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. 2014 Nov;196(22):3923–3936. doi: 10.1128/JB.01908-14

TABLE 1.

Bacterial strains and plasmids used in this study

Bacterial strain or plasmid Description or purpose Reference or source
Serratia sp. strains
    SCBI Wild type 3
    16-D2 Transposon mutant with disrupted aprE This study
    22-A7 Transposon mutant with disrupted bglB This study
    22-B9 Transposon mutant with disrupted inosine/xanthosine triphosphatase This study
    22-C7 Transposon mutant with disrupted gidA This study
    22-D7 Transposon mutant with disrupted MCP This study
    22-F6 Transposon mutant with disrupted PIN protein This study
E. coli strains
    S17-1 λpir Tpr Smr recA thi pro hsdS(r m+) RP4::2-Tc::Mu::Km Tn7 λpir; donor strain for transposon mutagenesis 64
    DH5α λpir supE44 ΔlacU169lacZΔM15) recA1 endA1 hsdR17 thi-1 gyrA96 relA1; λpir phage lysogen; host strain for gene complementation 65
Plasmids
    pMiniHimar RB1 Transposon mutagenesis 35
    pCR2.1-TOPO TOPO cloning Invitrogen
    pBAD33-Cm Expression vector 37
    pBAD33-AprE pBAD33 vector containing cloned aprE plus tolC This study
    pBAD33-GidA pBAD33 vector containing cloned gidA This study
    pBAD33-MCP pBAD33 vector containing cloned gene (SCBI_0077) coding for MCP This study
    pBAD33-PIN pBAD33 vector containing cloned gene (SCBI_0044) coding for the PIN protein This study