChem","volume":" ","pages":"e202500332"},"PeriodicalIF":2.6000,"publicationDate":"2025-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Probing Unspecific Peroxygenases for Non-Natural Nitrene Chemistry.\",\"authors\":\"Pascal Püllmann, Dominik Homann, Lewis Thomas-Hargreaves\",\"doi\":\"10.1002/cbic.202500332\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Unspecific peroxygenases (UPOs) perform challenging oxyfunctionalization chemistry with high catalytic efficiency and reaction stability.[1-5] In this report, we add nitrene chemistry to the current repertoire of UPO chemistry, utilizing the inexpensive commodity chemical hydroxylamine as co-substrate. 1,2,3,4-tetrahydronaphthalene was investigated as model substrate employing a diverse panel of UPOs, reaching turnover numbers up to 745 and enantiomeric excess values up to 62 %. Overall, we report the first account of UPO activity regarding non-natural reactivities.</p>\",\"PeriodicalId\":140,\"journal\":{\"name\":\"ChemBioChem\",\"volume\":\" \",\"pages\":\"e202500332\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2025-06-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ChemBioChem\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1002/cbic.202500332\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemBioChem","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1002/cbic.202500332","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Probing Unspecific Peroxygenases for Non-Natural Nitrene Chemistry.
Unspecific peroxygenases (UPOs) perform challenging oxyfunctionalization chemistry with high catalytic efficiency and reaction stability.[1-5] In this report, we add nitrene chemistry to the current repertoire of UPO chemistry, utilizing the inexpensive commodity chemical hydroxylamine as co-substrate. 1,2,3,4-tetrahydronaphthalene was investigated as model substrate employing a diverse panel of UPOs, reaching turnover numbers up to 745 and enantiomeric excess values up to 62 %. Overall, we report the first account of UPO activity regarding non-natural reactivities.
期刊介绍:
ChemBioChem (Impact Factor 2018: 2.641) publishes important breakthroughs across all areas at the interface of chemistry and biology, including the fields of chemical biology, bioorganic chemistry, bioinorganic chemistry, synthetic biology, biocatalysis, bionanotechnology, and biomaterials. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and supported by the Asian Chemical Editorial Society (ACES).