Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Investigation of the specificity of the interaction between colicin E9 and its immunity protein by site‐directed mutagenesis

View through CrossRef
SummaryComparison of the amino acid sequences of the C‐terminal domain of three DNAase type E colicins has identified six candidate specificity determinants for the interaction of these E colicins with their homologous immunity proteins. We have changed these candidate specificity determinants of colicin E9, using site‐directed mutagenesis, to the corresponding amino‐acids of colicin E8. A‘mutant’colicin E9, in which four of the six candidate specificity determininants have been changed, demonstrated colicin activity against Escherichia coli indicator strains which carried either the E8imm or the E9imm genes, indicative of a‘novel’E colicin. After changing all six of the candidate specificity determinants, the resulting colicin E9‘mutant’exhibited a phenotype very similar to that of colicin E8.
Title: Investigation of the specificity of the interaction between colicin E9 and its immunity protein by site‐directed mutagenesis
Description:
SummaryComparison of the amino acid sequences of the C‐terminal domain of three DNAase type E colicins has identified six candidate specificity determinants for the interaction of these E colicins with their homologous immunity proteins.
We have changed these candidate specificity determinants of colicin E9, using site‐directed mutagenesis, to the corresponding amino‐acids of colicin E8.
A‘mutant’colicin E9, in which four of the six candidate specificity determininants have been changed, demonstrated colicin activity against Escherichia coli indicator strains which carried either the E8imm or the E9imm genes, indicative of a‘novel’E colicin.
After changing all six of the candidate specificity determinants, the resulting colicin E9‘mutant’exhibited a phenotype very similar to that of colicin E8.

Related Results

In vivo and in vitro characterization of overproduced colicin E9 immunity protein
In vivo and in vitro characterization of overproduced colicin E9 immunity protein
We report the overproduction of the immunity protein for the DNase colicin E9 and its characterization both in vivo and in vitro. The genes for colicin immunity proteins are normal...
Genetic analysis of ColN plasmid determinants for colicin production, release, and immunity
Genetic analysis of ColN plasmid determinants for colicin production, release, and immunity
Colicin N was identified as the 39,000-molecular-weight protein encoded by the 4,900-base-pair, multiple copy number, amplifiable plasmid ColN -284. Its production was controlled b...
Plasmid-encoded regulation of colicin E1 gene expression
Plasmid-encoded regulation of colicin E1 gene expression
A plasmid-encoded factor that regulates the expression of the colicin E1 gene was found in molecular cloning experiments. The 2,294-base-pair AvaII fragment of the colicin E1 plasm...
A single tryptic fragment of colicin E1 can form an ion channel: Stoichiometry confirms kinetics
A single tryptic fragment of colicin E1 can form an ion channel: Stoichiometry confirms kinetics
AbstractThe molecularity of the ion channel formed by peptide fragments of colicin has taken on particular significance since the length of the active peptide has been shown to be ...
Temporal changes in the frequency of colicinogeny in Escherichia coli from house mice
Temporal changes in the frequency of colicinogeny in Escherichia coli from house mice
Escherichia coli was isolated from feral house mice (Mus domesticus) during the course of a mouse plague in the state of Victoria, Australia. The isolates were characterized for th...
A very short peptide makes a voltage‐dependent ion channel: The critical length of the channel domain of colicin E1
A very short peptide makes a voltage‐dependent ion channel: The critical length of the channel domain of colicin E1
AbstractCleavage of colicin E1 molecules with a variety of proteases or with cyanogen bromide (CNBr) generates COOH‐terminal fragments which have channel‐forming activity similar t...
Exclusive Localization of Colicin A in Cell Cytoplasm of Producing Bacteria
Exclusive Localization of Colicin A in Cell Cytoplasm of Producing Bacteria
The production of colicin A in Citrobacter freundii and in Escherichia coli was studied. After induction with low concentrations of mitomycin C, these organisms differed with regar...
The effect of nonreceptor adsorption on the lethal action of colicin E1
The effect of nonreceptor adsorption on the lethal action of colicin E1
The survivability of Escherichia coli K12s cells has been studied after treatment with 125I‐labeled colicin E1. It has been shown that for low amounts of adsorbed colicin the survi...

Back to Top