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. 2016 Aug 19;84(9):2566–2574. doi: 10.1128/IAI.00297-16

TABLE 1.

Strains and plasmids used in this study

Strain or plasmid Description Source
B. burgdorferi
    297 Infectious, low-passage B. burgdorferi strain 51
    OY08 297; ΔbosR::Kan 37
    OY20 297 transformed with pOY63 53
    OY23 297 transformed with pOY69 53
    OY39 297 transformed with pOY90 This study
    OY44 297 transformed with pOY106 This study
    OY68 OY08 transformed with pOY69 This study
    OY69 OY08 transformed with pOY106 This study
    OY79 297 transformed with pOY89.2 This study
    OY81 OY08 transformed with pOY89.2 This study
    OY82 OY08 transformed with pOY90 This study
    OY318 297 transformed with pOY463 This study
    OY319 OY08 transformed with pOY463 This study
E. coli
    TOP10 F mcrA Δ(mrr-hsdRMS-mcrBC) f80lacZΔM15 ΔlacX74 recA1 araD139 Δ(ara-leu)7697 galU galK rpsL (Strr) endA1 nupG Thermo Fisher Scientific
Plasmids
    pGEM-Teasy TA cloning vector Promega
    pOY16 B. burgdorferi flaB cloned into pGEM-T Easy 27
    pPROEX HTb Cloning vector Thermo Fisher Scientific
    pOY21 bosR (PCR product from primers 26F and 26R) cloned into pPROEX HTb This study
    pOY63 Promoterless lucBb+ from pJD48 cloned into pJD54 at BglII and HindIII sites 53
    pOY69 pOY63::dbpBA minimal promoter 53
    pOY89.2 pOY63::UPbb0648 (PCR product from primers 91F and 91.2R) This study
    pOY90 pOY63::UPbosR (PCR product from primers 92F and 92R) This study
    pOY106 pOY63::ospC minimal promoter (PCR product from primers 108F and 108R) This study
    pOY463 pOY63::UPbb0648-bb0648-UPbosR (PCR product from primers 91F and 92R) This study