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. 2012 May 31;7(5):e38171. doi: 10.1371/journal.pone.0038171

Table 2. Plasmids used in this study.

Plasmid Description Source or reference
pCR®2.1-TOPO PCR cloning vector Invitrogen
pMAL-p2x Expression vector with an N-terminal maltose binding protein tag New England Biolabs
pET23a Expression vector with a C-terminal 6-His tag Novagen
pTV146 bb0685 cloned into pCR2.1 for protein expression This study
pTV147 bb0685 cloned into pMAL-p2x This study
pTV118 bb0686 cloned into pCR2.1 This study
pTV125 bb0686 cloned into pET23a This study
pTV119 bb0687 cloned into pCR2.1 This study
pTV101 bb0687 cloned into pET23a This study
pTV120 bb0688 cloned into pCR2.1 This study
pTV121 bb0688 cloned into pET23a This study
pTV131 bb0683 cloned into pET23a This study
pET45b/lmhmgr Lmhmgr cloned into pET45b [23]
pYL03 bb0589 cloned into pET23a This study
pYE04 bb0622 cloned into pET23a This study
pCR2.1/Pflac Pflac cloned into pCR2.1 Unpublished data, D. Scott Samuels
pTV142 Pflac cloned into pCR2.1 with KpnI and NheI restriction sites This study
pTV145 bb0685 cloned into pCR2.1 with NheI and EcoRV/KpnI restriction sites This study
pTV146 Pflac/bb0685 cloned into pCR2.1 with flanking KpnI sites This study
pBVS2/lacI Borrelial shuttle vector with kanr and lacI under the control of PflgB [55], [56]
pTR1 pBVS2/lacI with Pflac/bb0685 This study