{"title":"在NADPH再生过程中处理葡萄糖脱氢酶交叉反应的替代脱氢酶。","authors":"Jhilik Mondal, Piyal Das, Syed Masood Husain","doi":"10.1002/asia.202500654","DOIUrl":null,"url":null,"abstract":"<p><p>Biocatalytic reductions require NAD(P)H generation, which is usually achieved using a glucose/glucose dehydrogenase (GDH) system. However, certain GDHs exhibit cross-reactivity by reducing various keto or iminium substrates during NADPH regeneration, thereby altering the stereoselectivity of the final products. In this study, we evaluated two established NADPH regeneration enzymes-phosphite dehydrogenase (PTDH) and isocitrate dehydrogenase (ICDH) for their potential cross-reactivity with keto and iminium substrates. In contrast to glucose dehydrogenase (GDH), neither PTDH nor ICDH showed any reactivity toward the tested substrates. Consequently, phosphite/PTDH and isocitrate/ICDH systems were employed for NADPH regeneration during the biocatalytic reduction of keto compounds. These systems thus present effective alternatives to glucose/GDH, offering a solution to eliminate unwanted cross-reactivity during enzymatic reductions.</p>","PeriodicalId":145,"journal":{"name":"Chemistry - An Asian Journal","volume":" ","pages":"e00654"},"PeriodicalIF":3.3000,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Alternative Dehydrogenases to Address Glucose Dehydrogenase Cross-Reactivity During NADPH Regeneration.\",\"authors\":\"Jhilik Mondal, Piyal Das, Syed Masood Husain\",\"doi\":\"10.1002/asia.202500654\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Biocatalytic reductions require NAD(P)H generation, which is usually achieved using a glucose/glucose dehydrogenase (GDH) system. However, certain GDHs exhibit cross-reactivity by reducing various keto or iminium substrates during NADPH regeneration, thereby altering the stereoselectivity of the final products. In this study, we evaluated two established NADPH regeneration enzymes-phosphite dehydrogenase (PTDH) and isocitrate dehydrogenase (ICDH) for their potential cross-reactivity with keto and iminium substrates. In contrast to glucose dehydrogenase (GDH), neither PTDH nor ICDH showed any reactivity toward the tested substrates. Consequently, phosphite/PTDH and isocitrate/ICDH systems were employed for NADPH regeneration during the biocatalytic reduction of keto compounds. These systems thus present effective alternatives to glucose/GDH, offering a solution to eliminate unwanted cross-reactivity during enzymatic reductions.</p>\",\"PeriodicalId\":145,\"journal\":{\"name\":\"Chemistry - An Asian Journal\",\"volume\":\" \",\"pages\":\"e00654\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2025-09-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemistry - An Asian Journal\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://doi.org/10.1002/asia.202500654\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry - An Asian Journal","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1002/asia.202500654","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Alternative Dehydrogenases to Address Glucose Dehydrogenase Cross-Reactivity During NADPH Regeneration.
Biocatalytic reductions require NAD(P)H generation, which is usually achieved using a glucose/glucose dehydrogenase (GDH) system. However, certain GDHs exhibit cross-reactivity by reducing various keto or iminium substrates during NADPH regeneration, thereby altering the stereoselectivity of the final products. In this study, we evaluated two established NADPH regeneration enzymes-phosphite dehydrogenase (PTDH) and isocitrate dehydrogenase (ICDH) for their potential cross-reactivity with keto and iminium substrates. In contrast to glucose dehydrogenase (GDH), neither PTDH nor ICDH showed any reactivity toward the tested substrates. Consequently, phosphite/PTDH and isocitrate/ICDH systems were employed for NADPH regeneration during the biocatalytic reduction of keto compounds. These systems thus present effective alternatives to glucose/GDH, offering a solution to eliminate unwanted cross-reactivity during enzymatic reductions.
期刊介绍:
Chemistry—An Asian Journal is an international high-impact journal for chemistry in its broadest sense. The journal covers all aspects of chemistry from biochemistry through organic and inorganic chemistry to physical chemistry, including interdisciplinary topics.
Chemistry—An Asian Journal publishes Full Papers, Communications, and Focus Reviews.
A professional editorial team headed by Dr. Theresa Kueckmann and an Editorial Board (headed by Professor Susumu Kitagawa) ensure the highest quality of the peer-review process, the contents and the production of the journal.
Chemistry—An Asian Journal is published on behalf of the Asian Chemical Editorial Society (ACES), an association of numerous Asian chemical societies, and supported by the Gesellschaft Deutscher Chemiker (GDCh, German Chemical Society), ChemPubSoc Europe, and the Federation of Asian Chemical Societies (FACS).