Summary
The sensitivity of the capacity for forming galactokinase inE. coli was measured under various conditions. Differences were found between strains W 8 and Hfr 7 (λ) and between these strains and mutants, derived from them, which are partially constitutive for galactokinase. The same behavior as that of the constitutive mutants was also obtained for Hfr 7 (λ) induction of the genes for galactokinase or β-galactosidase prior to UV-irradiation. It was concluded that these genes exhibit different sensitivities toward UV, depending on whether they are in the repressed or de-repressed state. Pre-induction effects on UV-sensitivity are observed only in strain Hfr 7 (λ) and only if the latter is lysogenic for phage λ.
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Literature
Adams, M. H.: Bacteriophages. New York: Interscience Publ. 1959.
Attardi, G., S. Naono, Josette Rouviere, F. Jacob, andF. Gros: Production of messenger RNA and regulation of protein synthesis. Cold Spr. Harb. Symp. quant. Biol.28, 363–372 (1963).
Buttin, G.: Mécanismes régulaterus dans la biosynthèse des enzymes du métabolisme du galactose chez Escherichia coli K 12. II. Le déterminisme génétique de la régulation. J. molec. Biol.7, 183–205 (1963).
Clavilier, L., M. Luzzati etP. P. Slonimski: Sur la conversion du gène ad 3 chez la levure. C. R. Soc. Biol. (Paris)154, 1970–1974 (1960).
Kepes, A.: Kinetics of induced enzyme synthesis. Determination of the mean life of galactosidase-specific messenger RNA. Biochim. biophys. Acta (Amst.)76, 293–309 (1963).
Kölsch, E., andP. Starlinger: A difference in the photoreactivation of UV-damage between genes in the repressed and genes in the de-repressed state. Z. Vererbungsl.96, 304–306 (1965).
Luzzati, M., L. Clavilier, andG. Pere: On the possibility of a specific repression at the genetic level. In:S. J. Geerts (Editor), Genetics today. Proc. XIth Int. Congr. of Genetics, vol. 1, p. 40. Oxford: Pergamon Press 1963.
Nakada, D., andB. Magasanik: The roles of inducer and catabolite repressor in the synthesis of β-galactosidase by Escherichia coli. J. molec. Biol.8, 105–127 (1964).
Pardee, A. B., F. Jacob, andJ. Monod: The genetic control and cytoplasmatic expression of “inducibility” in the synthesis of β-galactosidase by E. coli. J. molec. Biol.1, 165–178 (1959).
Rupert, C. S.: Questions regarding the presumed role of thymine dimer in photoreactivable UV damage to DNA. Photochem. Photobiol.3, 399–403 (1964).
Sherman, J. R.: Rapid enzyme assay technique utilizing radioactive substrate, ion-exchange paper and liquid scintillation counting. Analyt. Biochem.5, 548–554 (1963).
Starlinger, P., andE. Kölsch: The sensitivity of the galactose operon of E. coli to UV-light. Biochem. biophys. Res. Commun.17, 508–511 (1964).
Winkler, U.: Über die fehlende Photo- und Wirtszellreaktivierbarkeit des UV-inaktivierten RNS-Phagen fr. Photochem. Photobiol.3, 37–43 (1964).
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Kölsch, E., Starlinger, P. A difference in UV-sensitivity between genes in the repressed and genes in the de-repressed state. Zeitschrift für Vererbungslehre 96, 297–303 (1965). https://doi.org/10.1007/BF00895045
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DOI: https://doi.org/10.1007/BF00895045