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Journal of Bacteriology, September 1998, p. 4460-4465, Vol. 180, No. 17
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Farnesol-Induced Generation of Reactive Oxygen Species via
Indirect Inhibition of the Mitochondrial Electron Transport Chain
in the Yeast Saccharomyces cerevisiae
Kiyotaka
Machida,
Toshio
Tanaka,*
Ken-ichi
Fujita, and
Makoto
Taniguchi
Department of Biology, Graduate School of
Science, Osaka City University, 3-3-138 Sugimoto, Sumiyoshi-ku,
Osaka 558-8585, Japan
Received 5 May 1998/Accepted 3 July 1998
The mechanism of farnesol (FOH)-induced growth inhibition of
Saccharomyces cerevisiae was studied in terms of its
promotive effect on generation of reactive oxygen species (ROS). The
level of ROS generation in FOH-treated cells increased five- to
eightfold upon the initial 30-min incubation, while cells treated with
other isoprenoid compounds, like geraniol, geranylgeraniol, and
squalene, showed no ROS-generating response. The dependence of
FOH-induced growth inhibition on such an oxidative stress was confirmed
by the protection against such growth inhibition in the presence of an
antioxidant such as
-tocopherol, probucol, or
N-acetylcysteine. FOH could accelerate ROS generation only
in cells of the wild-type grande strain, not in those of the
respiration-deficient petite mutant ([rho0]),
which illustrates the role of the mitochondrial electron transport chain as its origin. Among the respiratory chain inhibitors, ROS generation could be effectively eliminated with myxothiazol, which inhibits oxidation of ubiquinol to the ubisemiquinone radical by the
Rieske iron-sulfur center of complex III, but not with antimycin A, an
inhibitor of electron transport that is functional in further oxidation
of the ubisemiquinone radical to ubiquinone in the Q cycle of complex
III. Cellular oxygen consumption was inhibited immediately upon
extracellular addition of FOH, whereas FOH and its possible
metabolites failed to directly inhibit any oxidase activities detected
with the isolated mitochondrial preparation. A protein kinase C
(PKC)-dependent mechanism was suggested to exist in the inhibition of
mitochondrial electron transport since FOH-induced ROS
generation could be effectively eliminated with a membrane-permeable
diacylglycerol analog which can activate PKC. The present study
supports the idea that FOH inhibits the ability of the electron
transport chain to accelerate ROS production via interference with a
phosphatidylinositol type of signal.
*
Corresponding author. Mailing address: Department of
Biology, Graduate School of Science, Osaka City University, 3-3-138 Sugimoto, Sumiyoshi-ku, Osaka 558-8585, Japan. Phone: 81-6-605-3163. Fax: 81-6-605-3164. E-mail:
tanakato{at}sci.osaka-cu.ac.jp.
Journal of Bacteriology, September 1998, p. 4460-4465, Vol. 180, No. 17
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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