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Recombinant protein expression in proteome-reduced cells under aerobic and oxygen-limited regimes.
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Transport-controlled growth decoupling for self-induced protein expression with a glycerol-repressible genetic circuit.
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Physiological response of escherichia coli W3110 and BL21 to the aerobic expression of vitreoscilla hemoglobin.
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Fast dynamic response of the fermentative metabolism of Escherichia coli to aerobic and anaerobic glucose pulses.
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Engineering Escherichia coli to improve culture performance and reduce formation of by-products during recombinant protein production under transient intermittent anaerobic conditions.
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Effect of the oxygen transfer rate on oxygen-limited production of plasmid DNA by Escherichia coli.
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Characterization of Endogenous and Reduced Promoters for Oxygen-Limited Processes Using Escherichia coli.
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Design of a synthetic miniR1 plasmid and its production by engineered Escherichia coli.
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Transcriptional and metabolic response of recombinant Escherichia coli to spatial dissolved oxygen tension gradients simulated in a scale-down system.
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Comparison of oxygen enriched air vs. pressure cultivations to increase oxygen transfer and to scale-up plasmid DNA production fermentations.
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Evaluation of microbial globin promoters for oxygen-limited processes using Escherichia coli.
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Utility of an Escherichia coli strain engineered in the substrate uptake system for improved culture performance at high glucose and cell concentrations: An alternative to fed-batch cultures.
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Biomanufacturing Potential of Streamlined Cells.
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Model-Based Characterization of E. coli Strains with Impaired Glucose Uptake.
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High cell-density processes in batch mode of a genetically engineered Escherichia coli strain with minimized overflow metabolism using a pressurized bioreactor.
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Aerobic expression of Vitreoscilla hemoglobin improves the growth performance of CHO-K1 cells.
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Heterogeneous oxygen availability affects the titer and topology but not the fidelity of plasmid DNA produced by Escherichia coli.
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Engineering E. coli for improved microaerobic pDNA production.
Bioprocess and Biosystems Engineering,
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High kanamycin concentration as another stress factor additional to temperature to increase pdna production in e. Coli dh5α batch and fed-batch cultures.
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