EXPRESSION OF THE TURNIP YELLOW MOSAIC-VIRUS PROTEINASE IN ESCHERICHIA-COLI AND DETERMINATION OF THE CLEAVAGE SITE WITHIN THE 206-KDA PROTEIN

The large non-structural polyprotein (206 kDa) of turnip yellow mosaic tymovirus (TYMV) undergoes auto-cleavage, producing N- and C-terminal proteins. Here we show that the viral proteinase responsible for this event is active when produced in Escherichia coli, as monitored in We stern blots by examining the generation of the C-terminal cleavage pro duct after induction by IPTG. The outer boundaries and critical amino acids of the proteinase domain were characterized by deletion analysis and site-directed mutagenesis. A miniproteinase of 273 residues resul ting from combined N- and C-terminal deletions still performed efficie nt cleavage. Sequence analysis of the bacterially-purified C-terminal cleavage product indicated that cleavage occurs between Ala(1259) and Thr(1260) of the non-structural protein.