The light utilising DNA repair enzyme known as DNA photolyase induces
the reversion of cyclobutane-type pyrimidine dimers in DNA back to pyr
imidines thus restoring the DNA function. Either by direct excitation
or energy transfer, a noncovalently bound flavin cofactor becomes a po
werful reducing agent. Electron transfer to the pyrimidine dimer produ
ces an unstable radical anion and thereby initiates bond cleavage in t
he dimer. The substrate binding, dimer splitting mechanism, and energe
tics of the individual steps constitute a fascinating picture of photo
enzymic repair of UV damaged DNA.