Acute virus necrosis virus (AVNV) was reported as one causative agent responsible for summer mass mortality of adult Zhikong scallop (Chlamysfarreri), which is widely cultured on northern China coast.To explore its pathogenesis at the molecular level, we cloned a gene which was predicted to encode AVNV dUTPase based on the genomic sequence of C.farreri AVNV completed by our laboratory.The gene encodes a protein of 248aa with a predicted molecular mass of 26.4 kDa.To obtain the C.farreri AVNV Open Reading Frame 074, which supposed encodes AVNV dUTPase, a pair of specific primers was designed based on the genomic sequence of C.farreri AVNV.Then we amplified the expected DNA by PCR, using the total genomic DNA extracted from infected C.farreri tissues as template.Amplified PCR fragments were subcloned into the prokaryotic expression vector pET-32a (+).After that we transformed the recombinant plasmid pET32a-dut into E.coli BL21 (DE3) strain and expressed it under IPTG induction.SDS-PAGE analysis showed that the molecular mass of the induced recombinant protein was about 46 kDa.The western-blot and mass spectrometry analysis proved that the expressed protein is the target protein.Then we purified recombinant protein with Co2+ purification column and got the recombinant protein with a purity of more than 90%.The analysis of the enzymatic activity indicated that the recombinant dUTPase could specifically catalyse the hydrolysis of dUTP and the activity of enzyme was enhanced by Mg2+ while inhibited by EDTA.