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Interactions Between Natural Herbicides and Lipid Bilayers Mimicking the Plant Plasma Membrane

Natural phytotoxic compounds could become an alternative to traditional herbicides in the framework of sustainable agriculture. Nonanoic acid, sarmentine and sorgoleone are such molecules extracted from plants and able to inhibit the growth of various plant species. However, their mode of action is...

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Autores principales: Lebecque, Simon, Lins, Laurence, Dayan, Franck E., Fauconnier, Marie-Laure, Deleu, Magali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6431664/
https://www.ncbi.nlm.nih.gov/pubmed/30936889
http://dx.doi.org/10.3389/fpls.2019.00329
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author Lebecque, Simon
Lins, Laurence
Dayan, Franck E.
Fauconnier, Marie-Laure
Deleu, Magali
author_facet Lebecque, Simon
Lins, Laurence
Dayan, Franck E.
Fauconnier, Marie-Laure
Deleu, Magali
author_sort Lebecque, Simon
collection PubMed
description Natural phytotoxic compounds could become an alternative to traditional herbicides in the framework of sustainable agriculture. Nonanoic acid, sarmentine and sorgoleone are such molecules extracted from plants and able to inhibit the growth of various plant species. However, their mode of action is not fully understood and despite clues indicating that they could affect the plant plasma membrane, molecular details of such phenomenon are lacking. In this paper, we investigate the interactions between those natural herbicides and artificial bilayers mimicking the plant plasma membrane. First, their ability to affect lipid order and fluidity is evaluated by means of fluorescence measurements. It appears that sorgoleone has a clear ordering effect on lipid bilayers, while nonanoic acid and sarmentine induce no or little change to these parameters. Then, a thermodynamic characterization of interactions of each compound with lipid vesicles is obtained with isothermal titration calorimetry, and their respective affinity for bilayers is found to be ranked as follows: sorgoleone > sarmentine > nonanoic acid. Finally, molecular dynamics simulations give molecular details about the location of each compound within a lipid bilayer and confirm the rigidifying effect of sorgoleone. Data also suggest that mismatch in alkyl chain length between nonanoic acid or sarmentine and lipid hydrophobic tails could be responsible for bilayer destabilization. Results are discussed regarding their implications for the phytotoxicity of these compounds.
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spelling pubmed-64316642019-04-01 Interactions Between Natural Herbicides and Lipid Bilayers Mimicking the Plant Plasma Membrane Lebecque, Simon Lins, Laurence Dayan, Franck E. Fauconnier, Marie-Laure Deleu, Magali Front Plant Sci Plant Science Natural phytotoxic compounds could become an alternative to traditional herbicides in the framework of sustainable agriculture. Nonanoic acid, sarmentine and sorgoleone are such molecules extracted from plants and able to inhibit the growth of various plant species. However, their mode of action is not fully understood and despite clues indicating that they could affect the plant plasma membrane, molecular details of such phenomenon are lacking. In this paper, we investigate the interactions between those natural herbicides and artificial bilayers mimicking the plant plasma membrane. First, their ability to affect lipid order and fluidity is evaluated by means of fluorescence measurements. It appears that sorgoleone has a clear ordering effect on lipid bilayers, while nonanoic acid and sarmentine induce no or little change to these parameters. Then, a thermodynamic characterization of interactions of each compound with lipid vesicles is obtained with isothermal titration calorimetry, and their respective affinity for bilayers is found to be ranked as follows: sorgoleone > sarmentine > nonanoic acid. Finally, molecular dynamics simulations give molecular details about the location of each compound within a lipid bilayer and confirm the rigidifying effect of sorgoleone. Data also suggest that mismatch in alkyl chain length between nonanoic acid or sarmentine and lipid hydrophobic tails could be responsible for bilayer destabilization. Results are discussed regarding their implications for the phytotoxicity of these compounds. Frontiers Media S.A. 2019-03-18 /pmc/articles/PMC6431664/ /pubmed/30936889 http://dx.doi.org/10.3389/fpls.2019.00329 Text en Copyright © 2019 Lebecque, Lins, Dayan, Fauconnier and Deleu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Lebecque, Simon
Lins, Laurence
Dayan, Franck E.
Fauconnier, Marie-Laure
Deleu, Magali
Interactions Between Natural Herbicides and Lipid Bilayers Mimicking the Plant Plasma Membrane
title Interactions Between Natural Herbicides and Lipid Bilayers Mimicking the Plant Plasma Membrane
title_full Interactions Between Natural Herbicides and Lipid Bilayers Mimicking the Plant Plasma Membrane
title_fullStr Interactions Between Natural Herbicides and Lipid Bilayers Mimicking the Plant Plasma Membrane
title_full_unstemmed Interactions Between Natural Herbicides and Lipid Bilayers Mimicking the Plant Plasma Membrane
title_short Interactions Between Natural Herbicides and Lipid Bilayers Mimicking the Plant Plasma Membrane
title_sort interactions between natural herbicides and lipid bilayers mimicking the plant plasma membrane
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6431664/
https://www.ncbi.nlm.nih.gov/pubmed/30936889
http://dx.doi.org/10.3389/fpls.2019.00329
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