Mechanism of Conversion of the Salmonella O Antigen by Bacteriophage ε 34

Author:

Wright Andrew1

Affiliation:

1. Department of Molecular Biology and Microbiology, Tufts University Medical School, Boston, Massachusetts 02111

Abstract

The structural determinants for antigen 34 in the E group salmonella are glucosyl substituents on the galactosyl units of the O antigen which has a mannosylrhamnosylgalactose repeating sequence. The temperate bacteriophage ε 34 brings about the production of antigen 34. It has been shown here that glucose is transferred from uridine diphosphate glucose to the O antigen via a glucosyl-lipid intermediate in a two-step reaction. Glucose is linked through carbon 1 to the lipid by a phosphodiester bridge, the glucosyl bond having the β-anomeric configuration. The lipid is a C 55 -polyisoprenoid alcohol, each isoprene unit having one double bond. It is the same lipid which is involved in the synthesis of the O antigen repeating sequence.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

Reference29 articles.

1. Adams M. H. 1966. Bacteriophages p. 454-456. Interscience Publishers New York.

2. Ames B. N. 1966. Assay of inorganic phosphate total phosphate and phosphatases p. 115-118. In E. F. Neufeld and V. Ginsburg (ed.) Methods in enzymology vol. 8. Academic Press Inc. New York.

3. Rough mutants of Salmonella typhimurium;Beckmann I.;Nature (London),1964

4. Control aspects of uridine 5'-diphosphate glucose and thymidine 5'-diphosphate glucose synthesis by microbial enzymes;Bernstein R. L.;J. Biol. Chem.,1965

5. Mechanism of (e5 conversion studied with bacteriophage mutants;Bray D.;J. Mol. Biol.,1967

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