Conserved specificity of extracellular wastewater peptidases revealed by multiplex substrate profiling by mass spectrometry

Natalie Wichmann, Josephine Meibom, Tamar Kohn, Michael Zumstein (Corresponding author)

Publications: Contribution to journalArticlePeer Reviewed

Abstract

Peptide-based chemicals are promising for numerous applications including home and personal care and medical treatments. To better understand and control the environmental fate of peptide-based chemicals, in-depth knowledge on the specificity of wastewater peptidases is needed. Here, we employed multiplex substrate profiling by mass spectrometry to obtain specificity profiles of extracellular peptidases derived from influent and aeration tanks of three full-scale wastewater treatment plants. Specificities were confirmed by fluorogenic peptidase substrates. Our results revealed highly similar specificity profiles across wastewater treatment plants. We found that hydrolysis by extracellular wastewater peptidases is favored when positively charged amino acid residues surround the cleavage site and disfavored when negatively charged amino acid residues surround the cleavage site.

Original languageEnglish
Article number100210
Pages (from-to)953-959
Number of pages7
JournalEnvironmental Chemistry Letters
Volume23
Issue number4
DOIs
Publication statusPublished - Aug 2025

Austrian Fields of Science 2012

  • 104023 Environmental chemistry

Keywords

  • Benign-by-design
  • Environmental fate
  • Multiplex substrate profiling by mass spectrometry
  • Peptidase specificity
  • Peptide-based chemicals
  • Wastewater systems

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