Abstract
Berk, Richard S. (Wayne State University, College of Medicine, Detroit, Mich.). Partial purification of the extracellular hemolysin of Pseudomonas aeruginosa. J. Bacteriol. 88:559-565. 1964.-Through a series of chemical fractionation steps, the extracellular hemolysin of Pseudomonas aeruginosa was purified 126-fold with a recovery of 49%. Hemolytic activity of crude preparations was irreversibly lost upon contact with anionic exchange materials such as diethylaminoethyl Sephadex or ECTEOLA-Cellulose, but traveled with the solvent front during passage through Sephadex G-200 and carboxymethyl Sephadex. The hemolysin was soluble in water and ethanol, and was partially extractable with ether, but not with trichlorotrifluoroethane (Freon). Although normal serum and serum albumin blocked hemolytic activity, it was unaffected by trypsin, deoxyribonuclease, or ribonuclease. Partially purified hemolysin was studied in vivo, but did not exert dermonecrotic activity in mice or rabbits in the concentrations tested. Although preparations were toxic to mice, lethality appeared to be more a reflection of the nonhemolytic protein content of the preparations rather than of hemolytic activity.
Keywords
BLOOD
CELL MEMBRANE PERMEABILITY
CHLORIDES
DEOXYRIBONUCLEASE
EXPERIMENTAL LAB STUDY
HEMOLYSINS
ION EXCHANGE RESINS
MICE
PHARMACOLOGY
PSEUDOMONAS AERUGINOSA
RABBITS
RIBONUCLEASE
SERUM ALBUMIN
SPECTROPHOTOMETRY
TOXICOLOGIC REPORT
TRYPSIN
MeSH Terms
Animals
Blood
Cell Membrane Permeability
Cellulose
Chlorides
DNA
Deoxyribonucleases
Hemolysin Proteins
Ion Exchange Resins
Mice
Pharmacology
Proteins
Pseudomonas aeruginosa
Rabbits
Research
Ribonucleases
Serum Albumin
Spectrophotometry
Toxicology
Trypsin
Chemicals
Chlorides
Hemolysin Proteins
Ion Exchange Resins
Proteins
Serum Albumin
Cellulose
DNA
epichlorohydrin triethanolamine cellulose
Deoxyribonucleases
Ribonucleases
Trypsin
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
BERK R S
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16 references, click to expand
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