Time-Resolved Examination of Fungal Selenium Redox Transformations

Cara M. Santelli, Mary Sabuda, Carla Rosenfeld

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

Selenium (Se) is both a micronutrient required for most life and an element of environmental concern due to its toxicity at high concentrations, and both bioavailability and toxicity are largely influenced by the Se oxidation state. Environmentally relevant fungi have been shown to aerobically reduce Se(IV) and Se(VI), the generally more toxic and bioavailable Se forms. The goal of this study was to shed light on fungal Se(IV) reduction pathways and biotransformation products over time and fungal growth stages. Two Ascomycete fungi were grown with moderate (0.1 mM) and high (0.5 mM) Se(IV) concentrations in batch culture over 1 month. Fungal growth was measured throughout the experiments, and aqueous and biomass-associated Se was quantified and speciated using analytical geochemistry, transmission electron microscopy (TEM), and synchrotron-based X-ray absorption spectroscopy (XAS) approaches. The results show that Se transformation products were largely Se(0) nanoparticles, with a smaller proportion of volatile, methylated Se compounds and Se-containing amino acids. Interestingly, the relative proportions of these products were consistent throughout all fungal growth stages, and the products appeared stable over time even as growth and Se(IV) concentration declined. This time-series experiment showing different biotransformation products throughout the different growth phases suggests that multiple mechanisms are responsible for Se detoxification, but some of these mechanisms might be independent of Se presence and serve other cellular functions. Knowing and predicting fungal Se transformation products has important implications for environmental and biological health as well as for biotechnology applications such as bioremediation, nanobiosensors, and chemotherapeutic agents.

Original languageEnglish (US)
Pages (from-to)960-971
Number of pages12
JournalACS Earth and Space Chemistry
Volume7
Issue number5
DOIs
StatePublished - May 18 2023

Bibliographical note

Funding Information:
Research was supported by a NSF CAREER award to CMS (NSF #1749727) and a University of Minnesota Informatics Institute - MnDRIVE Fellowship to MCS. The funders had no role in project design, implementation, or analysis. Parts of this work were carried out in the Characterization Facility, University of Minnesota, which receives partial support from NSF through the MRSEC program. We thank Fang Zhou and Bob Hafner for assistance and training with TEM sample preparation and imaging. We thank Jason Myers for help with TEM analysis. This research used resources of the Advanced Photon Source, a U.S. Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Argonne National Laboratory under Contract No. DE-AC02-06CH11357. We thank Ben Reinhart for his help with XAS data collection, and Christine Hitomi and Josh Torgeson for experimental assistance.

Publisher Copyright:
© 2023 The Authors. Published by American Chemical Society.

Keywords

  • bioremediation
  • fungi
  • organic Se
  • redox
  • Se nanoparticles
  • selenite reduction
  • time series

PubMed: MeSH publication types

  • Journal Article

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