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. 2015 Nov 3;291(1):29–40. doi: 10.1074/jbc.M115.696625

TABLE 1.

Bacterial strains, plasmids, and primers used in this study

The following abbreviations are used: ApR, ampicillin resistance; CmR, chloramphenicol resistance; EryR, erythromycin resistance; KmR, kanamycin resistance; TetR, tetracycline resistance; AUAP, abridged universal anchor primer; UAP, universal anchor primer.

Bacterial strains, plasmids, oligonucleotides Description Source or Ref.
E. coli
    DH5α F-Ф80 dLacZΔM15 recA1 endA1 nupG gyrA96 glnV44 thi-1 hsdR17 (rk mk+) λsupE44 relA1 deoR Δ (lacZYA-argF)U169 Promega
    BL21(DE3) F ompT gal dcm lon hsdSB (rB mB+)λ (DE3 [lacI lacUV5-T7 gene 1 ind1 sam7 nin5]) Novagen

S. aureus
    RN4220 rkmk+ accepts foreign DNA 47
    RN6390 Prophage-cured wild-type strain 48
    H306 RN6390 sirA::Km; KmR 25
    H984 RN6390 sbnI::Tet; TetR This study
    H1312 H984/pSbnI; sbnI mutant complemented with sbnI This study
    H1313 H187 containing pCN51 This study
    H1317 H984 containing pCN51 This study
    H1324 RN6390 sbn; TetR 23
    H1448 RN6390 hts::Tet; TetR 23

Plasmids
    pET28a(+) Overexpression vector for His6-tagged proteins; KmR Novagen
    pCN51 Cadmium-inducible expression vector; EryR 49
    psbnI (pAB1) pCN51-sbnI; pCN51 vector for expression of sbnI; EryR This study
    pGylux Promoterless E. coli/S. aureus shuttle vector for luminescence, ApR, CmR 33
    pCM326 1479-bp sbnA/B cloned into pGylux; ApR, CmR (fragment A) This study
    pCM328 2322-bp sbnA/B/C cloned into pGylux; ApR, CmR (fragment B) This study
    pCM330 2389-bp sbnC/D cloned into pGylux; ApR, CmR (fragment C) This study
    pCM332 2395-bp sbnD/E cloned into pGylux; ApR, CmR (fragment D) This study

Oligonucleotides
    Cloning of sbnI from S. aureus for pET28a(+) GC AGC CAT ATG AAT CAT ATT GCT GAA CAT TTA A (forward)
TTG TGT CTC GAG TCA TCA TAT TTC CCT CAA CAT (reverse)
    Cloning of sbnI from S. aureus for complementing vector (psbnI) TTG AGC GGA TCC CTT AAG CCA TCC ACA TCC TG (forward)
TTG CGC GAA TTC TCG CTA TCA ATA CCG TAA ATC (reverse)
    Cloning of fragment A GCC TCC CGGGTCAATAAAATATTTATGATTTACATGC (forward)
GACTCCCGGGAACTTGCTTCCATAACTGCAATT (reverse)
    Cloning of fragment B GACTCCCGGGTAATTTAGGCATTGCGTTG (forward)
GACTCCCGGGCTGCAACCATTAAAGG (reverse)
    Cloning of fragment C GACTCCCGGGTGTCTGAACATTGCAG (forward)
GACTCCCGGGAAATGAACGGCGAATAC (reverse)
    Cloning of fragment D GACTCCCGGGACTGACAGTACTTGT (forward)
GACTCCCGGGCCTGTGTTACTAAAC (reverse)
    RT-PCR: sbnA ACTTCTGGTAATTTAGGCATTGCG (forward)
TGCATCAGGTTCTTCAACCATTTC (reverse)
    RT-PCR: sbnB CCTGAAAATGGACACATCGC (forward)
CAAAATAATGACGCCACTTGC (reverse)
    RT-PCR: sbnC ATGAATGGGAAGTGGCTCG (forward)
GCTAATGGATGAAATGGACGAT (reverse)
    RT-PCR: sbnD CGTAGAAATACAGTTGTGGAGTGG (forward)
AAATAAGCATACCGCCAAACC (reverse)
    RT-PCR: sbnE CGAATCCATTAGGGCAAACAG (forward)
CTTAACATCGGTGAATCAGGC (reverse)
    RT-PCR: sbnF TTTTATGCGATGGAAGGG (forward)
CGTCGTTTCTACTTTATCTTTGTCG (reverse)
    RT-PCR: sbnG TCATTAAAGTGTTGGATATGGGTGC (forward)
TTAGCCATCTCCATTGCATCAAG (reverse)
    RT-PCR: sbnH CGCTCGCAATGCCAAAGATTC (forward)
TAACGCCTATGCCACCACCAAG (reverse)
    RT-PCR: rpoB AGAGAAAGACGGCACTGAAAACAC (forward)
ATAACGACCCACGCTTGCTAAG (reverse)
    GSP1 GAAAGCTGATGTGCTGTTAG
    GSP2 GAGCCCGGGTCTAGACGCATACTTGAAGACGACAG
    AUAP GATACCCGGGCCACGCGTCGACTAGTAC
    UAP GGCCACGCGTCGACTAGTACGGGIIGGGIIGGGIIG