Abstract
A replicative DNA-nucleotidyl transferase free from detectable endonuclease activity has been partially purified from the nonhistone chromosomal proteins of rat liver. The polymerase preparation can form complexes with both DNA and RNA, but only DNA is functional in the enzymic reaction. The reaction product is in association with the DNA template and is heterogeneous, consisting of small fragments of molecular weights of less than 2.5 × 10 5.
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