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Cloning and expression of the genes specifying Shiga-like toxin production in Escherichia coli H19
- Source :
- Scopus-Elsevier
- Publication Year :
- 1986
- Publisher :
- American Society for Microbiology, 1986.
-
Abstract
- Some strains of Escherichia coli produce a protein which is cytotoxic for Vero cell and HeLa cell monolayers. This toxin is very similar to the toxin of Shigella dysenteriae 1 and has been named verotoxin or E. coli Shiga-like toxin. It has been shown that toxin conversion is due to a group of bacteriophages, one of which has been designated H-19B. In this study we report hybridization experiments showing that part of the H-19B genome is homologous to phage lambda. We have cloned a 1.7-kilobase BalI-BglII fragment from the genome of H-19B into pUC18. The recombinant plasmid confers the ability to produce high levels of Shiga-like toxin on transformed E. coli cells. We demonstrate using an in vitro transcription/translation system that the cloned fragment specifies the two verotoxin subunit peptides which have masses of 31 and 5.5 kilodaltons. The identity of peptides was confirmed by immunoprecipitation with verotoxin antiserum and protein A-Sepharose beads.
- Subjects :
- Shigella dysenteriae
Bacterial Toxins
DNA, Recombinant
Molecular cloning
Shiga Toxin 1
Shiga Toxins
medicine.disease_cause
Microbiology
chemistry.chemical_compound
Shiga-like toxin
Plasmid
Bacterial Proteins
Escherichia coli
medicine
Animals
Humans
Cloning, Molecular
Deoxyribonucleases, Type II Site-Specific
Molecular Biology
biology
Toxin
Genetic transfer
Nucleic Acid Hybridization
DNA Restriction Enzymes
Haplorhini
Lambda phage
Cell Transformation, Viral
biology.organism_classification
Bacteriophage lambda
Molecular biology
Gene Expression Regulation
chemistry
Research Article
HeLa Cells
Subjects
Details
- ISSN :
- 10985530 and 00219193
- Volume :
- 166
- Database :
- OpenAIRE
- Journal :
- Journal of Bacteriology
- Accession number :
- edsair.doi.dedup.....25e7af204f5fa74f7826adc3b3b9f991
- Full Text :
- https://doi.org/10.1128/jb.166.2.375-379.1986