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. 2016 Jun 3;11(6):e0157016. doi: 10.1371/journal.pone.0157016

Table 1. Strains and plasmids used in this study.

Strain or plasmid Description Source
Strains
Escherichia coli M182 Δlac galK galU strA [39]
Escherichia coli M182Δcrp [39]
Plasmids
pRW50 Broad-host-range lac fusion vector for cloning promoters on EcoRI–HindIII fragments: contains the RK2 origin of replication and encodes TcR. [40]
pSR pBR322-derived plasmid containing an EcoRI–HindIII fragment upstream of the λoop transcription terminator [17]
pRW225 pRW50-derived plasmid in which the ribosome binding site upstream of lacZ has been deleted. [23]
pDCRP crp gene preceding its native promoter (located on EcoRI-SalI flanked fragment). pBR322 derived. Encodes AmpR. ColE1 origin. [41]