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Table 5 Bacterial strains and plasmids used in this study.

From: Thioredoxin reductase is a key factor in the oxidative stress response of Lactobacillus plantarum WCFS1

Strain and Plasmids

Characteristics

Reference

Strains

  

E. coli DH5α

  

E. coli E10

  

L. lactis NZ9000

MG1363 pepn::nisRK

[35, 36]

L. plantarum WCFS1

Sequenced wild-type strain single colony isolate of NCIMB8826 form human saliva.

[10]

NZ7100

L. plantarum WCFS1 derivative with chromosomal integration of pEMnisRK plasmid.

This work

NZ7606

CmR, L. plantarum NZ7100 derivative carrying the pNZ8150 plasmid.

This work

NZ7601

CmR, L. plantarum NZ7100 derivative carrying the pMS011 plasmid.

This work

NZ7607

CmR, L. plantarum WCFS1 derivative carrying the pNZ7021 plasmid.

This work

NZ7602

CmR, L. plantarum WCFS1 derivative carrying the pMS040 plasmid.

This work

Plasmids

  

pUC18Ery

AmpR, EmR

[26]

pACYC184

CmR, TetR

[37]

pNZ84

CmR, pACYC184 derivative with deletion of Tetracycline resistance gene and BamhI site.

[38]

pNZ9521

EmR, nisRK cloned in pIL253, expression of nisRK driven by rep read-through.

[27]

pNZ7130

AmpR, EmR pUC18EM derivative carrying 1.0 kb DNA fragments of both L. plantarum WCFS1 lp_0075 and lp_0077 genes.

This work

pNZ7131

AmpR, EmR, pNZ7130 derivative with extra cloning sites Nsa1 and NsiI.

This work

ppNZ7132

CmR, Em R, pNZ84 derivative carrying 1.0 kb DNA fragments of L. plantarum WCFS1 (lp_0075) and (lp_0077) genes and the EryR resistance marker.

This work

pNZ7133

CmR, Em R p7132 derivative carrying the whole genes nisRK from L. lactis.

This work

pNZ8150

CmR, pNZ8148 derivative lactococcal cloning and expression vector with nisA promoter upstream of a multiple cloning site and Sca1 restriction site.

[39]

pMS011

CmR, pNZ8150 derivative carrying L. plantarum (lp_0761) trxB1 gene, translation fused to the nisA promoter.

This work

pNZ7021

CmR, pNZ8148 derivative carrying nisA::pepN.

[40]

pMS040

CmR, pNZ7021 derivative carrying L. plantarum lp_0761 trxB1 gene, translational fused to the pPEPN promoter.

This work