We have isolated a large number of polynucleotide kinase ribozymes fro
m a pool of RNA molecules consisting of an ATP-binding domain flanked
by regions of random sequence. Different classes of kinases catalyse t
he transfer of the gamma-thiophosphate of ATP-gamma S to the 5'-hydrox
yl or to internal 2'-hydroxyls. An engineered version of one class is
able to catalyse the transfer of thiophosphate from ATP-gamma S to the
5'-hydroxyl of an exogenous oligoribonucleotide substrate with multip
le turnover, thus acting as a true enzyme.