4.8 Article

Effect of fluoxetine on enhanced biological phosphorus removal using a sequencing batch reactor

Journal

BIORESOURCE TECHNOLOGY
Volume 320, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biortech.2020.124396

Keywords

Anaerobic phosphorus release; Polyhydroxyalkanoates; Glycogen; Polyhydroxyvalerate; Enzymes

Funding

  1. National Natural Science Foundation of China (NSFC) [51908305]
  2. Open Fund of Innovation Institute for Sustainable Maritime Architecture Research and Technology (iSMART), Qingdao University of Technology [Nu. 2020-042]
  3. China Postdoctoral Science Foundation [2019 M660162]
  4. Shanghai Engineering Research Center of Biotransformation of Organic Solid Waste [SERC2020C05]
  5. Open Project Fund of Qingdao University of Technology [QUTSEME201906]

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The study investigated the impact of Fluoxetine on enhanced biological phosphorus removal. Short-term exposure had no significant effect, but long-term exposure inhibited EBPR efficiency. High FLX concentrations reduced anaerobic phosphorus release and affected microbial populations, leading to decreased performance in the EBPR system.
In this work, the potential impact of emerging pollutant Fluoxetine (FLX) on enhanced biological phosphorus removal (EBPR) was systematically investigated using the sequencing batch reactor. The experimental results showed that even 200 mu g/L FLX had no significant effect on EBPR during the short-term exposure. However, in the long-term exposure test, high dosage of FLX inhibited EBPR. 200 mu g/L FLX induced biological phosphorus removal efficiency dropped to 71.3 +/- 2.1%, significantly lower than that of the blank. The mechanism investigation showed that high concentration of FLX reduced anaerobic phosphorus release and oxic phosphorus absorption, and the consumption of organic matter during the anaerobic period. In addition, FLX decreased the synthesis of intracellular polymer polyhydroxyalkanoates (PHA), but promoted the metabolism of glycogen and polyhydroxyvalerate. FLX reduced the activity of key enzymes in EBPR and the relative abundance of Accumulibacter, but improved the relative abundance of Candidatus Competibacter.

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