Table 1. Bacterial strains and plasmids used in this study.
Strains and plasmids | Relevant genotype or description | Reference |
---|---|---|
Escherichia coli strains | ||
MG1656 | ΔlacMluI derivative of Escherichia coli MG1655 (K-12F– λ– ilvG−rfb-50 rph-1) | [35] |
MG/pZE1 | MG1656 carrying p6851 and pZE1 plasmids | This work. |
MG/intI1 | MG1656 carrying p6851 and pZE1intI1 plasmids | This work. |
MG/intI1* | MG1656 carrying p6851 and pZE1intI1* plasmids | This work. |
MG1656λatt::gfp | MG1656 containing the gfpmut3 gene at the λatt site; expression of gfpmut3 from Pλ promoter. Green fluorescent bacteria. | [36] |
Plasmids | ||
p6851 | Cassette recombination reporter (pSU38::aac(6’)-Ib*::attCaadA7-cat(T4)-attCVCR2); CmR, KmR | [24] |
Recombined p6851 | Plasmid resulting from deletion of the resistance gene cassette cat(T4)-attCVCR2 in native p6851; expression of the resistance gene cassette aac(6’)-Ib* from PlacZ promoter; TobraR, KmR | This work. |
pZE1 | Promoterless derivative of pZE12 plasmid, carrying a multiple cloning site (mcs1); AmpR | [24] |
pZE1intI1 | attI site + intI1 gene from In40 class 1 integron cloned into pZE1 plasmid; this intI1 gene encodes the most active variant of the integrase, IntI1R32_H39; AmpR | [24,37] |
pZE1intI1* | pZE1intI1 plasmid carrying the LexAmut2 mutation in the LexA binding site of the class 1 integron integrase promoter PintI1, leading to constitutive expression of the intI1 gene; AmpR | [24] |
CmR: confers resistance to chloramphenicol; KmR: confers resistance to kanamycin; TobraR: confers resistance to tobramycin; AmpR: confers resistance to ampicillin