Temperature and oxygen regulated expression of a glutamine synthetase gene fromVibrio alginolyticus cloned inEscherichia coli |
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Authors: | Romilla Maharaj Frank T. Robb David R. Woods |
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Affiliation: | (1) UCT/CSIR Microbial Genetics Research Unit, Department of Microbiology, University of Cape Town, 7700 Rondebosch, South Africa |
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Abstract: | Glutamine synthetase (GS) synthesis inVibrio alginolyticus was regulated by temperature, oxygen and nitrogen levels. A GS gene,glnA fromV. alginolyticus was cloned on a 5.67 kb insert in the recombinant plasmid pRM210, which enabledEscherichia coli glnA, ntrB, ntrC deletion mutants to utilize (NH4)2SO4 as a sole source of nitrogen. TheV. alginolyticus glnA gene was expressed from a regulatory region contained within the cloned fragment.V. alginolyticus glnA expression from pRM210 was subject to regulation by temperature, oxygen and nitrogen levels. GS specific activity in anE. coli wild-type strain was not affected by temperature or oxygen. pRM211 was a deletion derivative of pRM210 and GS production by pRM211 was not regulated by temperature, oxygen or nitrogen levels inE. coli.Abbreviation GS glutamine synthetase |
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Keywords: | Vibrio alginolyticus Glutamine synthetase Cloning glutamine synthetase Temperature and oxygen regulation glutamine synthetase |
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