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Saccharomyces cerevisiae strains sensitive to inorganic mercury

III. Tyrosine uptake

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Summary

In Saccharomyces cerevisiae, the HGS2-1 allele confers sensitivities to inorganis mercury (Ono and Sakamoto 1985) and to excess fermentable sugars such as glucose (Sakamoto et al. 1985); exogenous tyrosine antagonizes both inorganic mercury and excess glucose. In this sutdy, the inorganic mercury sensitive strain has been shown to have about twice more glucose-1,6-bisphosphate and slightly less pyruvate than the normal strains, suggesting that the inorganic mercury sensitive strain has the reduced aldolase activity. It has been also shown that the growth retarded cells accumulate trehalose, by which the lower level of glucos-6-phosphate in the inorganic mercury sensitive strain is accounted for, and that inorganic mercury, presumably excess glucose also, causes growth inhibition via depletion of cellular tyrosine. The mechanism how cellular tyrosine is depleted by inorganic mercury or excess glucose is accounted for by the facts that (1) the tyrosine uptake activity is decreased with increase of glucose concentration in growth medium, (2) HGS2-1 enhances the effect of glucose on the tyrosine uptake activity, and (3) inorganic mercury inhibits the tyrosine uptake system by binding to its SH-group(s). Thus, it is concluded that the role of tyrosine is not to detoxify inorganic mercury nor excess fermentable sugars but simply to counteract depletion of cellular tyrosine induced by them.

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References

  • Cooper TG (1982) In: Strathern JN, Jones EW, Broach JR (eds) The molecular biology of the yeast Saccharomyces, pt 2. Cold Spring Harbor Laboratory, Cold Spring Harbor, New York, pp 399–461

    Google Scholar 

  • Entian K-D (1977) Mol Gen Genet 158:201–210

    Google Scholar 

  • Fonzi WA, Shanley M, Opheim DJ (1979) J Bacteriol 173:285–294

    Google Scholar 

  • Fraenkel DG (1982) In: Strathern JN, Jones EW, Broach JR (eds) The molecular biology of the yeast Saccharomyces, pt 2. Cold Spring Harbor Laboratory, Cold Spring Harbor, New York, pp 1–37

    Google Scholar 

  • Grenson M, Hou C, Crabeel M (1970) J Bacteriol 103:770–777

    Google Scholar 

  • Gresham RL, Moat AG (1973) J Bacteriol 115:975–981

    Google Scholar 

  • Jones EW, Fink RF (1982) In: Strathern JN, Jones EW, Broach JR (eds) The molecular biology of yeast Saccharomyces, pt 2. Cold Spring Harbor Laboratory, Cold Spring Harbor, New York, pp 181–299

    Google Scholar 

  • Kane M, Roth B (1974) J Bacteriol 118:8–14

    Google Scholar 

  • Lang G, Michal G (1965) In: Bergmeyer HU (ed) Methods of enzymatic analysis. Academic Press, London, pp 1239–1242

    Google Scholar 

  • Michal G, Beutler H-O (1965) In: Bergmeyer HU (ed) Methods of enzymatic analysis. Academic Press, London, pp 1314–1319

    Google Scholar 

  • Ono B, Sakamoto E (1985) Curr Genet 10:179–185

    Google Scholar 

  • Roon RG, Meyer GM, Larimore FS (1977) Mol Gen Genet 158:185–191

    Google Scholar 

  • Sakamoto E, Urata H, Ono B (1985) Curr Genet 10:187–195

    Google Scholar 

  • Scott Jr, TA, and Melvin EH (1953) Anal Chem 25:1656–1661

    Google Scholar 

  • Trevelyan WE, Harrison JS (1956) Biochem J 63:23–33

    Google Scholar 

Download references

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Ono, Bi., Sakamoto, E. & Yamaguchi, K. Saccharomyces cerevisiae strains sensitive to inorganic mercury. Curr Genet 11, 399–406 (1987). https://doi.org/10.1007/BF00378183

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  • DOI: https://doi.org/10.1007/BF00378183

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