1. Studies on deoxyribonucleic acid-dependent ribonucleic acid polymerase from Escherichia coli. Variations of the enzyme activity during growth
- Author
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A. Rognes, K A Abraham, and K. J. Andersen
- Subjects
DNA, Bacterial ,History ,Chemical Phenomena ,Uracil Nucleotides ,medicine.disease_cause ,Tritium ,Coliphages ,Education ,chemistry.chemical_compound ,RNA polymerase ,medicine ,Escherichia coli ,Methods ,Polymerase ,chemistry.chemical_classification ,Chromatography ,DNA clamp ,biology ,DNA-Directed RNA Polymerases ,Articles ,Molecular biology ,Enzyme assay ,Computer Science Applications ,Chemistry ,Enzyme ,chemistry ,Biochemistry ,biology.protein ,RNA ,Electrophoresis, Polyacrylamide Gel ,Uracil nucleotide ,DNA - Abstract
1. RNA polymerase activity of Escherichia coli extracts prepared from cells in exponential and stationary phases of growth, when measured in the presence and absence of external template, showed significant qualitative differences. 2. In both extracts, polymerase activity was higher when assayed with external template, suggesting the presence of a pool of enzyme not bound to cellular DNA. 3. In the crude extract, the fraction of enzyme bound to cellular DNA is higher during the exponential phase of growth. 4. A method is described for the purification of enzyme molecules not tightly bound to cellular DNA from exponential- and stationary-phase cultures. 5. Purified enzyme preparations showed differences in template requirement and subunit composition. 6. On phosphocellulose chromatography of stationary-phase enzyme, a major portion of polymerase activity eluted from the column with 0.25m-KCl. In the case of exponential-phase enzyme, polymerase activity eluted from a phosphocellulose column mainly with 0.35m-KCl. 7. Enzyme assays done with excess of bacteriophage T4 DNA showed a strong inhibition of stationary-phase enzyme by this template. The exponential-phase enzyme was only slightly inhibited by excess of bacteriophage T4 DNA.
- Published
- 1972