Determination of the free-energy change for repair of a DNA phosphodiester bond

J Biol Chem. 2000 May 26;275(21):15828-31. doi: 10.1074/jbc.M910044199.

Abstract

The repair of phosphodiester bonds in nicked DNA is catalyzed by DNA ligases. Ligation is coupled to cleavage of a phosphoanhydride bond in a nucleotide cofactor resulting in a thermodynamically favorable process. A free energy value for phosphodiester bond formation was calculated using the reversibility of the T4 DNA ligase reaction. The relative number of DNA nicks to phosphodiester bonds in a circular plasmid DNA, formed during this reaction at fixed concentrations of ATP to AMP and PP(i), was quantified. At 25 degrees C, pH 7, the equilibrium constant (K(eq)) for the ligation reaction is 3.89 x 10(4) m. This value corresponds to a standard free energy (DeltaG degrees ') of -6.3 kcal mol(-1). By subtracting the known energy contribution due to hydrolysis of ATP to AMP and PP(i), DeltaG degrees ' for the hydrolysis of a DNA phosphodiester bond is -5.3 kcal mol(-1).

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Monophosphate / chemistry
  • Adenosine Triphosphate / chemistry
  • DNA Ligases / chemistry*
  • DNA Repair*
  • DNA, Circular / chemistry*
  • Nucleic Acid Conformation
  • Thermodynamics

Substances

  • DNA, Circular
  • Adenosine Monophosphate
  • Adenosine Triphosphate
  • DNA Ligases