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. 2004 Mar;186(6):1620–1628. doi: 10.1128/JB.186.6.1620-1628.2004

TABLE 1.

Bacterial strains and plasmids used in this study

Strain or plasmid Relevant characteristics Source or reference
Strains
    M182 Δlac 5
    JRG4830 M182 Δlac Δcrp 5
    JRG4864 M182 Δlac Δhns; Cmr This work
    JRG2631 M182 Δlac Δfnr Δcrp; Tetr Jeff Cole
    JRG4865 M182 Δlac Δfnr Δhns; Cmr Tetr This work
    JRG4732 M182 Δlac Δcrp Δhns; Cmr This work
    JRG4866 M182 Δlac Δfnr Δcrp Δhns; Cmr Tetr This work
    JRG4747 M182 Δlac Δfnr; Cmr This work
    JRG3212 M182 Δlac Δfnr Δcrp; Cmr This work
    JRG4385 JM109 (pGS1482); Apr 32
Plasmids
    pRS415 Medium-copy-number vector (15 to 20 copies per cell; pBR322 origin of replication) for construction of hlyE::lacZ reporter plasmid pGS1629; Apr 29
    pGS1629 pRS415 containing PhlyE (−299 to +82); Apr This work
    pRW50 Low-copy-number (2 to 5 copies per cell; pSC101 origin of replication), lac reporter vector; Tetr 15
    pGS1065 pRW50 containing PhlyE (−97 to +61); Tetr 10
    pGS1064 pUC118 containing PhlyE (−97 to +61, start codon is +1); Apr 10
    pGS1482 pGEX-KG (13) containing the slyA coding region; Apr 32
    pGS1657 pBluescript containing S. enterica slyA coding region and promoter; Apr This work