A host factor absent from Lactococcus lactis subspecies lactis MG1363 is required for conjugative transposition
- 1 December 1991
- journal article
- research article
- Published by Wiley in Molecular Microbiology
- Vol. 5 (12) , 2983-2993
- https://doi.org/10.1111/j.1365-2958.1991.tb01858.x
Abstract
In matings between Lactococcus lactis strains, the conjugative transposons Tn916 and Tn919 are found in the chromosome of the transconjugants in the same place as in the chromosome of the donor, indicating that no transposition has occurred. In agreement with this, the frequency of L. lactis transconjugants from intraspecies matings is the same whether the donor contains the wild-type form of the transposon or the mutant Tn916-int1, which has an insertion in the transposon's integrase gene. However, in intergeneric crosses with Bacillus subtilis or Enterococcus faecalis donors, Tn916 and Tn919 transpose to different locations on the chromosome of the L. lactis transconjugants. Moreover, Tn916 and Tn919 could not be transferred by conjugation from L. lactis and B. subtilis, E. faecalis or Streptococcus pyogenes. This suggests that excision of these elements does not occur in L. lactis. When cloned into E. coli with adjacent chromosomal DNA from L. lactis, the conjugative transposons were able to excise, transpose and promote conjugation. Therefore, the inability of these elements to excise in L. lactis is not caused by a permanent structural alteration in the transposon. We conclude that L. lactis lacks a factor required for excision of conjugative transposons.Keywords
This publication has 53 references indexed in Scilit:
- Studies on transformation of Escherichia coli with plasmidsPublished by Elsevier ,2006
- The integration‐excision system of the conjugative transposon Tn 1545 is structurally and functionally related to those of lambdoid phagesMolecular Microbiology, 1990
- Tn10 transposition and circle formation in vitroCell, 1987
- Escherichia coli integration host factor binds specifically to the ends of the insertion sequence IS1 and to its major insertion hot-spot in pBR322Journal of Molecular Biology, 1987
- Conjugative transfer of the transposon Tn919to lactic acid bacteriaFEMS Microbiology Letters, 1985
- Size variation of the M protein in group A streptococci.The Journal of Experimental Medicine, 1985
- Extent of sequence homology required for bacteriophage lambda site-specific recombinationJournal of Molecular Biology, 1985
- TECHNOLOGICAL EXAMINATION OF LOW‐FIRED TERRACOTTA STATUES FROM AYIA IRINI, KEAArchaeometry, 1982
- Plasmids useable as gene-cloning vectors in an in vitro packaging by coliphage λ: “cosmids”Gene, 1978
- (Symposium on Bacterial Spores: Paper II). Genetics of Sporulation inBacillus subtilisMarburgJournal of Applied Bacteriology, 1970