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91探花
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Dr Jon Bath

Group Leader

Research theme

  • Biological physics

Sub department

  • Condensed Matter Physics

Research groups

  • Nucleic acid nanotechnology
jonathan.bath@physics.ox.ac.uk
Biochemistry Building, room 30-092
  • About
  • Publications

Topology of Xer recombination on catenanes produced by lambda integrase.

J Mol Biol 289:4 (1999) 873-883

Authors:

J Bath, DJ Sherratt, SD Colloms

Abstract:

Xer site-specific recombination at the psi site from plasmid pSC101 displays topological selectivity, such that recombination normally occurs only between directly repeated sites on the same circular DNA molecule. This intramolecular selectivity is important for the biological role of psi, and is imposed by accessory proteins PepA and ArcA acting at accessory DNA sequences adjacent to the core recombination site. Here we show that the selectivity for intramolecular recombination at psi can be bypassed in multiply interlinked catenanes. Xer site-specific recombination occurred relatively efficiently between antiparallel psi sites located on separate rings of right-handed torus catenanes containing six or more nodes. This recombination introduced one additional node into the catenanes. Antiparallel sites on four-noded right-handed catenanes, the normal product of Xer recombination at psi, were not recombined efficiently. Furthermore, parallel psi sites on right-handed torus catenanes were not substrates for Xer recombination. These findings 91探花 a model in which psi sites are plectonemically interwrapped, trapping a precise number of supercoils that are converted to four catenation nodes by Xer strand exchange.

Topological selectivity in Xer site-specific recombination.

Cell 88:6 (1997) 855-864

Authors:

SD Colloms, J Bath, DJ Sherratt

Abstract:

The product topology of Xer-mediated site-specific recombination at plasmid sites has been determined. The product of deletion at pSC101 psi is a right-handed antiparallel 4-noded catenane. The ColE1 cer deletion product has an identical topology, except that only one pair of strands is exchanged. These specific product topologies imply that the productive synaptic complex and the strand exchange mechanism have fixed topologies. Further analysis suggests that synapsis traps exactly three negative supercoils between recombining sites, and that strand exchange introduces a further negative topological node in the deletion reaction. We present a model in which the requirement for a specific synaptic stucture, with two recombination sites interwrapped around the accessory proteins ArgR and PepA, ensures that recombination only occurs efficiently between directly repeated sites on the same DNA molecule.

A DNA-based optical force sensor for live-cell applications

Authors:

Christina Jayachandran, Arindam Ghosh, Meenakshi Prabhune, Jonathan Bath, Andrew J Turberfield, Lara Hauke, J枚rg Enderlein, Florian Rehfeldt, Christoph F Schmidt

Controlling DNA-RNA strand displacement kinetics with base distribution

Authors:

Eryk J Ratajczyk, Jonathan Bath, Petr 艩ulc, Jonathan PK Doye, Ard A Louis, Andrew J Turberfield

Rational design of hidden thermodynamic driving through DNA mismatch repair

Authors:

Natalie EC Haley, Thomas E Ouldridge, Alessandro Geraldini, Ard A Louis, Jonathan Bath, Andrew J Turberfield

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