Previous Article | Next Article ![]()
Applied and Environmental Microbiology, January 2001, p. 51-58, Vol. 67, No. 1
Estuarine Research Center, Academy of Natural
Sciences, St. Leonard, Maryland 20685,1 and
Chesapeake Biological Laboratory, University of Maryland,
Solomons, Maryland 206882
Received 20 June 2000/Accepted 17 October 2000
We have previously hypothesized that sulfide inhibits Hg
methylation by decreasing its bioavailability to sulfate-reducing bacteria (SRB), the important methylators of Hg in natural sediments. With a view to designing a bioassay to test this hypothesis, we investigated a number of aspects of Hg methylation by the SRB Desulfobulbus propionicus, including (i) the relationship
between cell density and methylmercury (MeHg) production, (ii) the time course of Hg methylation relative to growth stage, (iii) changes in the
bioavailability of an added inorganic Hg (HgI) spike over time, and (iv) the dependence of methylation on the concentration of
dissolved HgI present in the culture. We then tested the
effect of sulfide on MeHg production by this microorganism. These
experiments demonstrated that under conditions of equal
bioavailability, per-cell MeHg production was constant through
log-phase culture growth. However, the methylation rate of a new Hg
spike dramatically decreased after the first 5 h. This result was
seen whether methylation rate was expressed as a fraction of the total
added Hg or the filtered HgI concentration, which suggests
that Hg bioavailability decreased through both changes in Hg
complexation and formation of solid phases. At low sulfide
concentration, MeHg production was linearly related to the
concentration of filtered HgI. The methylation of filtered
HgI decreased about fourfold as sulfide concentration was
increased from 10
0099-2240/01/$04.00+0 DOI: 10.1128/AEM.67.1.51-58.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Aspects of Bioavailability of Mercury for
Methylation in Pure Cultures of Desulfobulbus
propionicus (1pr3)
6 to 10
3 M. This decline
is consistent with a decrease in the bioavailability of
HgI, possibly due to a decline in the dissolved neutral
complex, HgS0.
*
Corresponding author. Present address: Princeton
University, Department of Geosciences, Guyot Hall, Princeton, NJ 08544. Phone: (609) 258-2489. Fax: (609) 258-1274. E-mail:
jbenoit{at}princeton.edu.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»