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. 2013 Sep 19;9(9):e1003802. doi: 10.1371/journal.pgen.1003802

Table 2. Plasmids used in this work.

Plasmid Relevant characteristicsa Reference
pKA52 Overproduction of His6-ParB (based on pET45b(+)) This study
pAH7 Pnat-parB-YFP, Mx8 attB, (Pnat 1097 bp)b [39]
pAH59 Pnat-parA-mCherry, Mx8 attB, (Pnat 1097 bp)b This study
pAH73 PcuoA-parB-YFP, copper-dependent expression of parB-YFP c This study
pNV3 tetO-array+fragment of mxan0733 region (33°) This study
pMAT20 tetO-array+fragment of mxan1968 region (90°) This study
pMAT19 tetO-array+fragment of mxan3779 region (180°) This study
pMAT13 tetO-array+fragment of mxan4000 region (192°) This study
pMAT18 tetO-array+fragment of mxan5499 region (270°) This study
pMAT6 PcuoA-tetR-YFP, Mx8 attB This study
pEB8 Pnat-ssb-YFP for integration at native site (Pnat 303 bp)d This study
pAH57 PcuoA-parB, copper-dependent expression of parB, Mx8 attB This study
pAH18 Construct for in-frame deletion of parB This study
pAH17 Overproduction of His6-ParA (based on pET45b(+)) This study
pMAT15 Vector for copper-dependent expressionc This study
pLAU53 lacI-ECFP and tetR-YFP [51]
pLAU44 tetO-array (240 copies of 19 bp tetO operator)e [51]
a

Promoters for the expression of a particular construct are indicated together with the integration site on the chromosome.

b

The promoter Pnat comprises 1097 bp upstream of the parA-gene.

c

The plasmid integrates at cuoA locus.

d

The promoter Pnat comprises 303 bp upstream of the ssb-gene.

e

The operators are separated by a 10 bp random sequence.