Microbial degradation of 17β-estradiol and 17α-ethinylestradiol followed by a validated HPLC-DAD method

Ana R. Ribeiro, Maria F. Carvalho, Carlos M.M. Afonso, Maria E. Tiritan, Paula M.L. Castro

Research output: Contribution to journalArticlepeer-review

22 Citations (Scopus)

Abstract

This work aimed at studying the biodegradation of two estrogens, 17α-estradiol (E2) and 17β-ethinylestradiol (EE2), and their potential metabolism to estrone (E1) by microbial consortia. The biodegradation studies were followed by High Performance Liquid Chromatography-Diode Array Detector (HPLC-DAD) using a specifically developed and validated method. Biodegradation studies of the estrogens (E2 and EE2) were carried out with activated sludge (consortium A, CA) obtained from a Wastewater Treatment Plant (WWTP) and with a microbial consortium able to degrade recalcitrant compounds, namely fluorobenzene (consortium B, CB). E2 was more extensively degraded than EE2 by CA whereas CB was only able to degrade E2. The addition of acetate as a supplementary carbon source led to a faster biodegradation of E2 and EE2. E1 was detected as a metabolite only during the degradation of E2. The 16S rRNA gene sequence analyses of strains recovered from the degrading cultures revealed the presence of the genera Pseudomonas, Chryseobacterium and Alcaligenes. The genera Pseudomonas and Chryseobacterium were retrieved from cultures supplied with E2 and EE2, while the genus Alcaligenes was found in the presence of E2, suggesting that they might be involved in the degradation of these compounds.

Original languageEnglish
Pages (from-to)265-273
Number of pages9
JournalJournal of Environmental Science and Health - Part B Pesticides, Food Contaminants, and Agricultural Wastes
Volume45
Issue number4
DOIs
Publication statusPublished - May 2010

Keywords

  • 17α-ethinylestradiol
  • 17β-estradiol
  • Biodegradation
  • Endocrine disrupting chemicals
  • Estrone
  • HPLC-DAD

Fingerprint

Dive into the research topics of 'Microbial degradation of 17β-estradiol and 17α-ethinylestradiol followed by a validated HPLC-DAD method'. Together they form a unique fingerprint.

Cite this