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. 2015 Sep 15;4:e10514. doi: 10.7554/eLife.10514

Table 1.

Plasmid Description Source
pLHN12-His pT7-His6-rpoD (Panaghie et al., 2000)
pET15b-His-fliA pT7-His6-fliA This work
pFW11tet-PR′_+19 λPR′ promoter and native σ70-dependent pause element with a second σ70-dependent pause element located 19 bp downstream of the +1 transcription start site. The tR′ intrinsic terminator is positioned to terminate transcription ∼116 bp downstream of +1. (Deighan et al., 2011)
pFW11tet-mutPR′_+19 Same as pFW11tet-PR′_+19 but with A+2 G/T+6 G mutations in the native σ70-dependent pause element. (Deighan et al., 2011)
pFW11tet-Ptar_+19 (pNUN175) Same as pFW11tet-PR′_+19 except that the promoter (up to and including +1) has been replaced with the σ28-dependent Ptar promoter. This work
pFW11tet-Ptar_mut+19 (pNUN176) Same as pFW11tet-Ptar_+19 but with mutations in the pause element. This work
pBR-fliA pSG585-fliA This work
pSG585 colE1 origin plasmid with lacUV5 upstream of multiple cloning site This work
pNUN191 pCDFlacMUT3-rpoD This work
pCDFlacMUT3 pCDFlac with attenuated −35 element (AATACA) This work
pCDFlac derivative of pCDF-1b into which the lacUV5 promoter has been inserted (Montero-Diez et al., 2013)