A plasmid able to transform and to be stably maintained both in Sulfol
obus solfataricus and in Escherichia coli was constructed by insertion
into an E. coli plasmid of the autonomously replicating sequence of t
he virus particle SSV1 and a suitable mutant of the hph (hygromycin ph
osphotransferase) gene as the transformation marker. The vector suffer
ed no rearrangement and/or chromosome integration, and its copy number
in Sulfolobus was increased by exposure of the cells to mitomycin C.