Pseudopterosin Biosynthesis: Unravelling a Decades Old Problem in Animal Specialized Metabolism

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Journal of the American Chemical Society Pub Date : 2025-01-16 DOI:10.1021/jacs.4c09925
Paul D. Scesa, Eric W. Schmidt
{"title":"Pseudopterosin Biosynthesis: Unravelling a Decades Old Problem in Animal Specialized Metabolism","authors":"Paul D. Scesa, Eric W. Schmidt","doi":"10.1021/jacs.4c09925","DOIUrl":null,"url":null,"abstract":"Soft corals are prolific producers of terpenoids, such as pseudopterosins. The exact biosynthetic pathway of these anti-inflammatory diterpene glycosides has eluded the scientific community for decades. Using a forward genetic approach, we have identified, cloned, and expressed the key genes involved in pseudopterosin biosynthesis. We characterized a unique class of multifunctional cytochrome P450 enzymes that catalyze a cascade reaction that produces a nearly mature natural product using a single enzyme. This clarifies the previously proposed biosynthetic pathways to pseudopterosin A and its relatives. The mechanism of the oxidative cascade was probed using in vivo feeding studies in <i>Saccharomyces cerevisiae</i> expressing heterologous coral genes. The cascade produces the pseudopterosin aglycone 7,8-dihydroxyerogorgiaene via elisabethatrienol and its epimer, starting from elisabethatriene. This discovery demonstrates the potential to produce this valuable class of natural products using fermentation.","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":"98 1","pages":""},"PeriodicalIF":14.4000,"publicationDate":"2025-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/jacs.4c09925","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

Soft corals are prolific producers of terpenoids, such as pseudopterosins. The exact biosynthetic pathway of these anti-inflammatory diterpene glycosides has eluded the scientific community for decades. Using a forward genetic approach, we have identified, cloned, and expressed the key genes involved in pseudopterosin biosynthesis. We characterized a unique class of multifunctional cytochrome P450 enzymes that catalyze a cascade reaction that produces a nearly mature natural product using a single enzyme. This clarifies the previously proposed biosynthetic pathways to pseudopterosin A and its relatives. The mechanism of the oxidative cascade was probed using in vivo feeding studies in Saccharomyces cerevisiae expressing heterologous coral genes. The cascade produces the pseudopterosin aglycone 7,8-dihydroxyerogorgiaene via elisabethatrienol and its epimer, starting from elisabethatriene. This discovery demonstrates the potential to produce this valuable class of natural products using fermentation.

Abstract Image

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
伪蝶蛋白生物合成:解开动物特殊代谢的一个几十年的问题
软珊瑚是萜类化合物的多产生产者,例如伪翅皂甙。这些抗炎二萜苷的确切生物合成途径几十年来一直困扰着科学界。利用正向遗传方法,我们已经鉴定、克隆并表达了参与伪蝶蛋白生物合成的关键基因。我们鉴定了一类独特的多功能细胞色素P450酶,该酶催化级联反应,使用单一酶产生接近成熟的天然产物。这澄清了先前提出的伪蝶蛋白A及其亲戚的生物合成途径。通过对表达异源珊瑚基因的酿酒酵母的体内摄食研究,探讨了氧化级联反应的机制。该级联反应从伊丽莎白三烯开始,通过伊丽莎白三烯醇和它的外聚体产生伪蝶苷元7,8-二羟基山茱萸烯。这一发现证明了利用发酵生产这类有价值的天然产品的潜力。
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
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
期刊最新文献
Breaking the Scaling Relationship for Oxygen Reduction Reaction Using Molecular Cobalt Complexes Synthesis of Cationic Cyclic Oligo(disulfide)s via Cyclo-Depolymerization: A Redox-Responsive and Potent Antibacterial Reagent From Bis(borylene)-Substituted Xanthenes as Reactive Intermediates to Diboraoxirane Complexes Achieving Higher Activity of Acidic Oxygen Evolution Reaction Using an Atomically Thin Layer of IrOx over Co3O4 Reconfigured Spin-Flip Process Enables Efficient and Persistent Triplet Excitons in Organic–Inorganic Metal Halides
×
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