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- W2921384116 abstract "Although increasing attention has been paid to the nanotoxicity of graphene oxide quantum dots (GOQDs) due to their broad range of applications, the persistence and recoverability associated with GOQDs had been widely ignored. Interestingly, stress-response hormesis for algal growth was observed for Chlorella vulgaris as a single-celled model organism. Few physiological parameters, such as algal density, plasmolysis, and levels of reactive oxygen species, exhibited facile recovery. In contrast, the effects on chlorophyll a levels, permeability, and starch grain accumulation exhibited persistent toxicity. In the exposure stage, the downregulation of genes related to unsaturated fatty acid biosynthesis, carotenoid biosynthesis, phenylpropanoid biosynthesis, and binding contributed to toxic effects on photosynthesis. In the recovery stage, downregulation of genes related to the cis-Golgi network, photosystem I, photosynthetic membrane, and thylakoid was linked to the persistence of toxic effects on photosynthesis. The upregulated galactose metabolism and downregulated aminoacyl-tRNA biosynthesis also indicated toxicity persistence in the recovery stage. The downregulation and upregulation of phenylalanine metabolism in the exposure and recovery stages, respectively, reflected the tolerance of the algae to GOQDs. The present study highlights the importance of studying nanotoxicity by elucidation of stress and recovery patterns with metabolomics and transcriptomics." @default.
- W2921384116 created "2019-03-22" @default.
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- W2921384116 date "2019-03-14" @default.
- W2921384116 modified "2023-10-07" @default.
- W2921384116 title "Study of the Persistence of the Phytotoxicity Induced by Graphene Oxide Quantum Dots and of the Specific Molecular Mechanisms by Integrating Omics and Regular Analyses" @default.
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- W2921384116 doi "https://doi.org/10.1021/acs.est.8b06023" @default.
- W2921384116 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30870590" @default.
- W2921384116 hasPublicationYear "2019" @default.
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