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. 2007 Sep 28;73(23):7781–7784. doi: 10.1128/AEM.01247-07

TABLE 1.

Lactococcal strains used in this study

Strain Host Plasmid Presence of gene(s)a
mIL-2 concn (pg/ml)b Reference or source
L-mIL-2 mIL-2 usp-mIL-2 lcnCD nis Δnis nisRK
FI5876 + 0 6
FI7847 + 0 8
UKLc10 + 0 29
FI9955 FI5876 +
pFI2398 + 160 This study
FI9957 FI5876 +
pFI2398 +
pFI2148 + 215 This study
FI9947 FI7847 +
pFI2398 + 150 This study
FI9949 FI7847 +
pFI2398 +
pFI2148 + 180 This study
FI10537 UKLc10 +
pFI2398 + 195 This study
FI10538 UKLc10 +
pFI2398 +
pFI2148 + 355 This study
FI10585 FI5876 +
pFI2584 + 175 This study
FI10584 FI7847 +
pFI2584 + 140 This study
FI10586 UKLc10 +
pFI2584 + 285 This study
FI10608 FI5876 +
pFI2593 + 490 This study
a

L-mIL-2 contains the lcnA leader and mIL-2 genes preceded by the nisin promoter; mIL-2 contains the mIL-2 gene preceded by the nisin promoter; usp-mIL-2 contains the usp45 leader and mIL-2 genes preceded by the nisin promoter; nis is the nisin gene cluster; Δnis is the nisin gene cluster with a frameshift mutation in codon 16 of the nisin structural gene impeding nisin biosynthesis (the sequences of the downstream nisin cluster genes are not affected); nisRK is the nisRK genes integrated into the fivefold peptidase-deficient mutant IM16, a derivative of L. lactis MG1363.

b

The concentration of mIL-2 (pg ml−1) in culture supernatants of lactococcal strains was determined by a sandwich ELISA. The values are the means from quadruplicate samples (standard deviation, ≤8%).