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. 2017 Sep 18;7(1):153–165. doi: 10.1021/acssynbio.7b00265

Table 2. Cloning and Expression Vectors Used in This Study.

plasmid description reference
pRSF-Duet-1 Expression vector (KanR), T7 promoter Novagen
pET-Duet-1 Expression vector (AmpR), T7 promoter Novagen
pET-28b Expression vector (KanR), T7 promoter Novagen
pACYC-Duet-1 Expression vector (CmR), T7 promoter Novagen
pME001 fadD gene with C-terminus His-tag from E. coli MG1655 cloned into pRSF-Duet-1 vector using the primers PrME001 and PrME002 This study
pME002 plsB gene with C-terminus His-tag from E. coli MG1655 cloned into pet-28b vector using the primers PrME003 and PrME004 This study
pME003 plsC gene with C-terminus His-tag from E. coli MG1655 cloned into pet-28b vector using the primers PrME005 and PrME006 This study
pSJ148 cdsA gene with N-terminus His-tag from E. E. coli MG1655 cloned into pACYC-Duet vector using the primers 103 and 106 Caforio et al.a
pAC004 pss gene with C-terminus His-tag from B. subtilis cloned into pACYC-Duet vector using the primers 89 and 90 Caforio et al.a
pAC008 psd gene with C-terminus His-tag from E. coli MG1655 cloned into pACYC-Duet vector using the primers 533 and 534 Caforio et al.a
pAC015 pgsA gene with C-terminus His-tag from E. coli MG1655 cloned into pRSF-Duet vector using the primers 551 and 552 Caforio et al.a
pAC017 pgpA gene with C-terminus His-tag from E. coli MG1655 cloned into pET-Duet vector using the primers 562 and 563 Caforio et al.a
a

Ref (24).