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J Eukaryot Microbiol ; 42(3): 257-60, 1995.
Article in English | MEDLINE | ID: mdl-12075624

ABSTRACT

Phytomonas sp. membranes have an adenylyl cyclase activity which is greater in the presence of Mn2+ than with Mg2+. The Mg2+ and Mn2+ activity ratio varies from one membrane preparation to another, suggesting that the adenylyl cyclase has a variable activation state. A[35S]GTP-gamma-S-binding activity with a Kd of 171 nM was detected in Phytomonas membranes. Incubation of these membranes with activated cholera or pertussis toxin and [adenylate 23P]NAD+ led to incorporation of radioactivity into bands of about 40-44 kDa. Crude membranes were electrophoresed on SDS-polyacrylamide gels and analyzed, by Western blotting, with the 9188 anti-alpha[s] antibody and the AS/7 antibody (anti-alpha[i], anti-alpha[i1], and anti-alpha[i2]. These procedures resulted in the identification of polypeptides of approximately 40-44 kDa. Phytomonas adenylyl cyclase could be activated by treatment of membrane preparations with cholera toxin, in the presence of NAD+, while similar treatment with pertussis toxin did not affect this enzyme activity. These studies indicate that in Phytomonas, adenylyl cyclase activity is coupled to an unknown receptor entity through G alpha[s] proteins.


Subject(s)
Adenylyl Cyclases/metabolism , Heterotrimeric GTP-Binding Proteins/metabolism , Trypanosomatina/enzymology , Adenosine Diphosphate/metabolism , Adenylate Cyclase Toxin , Animals , Bacterial Toxins/pharmacology , Cations, Divalent/pharmacology , Cell Membrane/drug effects , Cell Membrane/enzymology , Cholera Toxin/pharmacology , Enzyme Activation/drug effects , Guanosine Triphosphate/metabolism , Magnesium/pharmacology , Manganese/pharmacology , Molecular Weight , NAD/metabolism , NAD/pharmacology , Pertussis Toxin , Protein Binding , Trypanosomatina/cytology , Trypanosomatina/metabolism , Virulence Factors, Bordetella/pharmacology
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