Unveiling the role of vermicompost in modulating phenylpropanoid metabolism in basil (Ocimum basilicum L.): A single-cell type PGT approach

IF 5.4 Q1 PLANT SCIENCES Current Plant Biology Pub Date : 2024-03-05 DOI:10.1016/j.cpb.2024.100335
İlker TÜRKAY , Lokman ÖZTÜRK , Fevziye Şüheda HEPŞEN TÜRKAY
{"title":"Unveiling the role of vermicompost in modulating phenylpropanoid metabolism in basil (Ocimum basilicum L.): A single-cell type PGT approach","authors":"İlker TÜRKAY ,&nbsp;Lokman ÖZTÜRK ,&nbsp;Fevziye Şüheda HEPŞEN TÜRKAY","doi":"10.1016/j.cpb.2024.100335","DOIUrl":null,"url":null,"abstract":"<div><p>This research delves into phenylpropanoid metabolism, focusing on phenylpropene biosynthesis in the methyleugenol chemotype of basil (<em>Ocimum basilicum</em> L.). We isolated peltate glandular trichomes (PGTs) from basil leaves to eliminate primary metabolic influences, offering a unique perspective into these complex processes. Vermicompost, chosen for its eco-friendly composition and superiority in invigorating phenylpropanoid metabolism. In this study, we investigated the impacts of solid and tea-form vermicompost applications at 0%, 10%, and 25% doses on the methyleugenol chemotype of basil, focusing on the expression levels of <em>PAL</em>, <em>4CL</em>, <em>EGS</em>, <em>EOMT</em>, and <em>CVOMT</em> genes and phenylpropene accumulation in the peltate glandular trichomes. Results showed that 10% solid vermicompost (SV) application increased <em>4CL</em> expression level at 236%, while 25% SV application further enhanced <em>EOMT</em> and <em>CVOMT</em> expressions to towering values by 7,494-fold and 19,643-fold, respectively. SV applications did not significantly impact eugenol accumulation but suppressed chavicol biosynthesis. Methyleugenol and methylchavicol accumulation rose in a dose-dependent manner, with significant increases observed in the 25% SV application. A positive correlation was found between <em>CVOMT</em> expression and accumulation rates of methyleugenol and methylchavicol phenylpropenes following SV applications. Conversely, vermicompost tea (VT) applications led to mixed gene expression patterns and reduced eugenol and methyleugenol ratios in peltate glandular trichomes compared to control. In summary, the notably high gene expressions observed in the results of our preliminary study offer a new perspective in the field of phenylpropanoid metabolism. This underscores the value of utilizing single-cell type PGTs for examining secondary metabolic pathways in plants and demonstrates the impact of vermicompost on phenylpropene production.</p></div>","PeriodicalId":38090,"journal":{"name":"Current Plant Biology","volume":"38 ","pages":"Article 100335"},"PeriodicalIF":5.4000,"publicationDate":"2024-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214662824000173/pdfft?md5=2175869e5669cd725e0be3af99d9f749&pid=1-s2.0-S2214662824000173-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Plant Biology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2214662824000173","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

This research delves into phenylpropanoid metabolism, focusing on phenylpropene biosynthesis in the methyleugenol chemotype of basil (Ocimum basilicum L.). We isolated peltate glandular trichomes (PGTs) from basil leaves to eliminate primary metabolic influences, offering a unique perspective into these complex processes. Vermicompost, chosen for its eco-friendly composition and superiority in invigorating phenylpropanoid metabolism. In this study, we investigated the impacts of solid and tea-form vermicompost applications at 0%, 10%, and 25% doses on the methyleugenol chemotype of basil, focusing on the expression levels of PAL, 4CL, EGS, EOMT, and CVOMT genes and phenylpropene accumulation in the peltate glandular trichomes. Results showed that 10% solid vermicompost (SV) application increased 4CL expression level at 236%, while 25% SV application further enhanced EOMT and CVOMT expressions to towering values by 7,494-fold and 19,643-fold, respectively. SV applications did not significantly impact eugenol accumulation but suppressed chavicol biosynthesis. Methyleugenol and methylchavicol accumulation rose in a dose-dependent manner, with significant increases observed in the 25% SV application. A positive correlation was found between CVOMT expression and accumulation rates of methyleugenol and methylchavicol phenylpropenes following SV applications. Conversely, vermicompost tea (VT) applications led to mixed gene expression patterns and reduced eugenol and methyleugenol ratios in peltate glandular trichomes compared to control. In summary, the notably high gene expressions observed in the results of our preliminary study offer a new perspective in the field of phenylpropanoid metabolism. This underscores the value of utilizing single-cell type PGTs for examining secondary metabolic pathways in plants and demonstrates the impact of vermicompost on phenylpropene production.

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
揭示蛭石在调节罗勒(Ocimum basilicum L.)苯丙类代谢中的作用:单细胞型 PGT 方法
本研究深入研究了苯丙类化合物的代谢,重点是罗勒(Ocimum basilicum L.)甲基丁香酚化学型中的苯丙烯生物合成。我们从罗勒叶片中分离出盾状腺毛体(PGTs),以消除主要代谢影响因素,为这些复杂过程提供了一个独特的视角。蛭石堆肥因其环保成分和在促进苯丙类代谢方面的优越性而被选用。在这项研究中,我们研究了固体和茶状蛭石堆肥在 0%、10% 和 25% 的剂量下对罗勒甲基丁香酚化学型的影响,重点研究了 PAL、4CL、EGS、EOMT 和 CVOMT 基因的表达水平以及盾状腺毛中苯丙烯的积累。结果表明,施用 10%的固体蛭石堆肥(SV)可使 4CL 的表达水平提高 236%,而施用 25% 的 SV 可使 EOMT 和 CVOMT 的表达水平进一步提高,分别提高了 7494 倍和 19643 倍。施用 SV 对丁香酚的积累没有明显影响,但抑制了辣椒素的生物合成。甲基丁香酚和甲基黄烷醇的积累以剂量依赖的方式上升,在施用 25% SV 的情况下观察到显著增加。施用 SV 后,发现 CVOMT 的表达与甲基丁香酚和甲基泽泻醇苯丙烯的积累率呈正相关。相反,与对照组相比,施用蛭石茶(VT)会导致混合基因表达模式以及盾状腺毛中丁香酚和甲基丁香酚比率的降低。总之,在我们的初步研究结果中观察到的明显的高基因表达为苯丙类代谢领域提供了一个新的视角。这凸显了利用单细胞型 PGTs 研究植物次生代谢途径的价值,并证明了蛭霉对苯丙烯生产的影响。
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 Plant Biology
Current Plant Biology Agricultural and Biological Sciences-Plant Science
CiteScore
10.90
自引率
1.90%
发文量
32
审稿时长
50 days
期刊介绍: Current Plant Biology aims to acknowledge and encourage interdisciplinary research in fundamental plant sciences with scope to address crop improvement, biodiversity, nutrition and human health. It publishes review articles, original research papers, method papers and short articles in plant research fields, such as systems biology, cell biology, genetics, epigenetics, mathematical modeling, signal transduction, plant-microbe interactions, synthetic biology, developmental biology, biochemistry, molecular biology, physiology, biotechnologies, bioinformatics and plant genomic resources.
期刊最新文献
Sulfur redirects carbon metabolism to optimize nitrogen utilization and promote andrographolide biosynthesis in Andrographis paniculata seedlings Advancing sustainability: The impact of emerging technologies in agriculture Rock dust-based potting media enhances agronomic performance and nutritional quality of horticultural crops Probing marine macroalgal phlorotannins as an antibacterial candidate against Salmonella typhi: Molecular docking and dynamics simulation approach Integrated transcriptomic and metabolomic analysis reveals the effects of forchlorfenuron and thidiazuron on flavonoid biosynthesis in table grape skins
×
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