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. 2010 Nov 19;193(3):768–773. doi: 10.1128/JB.01196-10

TABLE 1.

Bacterial strains and plasmids

Strain or plasmid Genotype Resistancea Source
Escherichia coli strains
    CV1 Chemotaxis wild type (same as RP437) Str 24
    TG1/pDS-Red Express Wild type; dead-cell control Amp Stratagene
    CV5 CV1 Δtsr Str This studyb
    CV12 CV1 Δtar-tap trg::Tn10 Str, Tet This studyc
    MJ101 CV1 lsrBΩKanr Str, Kan This studyd
    MJ102 CV1 lsrCΩKanr Str, Kan This studye
    BW25113 ΔlsrB lsrBΩKanr Kan 3
    BW25113 ΔlsrC lsrCΩKanr Kan 3
Plasmids
    pCM18 GFP-expressing vector Erm 12
    pDS-RedExpress RFP-expressing vector Amp Clontech
    pCA24N-lsrB pCA24N PT5-lac::lsrB; expresses E. coli lsrB from placZYA Cm 15
a

Str, streptomycin; Tet, tetracycline; Kan, kanamycin; Erm, erythromycin; Amp, ampicillin; Cm, chloramphenicol.

b

Made by introducing Δtsr9101 (7) into CV1 by phage P1 transduction (16), with selection for Thr+ and screening for Tsr.

c

Made in two steps: Δtar-tap5201 (26) was introduced into CV1 by phage P1 transduction with selection for Eda+, followed by screening for Tar, and then trg::Tn10 was introduced by phage P1 transduction followed by selection for Tetr on lysis broth (LB) (20) agar plates containing 10 μg/ml tetracycline, followed by screening for Trg.

d

Made by introducing lsrBΩKanr (3) into CV1 by phage P1 transduction, with selection for Kanr and confirmation of lsrB gene disruption by PCR.

e

Made by introducing lsrCΩKanr (3) into CV1 by phage P1 transduction, with selection for Kanr and confirmation of lsrC gene disruption by PCR.