Production of cloned carboxypeptidase G2 by Escherichia coli: Genetic and environmental considerations
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Summary
The optimum production of cloned carboxypeptidase G2 from plasmid pNM21 byEscherichiacoli was found to be strongly strain- and temperature-dependent. The superior host was strain RV308 and the preferred growth temperature 28°C. Copy number, which decreased during exponential growth of all strains examined, did not relate in these studies to the level of enzyme production: the strain with the highest enzyme yield also having the lowest overall copy number.
Keywords
Enzyme Escherichia Coli Exponential Growth Growth Temperature Enzyme Production
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References
- Cesarini, G. and Banner, D. W. (1985). Trends in Biochem. Sci.10, 303–306.Google Scholar
- Della Latta, P., Bouanchaud, D. and Novick, R. P. (1978). Plasmid1, 366–375.PubMedGoogle Scholar
- Ford, J. (1967). Chem. and Ind., 1556–1557.Google Scholar
- Imanaka, T. (1986). Advances in Biochemical Engineering. Biotechnology, Vol. 33, p. 1–27. Fiechter, A. (Ed) Berlin, Springer Verlag.Google Scholar
- Imanaka, T., Tsunekawa, H. and Schuichi, A. (1980). J. Gen. Microbiol.118, 253–261.PubMedGoogle Scholar
- Kalghati, K. K. and Bertino, J. R. (1981). Folate degrading enzymes: a review with special emphasis on carboxypeptidase G, p 77–102.In: Enzymes as drugs, Mopcenburg, J. S. and Roberts, J. (eds.), New York, John Wiley.Google Scholar
- Mandel, M. and Higa, A. (1970). J. Mol. Biol.53, 159–162.PubMedGoogle Scholar
- McEntee, J. D., McEntee, I. D. and Sharp, R. J. (1989). Monitoring of ATP in fermentation seed cultures and in bacterial fermentations. (in press). Conference Proceedings of the Society for Applied Bacteriology. (April 1988).Google Scholar
- Meacock, P. A. and Cohen, S. N. (1980). Cell20, 529–542.PubMedGoogle Scholar
- Miles, A. A. and Misra, S. S. (1938). J. Hygiene38, 732–749.Google Scholar
- Minton, N. P., Atkinson, T. and Sherwood, R. F. (1983). J. Bact.156, 1222–1227.PubMedGoogle Scholar
- Minton, N. P., Atkinson, T., Bruton, C. J. and Sherwood, R. F. (1984). Gene31, 31–38.PubMedGoogle Scholar
- Noack, D., Roth, M., Geuther, R., Muller, G., Undisz, K., Hoffmeier, C. and Gaspar, S. Mol. Gen. Genet.184, 121–124.Google Scholar
- Nordstrom, K. and Aagaard-Hansen, H. (1984). Mol. Gen. Genet.197, 1–7.PubMedGoogle Scholar
- Nordstrom, K., Molin, S. and Aagaard-Hansen, H. (1988). Plasmid,4, 215–227.Google Scholar
- Projan, S. J., Carleton, S. and Novick, R. P. (1983). Plasmid,9, 182–190.PubMedGoogle Scholar
- Scott, J. R. (1984). Microbiol. Revs.48, 1–23.Google Scholar
- Sherwood, R. F., Melton, R. G., Alwan, S. M. and Hughes, P. (1985). Eur. J. Biochem.148, 447–453.PubMedGoogle Scholar
- Uhlin, B. and Nordstrom, K. (1977). Plasmid,1, 1–7.PubMedGoogle Scholar
- Weichselbaum, T. E. (1946). Amer. J. Clin. Path.16, 40.Google Scholar
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