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A novel nanoparticle loaded with methyl caffeate and caffeic acid phenethyl ester against Ralstonia solanacearum—a plant pathogenic bacteria

Developing a novel agent and understanding the interaction model between multipolymer nanoparticles and bacteria could be worthwhile to induce the protection of crops with the prevalence of frequent hazards because of the use of pesticides and chemical resistance. Unlike metal nanoparticles, multipo...

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Autores principales: Wang, Jin-Zheng, Yan, Cheng-Hai, Zhang, Xiao-Rui, Tu, Qing-Bo, Xu, Yan, Sheng, Sheng, Wu, Fu-An, Wang, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049244/
https://www.ncbi.nlm.nih.gov/pubmed/35492651
http://dx.doi.org/10.1039/c9ra09441e
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author Wang, Jin-Zheng
Yan, Cheng-Hai
Zhang, Xiao-Rui
Tu, Qing-Bo
Xu, Yan
Sheng, Sheng
Wu, Fu-An
Wang, Jun
author_facet Wang, Jin-Zheng
Yan, Cheng-Hai
Zhang, Xiao-Rui
Tu, Qing-Bo
Xu, Yan
Sheng, Sheng
Wu, Fu-An
Wang, Jun
author_sort Wang, Jin-Zheng
collection PubMed
description Developing a novel agent and understanding the interaction model between multipolymer nanoparticles and bacteria could be worthwhile to induce the protection of crops with the prevalence of frequent hazards because of the use of pesticides and chemical resistance. Unlike metal nanoparticles, multipolymer nanoparticles have bacteriostatic properties against Ralstonia solanacearum that can trigger bacterial wilt by infecting the plant. Therefore, a novel poly(lactic-co-glycolic acid) nanoparticle containing caffeic acid phenethyl ester (CAPE) and methyl caffeate (MC) was prepared with the sustained-release property (for 10 d at pH 6.5); here, 50% of the cumulative release rate was achieved. It was observed that the cytomembrane of R. solanacearum was jeopardized by the nanoparticle by the creation of large holes on the bacterial surface. The nanoparticle has an approximate EC(50) value of 0.285 mg mL(−1) with active pharmaceutical ingredients (APIs), while the drug dosage could be reduced by 2/3. Furthermore, to reveal the possible mechanism of interaction between the multipolymer nanoparticles and bacteria, a formidable inhibition effect was observed; the pathogenicity-related genes, namely, phcA, phcB, pehC, egl, pilT, and polA, of R. solanacearum were downregulated by 1/2, 1/42, 1/13, 1/6, 1/2, and 1/8, respectively, showing significant effects on the major virulence-related genes. Hence, a novel nanoparticle with excellent antibacterial and sustained-release properties has been prepared, possessing the potential to replace chemical pesticides and serve as a new control strategy for mulberry blight disease.
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spelling pubmed-90492442022-04-29 A novel nanoparticle loaded with methyl caffeate and caffeic acid phenethyl ester against Ralstonia solanacearum—a plant pathogenic bacteria Wang, Jin-Zheng Yan, Cheng-Hai Zhang, Xiao-Rui Tu, Qing-Bo Xu, Yan Sheng, Sheng Wu, Fu-An Wang, Jun RSC Adv Chemistry Developing a novel agent and understanding the interaction model between multipolymer nanoparticles and bacteria could be worthwhile to induce the protection of crops with the prevalence of frequent hazards because of the use of pesticides and chemical resistance. Unlike metal nanoparticles, multipolymer nanoparticles have bacteriostatic properties against Ralstonia solanacearum that can trigger bacterial wilt by infecting the plant. Therefore, a novel poly(lactic-co-glycolic acid) nanoparticle containing caffeic acid phenethyl ester (CAPE) and methyl caffeate (MC) was prepared with the sustained-release property (for 10 d at pH 6.5); here, 50% of the cumulative release rate was achieved. It was observed that the cytomembrane of R. solanacearum was jeopardized by the nanoparticle by the creation of large holes on the bacterial surface. The nanoparticle has an approximate EC(50) value of 0.285 mg mL(−1) with active pharmaceutical ingredients (APIs), while the drug dosage could be reduced by 2/3. Furthermore, to reveal the possible mechanism of interaction between the multipolymer nanoparticles and bacteria, a formidable inhibition effect was observed; the pathogenicity-related genes, namely, phcA, phcB, pehC, egl, pilT, and polA, of R. solanacearum were downregulated by 1/2, 1/42, 1/13, 1/6, 1/2, and 1/8, respectively, showing significant effects on the major virulence-related genes. Hence, a novel nanoparticle with excellent antibacterial and sustained-release properties has been prepared, possessing the potential to replace chemical pesticides and serve as a new control strategy for mulberry blight disease. The Royal Society of Chemistry 2020-01-23 /pmc/articles/PMC9049244/ /pubmed/35492651 http://dx.doi.org/10.1039/c9ra09441e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Wang, Jin-Zheng
Yan, Cheng-Hai
Zhang, Xiao-Rui
Tu, Qing-Bo
Xu, Yan
Sheng, Sheng
Wu, Fu-An
Wang, Jun
A novel nanoparticle loaded with methyl caffeate and caffeic acid phenethyl ester against Ralstonia solanacearum—a plant pathogenic bacteria
title A novel nanoparticle loaded with methyl caffeate and caffeic acid phenethyl ester against Ralstonia solanacearum—a plant pathogenic bacteria
title_full A novel nanoparticle loaded with methyl caffeate and caffeic acid phenethyl ester against Ralstonia solanacearum—a plant pathogenic bacteria
title_fullStr A novel nanoparticle loaded with methyl caffeate and caffeic acid phenethyl ester against Ralstonia solanacearum—a plant pathogenic bacteria
title_full_unstemmed A novel nanoparticle loaded with methyl caffeate and caffeic acid phenethyl ester against Ralstonia solanacearum—a plant pathogenic bacteria
title_short A novel nanoparticle loaded with methyl caffeate and caffeic acid phenethyl ester against Ralstonia solanacearum—a plant pathogenic bacteria
title_sort novel nanoparticle loaded with methyl caffeate and caffeic acid phenethyl ester against ralstonia solanacearum—a plant pathogenic bacteria
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049244/
https://www.ncbi.nlm.nih.gov/pubmed/35492651
http://dx.doi.org/10.1039/c9ra09441e
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