Literature DB >> 2506593

Characterization of the genetic element coding for lactose metabolism in Lactococcus lactis subsp. lactis KP3.

J L Steele1, K M Polzin, L L McKay.   

Abstract

The Lactococcus lactis subsp. lactis KP3 Lac genetic element was investigated. KP3 is a lactose-positive (Lac+) transconjugant which contains no detectable plasmid DNA. The KP3 Lac genetic element was self-transmissible (Tra+) and encoded a reduced bacteriophage sensitivity (Rbs+) phenotype. Matings of KP3 with a recombination-deficient (Rec-) recipient resulted in Lac+ transconjugants which were phenotypically indistinguishable from KP3 and contained a 96-MDa plasmid (pJS96). Phenotypic and physical analyses of pJS96 indicated that it was a deletion derivative of a putative pKB32::pJS88 Lac+ Tra+ cointegrate. pKB32 is the Lac plasmid and pJS88 is the Tra+ Rbs+ plasmid in L. lactis subsp. lactis 11007, the donor used in obtaining KP3. The results presented suggest that pJS96 is an episome, since it appeared to replicate both as a plasmid and as an integrated part of the chromosome. Conjugal transfer of chromosomal DNA mediated by pJS96 was not observed. Conjugal transfer of pJS96 resulted in Lac+ transconjugants containing plasmids ranging in size from 21 to 90 MDa. Only in Rec+ recipients were transconjugants isolated which appeared to contain pJS96 integrated into the host chromosome. Restriction analysis of several plasmids in the 21 to 90 MDa range suggested the deletions were due to intramolecular transposition of a transposable element on pJS96. This report suggests that a self-transmissible episome exists in KP3 and provides an explanation of how plasmids which vary in size yet encode similar phenotypes may be formed and disseminated.

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Year:  1989        PMID: 2506593     DOI: 10.1016/0147-619x(89)90034-6

Source DB:  PubMed          Journal:  Plasmid        ISSN: 0147-619X            Impact factor:   3.466


  4 in total

1.  Simultaneous loss of N5-(carboxyethyl)ornithine synthase, nisin production, and sucrose-fermenting ability by Lactococcus lactis K1.

Authors:  J A Donkersloot; J Thompson
Journal:  J Bacteriol       Date:  1990-07       Impact factor: 3.490

2.  Insertion elements on lactococcal proteinase plasmids.

Authors:  A J Haandrikman; C van Leeuwen; J Kok; P Vos; W M de Vos; G Venema
Journal:  Appl Environ Microbiol       Date:  1990-06       Impact factor: 4.792

3.  Molecular characterization of the integration of the lactose plasmid from Lactococcus lactis subsp. cremoris SK11 into the chromosome of L. lactis subsp. lactis.

Authors:  J P Petzel; L L McKay
Journal:  Appl Environ Microbiol       Date:  1992-01       Impact factor: 4.792

4.  Characterization of the Lactococcus lactis lactose operon promoter: contribution of flanking sequences and LacR repressor to promoter activity.

Authors:  R J van Rooijen; M J Gasson; W M de Vos
Journal:  J Bacteriol       Date:  1992-04       Impact factor: 3.490

  4 in total

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