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1 he obtained advances in our understanding of lactococcal antiphage mechanisms provide fundamental ins
2                LsbB is a class II leaderless lactococcal bacteriocin of 30 amino acids.
3        An inducible middle promoter from the lactococcal bacteriophage phi31 was isolated previously
4 ng phage resistance against three species of lactococcal bacteriophages.
5 nding to type I collagen when present on the lactococcal cell surface.
6  involved in the conjugative transfer of the lactococcal conjugative element pRS01 has revealed a bac
7          Previous studies have reported that lactococcal CWPS consists of two distinct components, a
8                           Replacement of the lactococcal DpsA Lys residues 9, 15 and 16 by Glu did no
9 ative relaxase essential for transfer of the lactococcal element pRSO1.
10                                          The lactococcal group II intron Ll.ltrB interrupts the ltrB
11  Escherichia coli, retrotransposition of the lactococcal group II intron, Ll.LtrB, occurs preferentia
12                             Splicing of this lactococcal intron (designated Ll.ltrB) in vivo resulted
13                       Here, we show that the Lactococcal intron can be expressed and spliced efficien
14                                          The Lactococcal intron endonuclease can be obtained in large
15 ntrons, the DNA endonuclease activity of the Lactococcal intron is associated with RNP particles cont
16 drophobic cavity of the transcription factor Lactococcal multidrug resistance Regulator (LmrR) as a g
17   This result is in marked contrast with the lactococcal phage p2 situation, whose baseplate is known
18                  A spontaneous mutant of the lactococcal phage phi31 that is insensitive to the phage
19  insensitive to 13 distinct, plasmid-encoded lactococcal phage resistance systems (i.e. Rhea, Kamadhe
20  host adsorption device (baseplate) from the lactococcal phage TP901-1 shows that the receptor-bindin
21                                              Lactococcal phages belong to a large family of Siphoviri
22 ave recently emerged as important taxa among lactococcal phages that disrupt dairy fermentations.
23                                              Lactococcal phages Tuc2009 and TP901-1 possess a conserv
24 practical use of nanobodies in circumventing lactococcal phages viral infection in dairy fermentation
25 nal changes or Ca(2+), which contrasts other lactococcal phages.
26 urthermore, subclones of the native parental lactococcal plasmid pKR223, which encode M.
27                                   The native lactococcal plasmid, pKR223, from Lactococcus lactis sub
28 study reveals, for the first time, the dairy lactococcal plasmidome to be a rich reservoir of orphan
29 as significant identity (45%) to that of the lactococcal PrtP proteinases.
30                                      We used lactococcal recombinant strains, a protein-protein inter
31                   Thus, we hypothesized that lactococcal SodA played a role in attenuating colitis.
32 eins (RBPs) promoting adhesion to a specific lactococcal strain.
33                   The genomes of 43 distinct lactococcal strains were reconstructed by a combination
34 pecific glycosyltransferases that vary among lactococcal strains, resulting in PSPs with diverse stru
35 a, defence-associated sirtuins and classical lactococcal/streptococcal abortive infection systems.
36  assay with VAD membranes and a heterologous lactococcal system of expression, we identify 3 S. aureu
37 ino acid and DNA level homologies with other lactococcal temperate phage repressors suggest that evol
38 her evidence of the potential of recombinant lactococcal vaccines for inducing systemic and mucosal i
39 to both the dipeptidyl-peptidase IV/CD26 and lactococcal x-prolyl dipeptidyl-peptidase families.