Adenylic acid: deoxythymidine 5'-phosphotransferase: evidence for the existence of a novel herpes simplex virus-induced enzyme

Abstract

BHK (dPyK-) cells infected with herpes simplex virus type 1 (HSV-1) contain a virus-induced deoxythymidine (dThd)-phosphorylating enzyme. This enzyme uses AMP as phosphate donor and is called AMP :deoxythymidine 5'-phosphotransferase (or kinase). The enzyme was purified over 1300-fold and was found to be specific for an AMP substrate. It can thus be distinguished from virus-specific deoxypyrimidine kinase (dPyK). It is shown that the two substrates AMP and dThd participate in the reaction at a 1 : 1 molar ratio; the Km for AMP was 2 X 3 muM and for dThd it was 2 X 1 muM. The mol. wt. of the enzyme was estimated to be between 110 000 (by glycerol gradient centrifugation) and 90 000 (by gel filtration). For optimum activity, the phosphotransferase required an alkaline pH, and 37 degrees C; the activation energy of the reaction was 18 450 cal/mol. The appearance of the enzyme after infection parallels that of viral DNA synthesis-related functions.