Study on active response of superoxide dismutase and relevant binding interaction with bioaccumulated phthalates and key metabolites in Eisenia fetida

• Published in: Ecotoxicology and environmental safety Vol. 223; p. 112559
• Main Authors: Fan, Xiuli, Gu, Chenggang, Cai, Jun, Bian, Yongrong, Yang, Xinglun, Sun, Cheng, Jiang, Xin
• Format: Journal Article
• Language: English
• Published: Elsevier Inc 15.10.2021; Elsevier
• Subjects: Activity inhibition; Binding interactions; Biotransformation; PAEs; SOD; Binding interactions; SOD; PAEs; Activity inhibition; Biotransformation
• ISSN: 0147-6513; 1090-2414; 1090-2414
• DOI: 10.1016/j.ecoenv.2021.112559

Phthalic acid esters (PAEs) are a group of widespread persistent organic pollutants in the environment. Though the harmful effect of PAEs including activity inhibition of superoxide dismutase (SOD) to arouse oxidative stress were well documented, the deep insights into mechanisms that are relevant with SOD activity are still lacking. By 7d-cultivation of Eisenia fetida in artificially-polluted soil, the different active responses of SOD in earthworm were shown to PAE congeners. Despite the less bioaccumulation and bioavailability, the di-butyl phthalate (DBP) etc. structurally coupled with longer ester-chains appeared more effective to trigger the up-regulation and then the slight decline of SOD activity. Given the remarkable biotransformation especially for short-chain PAEs, the SOD activity response in earthworm should be regarded as joint effect with their metabolites, e.g. monophthalates (MAEs) and phthalic acid (PA). The in vitro SOD activity was shown with the obvious inhibition of 21.31% by DBP, 88.93% by MBP, and 58.57% by PA respectively when the concentrations were elevated up to 0.03 mM. The SOD activity inhibition confirmed the molecular binding with pollutants as an essential event besides the biological regulation for activity. The binding interaction was thermodynamically exothermic, spontaneous and strengthened primarily by Van der Waals force and hydrogen bonds, and was spectrally diagnosed with the conformational changes including diminution of α-helix content and spatial reorientation of fluorophore tryptophan. As coherently illustrated with the larger fluorescence quenching constants (3.65*104–4.47*104/mol) than DBP, the metabolites should be the priority concern due to stronger activity inhibition and toxicological risks. [Display omitted] •Active responses of SOD were shown for PAEs in congener-specificity.•Binding interaction was regarded as associative molecular event with SOD activity.•Conformational changes and thermodynamics variation in binding were revealed.•Metabolites have higher binding affinity with SOD and larger potency in inhibition.