Summary
Two active enzymes of the galactose operon of Escherichia coli, uridyl transferase and galactokinase have been synthesized with high yields in a DNA dependent system for protein synthesis. The unspecific blank values amount to less than two percent of the rate obtained under optimal conditions and permit the accurate determination of even a small fraction of the maximum synthesis rate. Therefore this system provides a sensitive assay for the biological activity of DNA that contains the intact galactose operon of Escherichia coli.
The synthesis of these galactose enzymes is to a high extent dependent on the presence of cyclic adenosine-3′:5′-monophosphate.
D-fucose, known as an inducer of the galactose operon in vivo, stimulates the synthesis of galactokinase, indicating that the repressor of the galactose operon in active under these conditions. This stimulation is not observed, if the bacterial extract is prepared from a strain defective for the galactose repressor or if the DNA carries an operator constitutive mutation in the galactose operon. Therefore the stimulation by D-fucose is true derepression.
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Communicated by H. G. Wittmann
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Wetekam, W., Staack, K. & Ehring, R. DNA-dependent in vitro synthesis of enzymes of the galactose operon of Escherichia coli . Molec. Gen. Genet. 112, 14–27 (1971). https://doi.org/10.1007/BF00266928
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DOI: https://doi.org/10.1007/BF00266928