Skip to main content
. 1998 Jan;180(2):377–387. doi: 10.1128/jb.180.2.377-387.1998

TABLE 2.

Plasmids used in this work

Plasmid Descriptiona Source or reference
pGP1-3 Tcr plasmid carrying T7 RNA polymerase gene under λcI857 control 44
pWSK29 Apr low-copy-number vector 47
pGZK20 Apr low-copy-number uvrD+ plasmid uvrD+ cloned in SalI site of pWSK29
pGZK28 ApruvrD300 (A406T) substitution in pGZK20 Isolated by EMS mutagenesis
pGZK29 ApruvrD301 (A406V) substitution in pGZK20 Site-directed mutagenesis
pGZK30 ApruvrD302 (A406S) substitution in pGZK20 Site-directed mutagenesis
pGZK31 ApruvrD303 (D403AD404A) substitution in pGZK20 Site-directed mutagenesis
pGZK32 ApruvrD304 (E408AR409A) substitution in pGZK20 Site-directed mutagenesis
pGZK33 ApruvrD+ (T406A) substitution in pGZK28 Site-directed mutagenesis
a

Mutationally altered uvrD genes were isolated as described in Materials and Methods. The positions of amino acid substitutions are indicated in parentheses.