Using promoter libraries to reduce metabolic burden due to plasmid-encoded proteins in recombinant Escherichia coli

Keyphrases

• Plasmid Encoded 100%
• Glycine 100%
• Encoded Protein 100%
• Repressor Protein 100%
• Promoter Library 100%
• Metabolic Burden 100%
• Plasmid Maintenance 100%
• Auxotrophic Marker 100%
• Recombinant Escherichia Coli 100%
• Maintenance Mechanism 50%
• Phosphate 50%
• Overexpression 50%
• Growth Inhibition 50%
• Host Cell 50%
• Protein Production 50%
• Recombinant 50%
• Metabolic Pathway 50%
• LacI 50%
• Expression Level 50%
• Overproduction 50%
• Growth Kinetics 50%
• Production Increase 50%
• Physiological Response 50%
• Fucose 50%
• Expression System 50%
• Acetic Acid Production 50%
• Metabolic Load 50%
• Mechanism-based 50%
• Heterologous Protein Expression 50%
• Antibiotic Resistance Genes 50%
• Growth Parameters 50%
• Antibiotic-free 50%
• Generation System 50%
• Free Expression 50%
• Synthetic Biology Tools 50%
• Aldolase 50%
• Antibiotic-free Plasmid 50%
• Rapid Construction 50%
• Escherichia Coli Expression 50%
• Maintenance Proteins 50%
• Secondary Metabolism 50%

Biochemistry, Genetics and Molecular Biology

• Escherichia coli 100%
• Plasmid 100%
• Promoter Region 100%
• Repressor Protein 50%
• Acetic Acid 25%
• Growth Inhibition 25%
• Protein Expression 25%
• Gene Expression System 25%
• Antibiotic Resistance Gene 25%
• Fructose-Bisphosphate Aldolase 25%
• Aldolase 25%
• Secondary Metabolism 25%

Immunology and Microbiology

• Escherichia coli 100%
• Plasmid 100%
• Promoter Region 100%
• Repressor Gene 50%
• Growth Inhibition 25%
• Acetic Acid 25%
• Host Cell 25%
• Protein Expression 25%
• Antimicrobial Resistance 25%
• Gene Expression System 25%
• Secondary Metabolism 25%