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Table 1 Strains and plasmids used in this study

From: Development of an efficient autoinducible expression system by promoter engineering in Bacillus subtilis

Strains and plasmids

Relevant properties

Reference

Strains

 E. coli JM109

recA1, endA1, gyrA96, thi-1, hsdR17(rk-mk-), e14−(mcrA −), supE44, relA1, Δ(lac-proAB)/F’ [traD36, proAB+, lacIq, lacZΔM15]

 

 B. subtilis 168

trpC2

This work

 BSG1682

(B. subtilis 168) Δσ F

This work

 BSG1683

The chromosome of B. subtilis 168 integrated with the fragment containing the P srfA and the gfp gene

This work

 BSG1684

The chromosome of BSG1682 integrated with the fragment containing the P srfA and the gfp gene

This work

 BSG101

B. subtilis 168, pBSG03 (P srfA -GFP)

[18]

 BSG303

BSG1682, pBSG03 (P srfA -GFP)

This work

 BSG305

BSG1682, pBSG05 (mutP srfA -GFP)

This work

 BSG3x

BSG1682, pBSGx (Px-GFP)

This work

 BSG328

BSG1682, pBSG28 (P23-NK)

This work

 BSG329

BSG1682, pBSG29 (P23-AP)

This work

Plasmids

 P7Z6

zeo r, bla r, Cre/lox

[40]

 pUC19

pUC origin, P lac , Ap r

Takara

 pAX01

P xylA , erm r, bla r, lacA

[45]

 pAX01-GFP

pAX01 containing P srfA and GFP

This work

 pET-24a-nk

pET-24a containing signal peptide of Bpr and the CDS of NK

In our lab

 pBSG03

GFP ligated downstream of P srfA

[18]

 pBSG04

pBSG03 with P srfA replaced by P HpaII

[18]

 pBSG05

pBSG03 with mutP srfA (mutP srfA was referred as P05 in this work)

[18]

 pBSG06

pBSG05 with GFP replaced by the sequence containing the intrinsic signal peptide and the CDS of AP

[18]

 pBSG3x

The derivatives of pBSG03 containing parallel promoter of Px (from P11 to P27)

This work

 pBSG28

Derivative of pBSG23 with GFP replaced by the fragment containing the signal peptide of Bpr and the CDS of NK

This work

 pBSG29

Derivative of pBSG23 with GFP replaced by the sequence loading the signal peptide and the CDS of AP

This work