Poster: Phytoremediation
Abs #
983: Biotransformation of Hg2+ by selected cyanobacteria.
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Presenter: |
Lefebvre, Daniel D., lefebvre@biology.queensu.ca |
Authors | Lefebvre, Daniel D. (A) Kelly, David (A) Budd, Kenneth (A) | | Affiliations: |
(A): Dept. Biology, Queen's University
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The biotransformation of Hg2+ by selected cyanobacteria was investigated under pH-stat culture conditions at environmentally relevant Hg2+:chl a ratios. A novel method permitted the selective, quantitative determination of b-HgS. A direct, simultaneous determination of this pathway together with losses to the well-known reductive Hg° pathway was made, thereby assessing the fate of Hg2+ doses in real time.
Upon exposure of cyanobacteria to Hg2+, acid SnCl2 reducible Hg signal (free ions and complexes) was transformed to alkaline SnCl2 reducible Hg signal consistent with b-HgS and inconsistent with other biologically-reported mercury compounds and complexes. The initial biotransformation process included a rapid phase for b-HgS synthesis (K1/2 of minutes) and high Hg° evolution, but the rate of the latter decreased rapidly. This is consistent with ecological literature from which Hg° volatilization would be expected to occur from the surface-water interface for only a short time following precipitation.
The synthesis of b-HgS appears to require intracellular thiols and active metabolism as interference with either requirement favored Hg° volatilization. Therefore, in the environment cyanobacteria at the air-water interface would primarily act to sediment Hg2+ as b-HgS. This suggests that b-HgS, not chelated Hg2+ , is the relevant dietary mercurial for algal grazers. In addition, direct exposure to Hg2+ may not be appropriate for methylation studies in sediments.