(Q54431432)

29 May 2018

title

The transcriptional response of Escherichia coli to recombinant protein insolubility. (English)

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29 May 2018

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Harold E Smith

1

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29 May 2018

publication date

1 March 2007

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29 May 2018

Journal of Structural and Functional Genomics

published in

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29 May 2018

volume

8

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29 May 2018

issue

1

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29 May 2018

page(s)

27-35

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29 May 2018

https://scigraph.springernature.com/pub.10.1007/s10969-007-9030-7

exact match

0 references

cites work

ClpB cooperates with DnaK, DnaJ, and GrpE in suppressing protein aggregation. A novel multi-chaperone system from Escherichia coli

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12 December 2020

Strategies for efficient production of heterologous proteins in Escherichia coli

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Regulon and promoter analysis of the E. coli heat-shock factor, sigma32, reveals a multifaceted cellular response to heat stress

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The global transcriptional response of Escherichia coli to induced sigma 32 protein involves sigma 32 regulon activation followed by inactivation and degradation of sigma 32 in vivo.

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Identification of protein-protein interactions of the major sperm protein (MSP) of Caenorhabditis elegans

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Protein misfolding and inclusion body formation in recombinant Escherichia coli cells overexpressing Heat-shock proteins.

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In vivo observation of polypeptide flux through the bacterial chaperonin system.

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Use of bacteriophage T7 lysozyme to improve an inducible T7 expression system

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Roles and applications of small heat shock proteins in the production of recombinant proteins in Escherichia coli.

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Back to log phase: sigma S as a global regulator in the osmotic control of gene expression in Escherichia coli

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A novel strategy for production of a highly expressed recombinant protein in an active form

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A chaperone network controls the heat shock response in E. coli

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Polypeptide flux through bacterial Hsp70: DnaK cooperates with trigger factor in chaperoning nascent chains

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Two novel heat shock genes encoding proteins produced in response to heterologous protein expression in Escherichia coli

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Levels of DnaK and DnaJ provide tight control of heat shock gene expression and protein repair in Escherichia coli.

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12 December 2020

DnaK, DnaJ, and GrpE heat shock proteins negatively regulate heat shock gene expression by controlling the synthesis and stability of sigma 32.

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Chaperone-based procedure to increase yields of soluble recombinant proteins produced in E. coli

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Gene expression response to misfolded protein as a screen for soluble recombinant protein.

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2.5 A resolution crystal structure of the motile major sperm protein (MSP) of Ascaris suum

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Soluble expression of recombinant proteins in the cytoplasm of Escherichia coli

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12 December 2020

Physical interaction between heat shock proteins DnaK, DnaJ, and GrpE and the bacterial heat shock transcription factor sigma 32

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Overexpression of trigger factor prevents aggregation of recombinant proteins in Escherichia coli

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12 December 2020

IbpA and IbpB, the new heat-shock proteins, bind to endogenous Escherichia coli proteins aggregated intracellularly by heat shock

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12 December 2020

Use of bacteriophage T7 RNA polymerase to direct selective high-level expression of cloned genes

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12 December 2020

Trigger factor and DnaK cooperate in folding of newly synthesized proteins.

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12 December 2020

Inclusion body anatomy and functioning of chaperone-mediated in vivo inclusion body disassembly during high-level recombinant protein production in Escherichia coli

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12 December 2020

Sigma 32 synthesis can regulate the synthesis of heat shock proteins in Escherichia coli.

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12 December 2020

Roles of heat-shock chaperones in the production of recombinant proteins in Escherichia coli.

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12 December 2020

Recombinant protein folding and misfolding in Escherichia coli

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12 December 2020

10.1007/S10969-007-9030-7

Identifiers

DOI

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29 May 2018

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29 May 2018