Purification, crystallization and preliminary crystallographic analysis of a multiple cofactor-dependent DNA ligase from Sulfophobococcus zilligii

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2010 Dec 1;66(Pt 12):1583-5. doi: 10.1107/S1744309110034135. Epub 2010 Nov 16.

Abstract

A recombinant DNA ligase from Sulfophobococcus zilligii that shows multiple cofactor specificity (ATP, ADP and GTP) was expressed in Escherichia coli and purified under reducing conditions. Crystals were obtained by the microbatch crystallization method at 295 K in a drop containing 1 µl protein solution (10 mg ml(-1)) and an equal volume of mother liquor [0.1 M HEPES pH 7.5, 10%(w/v) polyethylene glycol 10 000]. A data set was collected to 2.9 Å resolution using synchrotron radiation. The crystals belonged to space group P1, with unit-cell parameters a=63.7, b=77.1, c=77.8 Å, α=83.4, β=82.4, γ=74.6°. Assuming the presence of two molecules in the unit cell, the solvent content was estimated to be about 53.4%.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Coenzymes / metabolism*
  • Crystallization
  • Crystallography, X-Ray
  • DNA Ligase ATP
  • DNA Ligases / chemistry*
  • DNA Ligases / isolation & purification*
  • Desulfurococcaceae / enzymology*

Substances

  • Coenzymes
  • DNA Ligases
  • DNA Ligase ATP