Sanrunyi Gong , Tianzhen Li , Zijing Tang , Zijian Tan , Ruke Zhang , Karsten Olsen , Haifeng Liu , Leilei Zhu
{"title":"One-pot enzymatic synthesis of l-threitol from C1 formaldehyde†","authors":"Sanrunyi Gong , Tianzhen Li , Zijing Tang , Zijian Tan , Ruke Zhang , Karsten Olsen , Haifeng Liu , Leilei Zhu","doi":"10.1039/d4gc05638h","DOIUrl":null,"url":null,"abstract":"<div><div>Here, we report an enzymatic cascade reaction converting a high concentration of formaldehyde into <span>l</span>-threitol. The cascade reaction starts with the carboligation of formaldehyde catalyzed by formolase and fructose-6-phosphate aldolase, generating <span>l</span>-erythrulose. Subsequently, a newly identified <span>l</span>-threitol dehydrogenase facilitates the conversion of <span>l</span>-erythrulose into <span>l</span>-threitol, utilizing NADH as a coenzyme. Three types of NADH regeneration systems were investigated to facilitate the recycling of NADH in the reaction system. 405.7 mM (49.6 g L<sup>−1</sup>) <span>l</span>-threitol was achieved from the conversion of formaldehyde in a one-pot reaction system with a self-sufficient NADH recycling system, which is based on the oxidation of glycerol catalyzed by glycerol dehydrogenase. Furthermore, the highest yield (89.4%; 251.3 mM) of <span>l</span>-threitol from formaldehyde was achieved in the one-pot two-step reaction system in which NADH was efficiently recycled by using methanol dehydrogenase and isopropanol.</div></div>","PeriodicalId":78,"journal":{"name":"Green Chemistry","volume":"27 8","pages":"Pages 2189-2196"},"PeriodicalIF":9.3000,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Green Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1463926225000615","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Here, we report an enzymatic cascade reaction converting a high concentration of formaldehyde into l-threitol. The cascade reaction starts with the carboligation of formaldehyde catalyzed by formolase and fructose-6-phosphate aldolase, generating l-erythrulose. Subsequently, a newly identified l-threitol dehydrogenase facilitates the conversion of l-erythrulose into l-threitol, utilizing NADH as a coenzyme. Three types of NADH regeneration systems were investigated to facilitate the recycling of NADH in the reaction system. 405.7 mM (49.6 g L−1) l-threitol was achieved from the conversion of formaldehyde in a one-pot reaction system with a self-sufficient NADH recycling system, which is based on the oxidation of glycerol catalyzed by glycerol dehydrogenase. Furthermore, the highest yield (89.4%; 251.3 mM) of l-threitol from formaldehyde was achieved in the one-pot two-step reaction system in which NADH was efficiently recycled by using methanol dehydrogenase and isopropanol.
期刊介绍:
Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.