Independent evolution of plant natural products: Formation of benzoxazinoids in Consolida orientalis (Ranunculaceae).

IF 4 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Biological Chemistry Pub Date : 2025-01-01 Epub Date: 2024-11-26 DOI:10.1016/j.jbc.2024.108019
Matilde Florean, Hedwig Schultz, Jens Wurlitzer, Sarah E O'Connor, Tobias G Köllner
{"title":"Independent evolution of plant natural products: Formation of benzoxazinoids in Consolida orientalis (Ranunculaceae).","authors":"Matilde Florean, Hedwig Schultz, Jens Wurlitzer, Sarah E O'Connor, Tobias G Köllner","doi":"10.1016/j.jbc.2024.108019","DOIUrl":null,"url":null,"abstract":"<p><p>Benzoxazinoids (BXDs) are important defense compounds produced by a number of species from different, evolutionarily unrelated plant families. While BXD biosynthesis has been extensively studied in the grasses (monocots) and core eudicots, the mechanism of BXD synthesis in the basal eudicots is still unclear. We used an integrated metabolomics and transcriptomics approach to elucidate the BXD pathway in Consolida orientalis, a Ranunculaceae species known to produce the BXD DIBOA-Glc. Overexpression of candidate genes in Nicotiana benthamiana identified a flavin-dependent monooxygenase (CoBX2-3) and two cytochrome P450 enzymes (CoBX4 and CoBX5) that catalyze the oxidation steps that transform indole into DIBOA. Co-expression of CoBx2-3, CoBx4, and CoBx5 with the previously described indole synthase gene CoBx1 and the UDP-glucosyltransferase gene CoBx8 in N. benthamiana resulted in the reconstitution of a fully active BXD pathway. The fact that CoBX2-3, CoBX4, and CoBX5 are not phylogenetically related to their counterparts in the grasses and core eudicots suggests independent evolution of benzoxazinoid biosynthesis in these three angiosperm lineages.</p>","PeriodicalId":15140,"journal":{"name":"Journal of Biological Chemistry","volume":" ","pages":"108019"},"PeriodicalIF":4.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11742589/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Biological Chemistry","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.jbc.2024.108019","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/26 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Benzoxazinoids (BXDs) are important defense compounds produced by a number of species from different, evolutionarily unrelated plant families. While BXD biosynthesis has been extensively studied in the grasses (monocots) and core eudicots, the mechanism of BXD synthesis in the basal eudicots is still unclear. We used an integrated metabolomics and transcriptomics approach to elucidate the BXD pathway in Consolida orientalis, a Ranunculaceae species known to produce the BXD DIBOA-Glc. Overexpression of candidate genes in Nicotiana benthamiana identified a flavin-dependent monooxygenase (CoBX2-3) and two cytochrome P450 enzymes (CoBX4 and CoBX5) that catalyze the oxidation steps that transform indole into DIBOA. Co-expression of CoBx2-3, CoBx4, and CoBx5 with the previously described indole synthase gene CoBx1 and the UDP-glucosyltransferase gene CoBx8 in N. benthamiana resulted in the reconstitution of a fully active BXD pathway. The fact that CoBX2-3, CoBX4, and CoBX5 are not phylogenetically related to their counterparts in the grasses and core eudicots suggests independent evolution of benzoxazinoid biosynthesis in these three angiosperm lineages.

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
植物天然产物的独立进化:毛茛科植物中苯并恶嗪类化合物的形成。
苯并恶嗪类化合物(BXDs)是一种重要的防御化合物,由来自不同的、进化上不相关的植物科的许多物种产生。虽然BXD在禾本科(单子叶)和核心花序中的生物合成已经得到了广泛的研究,但BXD在基部花序中的合成机制尚不清楚。我们使用综合代谢组学和转录组学方法来阐明毛茛科植物东方固结菌(Consolida orientalis)的BXD途径,该物种已知可产生BXD DIBOA-Glc。benthamiana中候选基因的过表达鉴定出一种黄素依赖性单加氧酶(CoBX2-3)和两种细胞色素P450酶(CoBX4和CoBX5),它们催化将吲哚转化为DIBOA的氧化步骤。在N. benthamiana中,CoBx2-3、CoBx4和CoBx5与先前描述的吲哚合成酶基因CoBx1和udp -葡萄糖基转移酶基因CoBx8共表达导致BXD通路的完全活性重建。cox2 -3、cox4和cox5与禾本科和核心菊科植物中的cox2 -3、cox4和cox5在系统发育上没有亲缘关系,这表明这三个被子植物谱系的苯并恶嗪类生物合成是独立进化的。
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
Journal of Biological Chemistry
Journal of Biological Chemistry Biochemistry, Genetics and Molecular Biology-Biochemistry
自引率
4.20%
发文量
1233
期刊介绍: The Journal of Biological Chemistry welcomes high-quality science that seeks to elucidate the molecular and cellular basis of biological processes. Papers published in JBC can therefore fall under the umbrellas of not only biological chemistry, chemical biology, or biochemistry, but also allied disciplines such as biophysics, systems biology, RNA biology, immunology, microbiology, neurobiology, epigenetics, computational biology, ’omics, and many more. The outcome of our focus on papers that contribute novel and important mechanistic insights, rather than on a particular topic area, is that JBC is truly a melting pot for scientists across disciplines. In addition, JBC welcomes papers that describe methods that will help scientists push their biochemical inquiries forward and resources that will be of use to the research community.
期刊最新文献
G protein regulatory network shapes magnitude and kinetics of behavioral responses in an engineered opioid receptor model. Endothelin-1 induces Zfp36 family RNA binding proteins and restrains cytokine and chemokine production in reactive astrocytes. PIEZO1 variants that reduce open channel probability are associated with familial osteoarthritis. Molecular mechanisms of immune evasion by host protein glycosylation of a bacterial immunogen used in nucleic acid vaccines. Prolyl-3-hydroxylase 1 is a central regulator of collagen post-translational modifications and the collagen biosynthetic network.
×
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:604180095
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