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. 2020 Mar 18;86(7):e02312-19. doi: 10.1128/AEM.02312-19

TABLE 3.

Plasmids used in this study

Plasmid Description Resistance toa: Source or reference
pCB578 E. coli-lactobacilli shuttle vector containing SpCas9, tracrRNA, and a repeat-spacer-repeat array Erm 40
pJV114 Shuttle vector with pCB578 base containing a spacer targeting mntH1 Erm This work
pCB591 E. coli-lactobacilli shuttle vector for homologous recombination template cloning Amp (E. coli) Cm (Lactobacillus) 40
pJV88 Shuttle vector with pCB591 base containing the mntH1 gene and 500-bp homology arms on either side Amp (E. coli) Cm (Lactobacillus) This work
pJV91 Shuttle vector with pCB591 base containing 500-bp homology arms on either side of mntH1 that serves as a recombination template to generate a clean deletion Amp (E. coli) Cm (Lactobacillus) This work
pNZ8148 Broad-host-range LAB expression vector containing NisA promoter and pepN terminator Cm Mobitech
pEFB021 pNZ8148 in which NisA promoter has been replaced by the 207-bp native mntH1 promoter followed by mntH1 Cm This work
a

Erm, erythromycin; Amp, ampicillin; Cm, chloramphenicol.