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filingDate 1986-01-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1989-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1c0175b00be1d244253094580e58f70b
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publicationDate 1989-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4831121-A
titleOfInvention Polydisperse native pseudomonas flagellar (H) antigens (FAg) and methods of producing them
abstract PCT No. PCT/AT86/00002 Sec. 371 Date Oct. 2, 1986 Sec. 102(e) Date Oct. 2, 1986 PCT Filed Jan. 13, 1986 PCT Pub. No. WO86/03974 PCT Pub. Date Jul. 17, 1986.Polydisperse native Pseudomonas flagellar (H) antigens (FAg) and methods of producing them are described, wherein each monomeric component contains certain amino acids, has a certain N-terminal amino acid sequence and a certain molecular weight and is free from pyrogenic substances. The ratio of the individual amino acids in the flagellar antigen of the individual H-serotypes is stated. For producing the polydisperse native Pseudomonas flagellar (H) antigens (FAg) methods are indicated, wherein Pseudomonas aeruginosa bacterial cultures or fractions thereof are treated with a detergent and the flagellar antigens are separated from the cultures. Prior to treatment or in the presence of the detergent, the bacterial culture is subjected to a shearing procedure, i.e. exposed to shearing forces. Thereafter, the flagellar antigens separated from the bacterial mass are isolated by a chromatographic treatment. For this chromatographic treatment a molecular sieve can be used and a further purification by chromatography on a column can be carried out for obtaining flagellar antigens of high purity.
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