Comprehensive Structural and Functional Characterization of a Seed γ-thionin as a Potent Bioactive Molecule Against Fungal Pathogens and Insect Pests.


Journal

Current medicinal chemistry
ISSN: 1875-533X
Titre abrégé: Curr Med Chem
Pays: United Arab Emirates
ID NLM: 9440157

Informations de publication

Date de publication:
2022
Historique:
received: 11 11 2021
revised: 28 04 2022
accepted: 05 05 2022
pubmed: 10 6 2022
medline: 27 10 2022
entrez: 9 6 2022
Statut: ppublish

Résumé

Fungi and insect pests ruin stored crop grain, which results in millions of dollars of damage, presenting an ongoing challenge for farmers in addition to diminishing the safety of stored food. A wide-range defensive system against pathogens is needed to reduce or even eliminate the dependence of the crop yield upon the use of pesticides. Plant defensins (γ-thionins) are antimicrobial peptides (AMPs) that are a component of the host defense system. They are known to interact with cell membranes to exhibit antifungal and insecticidal activity. They exhibit a broad range of activities against fungi and insects and are effective at low concentrations. Thionins act on membranes, greatly reducing the development of pathogen resistance. The aim of this study is to investigate a bioactive molecule that acts against fungal pathogens and stored grain insect pests. γ-thionin protein was extracted from Brassica oleracea L. var. capitata f. alba (white cabbage) seed powder in phosphate buffer (100 mM, pH 7.0) and was identified by MALDI-TOF/TOF. The crude extract was subjected to 70% ammonium sulfate saturation followed by gel filtration chromatography. The disc diffusion assay along with a microtiter bioassay was used to determine the antifungal activity of the protein against phytopathogenic fungi. The insecticidal efficacy was evaluated by feeding insect pests with food contaminated with the purified protein. Additionally, an in silico molecular structure prediction study of the protein was performed using Auto Dock Vina for molecular docking of the protein with either fungal membrane moieties or α-amylase from Tenebrio molitor L. MD simulations of protein-ligand complexes were conducted using Schrodinger's Desmond module. γ-Thionin (BoT) was purified from white cabbage seeds and showed 100% homology with thionin (Brassica oleracea L. var. viridis) and 80% homology with defensin-like protein 1 (Raphanus sativus L.), respectively. BoT significantly inhibited the mycelial growth of Aspergillus niger van Tieghem and Aspergillus flavus Link at a concentration of 2 μM. Similarly, 0.12 μM BoT treatment resulted in significant mortality of Tribolium castaneum Herbst and Sitophilus oryzae L. Molecular docking and MD simulation of BoT confirmed the strong binding affinity with fungal membrane moieties (phosphatidylinositol 4,5-bisphosphate and phosphatidic acid), which causes disruption of the cell membrane and leakage of the cellular contents, leading to cell death. BoT blocked the active site of α-amylase, and as a result of the inactivation of this gut enzyme, the digestive systems of insects were disturbed, resulting in their deaths. This study revealed that γ-thionin is a good antifungal and insecticidal agent that could be used as an alternate to fungicides and insecticides.

Sections du résumé

BACKGROUND BACKGROUND
Fungi and insect pests ruin stored crop grain, which results in millions of dollars of damage, presenting an ongoing challenge for farmers in addition to diminishing the safety of stored food. A wide-range defensive system against pathogens is needed to reduce or even eliminate the dependence of the crop yield upon the use of pesticides. Plant defensins (γ-thionins) are antimicrobial peptides (AMPs) that are a component of the host defense system. They are known to interact with cell membranes to exhibit antifungal and insecticidal activity. They exhibit a broad range of activities against fungi and insects and are effective at low concentrations. Thionins act on membranes, greatly reducing the development of pathogen resistance.
OBJECTIVE OBJECTIVE
The aim of this study is to investigate a bioactive molecule that acts against fungal pathogens and stored grain insect pests.
METHODS METHODS
γ-thionin protein was extracted from Brassica oleracea L. var. capitata f. alba (white cabbage) seed powder in phosphate buffer (100 mM, pH 7.0) and was identified by MALDI-TOF/TOF. The crude extract was subjected to 70% ammonium sulfate saturation followed by gel filtration chromatography. The disc diffusion assay along with a microtiter bioassay was used to determine the antifungal activity of the protein against phytopathogenic fungi. The insecticidal efficacy was evaluated by feeding insect pests with food contaminated with the purified protein. Additionally, an in silico molecular structure prediction study of the protein was performed using Auto Dock Vina for molecular docking of the protein with either fungal membrane moieties or α-amylase from Tenebrio molitor L. MD simulations of protein-ligand complexes were conducted using Schrodinger's Desmond module.
RESULTS RESULTS
γ-Thionin (BoT) was purified from white cabbage seeds and showed 100% homology with thionin (Brassica oleracea L. var. viridis) and 80% homology with defensin-like protein 1 (Raphanus sativus L.), respectively. BoT significantly inhibited the mycelial growth of Aspergillus niger van Tieghem and Aspergillus flavus Link at a concentration of 2 μM. Similarly, 0.12 μM BoT treatment resulted in significant mortality of Tribolium castaneum Herbst and Sitophilus oryzae L. Molecular docking and MD simulation of BoT confirmed the strong binding affinity with fungal membrane moieties (phosphatidylinositol 4,5-bisphosphate and phosphatidic acid), which causes disruption of the cell membrane and leakage of the cellular contents, leading to cell death. BoT blocked the active site of α-amylase, and as a result of the inactivation of this gut enzyme, the digestive systems of insects were disturbed, resulting in their deaths.
CONCLUSION CONCLUSIONS
This study revealed that γ-thionin is a good antifungal and insecticidal agent that could be used as an alternate to fungicides and insecticides.

Identifiants

pubmed: 35676855
pii: CMC-EPUB-124289
doi: 10.2174/0929867329666220608163645
doi:

Substances chimiques

Thionins 0
Antifungal Agents 0
Insecticides 0
Fungicides, Industrial 0
Powders 0
Ligands 0
Ammonium Sulfate SU46BAM238
Defensins 0
alpha-Amylases EC 3.2.1.1
Phosphatidic Acids 0
Complex Mixtures 0
Phosphatidylinositols 0
Phosphates 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

6446-6462

Subventions

Organisme : Higher Education Commission (HEC), Pakistan
ID : 112-22140-2BM1-565

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Binish Khaliq (B)

Botany Division, Institute of Pure and Applied Biology, Bahauddin Zakariya University, Multan, Pakistan.
Department of Botany, University of Okara, Okara, Pakistan.

Mohnad Abdalla (M)

School of Life Sciences and Hefei National Laboratory for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei, Anhui 230027, People\'s Republic of China.

Sohaib Mehmood (S)

Botany Division, Institute of Pure and Applied Biology, Bahauddin Zakariya University, Multan, Pakistan.

Ahsan Saeed (A)

Botany Division, Institute of Pure and Applied Biology, Bahauddin Zakariya University, Multan, Pakistan.

Aisha Munawar (A)

Department of Chemistry, University of Engineering and Technology, Lahore 54890, Pakistan.

Muhammad Qamar Saeed (MQ)

Department of Microbiology, Institute of Pure and Applied Biology, Bahauddin Zakariya University, Multan, Pakistan.

Qamar Saeed (Q)

Department of Entomology, Bahauddin Zakariya University, Multan, Pakistan.

Muhammad Ibrahim (M)

Department of Biosciences, COMSATS University Islamabad, Sahiwal Campus, Islamabad, Pakistan.

Zahid Ali (Z)

Plant Biotechnology & Molecular Pharming Lab, Department of Biosciences, COMSATS University Islamabad (CUI), Islamabad, Pakistan.

Saber Hussain (S)

Botany Division, Institute of Pure and Applied Biology, Bahauddin Zakariya University, Multan, Pakistan.
Institute of Botany, University of the Punjab, Lahore 54590, Punjab, Pakistan.

Wafa Ali Eltayb (WA)

Biotechnology Department, Faculty of Science and Technology, Shendi University, Shendi, Nher Anile, Sudan.

Christian Betzel (C)

Laboratory for Structural Biology of Infection and Inflammation, University Hamburg, DESY, Build. 22a, Notkestr. 85, 22603 Hamburg, Germany.

Ahmed Akrem (A)

Botany Division, Institute of Pure and Applied Biology, Bahauddin Zakariya University, Multan, Pakistan.

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Classifications MeSH