Literature DB >> 204402

DNA nicking--closing activity from salmon testis.

B Eskin, A R Morgan.   

Abstract

Salmon testis is a good source of DNA nicking--closing (N--C) enzyme, as expected for rapidly proliferating cells. Partial purification was obtained but it resulted in an unstable form of N--C enzyme. Cruder fractions are useful for relaxing supercoiled DNA under conditions where other N--C enzymes are inactive. The enzyme is very tolerant of salt concentration, with activity still detectable at 0.6 M NaCl. It is also active at low temperatures with reasonable activity at 0 degrees C. However, at temperatures greater than 25 degrees C it is rapidly inactivated. Otherwise, its properties are similar to other eucaryotic N--C enzymes.

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Year:  1978        PMID: 204402     DOI: 10.1139/o78-014

Source DB:  PubMed          Journal:  Can J Biochem        ISSN: 0008-4018


  2 in total

1.  A rapid method for the measurement of the unwinding angle of intercalating agents and the superhelix density of circular DNAs.

Authors:  J S Lee; A R Morgan
Journal:  Nucleic Acids Res       Date:  1978-07       Impact factor: 16.971

Review 2.  Review: ethidium fluorescence assay. Part II. Enzymatic studies and DNA-protein interactions.

Authors:  A R Morgan; D H Evans; J S Lee; D E Pulleyblank
Journal:  Nucleic Acids Res       Date:  1979-10-10       Impact factor: 16.971

  2 in total

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