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Applied and Environmental Microbiology, September 2001, p. 4030-4035, Vol. 67, No. 9
Environmental Research Center, Department of
Biology, Georgia State University, Atlanta, Georgia
Received 14 March 2001/Accepted 27 June 2001
The effects of Ag(I) and Hg(II) on membrane potential and integrity
of cells of Candida albicans and C.
maltosa were determined with a flow cytometric procedure that
employed an anionic membrane potential-sensitive dye,
bis-(1,3-dibutylbarbituric acid) trimethine oxonol, and a membrane
integrity indicator, propidium iodide. The membrane potentials of cells
of both species were reduced rapidly within 15 min of exposure to
Ag(I). No threshold dose for Hg(II) existed, and cells of both species
lost membrane potential gradually in Hg(II) solutions. Cells of both
species lost membrane integrity more rapidly in Ag(I) solutions than in
Hg(II) solutions. In Ag(I) solutions, the decrease in the numbers of
cells recoverable in culture occurred at a rate similar to the rate of
cell depolarization and membrane permeabilization. In Hg(II) solutions,
loss of cell recoverability preceded the loss of membrane potential and
membrane integrity. C. albicans, in contrast to
C. maltosa, showed no loss of membrane integrity after
exposure to Hg(II) solutions for 1 h. Different rates of binding
of Ag(I) and Hg(II) between the two species suggest that the two ions
target different primary sites.
0099-2240/01/$04.00+0 DOI: 10.1128/AEM.67.9.4030-4035.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Toxic Effects of Ag(I) and Hg(II) on Candida
albicans and C. maltosa: a Flow
Cytometric Evaluation
*
Corresponding author. Mailing address: Department of
Biology, P.O. Box 4010, Georgia State University, Atlanta, GA
30302-4010. Phone: (404) 651-3103. Fax: (404) 651-2509. E-mail:
biosac{at}panther.gsu.edu.
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