Cargando…

Identification of Pyruvate Dehydrogenase E1 as a Potential Target against Magnaporthe oryzae through Experimental and Theoretical Investigation

Magnaporthe oryzae (M. oryzae) is a typical cause of rice blast in agricultural production. Isobavachalcone (IBC), an active ingredient of Psoralea corylifolia L. extract, is an effective fungicide against rice blast. To determine the mechanism of IBC against M. oryzae, the effect of IBC on the meta...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Yuejuan, Hu, Baichun, Wang, Zhibin, He, Jianhua, Zhang, Yaoliang, Wang, Jian, Guan, Lijie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153330/
https://www.ncbi.nlm.nih.gov/pubmed/34068366
http://dx.doi.org/10.3390/ijms22105163
_version_ 1783698777318621184
author Li, Yuejuan
Hu, Baichun
Wang, Zhibin
He, Jianhua
Zhang, Yaoliang
Wang, Jian
Guan, Lijie
author_facet Li, Yuejuan
Hu, Baichun
Wang, Zhibin
He, Jianhua
Zhang, Yaoliang
Wang, Jian
Guan, Lijie
author_sort Li, Yuejuan
collection PubMed
description Magnaporthe oryzae (M. oryzae) is a typical cause of rice blast in agricultural production. Isobavachalcone (IBC), an active ingredient of Psoralea corylifolia L. extract, is an effective fungicide against rice blast. To determine the mechanism of IBC against M. oryzae, the effect of IBC on the metabolic pathway of M. oryzae was explored by transcriptome profiling. In M. oryzae, the expression of pyruvate dehydrogenase E1 (PDHE1), part of the tricarboxylic acid (TCA cycle), was significantly decreased in response to treatment with IBC, which was verified by qPCR and testing of enzyme activity. To further elucidate the interactions between IBC and PDHE1, the 3D structure model of the PDHE1 from M. oryzae was established based on homology modeling. The model was utilized to analyze the molecular interactions through molecular docking and molecular dynamics simulation, revealing that IBC has π-π stacking interactions with residue TYR139 and undergoes hydrogen bonding with residue ASP217 of PDHE1. Additionally, the nonpolar residues PHE111, MET174, ILE 187, VAL188, and MET250 form strong hydrophobic interactions with IBC. The above results reveal that PDHE1 is a potential target for antifungal agents, which will be of great significance for guiding the design of new fungicides. This research clarified the mechanism of IBC against M. oryzae at the molecular level, which will underpin further studies of the inhibitory mechanism of flavonoids and the discovery of new targets. It also provides theoretical guidance for the field application of IBC.
format Online
Article
Text
id pubmed-8153330
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-81533302021-05-27 Identification of Pyruvate Dehydrogenase E1 as a Potential Target against Magnaporthe oryzae through Experimental and Theoretical Investigation Li, Yuejuan Hu, Baichun Wang, Zhibin He, Jianhua Zhang, Yaoliang Wang, Jian Guan, Lijie Int J Mol Sci Article Magnaporthe oryzae (M. oryzae) is a typical cause of rice blast in agricultural production. Isobavachalcone (IBC), an active ingredient of Psoralea corylifolia L. extract, is an effective fungicide against rice blast. To determine the mechanism of IBC against M. oryzae, the effect of IBC on the metabolic pathway of M. oryzae was explored by transcriptome profiling. In M. oryzae, the expression of pyruvate dehydrogenase E1 (PDHE1), part of the tricarboxylic acid (TCA cycle), was significantly decreased in response to treatment with IBC, which was verified by qPCR and testing of enzyme activity. To further elucidate the interactions between IBC and PDHE1, the 3D structure model of the PDHE1 from M. oryzae was established based on homology modeling. The model was utilized to analyze the molecular interactions through molecular docking and molecular dynamics simulation, revealing that IBC has π-π stacking interactions with residue TYR139 and undergoes hydrogen bonding with residue ASP217 of PDHE1. Additionally, the nonpolar residues PHE111, MET174, ILE 187, VAL188, and MET250 form strong hydrophobic interactions with IBC. The above results reveal that PDHE1 is a potential target for antifungal agents, which will be of great significance for guiding the design of new fungicides. This research clarified the mechanism of IBC against M. oryzae at the molecular level, which will underpin further studies of the inhibitory mechanism of flavonoids and the discovery of new targets. It also provides theoretical guidance for the field application of IBC. MDPI 2021-05-13 /pmc/articles/PMC8153330/ /pubmed/34068366 http://dx.doi.org/10.3390/ijms22105163 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Li, Yuejuan
Hu, Baichun
Wang, Zhibin
He, Jianhua
Zhang, Yaoliang
Wang, Jian
Guan, Lijie
Identification of Pyruvate Dehydrogenase E1 as a Potential Target against Magnaporthe oryzae through Experimental and Theoretical Investigation
title Identification of Pyruvate Dehydrogenase E1 as a Potential Target against Magnaporthe oryzae through Experimental and Theoretical Investigation
title_full Identification of Pyruvate Dehydrogenase E1 as a Potential Target against Magnaporthe oryzae through Experimental and Theoretical Investigation
title_fullStr Identification of Pyruvate Dehydrogenase E1 as a Potential Target against Magnaporthe oryzae through Experimental and Theoretical Investigation
title_full_unstemmed Identification of Pyruvate Dehydrogenase E1 as a Potential Target against Magnaporthe oryzae through Experimental and Theoretical Investigation
title_short Identification of Pyruvate Dehydrogenase E1 as a Potential Target against Magnaporthe oryzae through Experimental and Theoretical Investigation
title_sort identification of pyruvate dehydrogenase e1 as a potential target against magnaporthe oryzae through experimental and theoretical investigation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153330/
https://www.ncbi.nlm.nih.gov/pubmed/34068366
http://dx.doi.org/10.3390/ijms22105163
work_keys_str_mv AT liyuejuan identificationofpyruvatedehydrogenasee1asapotentialtargetagainstmagnaportheoryzaethroughexperimentalandtheoreticalinvestigation
AT hubaichun identificationofpyruvatedehydrogenasee1asapotentialtargetagainstmagnaportheoryzaethroughexperimentalandtheoreticalinvestigation
AT wangzhibin identificationofpyruvatedehydrogenasee1asapotentialtargetagainstmagnaportheoryzaethroughexperimentalandtheoreticalinvestigation
AT hejianhua identificationofpyruvatedehydrogenasee1asapotentialtargetagainstmagnaportheoryzaethroughexperimentalandtheoreticalinvestigation
AT zhangyaoliang identificationofpyruvatedehydrogenasee1asapotentialtargetagainstmagnaportheoryzaethroughexperimentalandtheoreticalinvestigation
AT wangjian identificationofpyruvatedehydrogenasee1asapotentialtargetagainstmagnaportheoryzaethroughexperimentalandtheoreticalinvestigation
AT guanlijie identificationofpyruvatedehydrogenasee1asapotentialtargetagainstmagnaportheoryzaethroughexperimentalandtheoreticalinvestigation