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PMID: 6098527 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Cloning of the structural gene (hly) for the haemolysin of Vibrio cholerae El Tor strain 017.

Gene ·Vol. 31 ·No. 1-3 ·1984-11-00 ·Pages 225-31

Manning PA, Brown MH, Heuzenroeder MW

Abstract

We have cloned the DNA encoding the haemolysin of Vibrio cholerae El Tor strain 017 into the plasmid vector pBR322. The resultant plasmid, pPM431, has a 6.2-kb PstI DNA insert which leads to the production of the haemolysin in Escherichia coli K-12. Deletion analysis and transposon mutagenesis have allowed us to localize several regions affecting haemolysin production. A number of these mutants have been analysed in E. coli K-12 minicells. Three proteins have been identified: A, 80 kDal; B, 71 kDal; and C, 22 kDal. A is the haemolysin which appears to be cell-associated in E. coli K-12, and B and C are required for its efficient production. We suggest that the genes for proteins A, B and C be designated hlyA, hlyB and hlyC, respectively.

MeSH Terms
Cloning, Molecular DNA Transposable Elements Escherichia coli/genetics,metabolism Genes Genes, Bacterial Genetic Vectors Hemolysin Proteins/biosynthesis,genetics Plasmids Vibrio cholerae/genetics
Chemicals
DNA Transposable Elements Hemolysin Proteins
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Manning P A
Brown M H
Heuzenroeder M W
Article Info
Journal
Gene
Abbr.
Gene
ISSN
0378-1119
Published
1984-11-00
Pages
225-31
Language
English
Region
Netherlands
NLM ID
7706761
Subset
IM
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