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Table 1 Bacterial strains and plasmids used in this study

From: Rapid monitoring of the target protein expression with a fluorescent signal based on a dicistronic construct in Escherichia coli

 

Genotype/characteristics

Source

Strains

 Top10

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

Invitrogen

 BL21(DE3)pLysS

F ompT hsdS B (r B m B ) gal dcm (DE3) pLysS (CmR)

Novagen

 Rosetta(DE3)pLysS

F ompT hsdS B (r B m B ) gal dcm lacY1 (DE3) pLysSRARE (CmR)

Novagen

Plasmids

 pET-21a

Ampr T7 promoter lac operator

Novagen

 pUCm-T

TA cloning

Sangon

 pT-RFP

pUCm-T carrying mcherry

This study

 pET-RFP

pET-21a expressing mCherry

This study

 pO-RFP

pET-21a carrying mcherry in ORF2

This study

 pOI-RFP

pO-RFP with one rare codon in ORF1

This study

 pOII-RFP

pO-RFP with two consecutive rare codons in ORF1

This study

 pOIII-RFP

pO-RFP with three consecutive rare codons in ORF1

This study

 pT-GFP

pUCm-T carrying egfp

This study

 pGFP-RFP

pO-RFP carrying egfp in ORF1

This study

 pGFPI-RFP

pGFP-RFP with one rare codon preceding egfp

This study

 pGFPII-RFP

pGFP-RFP with two consecutive rare codons preceding egfp

This study