Skip to main content
. 1999 Aug;181(16):4949–4954. doi: 10.1128/jb.181.16.4949-4954.1999

TABLE 1.

Bacterial strains and plasmids used in this work

Strain Genotype Reference or source
S. typhimurium
 SL1344 Wild type 19
 SVM473 Cmr Φ(sigD-lacZYA)/sigDE+ This work
 SB154 Cmr StrRinvA::Ωcat J. Galán
 SVM514 Strr SprspaS::ΩStr/Sp This work
 SVM579 ΔinvF (in-frame deletion of 465 bp) This work
 VV302 ΔhilA-523 3
 BJ68 Tcr; sipC::Tn5lacZY 34
 SVM725 TcrsipC::Tn5lacZY ΔinvF This work
 SVM733 Strr SprspaS::ΩStr/Sp ΔinvF This work
 SVM754 Strr Spr Tcr ΔinvF spaS::ΩStr/Sp sipC::Tn5lacZY This work
 LB5000 LT2, flaA66 metA22 trp-2 rpsL xyl-401 ilv-452 leu hsd mod+ 37
Plasmids
 pHG329 Apr medium-copy-number cloning vector 39
 pWKS130 Knr, low-copy-number cloning vector 40
 pVV214 Apr, hilA in pACYC177 3
 philA Knr, 2.2-kb NsiI fragment from pVV214 cloned into the PstI site of pWSK130 This work
 pHH21 Apr, sigD-lacZYA, 0.9-kb EcoRI/PstI sigDE promoter and partial coding sequences in pRS415 20
 pVLT33 Knr, low-copy-vector for IPTG-inducible expression downstream of Ptac 9
 pHH37 Knr, 3.2-kb EcoRI-BamHI sigDE fragment in pVLT33 This work
 pRW50 Tcr, low-copy-number transcriptional reporter fusion vector 29
 pHD3 Tcr, Φ(invF-lacZYA) in pRW50 This work
 pHD11 Tcr, Φ(sicA-lacZYA) in pRW50 This work
 pFUSE Cmr, suicide vector for integration of lacZYA transcriptional reporters onto the chromosome 5
 pHD5 Cmr, 1-kb sequence including sigDE promoter in pFUSE This work
 pDL7-2 Tcr, cosmid clone containing inv-spa and sicAB genes 32
 pHD7 Knr, ∼8-kb EcoRI fragment from pDL7-2 containing invHFGEABC′ in pWKS130 This work
 pHD8 Knr, ∼6.7-kb EcoRI fragment from pDL7-2 containing invC′IJ spaOPQRS sicA sequence in pWSK130 This work
 pHD9-1 Knr, 1.7-kb PstI fragment from pHD7 containing invF in pWKS130 This work
 pHD10-1 Apr, 1.7-kb PstI fragment from pHD7 containing invF in pHG329 This work
 pHD17 Cmr, 1.7-kb HindIII invF fragment from pHD10-1 cloned into pACYC184 This work
 pHD13 Apr, same as pHD10-1 but with 465-bp deletion in invF This work
 pMAK705 Cmr, temperature-sensitive origin of replication vector used for gene replacement 16
 pHD15 Cmr, ∼1.25-kb PstI fragment from pHD13 cloned into pMAK705 This work