Skip to main content

Table 2 Plasmids and bacterial strains used in this study

From: Coupling the recombineering to Cre-lox system enables simplified large-scale genome deletion in Lactobacillus casei

Strain or plasmid

Characteristic(s)

Source

Strains

 Escherichia coli DH5α

F− supE44 ∆lacU169 Ф80lacZ ∆M15 hsdR17 recA1 endA1 gyrA96 thi-1 relA1

Novagen

 Lactobacillus casei BL23

Derivative of L. casei ATCC 393 (pLZ15−)

[44]

Plasmids

 pG+host9

Ermr; temperature-sensitive vector

[17]

 pUC19

Ampr; cloning vector

This study

 pSec:Leiss:Nuc

pWV01 replicon; expresses Nuc under PnisA control; Cmr

[28]

 pET-28a

Kanr; cloning vector

This study

 pTRKH2

Ermr; theta-replicating vector

[29]

 pMSP456

Expression LCABL_13040-50-60 under PnisA control

This study

 pMSPcre

Expression Cre under PnisA control

This study

 pUCgalK

Source of fragment loxP-cat-loxP

[15]

 pCD4033-gfp

Gene gfp as a reporter in the downstream of Pldh

[45]