Related Experiment Video
Updated: May 6, 2026

Transient Expression in Nicotiana Benthamiana Leaves for Triterpene Production at a Preparative Scale
Published on: August 16, 2018
Thiophene interconversion in elicitor-treated roots ofTagetes patula L
R R Arroo1, A P De Brouwer, A F Croes
1Department of Experimental Botany, NOVAPLANT Cell Biotechnology Group, University Toernooiveld, NL-6525 ED, Nijmegen, The Netherlands.
Fungal extracts trigger thiophene production in Tagetes plants, which then inhibit fungal growth. These thiophenes may act as a defense mechanism against pathogens.
Area of Science:
- Plant biochemistry
- Mycology
- Chemical ecology
Background:
- Thiophenes are heterocyclic metabolites related to polyacetylenes.
- Some thiophenes exhibit phototoxicity, but their role in planta is often limited by light exposure.
- Bithiophenes in Tagetes primarily accumulate in roots, where light is absent.
Purpose of the Study:
- To investigate the induction of thiophene biosynthesis in Tagetes patula.
- To determine the role of fungal elicitors in thiophene production.
- To assess the potential role of thiophenes in plant defense against fungal pathogens.
Main Methods:
- Utilized cell-free extracts from Fusarium oxysporum as an elicitor.
- Applied extracts to root cultures and intact seedlings of Tagetes patula.
- Analyzed the biosynthesis and excretion of thiophenes.
- Assayed fungal growth inhibition by excreted thiophenes in vitro.
Main Results:
- Fusarium oxysporum extract successfully induced the biosynthesis of hydrophilic thiophenes in Tagetes patula.
- Newly synthesized thiophenes were partially excreted into the culture medium.
- Excreted thiophenes demonstrated significant inhibition of fungal growth, even in the absence of light.
Conclusions:
- Fusarium oxysporum can stimulate thiophene production in Tagetes.
- Thiophenes produced by Tagetes may function as a non-phototoxic defense compound against fungal pathogens.
- This suggests a role for thiophenes in the biochemical defense strategy of plants.
More Related Videos
08:12Inducing Hairy Roots by Agrobacterium rhizogenes-Mediated Transformation in Tartary Buckwheat Fagopyrum tataricum
Published on: March 11, 2020
05:19Evaluation of Antioxidant and Anthelmintic Properties of Tithonia diversifolia Extracts Against Gastrointestinal Nematode Eggs Using In Vitro Assays
Published on: August 1, 2025
Related Concept Videos
Thermal and Photochemical Electrocyclic Reactions: Overview
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.