Abstract
The K88 antigen was carried by episomal transfer to D282, a nonmotile Escherichia coli strain without K antigen. D520, obtained by this episomal transfer, was used for the extraction of K88 antigen. It was shown by the agar gel precipitation technique that some K88 antigen was released from D520 into suspending aqueous medium. The amount of liberated material was increased by gentle heating (60 C) or treatment in a Waring Blendor. The antigen was obtained from the extracts in a purified form by making use of its insolubility between pH 3.5 and 5.5 and of its high sedimentation rate (S(0) (20,w) = 36.7S). The homogeneity of the material was demonstrated by agar gel precipitation with D520 antiserum, by analytical ultracentrifugation, and by moving-boundary electrophoresis. Chemical analysis revealed that K88 is a pure protein containing all the common amino acids with the exception of cysteine-cystine. Purified K88 selectively precipitated the K88 antibodies from D520 antiserum and was shown to be immunogenic in rabbits.
MeSH Terms
Amino Acids/analysis
Animals
Antigens/analysis
Bacterial Proteins/analysis
Electrophoresis
Escherichia coli/immunology
Hemagglutination Tests
Hexosamines/analysis
Immunodiffusion
Lipids/analysis
Molecular Biology
Rabbits
Ultracentrifugation
Chemicals
Amino Acids
Antigens
Bacterial Proteins
Hexosamines
Lipids
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Stirm S
Orskov F
Orskov I
Mansa B
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10 references, click to expand
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