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Table 1 Plasmids and strains used in this study

From: Characterization of a synthetic bacterial self-destruction device for programmed cell death and for recombinant proteins release

Strains

Name

Genotype

Source

TOP10

F- mcrA Δ(mrr-hsdRMS-mcrBC) φ80lacZΔM15 ΔlacX74 nupG recA1 araD139 Δ(ara-leu)7697 galE15 galK16 rpsL(StrR) endA1 λ-

Invitrogen

DB3.1

F- gyrA462 endA1 glnV44 Δ(sr1-recA) mcrB mrr hsdS20(rB-, mB-) ara14 galK2 lacY1 proA2 rpsL20(Smr) xyl5 Δleu mtl1

Invitrogen

DH5alpha

F- endA1 glnV44 thi-1 recA1 relA1 gyrA96 deoR nupG φ80dlacZΔM15 Δ(lacZYA-argF)U169, hsdR17(rK- mK+), λ-

Invitrogen

MG1655

F- λ- ilvG- rfb-50 rph-1

CGSC

Plasmids

Name

BioBrick™ code

Description

pLC-ccdB

pSB4C5(BBa_I52002)a

pUC19-derived pMB1 replication origin and ccdB toxin constitutive expression cassette in low copy vector

pHC-T4Lys-

pSB1A2(BBa_K112808)a

promoterless lysis device in high copy vector

pHC-HSL

pSB1A2(BBa_F2620)b

HSL-inducible promoter in high copy vector

pHC-RFP

BBa_J61002(BBa_J23118)a

RFP constitutive expression cassette

pHC-Heat

pSB1A2(BBa_ K098995)a

heat-inducible promoter in high copy vector

pHC-T4LysHSL

pSB1A2(BBa_K173015)c

HSL-inducible lysis device in high copy vector

pLC-HSL

pSB4C5(BBa_F2620)c

HSL-inducible promoter in low copy vector

pLC-T4Lys-

pSB4C5(BBa_K112808)c

promoterless lysis device in low copy vector

pLC-T4LysHSL

pSB4C5(BBa_K173015)c

HSL-inducible lysis device in low copy vector

pLC-T4LysHeat

pSB4C5(BBa_J107014)c

heat-inducible lysis device in low copy vector

  1. a taken from the Registry DNA Distribution 2009
  2. b given by the iGEM Headquarters, Massachusetts Institute of Technology, Cambridge, USA
  3. c constructed in this study
  4. The BioBrick™ code of the plasmids include the vector name (out of brackets) and insert name (in brackets). The prefix pHC- indicates a high copy vector backbone (pSB1A2 or BBa_J61002), while pLC- indicates a low copy vector backbone (pSB4C5).