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Table 1 Primers, plasmids and strains used in this study

From: Engineering E. coli cell surface in order to develop a one-step purification method for recombinant proteins

Primer, plasmid or strains

Description or Genotype

Source or reference

Primer

 P1 (LPO1-F) NdeI

ggggcatatgaaagctactaaactggtactgggcaacccgtatgttggctttgaaatggg

Tafakori et al. (2012)

 P2 (LPO3-R) EcoRI

gggggaattccggtctgcggcagcggaatgccgttgtccggacg

MWG

 P1(SRTA3-F) SphI

gggggcatgccaagctaaacctcaaattcc

MWG

 P2(SRTA2-R) PstI

ggggctgcagttatttgacttctgtagcta

MWG

Plasmid

 PQE

T5 promoter, 6×His-tag coding sequence, β-lactamase coding sequence, Amp r

Qiagen

 PET 26b

T7 promoter, an N-terminal pelB signal sequence for potential periplasmic localization, plus optional C-terminal His·Tag

Novagene

 PET 26b-lOAE (pLOAE)

Vector for construction and expressing of chimeric protein containing lpp′-ompA, Elongatus and Chitin Binding domain

Constructed in this study

Constructed in this srudy

 pSRTA

Vector for construction and expressing of SrtA

NIGEB collection

 SrtA∆N

Vector for construction and expressing of SrtAΔ59 (StrAT)

NIGEB collection

 pQE30

  

Strain

 BL21 DE3

F– ompT gal dcm lon hsdSB (rB- mB-) λ (DE3 [lacI lacUV5-T7 gene 1 ind1 sam7 nin5]

Stratagene

 Top 10

Staphylococcus aureus

F′[lacIq Tn10 (tetR)] mcrA Δ (mrr-hsdRMS-mcrBC) \( \varphi \) 80lacZΔM15 ΔlacX74 deoR nupG recA1 araD139 ∆(araleu) 7697 galU galK rpsL(StrR) endA1 λ−

Invitrogen