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Biomedical subjects

J Doskocil

Publications and source records attributed to J Doskocil.

At least 55 records · Page 3Linked to original sources

The metabolism of isocytidine in Escherichia coli.

Intact cells and cell-free extracts of E. coli convert isocytidine to isocytosine and uracil. The radioactive label of 5-[(3)H]isocytidine is incorporated into RNA and, DNA of growing bacteria at a rate equal to about 1.4% of that of cytidine under similar conditions; the radioactivity is found in uridylic, cytidylic and 2'-deoxythymidylic acids, while less than 0.4% of incorporated radioactive material might be due to possible incorporation of intact isocytidine. Uridine phosphorylase and cytidine deaminase apparently do not participate in the metabolic conversion of isocytidine.5-[(3)H]isocytidine was prepared by platinum-catalyzed dehalogenation of 5-bromoisocytidine in the presence of tritium. The 5-bromo derivative was obtained from 2',3'-0- -isopropylideneisocytidine by N-bromsuccinimide bromination followed by acidic hydrolysis.

Bacterial Proteins↗

Inducible and constitutive nucleoside-binding sites in Escherichia coli: differential inhibition by nucleoside analogues.

Constitutive and inducible nucleoside-binding sites on the surface of the cells of E. coli B have different patterns of inhibition by nucleoside analogues. 1(beta-D-Ribofuranosyl)-4-aminopyrimidine-6-one and isoguanosine preferentially inhibit the inducible binding sites while showdomycin and N(4)-dimethylcytidine interfere more strongly with the constitutive function.

Adenosine↗