Effect of glucose supply strategy on acetate accumulation, growth, and recombinant protein production by Escherichia coli BL21 (lambdaDE3) and Escherichia coli JM109.
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Improvement of Escherichia coli production strains by modification of the phosphoenolpyruvate:sugar phosphotransferase systemMinimal Escherichia coli cell for the most efficient production of ethanol from hexoses and pentosesExpression of Clostridium acetobutylicum ATCC 824 genes in Escherichia coli for acetone production and acetate detoxificationExpression, purification, and characterization of rhTyrRS.Glucose uptake regulation in E. coli by the small RNA SgrS: comparative analysis of E. coli K-12 (JM109 and MG1655) and E. coli B (BL21).Recombinant production of human interleukin 6 in Escherichia coliA comparative analysis of industrial Escherichia coli K-12 and B strains in high-glucose batch cultivations on process-, transcriptome- and proteome level.Construction of Escherichia coli Mutant with Decreased Endotoxic Activity by Modifying Lipid A Structure.Evaluating microarrays using a semiparametric approach: application to the central carbon metabolism of Escherichia coli BL21 and JM109.Fed-batch like cultivation in a micro-bioreactor: screening conditions relevant for Escherichia coli based production processes.Increasing recombinant protein production in Escherichia coli through metabolic and genetic engineering.Acetate metabolism regulation in Escherichia coli: carbon overflow, pathogenicity, and beyond.Evaluation of three industrial Escherichia coli strains in fed-batch cultivations during high-level SOD protein production.Comparative analysis of L-sorbose dehydrogenase by docking strategy for 2-keto-L-gulonic acid production in Ketogulonicigenium vulgare and Bacillus endophyticus consortium.Characterization of growth and acid formation in a Bacillus subtilis pyruvate kinase mutant.Expression of an anaplerotic enzyme, pyruvate carboxylase, improves recombinant protein production in Escherichia coliModification of glucose import capacity in Escherichia coli: physiologic consequences and utility for improving DNA vaccine productionEfficient process development of recombinant human granulocyte colony-stimulating factor (rh-GCSF) production in Escherichia coli.Multi-omics Quantification of Species Variation of Escherichia coli Links Molecular Features with Strain Phenotypes.The use of nano-sized acicular material, sliding friction, and antisense DNA oligonucleotides to silence bacterial genes.Direct measurements of IPTG enable analysis of the induction behavior of E. coli in high cell density cultures.Metabolic network capacity of Escherichia coli for Krebs cycle-dependent proline hydroxylation.Down Regulation of ackA-pta Pathway in Escherichia coli BL21 (DE3): A Step Toward Optimized Recombinant Protein Expression SystemFed-batch cultivation of Escherichia coli expressed designer hepatitis C virus diagnostic intermediate and its evaluation.Avoiding acetate accumulation in Escherichia coli cultures using feedback control of glucose feeding.Time-resolved selected ion flow tube mass spectrometric quantification of the volatile compounds generated by E. coli JM109 cultured in two different media.Optimization of expression of untagged and histidine-tagged human recombinant thrombin precursors in Escherichia coli.Online measurement of the respiratory activity in shake flasks enables the identification of cultivation phases and patterns indicating recombinant protein production in various E. coli host strains.High throughput automated microbial bioreactor system used for clone selection and rapid scale-down process optimization.Recombinant biosynthesis of bacterial cellulose in genetically modified Escherichia coli.Very high-level production and export in Escherichia coli of a cellulose binding domain for use in a generic secretion-affinity fusion system.Optimization of fermentation conditions for the production of curcumin by engineered Escherichia coli.Effect of iclR and arcA deletions on physiology and metabolic fluxes in Escherichia coli BL21 (DE3).Optimization of culture conditions for enhanced lysine production using engineered Escherichia coli.Two-stage cultivation of Pseudomonas sp. F12 for the production of enzymes converting DL-2-amino-Δ²-thiazoline-4-carboxylic acid to L-cysteine.Regulation of acetate metabolism in Escherichia coli BL21 by protein N(ε)-lysine acetylation.Using small molecules as a new challenge to redirect metabolic pathway.A Novel Process for Cadaverine Bio-Production Using a Consortium of Two Engineered Escherichia coli.E. coli HMS174(DE3) is a sustainable alternative to BL21(DE3)
P2860
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P2860
Effect of glucose supply strategy on acetate accumulation, growth, and recombinant protein production by Escherichia coli BL21 (lambdaDE3) and Escherichia coli JM109.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年学术文章
@wuu
1996年学术文章
@zh
1996年学术文章
@zh-cn
1996年学术文章
@zh-hans
1996年学术文章
@zh-my
1996年学术文章
@zh-sg
1996年學術文章
@yue
1996年學術文章
@zh-hant
name
Effect of glucose supply strat ...... 3) and Escherichia coli JM109.
@en
Effect of glucose supply strat ...... 3) and Escherichia coli JM109.
@nl
type
label
Effect of glucose supply strat ...... 3) and Escherichia coli JM109.
@en
Effect of glucose supply strat ...... 3) and Escherichia coli JM109.
@nl
prefLabel
Effect of glucose supply strat ...... 3) and Escherichia coli JM109.
@en
Effect of glucose supply strat ...... 3) and Escherichia coli JM109.
@nl
P2093
P2860
P1476
Effect of glucose supply strat ...... 3) and Escherichia coli JM109.
@en
P2093
P2860
P304
P356
10.1002/(SICI)1097-0290(19960220)49:4<421::AID-BIT9>3.0.CO;2-R
P577
1996-02-01T00:00:00Z