Use of new methods for construction of tightly regulated arabinose and rhamnose promoter fusions in studies of the Escherichia coli phosphate regulon.
about
A highly sensitive selection method for directed evolution of homing endonucleases.The X-ray Crystal Structures of Two Constitutively Active Mutants of the Escherichia coli PhoB Receiver Domain Give Insights into ActivationOne-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR productsAtypical Role for PhoU in Mutagenic Break Repair under Stress in Escherichia coliA nanobody:GFP bacterial platform that enables functional enzyme display and easy quantification of display capacityDirected evolution of the transcription factor XylS for development of improved expression systemsConditional-replication, integration, excision, and retrieval plasmid-host systems for gene structure-function studies of bacteriaIdentification of a Streptococcus pneumoniae gene locus encoding proteins of an ABC phosphate transporter and a two-component regulatory systemThe unphosphorylated receiver domain of PhoB silences the activity of its output domainRegulation of stalk elongation by phosphate in Caulobacter crescentus.Streptococcus pneumoniae PstS production is phosphate responsive and enhanced during growth in the murine peritoneal cavityLong-term and homogeneous regulation of the Escherichia coli araBAD promoter by use of a lactose transporter of relaxed specificityOrganization and coordinated assembly of the type III secretion export apparatus.Mapping of orthologous genes in the context of biological pathways: An application of integer programming.Mechanism of regulation of phosphate dissociation from actomyosin-ADP-Pi by thin filament proteins.Burkholderia cenocepacia conditional growth mutant library created by random promoter replacement of essential genes.Synthetic lac operator substitutions for studying the nitrate- and nitrite-responsive NarX-NarL and NarQ-NarP two-component regulatory systems of Escherichia coli K-12.Evolutionary tuning of protein expression levels of a positively autoregulated two-component system.Isolation of peptide aptamers that inhibit intracellular processes.Genetic analysis, structural modeling, and direct coupling analysis suggest a mechanism for phosphate signaling in Escherichia coli.Comparative Single-Cell Analysis of Different E. coli Expression Systems during Microfluidic Cultivation.Interplay between genetic regulation of phosphate homeostasis and bacterial virulence.In vivo characterization of the type A and B vancomycin-resistant enterococci (VRE) VanRS two-component systems in Escherichia coli: a nonpathogenic model for studying the VRE signal transduction pathwaysBreaking evolutionary constraint with a tradeoff ratchet.Substitutions at auxiliary operator O3 enhance repression by nitrate-responsive regulator NarL at synthetic lac control regions in Escherichia coli K-12Probing kinase and phosphatase activities of two-component systems in vivo with concentration-dependent phosphorylation profiling.Discovery of a rhamnose utilization pathway and rhamnose-inducible promoters in Pichia pastoris.Low-pH rescue of acid-sensitive Salmonella enterica Serovar Typhi Strains by a Rhamnose-regulated arginine decarboxylase system.Employment of a promoter-swapping technique shows that PhoU modulates the activity of the PstSCAB2 ABC transporter in Escherichia coliActivation of the Rcs signal transduction system is responsible for the thermosensitive growth defect of an Escherichia coli mutant lacking phosphatidylglycerol and cardiolipin.Positively regulated bacterial expression systems.Recent progress in synthetic biology for microbial production of C3-C10 alcohols.The HilA box and sequences outside it determine the magnitude of HilA-dependent activation of P(prgH) from Salmonella pathogenicity island 1.RpoS synthesis is growth rate regulated in Salmonella typhimurium, but its turnover is not dependent on acetyl phosphate synthesis or PTS function.Dual transcriptional-translational cascade permits cellular level tuneable expression control.Tunable recombinant protein expression in E. coli: promoter systems and genetic constraintsSingle-copy green fluorescent protein gene fusions allow accurate measurement of Salmonella gene expression in vitro and during infection of mammalian cellsCombined inactivation and expression strategy to study gene function under physiological conditions: application to identification of new Escherichia coli adhesins.The Escherichia coli rhaSR-PrhaBAD Inducible Promoter System Allows Tightly Controlled Gene Expression over a Wide Range in Pseudomonas aeruginosa.Rapid and efficient construction of markerless deletions in the Escherichia coli genome
P2860
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P2860
Use of new methods for construction of tightly regulated arabinose and rhamnose promoter fusions in studies of the Escherichia coli phosphate regulon.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
Use of new methods for constru ...... richia coli phosphate regulon.
@en
Use of new methods for constru ...... richia coli phosphate regulon.
@nl
type
label
Use of new methods for constru ...... richia coli phosphate regulon.
@en
Use of new methods for constru ...... richia coli phosphate regulon.
@nl
prefLabel
Use of new methods for constru ...... richia coli phosphate regulon.
@en
Use of new methods for constru ...... richia coli phosphate regulon.
@nl
P2093
P2860
P1476
Use of new methods for constru ...... erichia coli phosphate regulon
@en
P2093
A Haldimann
B L Wanner
L L Daniels
P2860
P304
P407
P577
1998-03-01T00:00:00Z