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Purification and properties of Epstein-Barr virus DNase expressed in Escherichia coli
1990
Journal of Virology
A cDNA corresponding to the BGLF5 open reading frame of the Epstein-Barr virus (EBV) genome and coding for an early DNase was inserted into the procaryotic expression vector pKK223-3. One bacterial clone producing the expected 52-kilodalton DNase was used as a source of EBV DNase. The 52-kilodalton DNase was purified in the active form to near homogeneity by ammonium sulfate precipitation and successive chromatographies on phosphocellulose, DNA-cellulose, and gel filtration columns. The
doi:10.1128/jvi.64.1.96-104.1990
fatcat:ka52nmhtmvcgfma4oaw4s4crmy