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Simultaneous selenate reduction and denitrification by a consortium of enriched mine site bacteria.

Authors :
Subedi G
Taylor J
Hatam I
Baldwin SA
Source :
Chemosphere [Chemosphere] 2017 Sep; Vol. 183, pp. 536-545. Date of Electronic Publication: 2017 May 25.
Publication Year :
2017

Abstract

Increasing selenium concentrations in aquatic environments downstream of mine sites is of great concern due to selenium's bioaccumulation propensity and teratogenic toxicity. Removal of selenium from mine influenced water is complicated by the presence of nitrate, which is also elevated in mine influenced water due to the use of explosives in mining. In many biological treatment processes, nitrate as a thermodynamically more preferable electron acceptor inhibits selenate reduction. Here we report on an enrichment of a bacterial assemblage from a mine impacted natural marsh sediment that was capable of simultaneous selenate reduction and denitrification. Selenate reduction followed first order kinetics with respect to the concentration of total dissolved selenium. The kinetic rate constant was independent of initial nitrate concentration over the range 3-143 mg L <superscript>-1</superscript> -NO <subscript>3</subscript> <superscript>-</superscript> -N. The initial concentration of selenate inhibited selenate reduction kinetics over the range 1-24 mg-Se L <superscript>-1</superscript> . Dominant taxa that grew in selenate only medium were classified in the genera Pseudomonas, Lysinibacillus and Thauera. When nitrate was introduced in addition to selenate, previously rare taxa that became dominant were relatives of Exiguobacterium, Tissierella and Clostridium. Open reading frames (ORFs) associated with dissimilatory denitrification were identified for Pseudomonas, Thauera and Clostridium. In addition, ORFs were found that were homologous with known selenate reductase subunits (SerA and SerB). These findings suggest that native mine site bacteria can be used for removing selenate and nitrate from mine wastewater.<br /> (Crown Copyright © 2017. Published by Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1879-1298
Volume :
183
Database :
MEDLINE
Journal :
Chemosphere
Publication Type :
Academic Journal
Accession number :
28570897
Full Text :
https://doi.org/10.1016/j.chemosphere.2017.05.144