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Table 1 Bacterial strains and plasmids utilized in this study

From: Functional characterization of a three-component regulatory system involved in quorum sensing-based regulation of peptide antibiotic production in Carnobacterium maltaromaticum

Bacterial strain or plasmid

Relevant characteristics

Reference, source

Strains

  

Escherichia coli DH5α

Cloning host

[25]

Lactococcus lactis MG1363

Gram-positive bacterium

[28]

Carnobacterium maltaromaticum LV17B

Carnobacteriocin producer carrying pCP40

[29]

Carnobacterium maltaromaticum LV17C

C. maltaromaticum LV17B derivative lacking pCP40

[29]

Plasmids

  

pUC18

E. coli cloning vector, Ampr

[25]

pNZ273

L. lactis promoter screening vector, gusA reporter, CmR

[24]

pIL253

L. lactis expression vector, cloned genes are transcribed from the rep promoter, EmR

[23]

pK194

E. coli cloning vector, KmR

[30]

pLQB14

pK194 carrying the 14-kbp Bam H1 fragment of pCP40

This study

pCbnKR

pUC18 with cbnK-cbnR insert, AmpR

This study

pBRKR

pIL253 expressing cbnK-cbnR, EmR

This study

pBRKA239R

pBRKR derivative with His 239 of CbnK replaced by Ala, Emr

This study

pBRKRN62

pBRKR derivative with Asp 62 of CbnR replaced by Asn, Emr

This study

pLQPBM1

pNZ273 with PBM1 promoter upstream of gusA, CmR

This study

pLQPB

pNZ273 with PB promoter upstream of gusA, CmR

[19]

pLQPS

pNZ273 with PS promoter upstream of gusA, CmR

[19]