Biotechnology and Applied Biochemistry · 2003 · 21 citations · 17 references
Life SciencesMicrobiologyMolecular BiologyBioenergeticsMicrobial GeneticsMicrobial PhysiologyCellular RespirationMicrobial GrowthPlasmid BiologyPlasmid GeneticsRespiratory MetabolismAerobic GrowthChemostat CultureChemostat Culture AnalysisOxygen Uptake RatePlasmid - Host InteractionsPlasmid Size OptimizationSpecific Oxygen Uptake Rate
Escherichia coli DH5alpha harbouring either pBGS18, a 4.4 kb pUC-based plasmid, or pQR150, a 20 kb derivative of pBGS18, were grown in glucose-limited chemostat culture to investigate the effects of plasmid size and recombinant protein production on oxygen demand. Under non-induced conditions, where no recombinant protein was expressed, the cellular oxygen demand of cells harbouring pBGS18 and pQR150 was not significantly different, mean specific oxygen uptake rate (OUR) being 0.75+/-0.24 and 0.78+/-0.32 mmol/h per mg of plasmid respectively. Under isopropyl beta-D-thiogalactoside-induced conditions, where recombinant protein was expressed, cells harbouring pBGS18 demonstrated a statistically insignificant 37% increase in mean specific OUR while those harbouring pQR150 demonstrated a statistically significant 415% increase. It is concluded that plasmid size does not significantly affect oxygen demand and that increasing oxygen demand observed with increasing plasmid size is due to production of recombinant protein.
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Molecular cloning: A laboratory manual
Prescott L. Deininger · Analytical Biochemistry · 1990 · 86.2K citations
Metabolic load and heterologous gene expression
Bernard R. Glick · Biotechnology Advances · 1995 · 677 citations