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Architecture and potential roles of a delta-class glutathione S-transferase in protecting honey bee from agrochemicals.

Authors :
Moural, Timothy W.
Koirala B K, Sonu
Bhattarai, Gaurab
He, Ziming
Guo, Haoyang
Phan, Ngoc T.
Rajotte, Edwin G.
Biddinger, David J.
Hoover, Kelli
Zhu, Fang
Source :
Chemosphere. Feb2024, Vol. 350, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

The European honey bee, Apis mellifera , serves as the principle managed pollinator species globally. In recent decades, honey bee populations have been facing serious health threats from combined biotic and abiotic stressors, including diseases, limited nutrition, and agrochemical exposure. Understanding the molecular mechanisms underlying xenobiotic adaptation of A. mellifera is critical, considering its extensive exposure to phytochemicals and agrochemicals present in the environment. In this study, we conducted a comprehensive structural and functional characterization of AmGSTD1, a delta class glutathione S-transferase (GST), to unravel its roles in agrochemical detoxification and antioxidative stress responses. We determined the 3-dimensional (3D) structure of a honey bee GST using protein crystallography for the first time, providing new insights into its molecular structure. Our investigations revealed that AmGSTD1 metabolizes model substrates, including 1-chloro-2,4-dinitrobenzene (CDNB), p -nitrophenyl acetate (PNA), phenylethyl isothiocyanate (PEITC), propyl isothiocyanate (PITC), and the oxidation byproduct 4-hydroxynonenal (HNE). Moreover, we discovered that AmGSTD1 exhibits binding affinity with the fluorophore 8-Anilinonaphthalene-1-sulfonic acid (ANS), which can be inhibited with various herbicides, fungicides, insecticides, and their metabolites. These findings highlight the potential contribution of AmGSTD1 in safeguarding honey bee health against various agrochemicals, while also mitigating oxidative stress resulting from exposure to these substances. [Display omitted] • The three-dimensional structure of AmGSTD1 was solved by X-ray crystallography. • G-site S34A and H-site F142A mutants exhibited the largest changes in kinetics. • Herbicides, fungicides, insecticides, and metabolites hindered AmGSTD1-ANS binding. • AmGSTD1 was highly expressed in the Malpighian tubules of both nurse and forager bees. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00456535
Volume :
350
Database :
Academic Search Index
Journal :
Chemosphere
Publication Type :
Academic Journal
Accession number :
174951284
Full Text :
https://doi.org/10.1016/j.chemosphere.2023.141089