Adenylyl Cyclase and G-Proteins in Phytomonas

MARISA D. FARBER; ANDREA E. MONTAGNA; CRISTINA PAVETO; MICHEL DOLLET; MANUEL SANCHEZ-MORENO; ANTONIO OSUNA; HECTOR N. TORRES; MIRTHA M. FLAWIA

JOURNAL OF EUKARYOTIC MICROBIOLOGY

Blackwell Publishing

Lugar: Oxford; Año: 1995 vol. 42 p. 257 - 260

1066-5234

Phytomonas sp. membranes have an adenylyl cyclase activity which is greater in the presence of Mn2+ than with Mg'+. The MgZ+ and Mnz+ activity ratio vanes from one membrane preparation to another, suggesting that the adenylyl cyclase has a variable activation state. A [35S]GTP-y-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 ',PINAD+ 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 9 188 anti-a, antibody and the AS/7 antibody (anti-a,, anti-a,,, anti-a,,). 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 Phytornonas, adenylyl cyclase activity is coupled to an unknown receptor entity through Gas proteins.