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PMID: 2838729 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Exotoxin A of Pseudomonas aeruginosa: evidence that domain I functions in receptor binding.

Molecular microbiology ·Vol. 1 ·No. 1 ·1987-07-00 ·Pages 67-72

Guidi-Rontani C, Collier RJ

Abstract

We have constructed defined deletions in the structural gene of Pseudomonas aeruginosa exotoxin A (ETA) in order to probe the function of Domain I of this protein. Three forms of the gene containing specific deletions were expressed in a strain of Escherichia coli K12 with lesions in the htpR and Ion genes; extracts containing the gene products were tested for ADP-ribosylation activity, cytotoxicity, and ability to protect sensitive cells from the cytotoxic action of authentic ETA. Two of the mutant ETAs gave concentration-dependent protection against authentic ETA, and protection correlated with the presence of the bulk of Domain I. The results support the notion that Domain I functions in binding the toxin to specific cell-surface receptors.

MeSH Terms
ADP Ribose Transferases Bacterial Toxins Carrier Proteins Chromosome Deletion DNA Restriction Enzymes Escherichia coli/genetics Exotoxins/genetics,metabolism Genes Genes, Bacterial Kinetics Mutation Plasmids Protein Binding Pseudomonas aeruginosa/genetics Receptors, Cell Surface Receptors, Cholinergic/metabolism Virulence Factors
Chemicals
Bacterial Toxins Carrier Proteins Exotoxins Pseudomonas exotoxin binding protein, mouse Receptors, Cell Surface Receptors, Cholinergic Virulence Factors ADP Ribose Transferases toxA protein, Pseudomonas aeruginosa DNA Restriction Enzymes
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Guidi-Rontani C
Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, Massachusetts 02115.
Collier R J
Article Info
Journal
Molecular microbiology
Abbr.
Mol Microbiol
ISSN
0950-382X
Published
1987-07-00
Pages
67-72
Language
English
Region
England
NLM ID
8712028
Subset
IM
Grants
NIAID NIH HHS · AI-22021 · United States
NIAID NIH HHS · AI-22848 · United States
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