Regulation of DNA Supercoiling in Escherichia coli

  1. M. Gellert,
  2. R. Menzel,
  3. K. Mizuuchi,
  4. M.H. O'Dea, and
  5. D.I. Friedman*
  1. Laboratory of Molecular Biology, National Institute of Arthritis, Diabetes, and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20205; *Department of Microbiology and Immunology, University of Michigan, Ann Arbor, Michigan 48109

This extract was created in the absence of an abstract.

Excerpt

DNA supercoiling in Escherichia coli is an active process mediated by DNA gyrase. Intracellular DNA is kept under torsional stress (Sinden et al. 1980); maintenance of that stress, in the presence of DNA-relaxing topoisomerases, requires the continued activity of DNA gyrase. When DNA gyrase activity is blocked by inhibitors or by mutational means, cellular DNA becomes at least partly relaxed (Drlica and Snyder 1978), and newly introduced DNA does not become supercoiled (Gellert et al. 1976b).

The cellular functions of DNA are greatly affected by its supercoiling. If DNA gyrase activity is blocked, chromosomal replication and some forms of recombination are halted, and the rate of transcription from some promoters is altered (for review, see Gellert 1981). Thus, the mechanisms by which the cellular level of DNA supercoiling is adjusted are worth studying. It is known that purified DNA gyrase can raise the level of DNA supercoiling considerably beyond that...

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