Metabolism of 17β-estradiol by Novosphingobium sp. ES2-1 as probed via HRMS combined with 13C3-labeling

J Hazard Mater. 2020 May 5:389:121875. doi: 10.1016/j.jhazmat.2019.121875. Epub 2019 Dec 10.

Abstract

This study investigated the biodegradation and metabolic mechanisms of 17β-estradiol (E2) by Novosphingobium sp. ES2-1 isolated from the activated sludge in a domestic sewage treatment plant (STP). It could degrade 97.1% E2 (73.5 μmol/L) in 7 d with a biodegradation half-life of 1.29 d. E2 was initially converted to estrone (E1), then to 4-hydroxyestrone (4-OH-E1), before subsequent monooxygenation reactions cleaved 4-OH-E1 into a metabolite with long-chain ketones structure (metabolite P8). However, when 4-OH-E1 was cleaved through the 4,5-seco pathway, the resulting phenol ring cleavage product could randomly condense with NH3 to yield a pyridine derivative, accompanied by the uncertain loss of a carboxy group at C4 before the condensation. The derivative was further oxidized into the metabolites with both pyridine and long-chain ketones structure (metabolite N5) through a similar formation mechanism as for P8 performed. This research presents several novel metabolites and shows that E2 can be biodegraded into the metabolite with long-chain structure through three optional pathways, thereby reducing E2 contamination.

Keywords: 17β-Estradiol biodegradation; High-resolution mass spectrometry; Mechanism; Sphingomonad; Stable isotope labeling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbon Isotopes
  • Estradiol / metabolism*
  • Estrogens / metabolism*
  • Estrone / metabolism
  • Hydroxyestrones / metabolism
  • Isotope Labeling
  • Mass Spectrometry / methods
  • Sphingomonadaceae / metabolism*

Substances

  • Carbon Isotopes
  • Estrogens
  • Hydroxyestrones
  • Estrone
  • 4-hydroxyestrone
  • Estradiol