Literature DB >> 6300092

Gyrase . DNA complexes visualized as looped structures by electron microscopy.

C L Moore, L Klevan, J C Wang, J D Griffith.   

Abstract

Gyrase bound to duplex DNA in the absence of ATP is seen by electron microscopy as a nearly spherical particle frequently located at the intersection of two duplex DNA strands. Such looped structures with gyrase situated at the base of the loops are observed with both linear and circular DNA substrates, and two or three individual DNA molecules bound to the same protein are also seen at high DNA concentrations. Addition of the nonhydrolyzable beta,gamma-imido analog of ATP to the gyrase . DNA reaction mixture prior to sample fixation for microscopy reduces the frequency of gyrase molecules found at DNA intersections. Looped structures similar to those of the gyrase . DNA complex are also seen with the complex of DNA and the A subunit of gyrase. When negatively supercoiled DNA which has been partially relaxed by gyrase in the absence of ATP is fixed for electron microscopic examination, intermediate forms are observed that contain both supercoiled and relaxed loops in a single DNA molecule, with the enzyme located at the common base of the loops. These results suggest that gyrase possesses multiple DNA-binding sites, a feature which allows the enzyme to hold DNA in constrained loops. The relation of these observations to the mechanism of gyrase action is discussed.

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Year:  1983        PMID: 6300092

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  9 in total

1.  The C-terminal domain of the Escherichia coli DNA gyrase A subunit is a DNA-binding protein.

Authors:  R J Reece; A Maxwell
Journal:  Nucleic Acids Res       Date:  1991-04-11       Impact factor: 16.971

Review 2.  DNA-protein interactions during replication of genetic elements of bacteria.

Authors:  J Nesvera; J Hochmannová
Journal:  Folia Microbiol (Praha)       Date:  1985       Impact factor: 2.099

3.  DNA gyrase binds to the family of prokaryotic repetitive extragenic palindromic sequences.

Authors:  Y Yang; G F Ames
Journal:  Proc Natl Acad Sci U S A       Date:  1988-12       Impact factor: 11.205

4.  DNA binding and antigenic specifications of DNA gyrase.

Authors:  H Lother; R Lurz; E Orr
Journal:  Nucleic Acids Res       Date:  1984-01-25       Impact factor: 16.971

5.  Eukaryotic topoisomerases recognize nucleic acid topology by preferentially interacting with DNA crossovers.

Authors:  E L Zechiedrich; N Osheroff
Journal:  EMBO J       Date:  1990-12       Impact factor: 11.598

6.  The key DNA-binding residues in the C-terminal domain of Mycobacterium tuberculosis DNA gyrase A subunit (GyrA).

Authors:  You-Yi Huang; Jiao-Yu Deng; Jing Gu; Zhi-Ping Zhang; Anthony Maxwell; Li-Jun Bi; Yuan-Yuan Chen; Ya-Feng Zhou; Zi-Niu Yu; Xian-En Zhang
Journal:  Nucleic Acids Res       Date:  2006-10-11       Impact factor: 16.971

7.  Binding of two DNA molecules by type II topoisomerases for decatenation.

Authors:  Rupesh Kumar; Jane E Riley; Damian Parry; Andrew D Bates; Valakunja Nagaraja
Journal:  Nucleic Acids Res       Date:  2012-09-18       Impact factor: 16.971

8.  The role of DNA bending in type IIA topoisomerase function.

Authors:  Imsang Lee; Ken C Dong; James M Berger
Journal:  Nucleic Acids Res       Date:  2013-04-10       Impact factor: 16.971

Review 9.  The why and how of DNA unlinking.

Authors:  Zhirong Liu; Richard W Deibler; Hue Sun Chan; Lynn Zechiedrich
Journal:  Nucleic Acids Res       Date:  2009-02       Impact factor: 16.971

  9 in total

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