Expression, high-pressure refolding, purification, crystallization and preliminary X-ray analysis of a novel single-strand-specific 3'-5' exonuclease PhoExo I from Pyrococcus horikoshii OT3.

ABSTRACT: PhoExo I is a single-strand-specific 3'-5' exonuclease from Pyrococcus horikoshii OT3 and is thought to be involved in a Thermococcales-specific DNA-repair pathway. The recombinant PhoExo I protein was produced as inclusion bodies in Escherichia coli cells. Solubilization of the inclusion bodies was performed by the high-pressure refolding method and highly purified protein was subjected to crystallization by the sitting-drop vapour-diffusion method at 20°C. A crystal of PhoExo I was obtained in a reservoir solution consisting of 0.1?M Tris-HCl pH 8.9, 27% PEG 6000 and diffracted X-rays to 1.52?Å resolution. The crystal of PhoExo I belonged to space group H32, with unit-cell parameters a = b = 112.07, c = 202.28?Å. The crystal contained two PhoExo I molecules in the asymmetric unit.

SUBMITTER: Miyazono K 

PROVIDER: S-EPMC4118808 | biostudies-literature | 2014 Aug

REPOSITORIES: biostudies-literature