Induction of somatic embryogenesis and ectopic proliferation in Tecoma stans (L.) Juss. ex Kunth cell suspension culture

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Rowida Omar, Ivan Kushkevych, Mohamed Abd El-Salam
{"title":"Induction of somatic embryogenesis and ectopic proliferation in Tecoma stans (L.) Juss. ex Kunth cell suspension culture","authors":"Rowida Omar, Ivan Kushkevych, Mohamed Abd El-Salam","doi":"10.1007/s11627-024-10421-4","DOIUrl":null,"url":null,"abstract":"<p>Somatic embryogenesis is a developmental pathway where somatic cells of plants generate embryogenic cells that subsequently mature into somatic embryos under favorable conditions. This process is one of the most important <i>in vitro</i> techniques for plant propagation, with diverse practical implications. In this study, ectopic proliferation and somatic embryos from <i>Tecoma stans</i> (L.) Juss. ex Kunth cell cultures were induced by employing primary conditioning Murashige and Skoog medium supplemented with 1.0 mg L<sup>−1</sup> 2,4-dichlorophenoxyacetic acid. Subsequently, a secondary induction medium supplemented with a combination of 1.0 mg L<sup>−1</sup> 2,4-dichlorophenoxyacetic acid with various concentrations of 6-benzyladenine cytokinin (1 to 5 mg L<sup>−1</sup>) was used to promote embryogenesis. The results revealed the successful formation of pre-embryonic and embryonic stages, including globular, heart, torpedo, and cotyledon stages within a 2-wk incubation period under the specified hormonal conditions, leading to subsequent development into the mature vegetative phase after an additional 4 wk. Significant embryo production (16 ± 2.0 torpedo stage embryos per 50 mL culture media) was observed in Murashige and Skoog medium enriched with 1.0 mg L<sup>−1</sup> 2,4-dichlorophenoxyacetic acid and 2.0 mg L<sup>−1</sup> 6-benzyladenine, surpassing the results observed with other concentrations (<i>p</i>-value &lt; 0.0001). The generated somatic embryos can serve as a potential <i>in vitro</i> tool for the propagation, generation, and organogenesis of <i>T. stans</i>, contributing to its role as both an ornamental and medicinal plant. Moreover, the induction of somatic embryogenesis opens avenues for the potential production of <i>T. stans</i> bioactive secondary metabolites and diverse applications in biotechnology, biotransformation, and biocatalysis, particularly in the conversion of both exogenous and endogenous substrates, such as tecomine—the principal antidiabetic alkaloid in the leaf extract.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s11627-024-10421-4","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0

Abstract

Somatic embryogenesis is a developmental pathway where somatic cells of plants generate embryogenic cells that subsequently mature into somatic embryos under favorable conditions. This process is one of the most important in vitro techniques for plant propagation, with diverse practical implications. In this study, ectopic proliferation and somatic embryos from Tecoma stans (L.) Juss. ex Kunth cell cultures were induced by employing primary conditioning Murashige and Skoog medium supplemented with 1.0 mg L−1 2,4-dichlorophenoxyacetic acid. Subsequently, a secondary induction medium supplemented with a combination of 1.0 mg L−1 2,4-dichlorophenoxyacetic acid with various concentrations of 6-benzyladenine cytokinin (1 to 5 mg L−1) was used to promote embryogenesis. The results revealed the successful formation of pre-embryonic and embryonic stages, including globular, heart, torpedo, and cotyledon stages within a 2-wk incubation period under the specified hormonal conditions, leading to subsequent development into the mature vegetative phase after an additional 4 wk. Significant embryo production (16 ± 2.0 torpedo stage embryos per 50 mL culture media) was observed in Murashige and Skoog medium enriched with 1.0 mg L−1 2,4-dichlorophenoxyacetic acid and 2.0 mg L−1 6-benzyladenine, surpassing the results observed with other concentrations (p-value < 0.0001). The generated somatic embryos can serve as a potential in vitro tool for the propagation, generation, and organogenesis of T. stans, contributing to its role as both an ornamental and medicinal plant. Moreover, the induction of somatic embryogenesis opens avenues for the potential production of T. stans bioactive secondary metabolites and diverse applications in biotechnology, biotransformation, and biocatalysis, particularly in the conversion of both exogenous and endogenous substrates, such as tecomine—the principal antidiabetic alkaloid in the leaf extract.

Abstract Image

在 Tecoma stans (L.) Juss. ex Kunth 细胞悬浮培养中诱导体细胞胚胎发生和异位增殖
体细胞胚胎发生是植物体细胞产生胚胎细胞的一种发育途径,胚胎细胞随后在有利条件下成熟为体细胞胚胎。这一过程是最重要的植物体外繁殖技术之一,具有多种实际意义。在本研究中,通过使用添加了 1.0 mg L-1 2,4-dichlorophenoxyacetic acid 的 Murashige 和 Skoog 一级调节培养基,诱导了 Tecoma stans (L.) Juss.随后,使用添加了 1.0 mg L-1 2,4-dichlorophenoxyacetic acid 和不同浓度 6-benzyladenine 细胞分裂素(1 至 5 mg L-1)的二级诱导培养基来促进胚胎发生。结果表明,在特定的激素条件下,胚胎前期和胚胎期(包括球茎期、心茎期、鱼雷期和子叶期)在 2 周的培养期内成功形成,随后经过 4 周的培养进入成熟的无性期。在富含 1.0 mg L-1 2,4-dichlorophenoxyacetic acid 和 2.0 mg L-1 6-benzyladenine 的 Murashige 和 Skoog 培养基中观察到了显著的胚胎生成(每 50 mL 培养基中有 16 ± 2.0 个鱼雷期胚胎),超过了在其他浓度下观察到的结果(p 值为 0.0001)。所生成的体细胞胚胎可作为一种潜在的体外工具,用于斯坦氏菌的繁殖、生成和器官形成,从而促进其作为观赏植物和药用植物的作用。此外,体细胞胚胎发生的诱导为 T. stans 生物活性次生代谢物的潜在生产以及在生物技术、生物转化和生物催化方面的多样化应用开辟了途径,特别是在外源性和内源性底物的转化方面,如叶提取物中的主要抗糖尿病生物碱 tecomine。
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 求助全文
来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信