Inductions of Superoxide Dismutase by Ultraviolet Irradiation and by Manganese.

Abstract

We have set out to study the inductions of superoxide dismutase and we have done that and a variety of other related projects. We find that the E. coli MnSOD gene is controlled by a repressor protein which can exist in two states i.e. reduced or oxidized. In the reduced state it blocks transcription of the MnSOD gene and in the oxidized state it does not. In soluble extracts of E. coli the repressor can be reduced by glutathione but not by cysteine and by NADPH but not by NADH. The redox active component of the repressor could be either a transition metal cation such as iron or a disulfide/thiol couple. This cannot yet be decided. The protein coded for by the MnSOD gene is first released in the form of an interactive precursor, distinct from the apoprotein and is then converted to the apoprotein. Final metal insertion to produce the active holoenzyme occurs much more readily under aerobic than under anaerobic conditions. As a consequence the inactive apoprotein, or a form with a metal other than manganese at the active site, accumulates under anaerobic conditions unless the medium is markedly enriched with Mn(II).

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Document Details

Document Type
Technical Report
Publication Date
Feb 01, 1988
Accession Number
ADA193707

Entities

People

  • Irwin Fridovich

Organizations

  • Duke University Hospital

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • Apoproteins
  • Availability
  • Biochemistry
  • Chain Reactions
  • Chemical Compounds
  • Chemical Reactions
  • Chemistry
  • Classification
  • Cysteine
  • Elements
  • Manganese
  • Metals
  • Military Research
  • Proteins
  • Security
  • Superoxides
  • Transition Metals

Fields of Study

  • Biology

Readers

  • Microbial Pathology
  • Molecular and Cellular Biochemistry
  • Prostate Cancer Biology.