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Purification of the Protective Antigen from Bacillus anthracis
Article in Ko | WPRIM | ID: wpr-164099
Responsible library: WPRO
ABSTRACT
Anthrax toxin consists of three separate proteins, protective antigen (PA), edema factor (EF), and lethal factor (LF). PA binds to the receptor on mammalian cells and facilitates translocation of EF or LF into its cytosol. PA is the primary component of anthrax vaccines. In this study we purified PA from culture filtrates of Bacillus anthracis. The purification involved sequential chromatography through hydroxylapatite, DEAE-Sepharose CL-4B, followed by Mono-Q. The purified PA was judged to be homogeneous on SDS-PAGE, and consisted of a single polypeptide chain with a relative molecular weight of 85,000.
Subject(s)
Full text: 1 Database: WPRIM Main subject: Bacillus / Bacillus anthracis / Chromatography / Durapatite / Anthrax Vaccines / Cytosol / Edema / Electrophoresis, Polyacrylamide Gel / Anthrax / Molecular Weight Language: Ko Journal: Journal of the Korean Society for Microbiology Year: 1998 Document type: Article
Full text: 1 Database: WPRIM Main subject: Bacillus / Bacillus anthracis / Chromatography / Durapatite / Anthrax Vaccines / Cytosol / Edema / Electrophoresis, Polyacrylamide Gel / Anthrax / Molecular Weight Language: Ko Journal: Journal of the Korean Society for Microbiology Year: 1998 Document type: Article