ABSTRACTBased on the well-documented hazards of microplastics and the importance and typicality of Saccharomyces cerevisiae (S. cerevisiae) in the environment, in this study, the influencing mechanisms of functional group, particle size and dosage of polystyrene microplastics (PS MPs) on S. cerevisiae were studied systematically. The results showed that compared with the bigger particle size and lower concentration of carboxylated PS MPs, the smaller particle size and higher concentration of aminated PS MPs had the most serious inhibition of the growth of S. cerevisiae, and their cell morphology was more abnormal, the more PS MPs attached to the yeast cells. The results of orthogonal experiment showed that the inhibitory effects of PS MPs on S. cerevisiae followed the order: functional groups > concentrations > particle sizes. Through the analysis of the antioxidant properties of S. cerevisiae, it was found that the activities of superoxide dismutase and catalase were first stimulated and then inhibited, and the concentrations of superoxide dismutase enzymes in the environment with bigger particle size and lower concentration of PS MPs was higher than that in the environment with smaller particle size and higher concentrations of PS MPs. catalase enzyme showed an opposite trend in particle sizes and a similar trend in concentrations. The concentrations of malondialdehyde increased with the increase of PS MPs concentrations and the decrease of particle sizes, indicating that PS MPs could induce S. cerevisiae to produce a large amount of reactive oxygen species, resulting in severe oxidative damage to S. cerevisiae.
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Evidence ID | Analyze ID | Gene/Complex | Systematic Name/Complex Accession | Qualifier | Gene Ontology Term ID | Gene Ontology Term | Aspect | Annotation Extension | Evidence | Method | Source | Assigned On | Reference |
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Evidence ID | Analyze ID | Gene | Gene Systematic Name | Phenotype | Experiment Type | Experiment Type Category | Mutant Information | Strain Background | Chemical | Details | Reference |
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Evidence ID | Analyze ID | Gene | Gene Systematic Name | Disease Ontology Term | Disease Ontology Term ID | Qualifier | Evidence | Method | Source | Assigned On | Reference |
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Evidence ID | Analyze ID | Regulator | Regulator Systematic Name | Target | Target Systematic Name | Direction | Regulation of | Happens During | Regulator Type | Direction | Regulation Of | Happens During | Method | Evidence | Strain Background | Reference |
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Site | Modification | Modifier | Source | Reference |
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Evidence ID | Analyze ID | Interactor | Interactor Systematic Name | Interactor | Interactor Systematic Name | Allele | Assay | Annotation | Action | Phenotype | SGA score | P-value | Source | Reference | Note |
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Evidence ID | Analyze ID | Interactor | Interactor Systematic Name | Interactor | Interactor Systematic Name | Assay | Annotation | Action | Modification | Source | Reference | Note |
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Complement ID | Locus ID | Gene | Species | Gene ID | Strain background | Direction | Details | Source | Reference |
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Evidence ID | Analyze ID | Dataset | Description | Keywords | Number of Conditions | Reference |
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