Construction and use of new cloning vectors for the rapid isolation of recombinant proteins from Escherichia coli. (Q38521352)

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3 January 2020

title

Construction and use of new cloning vectors for the rapid isolation of recombinant proteins from Escherichia coli (English)

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3 January 2020

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1

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3 January 2020

Ivan Rayment

4

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3 January 2020

author name string

K L Dennison

2

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3 January 2020

Vadim A Klenchin

3

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J C Escalante-Semerena

5

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publication date

4 March 2008

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3 January 2020

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volume

59

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issue

3

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3 January 2020

page(s)

231-237

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The three-dimensional crystal structure of the PrpF protein ofShewanella oneidensiscomplexed withtrans-aconitate: Insights into its biological function

3 January 2020

cites work

1 reference

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A combined approach to improving large-scale production of tobacco etch virus protease

6 September 2017

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Single-enzyme conversion of FMNH2 to 5,6-dimethylbenzimidazole, the lower ligand of B12

6 September 2017

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A family of E. coli expression vectors for laboratory scale and high throughput soluble protein production

6 September 2017

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Simplified screening for the detection of soluble fusion constructs expressed in E. coli using a modular set of vectors

6 September 2017

1 reference

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Improved solubility of TEV protease by directed evolution

6 September 2017

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Large-scale protein expression for proteome research

6 September 2017

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Studies on lysogenesis. I. The mode of phage liberation by lysogenic Escherichia coli

6 September 2017

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Lysogeny at mid-twentieth century: P1, P2, and other experimental systems

6 September 2017

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Release of proteins and peptides from fusion proteins using a recombinant plant virus proteinase

6 September 2017

1 reference

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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

6 September 2017

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Construction of Biologically Functional Bacterial Plasmids In Vitro

6 September 2017

1 reference

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

6 September 2017

1 reference

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Vectors for selective expression of cloned DNAs by T7 RNA polymerase

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2386272

Vectors that facilitate the expression and purification of foreign peptides in Escherichia coli by fusion to maltose-binding protein

6 September 2017

1 reference

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High efficiency transformation of Escherichia coli with plasmids

6 September 2017

1 reference

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Use of T7 RNA polymerase to direct expression of cloned genes

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2386272

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2386272

Utilizing the C-terminal cleavage activity of a protein splicing element to purify recombinant proteins in a single chromatographic step

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2386272

Tricarballylate catabolism in Salmonella enterica. The TcuB protein uses 4Fe-4S clusters and heme to transfer electrons from FADH2 in the tricarballylate dehydrogenase (TcuA) enzyme to electron acceptors in the cell membrane

14 September 2017

1 reference

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Large-scale purification of a stable form of recombinant tobacco etch virus protease

31 August 2018

1 reference

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Single-column purification of free recombinant proteins using a self-cleavable affinity tag derived from a protein splicing element

31 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18295882

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

An Escherichia coli vector to express and purify foreign proteins by fusion to and separation from maltose-binding protein

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18295882

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Structural characterization of the active site of the PduO-type ATP:Co(I)rrinoid adenosyltransferase from Lactobacillus reuteri.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18295882

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.PLASMID.2008.01.001

1 reference

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3 January 2020

1 reference

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3 January 2020

PubMed publication ID

18295882

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