• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

烯还原酶催化的非天然反应。

Ene-Reductases-Catalyzed Non-Natural Reactions.

作者信息

Chen Jie, Wu Wenjing, Peng Yongzhen, Fang Zheng, Hu Yujing, Guo Kai

机构信息

College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, Nanjing, Jiangsu, 211816, P. R. China.

State Key Laboratory of Materials-Oriented Chemical Engineering Institution, Nanjing Tech University, Nanjing, Jiangsu, 210009, P. R. China.

出版信息

Chemistry. 2025 May;31(25):e202500539. doi: 10.1002/chem.202500539. Epub 2025 Mar 30.

DOI:10.1002/chem.202500539
PMID:40105339
Abstract

Flavin-dependent ene-reductases (EREDs), members of the Old Yellow Enzyme (OYE) superfamily, are highly efficient biocatalysts primarily known for catalyzing the asymmetric reduction of activated alkenes. Beyond this native function, the chemical versatility of the flavin cofactor and the sophisticated architecture of their protein structures enable EREDs to exhibit catalytic multifunctionality. The catalytic promiscuity not only highlights the adaptability of these enzymes but also expands their potential to broaden the scope of enzyme-catalyzed reactions in organic synthesis. Given the inherent challenges associated with discovering novel enzyme activities, such catalytic promiscuity of EREDs offers a promising pathway for expanding their applications. This mini-review provides a comprehensive overview of the catalytic multifunctionality of flavin-dependent EREDs, with a particular focus on their "non-natural" functionalities in organic synthesis. This review is primarily divided into two main sections: hydride-dependent reactions and hydride-independent reactions. By highlighting these unconventional biocatalytic pathways, we aim to inspire further exploration into the untapped potential of EREDs and their role in advancing synthetic chemistry.

摘要

黄素依赖性烯还原酶(EREDs)是老黄色酶(OYE)超家族的成员,是高效的生物催化剂,主要以催化活化烯烃的不对称还原而闻名。除了这种天然功能外,黄素辅因子的化学多功能性及其蛋白质结构的复杂架构使EREDs能够展现出催化多功能性。催化多效性不仅突出了这些酶的适应性,还拓展了它们在有机合成中扩大酶催化反应范围的潜力。鉴于发现新酶活性存在内在挑战,EREDs的这种催化多效性为扩展其应用提供了一条有前景的途径。本综述简要概述了黄素依赖性EREDs的催化多功能性,特别关注它们在有机合成中的“非天然”功能。本综述主要分为两个主要部分:氢化物依赖性反应和氢化物非依赖性反应。通过强调这些非常规的生物催化途径,我们旨在激发对EREDs未开发潜力及其在推进合成化学中作用的进一步探索。

相似文献

1
Ene-Reductases-Catalyzed Non-Natural Reactions.烯还原酶催化的非天然反应。
Chemistry. 2025 May;31(25):e202500539. doi: 10.1002/chem.202500539. Epub 2025 Mar 30.
2
From Ground-State to Excited-State Activation Modes: Flavin-Dependent "Ene"-Reductases Catalyzed Non-natural Radical Reactions.从基态到激发态激活模式:黄素依赖的“Ene”-还原酶催化的非天然自由基反应。
Acc Chem Res. 2024 May 7;57(9):1446-1457. doi: 10.1021/acs.accounts.4c00129. Epub 2024 Apr 11.
3
E. coli Nickel-Iron Hydrogenase 1 Catalyses Non-native Reduction of Flavins: Demonstration for Alkene Hydrogenation by Old Yellow Enzyme Ene-reductases*.大肠杆菌镍铁氢化酶 1 可催化非天然黄素还原:通过老黄酶 Ene-还原酶证明烯烃加氢反应*。
Angew Chem Int Ed Engl. 2021 Jun 14;60(25):13824-13828. doi: 10.1002/anie.202101186. Epub 2021 May 11.
4
Photoenzymatic Synthesis of α-Tertiary Amines by Engineered Flavin-Dependent "Ene"-Reductases.通过工程化黄素依赖性“Ene”-还原酶的光酶合成 α-叔胺。
J Am Chem Soc. 2021 Dec 1;143(47):19643-19647. doi: 10.1021/jacs.1c09828. Epub 2021 Nov 16.
5
Recombinant S. cerevisiae expressing Old Yellow Enzymes from non-conventional yeasts: an easy system for selective reduction of activated alkenes.表达来自非常规酵母的 Old Yellow Enzymes 的重组 S. cerevisiae:一种用于选择性还原活化烯烃的简单系统。
Microb Cell Fact. 2014 Apr 25;13:60. doi: 10.1186/1475-2859-13-60.
6
Asymmetric redox-neutral radical cyclization catalysed by flavin-dependent 'ene'-reductases.黄素依赖型“ene”-还原酶催化的不对称氧化还原中性自由基环化反应。
Nat Chem. 2020 Jan;12(1):71-75. doi: 10.1038/s41557-019-0370-2. Epub 2019 Dec 2.
7
Bio-electrocatalytic Alkene Reduction Using Ene-Reductases with Methyl Viologen as Electron Mediator.利用甲基紫精作为电子介体的烯还原酶进行生物电化学烯烃还原。
Chembiochem. 2024 Nov 4;25(21):e202400458. doi: 10.1002/cbic.202400458. Epub 2024 Sep 12.
8
Flavin-dependent halogenases catalyze enantioselective olefin halocyclization.黄素依赖卤代酶催化对映选择性烯烃卤环化反应。
Nat Commun. 2021 Jun 1;12(1):3268. doi: 10.1038/s41467-021-23503-3.
9
Photoenzymatic Catalysis Enables Radical-Mediated Ketone Reduction in Ene-Reductases.光酶催化使烯还原酶中自由基介导的酮还原成为可能。
Angew Chem Int Ed Engl. 2019 Jun 24;58(26):8714-8718. doi: 10.1002/anie.201902005. Epub 2019 May 16.
10
BioLindlar Catalyst: Ene-Reductase-Promoted Selective Bioreduction of Cyanoalkynes to Give (Z)-Cyanoalkenes.BioLindlar 催化剂:促进氰基炔烃的选择性生物还原为(Z)-氰基烯烃的烯-还原酶。
Angew Chem Int Ed Engl. 2024 Sep 23;63(39):e202410283. doi: 10.1002/anie.202410283. Epub 2024 Aug 20.