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Pleiotropic phenotypes of fission yeast defective in ubiquinone-10 production. A study from the abc1Sp (coq8Sp) mutant
We previously constructed two Schizosaccahromyces pombe ubiquinone‐10 (or Coenzyme Q10) less mutants, which are either defective for decaprenyl diphosphate synthase or p‐hydroxybenzoate polyprenyl diphosphate transferase. To further confirm the roles of ubiquinone in S. pombe, we examined the phenot...
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Published in: | BioFactors (Oxford) 2003, Vol.18 (1-4), p.229-235 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | We previously constructed two Schizosaccahromyces pombe ubiquinone‐10 (or Coenzyme Q10) less mutants, which are either defective for decaprenyl diphosphate synthase or p‐hydroxybenzoate polyprenyl diphosphate transferase. To further confirm the roles of ubiquinone in S. pombe, we examined the phenotype of the abc1Sp (coq8Sp) mutant, which is highly speculated to be defective in ubiquinone biosynthesis. We show here that the abc1Sp defective strain did not produce UQ‐10 and could not grow on minimal medium. The abc1Sp‐deficient strain required supplementation with antioxidants such as cysteine or glutathione to grow on minimal medium. In support of the antioxidant function of ubiquinone, the abc1Sp‐deficient strain is sensitive to H2O2 and Cu2+. In addition, expression of the stress inducible ctt1 gene was much induced in the ubiquinone less mutant than wild type. Interestingly, we also found that the abc1‐deficient strain as well as other ubiquinone less mutants 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. Thus, analysis of the phenotypes of S. pombe ubiquinone less mutants clearly demonstrate that ubiquinone has multiple functions in the cell apart from being an integral component of the electron transfer system. |
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ISSN: | 0951-6433 1872-8081 |
DOI: | 10.1002/biof.5520180225 |