A Deinococcus radiodurans Nudix fehérjéjének klónozása, expressziója és enzimaktivitásának mérése

Abstract

The aim of my work was the experimental examination of the disordered regions to verify my hypothesis. For this it was necessary to produce the wild-type Nudix DR0550 protein. I cloned the DNA region coding for the enzyme, cloned it into an expression vector, purified the protein and measured the enzyme activity. I worked with the wild-type as well as with the Nudix-dN mutant which is truncated at its N-terminal, lacking the longer disordered region.