Abstract
The ether antigen ofFrancisella tularensis was submitted to fractionation using ammonium sulphate, ethanol and trichloracetic acid (TCA). A simple antigenic mixture was obtained by this fractionation from the original complex ether antigen. However, no separation of antigenically and chemically homogenous substances was achieved, by this procedure. The precipitation with TCA permitted the separation of an antigenic component that was found to be identical with the phenol antigen or its component migrating faster towards cathode in electrophoresis. The sediment obtained possessed common properties with the precipitate obtained by ethanol precipitation. The fraction having the highest anodic mobility could be obtained by salting out the original antigen with ammonium sulphate to 50% saturation. By increasing the concentration of ammonium sulphate to 60% saturation, all components of the ether antigen could be precipitated. The number of precipitation lines in the original antigen and its fractions depends both on the concentration of antigen and the quality of antisera.
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Procházka, O., Dubanská, H. The antigenic structure ofFrancisella tularensis . Folia Microbiol 17, 232–238 (1972). https://doi.org/10.1007/BF02875819
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DOI: https://doi.org/10.1007/BF02875819