The metabolic potential of Escherichia coli BL21 in defined and rich medium. - Wikidata - wikimedia - TriplyDB

The metabolic potential of Escherichia coli BL21 in defined and rich medium.

The metabolic potential of Escherichia coli BL21 in defined and rich medium.

http://www.wikidata.org/entity/Q39625992

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Proteomic analysis of enterotoxigenic Escherichia coli (ETEC) in neutral and alkaline conditions.Genomic and transcriptomic landscape of Escherichia coli BL21(DE3)Smart sustainable bottle (SSB) system for E. coli based recombinant protein production.A Minimalistic Resource Allocation Model to Explain Ubiquitous Increase in Protein Expression with Growth Rate.Constrained Allocation Flux Balance Analysis A peptide identification-free, genome sequence-independent shotgun proteomics workflow for strain-level bacterial differentiation.Efficient expression of sortase A from Staphylococcus aureus in Escherichia coli and its enzymatic characterizations.Structural and functional features of self-assembling protein nanoparticles produced in endotoxin-free Escherichia coli.Acetate metabolism regulation in Escherichia coli: carbon overflow, pathogenicity, and beyond.Proteome reallocation in Escherichia coli with increasing specific growth rate.Metabolic profiling of recombinant Escherichia coli cultivations based on high-throughput FT-MIR spectroscopic analysis.Challenges and Hallmarks of Establishing Alkylacetylphosphonates as Probes of Bacterial 1-Deoxy-d-xylulose 5-Phosphate Synthase.Rapid label-free quantitative analysis of the E. coli BL21(DE3) inner membrane proteome.Experimental design-aided systematic pathway optimization of glucose uptake and deoxyxylulose phosphate pathway for improved amorphadiene production.RNA Sequencing Identifies New RNase III Cleavage Sites in Escherichia coli and Reveals Increased Regulation of mRNA.Acetate: friend or foe? Efficient production of a sweet protein in Escherichia coli BL21 using acetate as a carbon source.Production of the short peptide surfactant DAMP4 from glucose or sucrose in high cell density cultures of Escherichia coli BL21(DE3).Increasing dissolved-oxygen disrupts iron homeostasis in production cultures of Escherichia coli.Interactions between genotype and environment drive the metabolic phenotype within Escherichia coli isolates.Improving Fab' fragment retention in an autonucleolytic Escherichia coli strain by swapping periplasmic nuclease translocation signal from OmpA to DsbA.High yield purification and first structural characterization of the full-length bacterial toxin CNF1.Systems assessment of transcriptional regulation on central carbon metabolism by Cra and CRP.Growth and Extended Survival of Escherichia coli O157:H7 in Soil Organic Matter.

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P2860

The metabolic potential of Escherichia coli BL21 in defined and rich medium.

http://www.wikidata.org/entity/Q39625992

description

2014 nî lūn-bûn

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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2014年论文

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2014年论文

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name

The metabolic potential of Escherichia coli BL21 in defined and rich medium.

@en

The metabolic potential of Escherichia coli BL21 in defined and rich medium.

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type

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The metabolic potential of Escherichia coli BL21 in defined and rich medium.

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The metabolic potential of Escherichia coli BL21 in defined and rich medium.

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The metabolic potential of Escherichia coli BL21 in defined and rich medium.

@en

The metabolic potential of Escherichia coli BL21 in defined and rich medium.

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Microbial Cell Factories

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The metabolic potential of Escherichia coli BL21 in defined and rich medium.

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Manfred Nimtz

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Zhaopeng Li

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P2860

High-level production of amorpha-4,11-diene, a precursor of the antimalarial agent artemisinin, in Escherichia coli

KEGG: kyoto encyclopedia of genes and genomes

Protein identification from two-dimensional gel electrophoresis analysis of Klebsiella pneumoniae by combined use of mass spectrometry data and raw genome sequences.

RegulonDB version 7.0: transcriptional regulation of Escherichia coli K-12 integrated within genetic sensory response units (Gensor Units)

Genomic comparisons among Escherichia coli strains B, K-12, and O157:H7 using IS elements as molecular markers.

Systems biology approach reveals that overflow metabolism of acetate in Escherichia coli is triggered by carbon catabolite repression of acetyl-CoA synthetase

Engineering a mevalonate pathway in Escherichia coli for production of terpenoids

Control of bacterial transcription, translation and replication by (p)ppGpp

A method for the quantitative recovery of protein in dilute solution in the presence of detergents and lipids

Metabolic deficiences revealed in the biotechnologically important model bacterium Escherichia coli BL21(DE3)

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