TABLE 1.
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 |
Str, streptomycin; Tet, tetracycline; Kan, kanamycin; Erm, erythromycin; Amp, ampicillin; Cm, chloramphenicol.
Made by introducing Δtsr9101 (7) into CV1 by phage P1 transduction (16), with selection for Thr+ and screening for Tsr−.
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−.
Made by introducing lsrBΩKanr (3) into CV1 by phage P1 transduction, with selection for Kanr and confirmation of lsrB gene disruption by PCR.
Made by introducing lsrCΩKanr (3) into CV1 by phage P1 transduction, with selection for Kanr and confirmation of lsrC gene disruption by PCR.