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Phenazine-1-Carboxylic Acid (PCA), Produced for the First Time as an Antifungal Metabolite by Truncatella angustata, a Causal Agent of Grapevine Trunk Diseases (GTDs) in Iran

[Image: see text] The phytopathogenic fungus Truncatella angustata, associated with grapevine trunk diseases (GTDs) in Iran, produces the well-known secondary metabolite isocoumumarin (+)-6-hyroxyramulosin and surprisingly also phenazine-1-carboxylic acid (PCA). PCA, identified by spectroscopic (ess...

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Autores principales: Cimmino, Alessio, Bahmani, Zeinab, Castaldi, Stefany, Masi, Marco, Isticato, Rachele, Abdollahzadeh, Jafar, Amini, Jahanshir, Evidente, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8532150/
https://www.ncbi.nlm.nih.gov/pubmed/34623150
http://dx.doi.org/10.1021/acs.jafc.1c03877
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author Cimmino, Alessio
Bahmani, Zeinab
Castaldi, Stefany
Masi, Marco
Isticato, Rachele
Abdollahzadeh, Jafar
Amini, Jahanshir
Evidente, Antonio
author_facet Cimmino, Alessio
Bahmani, Zeinab
Castaldi, Stefany
Masi, Marco
Isticato, Rachele
Abdollahzadeh, Jafar
Amini, Jahanshir
Evidente, Antonio
author_sort Cimmino, Alessio
collection PubMed
description [Image: see text] The phytopathogenic fungus Truncatella angustata, associated with grapevine trunk diseases (GTDs) in Iran, produces the well-known secondary metabolite isocoumumarin (+)-6-hyroxyramulosin and surprisingly also phenazine-1-carboxylic acid (PCA). PCA, identified by spectroscopic (essentially (1)H NMR and ESI MS) spectra, is a bacterial metabolite well known for its antifungal activity and was found for the first time in T. angustata culture filtrates. The antifungal activity of PCA was assayed against four different fungi responsible for GTDs, Phaeoacremonium minimum, Phaeoacremonium italicum, Fomitiporia mediterranea, involved in grapevine esca disease, and Neofusicoccum parvum, responsible for Botryosphaeria dieback. The activity was compared with that of the known commercial fungicide, pentachloronitrobenzene, and the close phenazine. PCA and phenazine exhibited strong antifungal activity against all phytopathogenic fungi, inhibiting the fungal growth by about 90–100% and 80–100%, respectively. These results suggested that T. angustata could use PCA to compete with other phytopathogenic fungi that attack grapevine and thus PCA could be proposed as a biofungicide against the fungi responsible for grapevine esca and Botryosphaeria dieback diseases.
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spelling pubmed-85321502021-10-22 Phenazine-1-Carboxylic Acid (PCA), Produced for the First Time as an Antifungal Metabolite by Truncatella angustata, a Causal Agent of Grapevine Trunk Diseases (GTDs) in Iran Cimmino, Alessio Bahmani, Zeinab Castaldi, Stefany Masi, Marco Isticato, Rachele Abdollahzadeh, Jafar Amini, Jahanshir Evidente, Antonio J Agric Food Chem [Image: see text] The phytopathogenic fungus Truncatella angustata, associated with grapevine trunk diseases (GTDs) in Iran, produces the well-known secondary metabolite isocoumumarin (+)-6-hyroxyramulosin and surprisingly also phenazine-1-carboxylic acid (PCA). PCA, identified by spectroscopic (essentially (1)H NMR and ESI MS) spectra, is a bacterial metabolite well known for its antifungal activity and was found for the first time in T. angustata culture filtrates. The antifungal activity of PCA was assayed against four different fungi responsible for GTDs, Phaeoacremonium minimum, Phaeoacremonium italicum, Fomitiporia mediterranea, involved in grapevine esca disease, and Neofusicoccum parvum, responsible for Botryosphaeria dieback. The activity was compared with that of the known commercial fungicide, pentachloronitrobenzene, and the close phenazine. PCA and phenazine exhibited strong antifungal activity against all phytopathogenic fungi, inhibiting the fungal growth by about 90–100% and 80–100%, respectively. These results suggested that T. angustata could use PCA to compete with other phytopathogenic fungi that attack grapevine and thus PCA could be proposed as a biofungicide against the fungi responsible for grapevine esca and Botryosphaeria dieback diseases. American Chemical Society 2021-10-08 2021-10-20 /pmc/articles/PMC8532150/ /pubmed/34623150 http://dx.doi.org/10.1021/acs.jafc.1c03877 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Cimmino, Alessio
Bahmani, Zeinab
Castaldi, Stefany
Masi, Marco
Isticato, Rachele
Abdollahzadeh, Jafar
Amini, Jahanshir
Evidente, Antonio
Phenazine-1-Carboxylic Acid (PCA), Produced for the First Time as an Antifungal Metabolite by Truncatella angustata, a Causal Agent of Grapevine Trunk Diseases (GTDs) in Iran
title Phenazine-1-Carboxylic Acid (PCA), Produced for the First Time as an Antifungal Metabolite by Truncatella angustata, a Causal Agent of Grapevine Trunk Diseases (GTDs) in Iran
title_full Phenazine-1-Carboxylic Acid (PCA), Produced for the First Time as an Antifungal Metabolite by Truncatella angustata, a Causal Agent of Grapevine Trunk Diseases (GTDs) in Iran
title_fullStr Phenazine-1-Carboxylic Acid (PCA), Produced for the First Time as an Antifungal Metabolite by Truncatella angustata, a Causal Agent of Grapevine Trunk Diseases (GTDs) in Iran
title_full_unstemmed Phenazine-1-Carboxylic Acid (PCA), Produced for the First Time as an Antifungal Metabolite by Truncatella angustata, a Causal Agent of Grapevine Trunk Diseases (GTDs) in Iran
title_short Phenazine-1-Carboxylic Acid (PCA), Produced for the First Time as an Antifungal Metabolite by Truncatella angustata, a Causal Agent of Grapevine Trunk Diseases (GTDs) in Iran
title_sort phenazine-1-carboxylic acid (pca), produced for the first time as an antifungal metabolite by truncatella angustata, a causal agent of grapevine trunk diseases (gtds) in iran
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8532150/
https://www.ncbi.nlm.nih.gov/pubmed/34623150
http://dx.doi.org/10.1021/acs.jafc.1c03877
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