Analysis by HPLC of Distributive Activities and the Synthetic (Back) Reaction of Pancreatic-Type Rib

Nucleic-acid cleavage can be processive, with the enzyme moving from one site to the next in the polymer before dissociating from the substrate, or distributive, with partially cleaved substrates released to the medium after the initial reaction. Kinetics indicate that either mechanism can be seen in reactions with polymerases, helicases, or nucleases (1 ). However, many factors affect these kinetics, including the strength of the enzyme-substrate binding, which can be altered by the salt concentration of the buffer, and intermediates in the formation of the complex or the release of the products that may be poorly characterized. The distinction between processivity and distributivity is based primarily on the ratio of rate constants for cleavage and dissociation. Unlike the distinction between endo- and exo-nucleases (i.e., those cleaving within or from one end of the nucleic acid), which will not change with reaction conditions, although in some cases enzymes show only a preference from one or the other activity, assay conditions can blur the distinction between processivity and distributivity.