Abstract
Radioactive labelling techniques are of major importance in the study of DNA synthesis in bacteria. In order to label DNA in Escherichia coli either radioactive thymine or thymidine is generally used because these compounds are specifically incorporated into DNA. The availability of mutants, unable to synthesize thymidylate (Thy-), makes possible the control of the specific activity of newly synthesized DNA by adjusting the specific activity of exogenously added thymine or thymidine. In experiments which measure the short-term incorporation of labelled precursors other factors must be considered. These include the intracellular precursor pool sizes of bases, nucleosides and nucleotides, the rates of uptake, as well as the points of entry of the particular exogenously labelled compounds. The transport of nucleosides and bases from the medium into the cells is of considerable importance since this may result in differences between strains in the incorporation of labelled precursors into DNA. This effect is evident only when extremely low exogenous concentrations of precursors are used and it can give the appearance of altered levels of DNA synthesis.
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O’Donovan, G.A. (1978). Thymidine Metabolism in Bacteria (and “How, or How Not, to Label DNA”). In: Molineux, I., Kohiyama, M. (eds) DNA Synthesis. NATO Advanced Study Institutes Series, vol 17. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-0844-7_17
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DOI: https://doi.org/10.1007/978-1-4684-0844-7_17
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