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Applied and Environmental Microbiology, November 2000, p. 4849-4853, Vol. 66, No. 11
Chemistry Department and Texas Research
Institute for Environmental Studies, Sam Houston State University,
Huntsville, Texas 773411; Stanford
Synchrotron Radiation Laboratory, Stanford Linear Accelerator Center,
Stanford, California 943092; and
ExxonMobil Research and Engineering Company, Annandale, New
Jersey 088013
Received 29 June 2000/Accepted 6 September 2000
Cultures of a purple nonsulfur bacterium, Rhodobacter
sphaeroides, amended with ~1 or ~100 ppm selenate or
selenite, were grown phototrophically to stationary phase. Analyses of
culture headspace, separated cells, and filtered culture supernatant
were carried out using gas chromatography, X-ray absorption
spectroscopy, and inductively coupled plasma spectroscopy-mass
spectrometry, respectively. While selenium-amended cultures showed much
higher amounts of SeO32
0099-2240/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Fate of Selenate and Selenite Metabolized by
Rhodobacter sphaeroides

bioconversion than
did analogous selenate experiments (94% uptake for
SeO32
as compared to 9.6% for
SeO42
-amended cultures from 100-ppm
solutions), the chemical forms of selenium in the microbial cells were
not very different except at exposure to high concentrations of
selenite. Volatilization accounted for only a very small portion of the
accumulated selenium; most was present in organic forms and the red
elemental form.
*
Corresponding author. Mailing address: Department of
Chemistry, Sam Houston State University, P.O. Box 2117, Huntsville, TX 77341. Phone: (936) 294-1533. Fax: (936) 294-4996. E-mail:
chm_tgc{at}shsu.edu.
Present address: Department of Biochemistry, Molecular Biology and
Biophysics, University of Minnesota, St. Paul, MN 55108-1022.
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