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l-Asparaginase II of Saccharomyces cerevisiae

Activity profile during growth using an ure 2 mutant P40-3C and a P40-3C+URE2p strain

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Abstract

The activity profile of the periplasmic asparaginase of Saccharomyces cerevisiae was determined during cell growth in an ure2 mutant; in an ure2 transformed with a plasmid containing the gene URE2 and, for comparison, in the strain D273-10B. Cells were cultivated in media presenting variable quantitative and qualitative nitrogen availability and the enzyme activity was evaluated in fresh and in nitrogen-starved cells. Nitrogen affected the asparaginase II level in fresh and starved cells of all strains. In the best condition, enzyme was produced by the wild-type cells at the late log-phase in the glucose/ammonium medium with a carbon to nitrogen ratio 4.3:1. Upon starvation, the activity doubled. The overall profile of the transformed strain was similar to that of the wild-type strain. In the ure2 mutant, highenzyme levels were observed during growth, as expected. However the activity level, upon starvation, in proline grown cells, increased sixfold, suggesting that in addition to the Ure2p-Gln3p system, another system regulates asparaginase II biosynthesis.

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References

  1. Bon, E. P. S., Carvajal, E., Stambrough, M., and Magasanik, B. (1997), Appl. Biochem. Biotechnol. 63/65, 1203–212.

    Article  Google Scholar 

  2. Magasanik, B. (1992), in The Molecular and Cellular Biology of the Yeast Saccharomyces: Gene Expression, vol. 2, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY pp. 283–317.

    Google Scholar 

  3. Coffman, J. A. and Cooper, T. G. (1997), J. Bacteriol. 179(17), 5609–5613.

    CAS  Google Scholar 

  4. Dunlop, P. C. and Roon, R. J. (1975), J. Bacteriol. 22, 1017–1024.

    Google Scholar 

  5. Pauling, K. D. and Jones, G. E. (1980), J. Gen. Microbiol. 117, 423–430.

    CAS  Google Scholar 

  6. Ito, H., Fukada, Y., Murato, K., and Kimiru, A. (1983), J. Bacteriol. 153, 163–168.

    CAS  Google Scholar 

  7. Jones, G. E. (1977), J. Bacteriol. 129, 1165–1167.

    CAS  Google Scholar 

  8. Kim, K. W., Kameruda, J. Q., Livingston, D. M., and Roon, R. J. (1988), J. Biol. Chem. 263, 11,948–11,953.

    CAS  Google Scholar 

  9. Stanbrough, M. and Magasanik, B. (1995), J. Bacteriol. 94, 102.

    Google Scholar 

  10. Stanbrough, M., Rowen, D. W., and Magazsanik, B. (1995), Proc. Natl. Acad. Sci. USA 92, 9450–9454.

    Article  CAS  Google Scholar 

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Correspondence to Elba P. S. Bon.

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Oliveira, E.M.M., Carvajal, E. & Bon, E.P.S. l-Asparaginase II of Saccharomyces cerevisiae . Appl Biochem Biotechnol 77, 311–316 (1999). https://doi.org/10.1385/ABAB:77:1-3:311

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  • DOI: https://doi.org/10.1385/ABAB:77:1-3:311

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