Literature DB >> 1558766

Gene expression in Lactococcus lactis.

M van de Guchte1, J Kok, G Venema.   

Abstract

Lactic acid bacteria are of major economic importance, as they occupy a key position in the manufacture of fermented foods. A considerable body of research is currently being devoted to the development of lactic acid bacterial strains with improved characteristics, that may be used to make fermentations pass of more efficiently, or to make new applications possible. Therefore, and because the lactococci are designated 'GRAS' organisms ('generally recognized as safe') which may be used for safe production of foreign proteins, detailed knowledge of homologous and heterologous gene expression in these organisms is desired. An overview is given of our current knowledge concerning gene expression in Lactococcus lactis. A general picture of gene expression signals in L. lactis emerges that shows considerable similarity to those observed in Escherichia coli and Bacillus subtilis. This feature allowed the expression of a number of L. lactis-derived genes in the latter bacterial species. Several studies have indicated, however, that in spite of the similarities, the expression signals from E. coli, B. subtilis and L. lactis are not equally efficient in these three organisms.

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Year:  1992        PMID: 1558766     DOI: 10.1111/j.1574-6968.1992.tb04958.x

Source DB:  PubMed          Journal:  FEMS Microbiol Rev        ISSN: 0168-6445            Impact factor:   16.408


  68 in total

1.  The pyrimidine operon pyrRPB-carA from Lactococcus lactis.

Authors:  J Martinussen; J Schallert; B Andersen; K Hammer
Journal:  J Bacteriol       Date:  2001-05       Impact factor: 3.490

2.  Bile salt hydrolase of Bifidobacterium longum-biochemical and genetic characterization.

Authors:  H Tanaka; H Hashiba; J Kok; I Mierau
Journal:  Appl Environ Microbiol       Date:  2000-06       Impact factor: 4.792

3.  Characterization of a new operon, as-48EFGH, from the as-48 gene cluster involved in immunity to enterocin AS-48.

Authors:  Marta Diaz; Eva Valdivia; Manuel Martínez-Bueno; Matilde Fernández; Andrés Santos Soler-González; Hilario Ramírez-Rodrigo; Mercedes Maqueda
Journal:  Appl Environ Microbiol       Date:  2003-02       Impact factor: 4.792

4.  Expression, regulation, and mode of action of the AbiG abortive infection system of lactococcus lactis subsp. cremoris UC653

Authors: 
Journal:  Appl Environ Microbiol       Date:  1999-01       Impact factor: 4.792

5.  The carB gene encoding the large subunit of carbamoylphosphate synthetase from Lactococcus lactis is transcribed monocistronically.

Authors:  J Martinussen; K Hammer
Journal:  J Bacteriol       Date:  1998-09       Impact factor: 3.490

6.  Distribution and evolution of nisin-sucrose elements in Lactococcus lactis.

Authors:  P J Rauch; M M Beerthuyzen; W M de Vos
Journal:  Appl Environ Microbiol       Date:  1994-06       Impact factor: 4.792

7.  Molecular characterization of lactococcal bacteriophage Tuc2009 and identification and analysis of genes encoding lysin, a putative holin, and two structural proteins.

Authors:  E K Arendt; C Daly; G F Fitzgerald; M van de Guchte
Journal:  Appl Environ Microbiol       Date:  1994-06       Impact factor: 4.792

8.  Tripeptidase gene (pepT) of Lactococcus lactis: molecular cloning and nucleotide sequencing of pepT and construction of a chromosomal deletion mutant.

Authors:  I Mierau; A J Haandrikman; O Velterop; P S Tan; K L Leenhouts; W N Konings; G Venema; J Kok
Journal:  J Bacteriol       Date:  1994-05       Impact factor: 3.490

9.  Cloning and characterization of the abortive infection genetic determinant abiD isolated from pBF61 of Lactococcus lactis subsp. lactis KR5.

Authors:  L A McLandsborough; K M Kolaetis; T Requena; L L McKay
Journal:  Appl Environ Microbiol       Date:  1995-05       Impact factor: 4.792

10.  Mutational analysis of cat-86 gene expression controlled by lactococcal promoters in Lactococcus lactis subsp. lactis and Escherichia coli.

Authors:  B Bojovic; G Djordjevic; A Banina; L Topisirovic
Journal:  J Bacteriol       Date:  1994-11       Impact factor: 3.490

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