Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2002-6-20
pubmed:abstractText
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.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Adenosine Diphosphate, http://linkedlifedata.com/resource/pubmed/chemical/Adenylate Cyclase, http://linkedlifedata.com/resource/pubmed/chemical/Adenylate Cyclase Toxin, http://linkedlifedata.com/resource/pubmed/chemical/Bacterial Toxins, http://linkedlifedata.com/resource/pubmed/chemical/Cations, Divalent, http://linkedlifedata.com/resource/pubmed/chemical/Cholera Toxin, http://linkedlifedata.com/resource/pubmed/chemical/Guanosine Triphosphate, http://linkedlifedata.com/resource/pubmed/chemical/Heterotrimeric GTP-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Magnesium, http://linkedlifedata.com/resource/pubmed/chemical/Manganese, http://linkedlifedata.com/resource/pubmed/chemical/NAD, http://linkedlifedata.com/resource/pubmed/chemical/Pertussis Toxin, http://linkedlifedata.com/resource/pubmed/chemical/Virulence Factors, Bordetella
pubmed:status
MEDLINE
pubmed:issn
1066-5234
pubmed:author
pubmed:issnType
Print
pubmed:volume
42
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
257-60
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:12075624-Adenosine Diphosphate, pubmed-meshheading:12075624-Adenylate Cyclase, pubmed-meshheading:12075624-Adenylate Cyclase Toxin, pubmed-meshheading:12075624-Animals, pubmed-meshheading:12075624-Bacterial Toxins, pubmed-meshheading:12075624-Cations, Divalent, pubmed-meshheading:12075624-Cell Membrane, pubmed-meshheading:12075624-Cholera Toxin, pubmed-meshheading:12075624-Enzyme Activation, pubmed-meshheading:12075624-Guanosine Triphosphate, pubmed-meshheading:12075624-Heterotrimeric GTP-Binding Proteins, pubmed-meshheading:12075624-Magnesium, pubmed-meshheading:12075624-Manganese, pubmed-meshheading:12075624-Molecular Weight, pubmed-meshheading:12075624-NAD, pubmed-meshheading:12075624-Pertussis Toxin, pubmed-meshheading:12075624-Protein Binding, pubmed-meshheading:12075624-Trypanosomatina, pubmed-meshheading:12075624-Virulence Factors, Bordetella
pubmed:articleTitle
Adenylyl cyclase and G-proteins in Phytomonas.
pubmed:affiliation
Instituto de Investigaciones en Ingeniería Genética y Biología Molecular and Facultad de Ciencias Exactas y Naturales, Obligado 2490, 1428 Buenos Aires, Argentina.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't