Journal of Bacteriology, December 2000, p. 6933-6939, Vol. 182, No. 24
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Department of Applied Bioscience and Biotechnology, Faculty of Life and Environmental Science, Shimane University, Matsue 690-8504, Japan
Received 13 June 2000/Accepted 26 September 2000
Ubiquinone is an essential component of the electron transfer
system in both prokaryotes and eukaryotes and is synthesized from
chorismate and polyprenyl diphosphate by eight steps.
p-Hydroxybenzoate (PHB) polyprenyl diphosphate
transferase catalyzes the condensation of PHB and polyprenyl
diphosphate in ubiquinone biosynthesis. We isolated the gene
(designated ppt1) encoding PHB polyprenyl diphosphate
transferase from Schizosaccharomyces pombe and constructed a strain with a disrupted ppt1 gene. This strain could not
grow on minimal medium supplemented with glucose. Expression of
COQ2 from Saccharomyces cerevisiae in the
defective S. pombe strain restored growth and enabled the
cells to produce ubiquinone-10, indicating that COQ2 and
ppt1 are functional homologs. The
ppt1-deficient strain required supplementation with
antioxidants, such as cysteine, glutathione, and
-tocopherol, to
grow on minimal medium. This suggests that ubiquinone can act as an
antioxidant, a premise supported by our observation that the
ppt1-deficient strain is sensitive to
H2O2 and Cu2+. Interestingly, we
also found that the ppt1-deficient strain produced a
significant amount of H2S, which suggests that oxidation of
sulfide by ubiquinone may be an important pathway for sulfur metabolism
in S. pombe. Ppt1-green fluorescent protein fusion proteins
localized to the mitochondria, indicating that ubiquinone biosynthesis
occurs in the mitochondria in S. pombe. Thus, analysis of
the phenotypes of S. pombe strains deficient in ubiquinone production clearly demonstrates that ubiquinone has multiple functions in the cell apart from being an integral component of the electron transfer system.
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