Bacterial Cpn60 proteins (homologues to the Escherichia coli GroEL protein) are often examined for function by testing their ability to complement a temperature sensitive mutation in the E. coli groEL gene. Such tests suffer from two drawbacks: the Cpn600 protein may come from a strain with a lower optimum growth temperature than E. coli, and the requirements for successful complementation in E. coli are likely to be more stringent at 43 degrees C than at lower temperatures. Here we describe the construction of a strain of E. coli where the chromosomal gene for the essential molecular chaperone GroEL has been deleted, with GroEL being expressed from a tightly regulated plasmid borne copy of the gene. The deletion can be transduced into stra...
The molecular mechanism supporting survival at a critical high temperature (CHT) in Escherichia coli...
Cochaperonins (cpn10) assist chaperonins (cpn60) in promoting folding and assembly of other proteins...
Barreiro C, Gonzalez-Lavado E, Brand S, Tauch A, Martin JF. Heat shock Proteome analysis of wild-typ...
Bacterial Cpn60 proteins (homologues to the Escherichia coli GroEL protein) are often examined for f...
Although many bacteria contain only a single groE operon encoding the essential chaperones GroES and...
Here, we demonstrate that the overexpression of the GroELS chaperone system, which assists the foldi...
The heat shock response of the psychrophilic bacterium Pseudoalteromonas haloplanktis TAC 125 (PhTAC...
The heat shock response of the psychrophilic bacterium Pseudoalteromonas haloplanktis TAC 125 (PhTAC...
Proteome analysis of Corynebacterium glutamicum ATCC 13032 showed that levels of several proteins in...
The GroES and GroEL proteins of Escherichia coli function together as the GroE molecular chaperone m...
The molecular mechanism supporting survival at a critical high temperature (CHT) in Escherichia coli...
Abstract GroEL is a multifunctional protein belonging to the conspicuous family of chaperones active...
We have recently identified a new gene of Escherichia coli, called greA, which is involved in the re...
[出版社版]The photosynthetic prokaryotic cyanobacteria generally have two copies of the groEL or chapero...
Cyanobacterial genomes generally contain two groEL genes, referred to as groEL1 and groEL2. The purp...
The molecular mechanism supporting survival at a critical high temperature (CHT) in Escherichia coli...
Cochaperonins (cpn10) assist chaperonins (cpn60) in promoting folding and assembly of other proteins...
Barreiro C, Gonzalez-Lavado E, Brand S, Tauch A, Martin JF. Heat shock Proteome analysis of wild-typ...
Bacterial Cpn60 proteins (homologues to the Escherichia coli GroEL protein) are often examined for f...
Although many bacteria contain only a single groE operon encoding the essential chaperones GroES and...
Here, we demonstrate that the overexpression of the GroELS chaperone system, which assists the foldi...
The heat shock response of the psychrophilic bacterium Pseudoalteromonas haloplanktis TAC 125 (PhTAC...
The heat shock response of the psychrophilic bacterium Pseudoalteromonas haloplanktis TAC 125 (PhTAC...
Proteome analysis of Corynebacterium glutamicum ATCC 13032 showed that levels of several proteins in...
The GroES and GroEL proteins of Escherichia coli function together as the GroE molecular chaperone m...
The molecular mechanism supporting survival at a critical high temperature (CHT) in Escherichia coli...
Abstract GroEL is a multifunctional protein belonging to the conspicuous family of chaperones active...
We have recently identified a new gene of Escherichia coli, called greA, which is involved in the re...
[出版社版]The photosynthetic prokaryotic cyanobacteria generally have two copies of the groEL or chapero...
Cyanobacterial genomes generally contain two groEL genes, referred to as groEL1 and groEL2. The purp...
The molecular mechanism supporting survival at a critical high temperature (CHT) in Escherichia coli...
Cochaperonins (cpn10) assist chaperonins (cpn60) in promoting folding and assembly of other proteins...
Barreiro C, Gonzalez-Lavado E, Brand S, Tauch A, Martin JF. Heat shock Proteome analysis of wild-typ...