Molecular cloning and high-level expression of G2 protein of Hantaan (HTN)virus 76-118 strain in the yeast Pichia pastoris KM71

Hantaan viral G2 envelope gene, which is known to be one of major antigens and induce neutralizing antibodies, was cloned into expression vector pHIL- S1 which consists of AOX1 promoter, PHO1 signal sequence, HIS4 gene and oth er components. The recombined plasmid was transformed into methylotropic ye ast, Pichia pastoris of KM71 and recombinant strains harboring multi-copy o f G2 gene were selected. Expression of the cloned G2 gene was confirmed wit h Western blot analysis using anti-sera of guinea pig immunized with the ca rboxyl terminal region of G2 protein expressed in Eschreichia coli. The exp ression of G2 gene from the recombinant strain was tightly repressed by dex trose and effectively induced by methanol, an inducer of AOX1 promoter. The highest expression level was observed from 1 day after induction and maint ained at the same level for up to 4 days.