Soluble adenylate cyclase from the culture medium of Bordetella pertussis: purification and characterization.
AUTOR(ES)
Hewlett, E
RESUMO
Culture medium of exponentially growing Bordetella pertussis (strain 114) contains significant quantities of soluble (100,000 X g for 1 h) adenylate cyclase. The enzyme was purified by chromatography on diethylaminoethyl-cellulose and Sephadex G-200. The purest material yielded a single band on sodium dodecyl sulfate-disc gel electrophoresis. It is heat labile, has a temperature optimum of 30 degrees C, a pH optimum of pH 7 to 8, and a Km for adenosine 5'-triphosphate of 0.4 mM, and requires Mg2+ for maximum activity. The molecular weight, by sodium dodecyl sulfate-disc gel electrophoresis and sucrose density gradient, is approximately 70,000. The enzyme is markedly inhibited by fluoride and weakly inhibited by monovalent salts, but its activity is not altered by alpha-keto acids of nonsubstrate nucleoside triphosphates. Thus, but its presence in the culture supernatant, its smaller molecular weight, and its insensitivity to alpha-keto acids and nucleotides, this enzyme differs from the bacterial adenylate cyclases previously described.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=232998Documentos Relacionados
- Adenylate cyclase toxin of Bordetella pertussis: production, purification, and partial characterization.
- Secreted adenylate cyclase of Bordetella pertussis: calmodulin requirements and partial purification of two forms.
- Bordetella pertussis adenylate cyclase: purification and characterization of the toxic form of the enzyme.
- Extracytoplasmic adenylate cyclase of Bordetella pertussis.
- Bordetella pertussis adenylate cyclase: isolation and purification by calmodulin-sepharose 4B chromatography.