Nucleic acid metabolism in uninfected and becteriophage OW-14 infected Pseudomonas acidovorans

Pseudomonas acidovorans was shown to be deficient in a number of enzymes of the salvage pathways of nucleic acid metabolism. These included uridine phosphorylase, purine nucleoside phosphorylase, cytidine (deoxycytidine) deaminase, and thymidine phosphorylase. The absence of uridine kinase and deoxy...

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Main Author: Kelln, Rodney Alexander
Language:English
Published: University of British Columbia 2011
Online Access:http://hdl.handle.net/2429/32034
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spelling ndltd-UBC-oai-circle.library.ubc.ca-2429-320342018-01-05T17:46:24Z Nucleic acid metabolism in uninfected and becteriophage OW-14 infected Pseudomonas acidovorans Kelln, Rodney Alexander Pseudomonas acidovorans was shown to be deficient in a number of enzymes of the salvage pathways of nucleic acid metabolism. These included uridine phosphorylase, purine nucleoside phosphorylase, cytidine (deoxycytidine) deaminase, and thymidine phosphorylase. The absence of uridine kinase and deoxycytidine kinase was also indicated. Pyrimidine requiring mutants were isolated and pyrimidine substitution patterns were examined in these auxotrophs. Concentrations of uracil of 50 µg/ml and greater had the unusual effect of inhibiting the growth of these strains, whereas no effect occurred with the wild-type. An inhibitory effect on the wild-type did result, however, when deoxyadenosine or adenosine was added at critical concentrations. Obligate thymidine auxotrophs were isolated using an adaptation of the aminopterin technique. These strains required very high concentrations of thymidine (250 to 1000 µg/ml) for growth. No change in the amount of aspartate transcarbamylase activity occurred during growth in the presence or absence of added uracil. No inhibition of aspartate transcarbamylase activity was evident in the presence of various nucleotides. Infection of cells by bacteriophage 0W-14 resulted in the apparent synthesis of a phage encoded thymidylate synthetase. In addition, an activity corresponding to deoxyuridyl ate hydroxymethylase was indicated. Thymidine was not a precursor for 5(4-aminobutylaminomethyl) uracil but the base was efficiently labelled by radioactive uracil or deoxyuridine. Pool studies indicated that the biosynthesis of the base occurred at the nucleotide level rather than the macromolecular level. Science, Faculty of Microbiology and Immunology, Department of Graduate 2011-03-04T03:15:40Z 2011-03-04T03:15:40Z 1973 Text Thesis/Dissertation http://hdl.handle.net/2429/32034 eng For non-commercial purposes only, such as research, private study and education. Additional conditions apply, see Terms of Use https://open.library.ubc.ca/terms_of_use. University of British Columbia
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language English
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description Pseudomonas acidovorans was shown to be deficient in a number of enzymes of the salvage pathways of nucleic acid metabolism. These included uridine phosphorylase, purine nucleoside phosphorylase, cytidine (deoxycytidine) deaminase, and thymidine phosphorylase. The absence of uridine kinase and deoxycytidine kinase was also indicated. Pyrimidine requiring mutants were isolated and pyrimidine substitution patterns were examined in these auxotrophs. Concentrations of uracil of 50 µg/ml and greater had the unusual effect of inhibiting the growth of these strains, whereas no effect occurred with the wild-type. An inhibitory effect on the wild-type did result, however, when deoxyadenosine or adenosine was added at critical concentrations. Obligate thymidine auxotrophs were isolated using an adaptation of the aminopterin technique. These strains required very high concentrations of thymidine (250 to 1000 µg/ml) for growth. No change in the amount of aspartate transcarbamylase activity occurred during growth in the presence or absence of added uracil. No inhibition of aspartate transcarbamylase activity was evident in the presence of various nucleotides. Infection of cells by bacteriophage 0W-14 resulted in the apparent synthesis of a phage encoded thymidylate synthetase. In addition, an activity corresponding to deoxyuridyl ate hydroxymethylase was indicated. Thymidine was not a precursor for 5(4-aminobutylaminomethyl) uracil but the base was efficiently labelled by radioactive uracil or deoxyuridine. Pool studies indicated that the biosynthesis of the base occurred at the nucleotide level rather than the macromolecular level. === Science, Faculty of === Microbiology and Immunology, Department of === Graduate
author Kelln, Rodney Alexander
spellingShingle Kelln, Rodney Alexander
Nucleic acid metabolism in uninfected and becteriophage OW-14 infected Pseudomonas acidovorans
author_facet Kelln, Rodney Alexander
author_sort Kelln, Rodney Alexander
title Nucleic acid metabolism in uninfected and becteriophage OW-14 infected Pseudomonas acidovorans
title_short Nucleic acid metabolism in uninfected and becteriophage OW-14 infected Pseudomonas acidovorans
title_full Nucleic acid metabolism in uninfected and becteriophage OW-14 infected Pseudomonas acidovorans
title_fullStr Nucleic acid metabolism in uninfected and becteriophage OW-14 infected Pseudomonas acidovorans
title_full_unstemmed Nucleic acid metabolism in uninfected and becteriophage OW-14 infected Pseudomonas acidovorans
title_sort nucleic acid metabolism in uninfected and becteriophage ow-14 infected pseudomonas acidovorans
publisher University of British Columbia
publishDate 2011
url http://hdl.handle.net/2429/32034
work_keys_str_mv AT kellnrodneyalexander nucleicacidmetabolisminuninfectedandbecteriophageow14infectedpseudomonasacidovorans
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