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Appl Environ Microbiol ; 66(4): 1253-8, 2000 Apr.
Article in English | MEDLINE | ID: mdl-10742196

ABSTRACT

We have previously reported the construction of a food-grade cloning vector for Lactococcus using the ochre suppressor, supB, as the selective marker. This vector, pFG1, causes only a slight growth inhibition in the laboratory strain MG1363 but is unstable in the industrial strains tested. As supB suppresses both amber and ochre stop codons, which are present in 82% of all known lactococcal genes, this undesirable finding may result from the accumulation of elongated mistranslated polypeptides. Here, we report the development of a new food-grade cloning vector, pFG200, which is suitable for overexpressing a variety of genes in industrial strains of Lactococcus lactis. The vector uses an amber suppressor, supD, as selectable marker and consists entirely of Lactococcus DNA, with the exception of a small polylinker region. Using suppressible pyrimidine auxotrophs, selection and maintenance are efficient in any pyrimidine-free medium including milk. Importantly, the presence of this vector in a variety of industrial strains has no significant effect on the growth rate or the rate of acidification in milk, making this an ideal system for food-grade modification of industrially relevant L. lactis strains. The usefulness of this system is demonstrated by overexpressing the pepN gene in a number of industrial backgrounds.


Subject(s)
Cloning, Molecular , Food Industry , Food Microbiology , Genetic Vectors , Lactococcus lactis/genetics , Amino Acid Sequence , Aminopeptidases/metabolism , Animals , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Base Sequence , Electroporation , Hydrogen-Ion Concentration , Lactococcus lactis/growth & development , Milk/microbiology , Molecular Sequence Data , Mutation , Plasmids/genetics , Pyrimidines/metabolism , Sequence Analysis, DNA , Transcription, Genetic
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