Making molecules with photodecarboxylases: A great start or a false dawn?

Tobias M. Hedison, Derren J. Heyes, Nigel S. Scrutton
{"title":"Making molecules with photodecarboxylases: A great start or a false dawn?","authors":"Tobias M. Hedison,&nbsp;Derren J. Heyes,&nbsp;Nigel S. Scrutton","doi":"10.1016/j.crchbi.2021.100017","DOIUrl":null,"url":null,"abstract":"<div><p>Photoenzymes are potentially attractive biocatalysts for chemicals synthesis and biomanufacturing. They do not require coenzymes such as NAD(P)H, or high energy molecules like ATP, and their activity can be controlled precisely in a temporal and spatial manner by light. The light-activated fatty acid photodecarboxylase (FAP) was discovered in 2017. Since its discovery, biophysical, structural, and computational methods have been used to understand how FAP uses blue light to catalyze the decarboxylation of fatty acid substrates. As a natural photobiocatalyst, FAP could offer insights into the design of new photoenzymes. Here, we provide a perspective on the structure, mechanism and biotechnological applications of FAP enzymes, and understanding from which new photobiocatalysts could be developed. We review early success in the engineering of FAPs but also identify major challenges for wider use of this recently discovered enzyme family in biotechnology and the chemical sciences. Based on these early insights, the reader is invited to consider if the use of FAPs will continue to flourish, or whether current limitations signify a false dawn.</p></div>","PeriodicalId":72747,"journal":{"name":"Current research in chemical biology","volume":"2 ","pages":"Article 100017"},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2666246921000173/pdfft?md5=453badeca147bd9e4ca22c7c760f6ca5&pid=1-s2.0-S2666246921000173-main.pdf","citationCount":"13","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current research in chemical biology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666246921000173","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 13

Abstract

Photoenzymes are potentially attractive biocatalysts for chemicals synthesis and biomanufacturing. They do not require coenzymes such as NAD(P)H, or high energy molecules like ATP, and their activity can be controlled precisely in a temporal and spatial manner by light. The light-activated fatty acid photodecarboxylase (FAP) was discovered in 2017. Since its discovery, biophysical, structural, and computational methods have been used to understand how FAP uses blue light to catalyze the decarboxylation of fatty acid substrates. As a natural photobiocatalyst, FAP could offer insights into the design of new photoenzymes. Here, we provide a perspective on the structure, mechanism and biotechnological applications of FAP enzymes, and understanding from which new photobiocatalysts could be developed. We review early success in the engineering of FAPs but also identify major challenges for wider use of this recently discovered enzyme family in biotechnology and the chemical sciences. Based on these early insights, the reader is invited to consider if the use of FAPs will continue to flourish, or whether current limitations signify a false dawn.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
用光脱羧酶制造分子:一个伟大的开始还是一个虚假的黎明?
光酶是化学合成和生物制造领域具有潜在吸引力的生物催化剂。它们不需要像NAD(P)H这样的辅酶,也不需要像ATP这样的高能分子,而且它们的活性可以通过光在时间和空间上精确地控制。光活化脂肪酸光脱羧酶(FAP)于2017年被发现。自发现以来,生物物理、结构和计算方法已被用于了解FAP如何利用蓝光催化脂肪酸底物的脱羧。作为一种天然的光生物催化剂,FAP可以为新型光酶的设计提供新的见解。本文就FAP酶的结构、作用机理、生物技术应用等方面进行了综述,并对开发新型光生物催化剂进行了展望。我们回顾了FAPs工程的早期成功,但也确定了在生物技术和化学科学中广泛使用这种最近发现的酶家族的主要挑战。基于这些早期的见解,请读者考虑fap的使用是否会继续蓬勃发展,或者当前的限制是否预示着虚假的曙光。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Current research in chemical biology
Current research in chemical biology Biochemistry, Genetics and Molecular Biology (General)
自引率
0.00%
发文量
0
审稿时长
56 days
期刊最新文献
Contents Covalent chemical probes for protein kinases Comparison of CX-4945 and SGC-CK2-1 as inhibitors of CSNK2 using quantitative phosphoproteomics: Triple SILAC in combination with inhibitor-resistant CSNK2 Methods of the enzymatic production of Ub-based tools Stability engineering of ferulic acid decarboxylase unlocks enhanced aromatic acid decarboxylation
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1