We have modified the positive-selection cloning vector pUN121 to expan
d the numbers of unique cloning sites by insertion of a multiple cloni
ng site into the h cl gene without disrupting its repressor function,
resulting in plasmid pSKM10. Plasmid pSKM10 has seven restriction enzy
me sites suitable for general cloning purposes. A mobilizable version
(pSKM11) of pSKM10 was constructed by insertion of the IncP mob sequen
ce which permitted mobilization of the plasmid into a wide variety of
Gram(-) bacteria.