E. Blum et al., PCR-DIRECTED PREPARATION AND SINGLE-STEP PURIFICATION OF HIGHLY-ACTIVE HISTIDINE-TAGGED RESTRICTION-ENDONUCLEASE HGIBI (GGWCC), Gene, 157(1-2), 1995, pp. 107-108
The polymerase chain reaction was used to produce His, fusion proteins
via deletion of an intervening piece of DNA. The generally applicable
method was performed using a standard primer with the advantage that
the fusion does not produce additional amino acids. In a single-step p
urification highly purified, enzymatically active restriction endonucl
ease was obtained.