摘要
The potential application of fungal laccase-assisted bioremediation for estrogen elimination has caused tremendous attention. Herein, naturally-occurring Trametes versicolor laccase ( Tv lac) was capable of significantly removing 17 β -estradiol (E2) and 17 α -ethynylestradiol (EE2) at pH 5. A lower (or higher) pH caused decline in the velocity constants ( k prcs ) by obstructing the single-electron oxidation of estrogen at Tv lac T1-Cu site (or intercepting the intramolecular-electron transfer between Tv lac T1-Cu and T2/T3-Cu sites). Humic acid (HA) and natural phenolic compounds (PCs) are omnipresent in water and can influence the conversion kinetics of estrogen in Tv lac-triggered reactions. Compared with HA-free, the k prcs values of E2 and EE2 in presence of HA respectively reduced 58.61%–83.72% and 69.72%–95.62% at different pH levels. Additionally, the k prcs values for estrogen were also hampered obviously by O -dihydroxyphenol structure of model PCs, owning to the created monomeric/polymeric O -quinones inverted estrogen phenoxy radicals. The generated carbon‑carbon/oxygen self-linking aggregates during Tv lac-mediated estrogen oxidative coupling were characterized, and the polymerization mechanisms were speculated. A fluid-bed reactor with cross-linked-entrapped Tv lac in Ca-alginate beads was established to treat E2 and EE2, respectively. Compared with free Tv lac, immobilized Tv lac prominently exhibited a higher pH and temperature stability. Especially, the fluid-bed reactor with immobilized Tv lac could be reused, keeping its high conversion efficiencies of E2 and EE2 in natural water, only changing from 99.2% to 73.6% and from 98.5% to 70.9% after 1 to 5 cycles, respectively. These findings present an alternative immobilized fungal laccase-based clean biotechnology for continuously handling estrogen-contaminated waterbodies at a large-scale.
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