Characterization of endogenous plasmids from Lactobacillus salivarius UCC118

Typeset version

 

TY  - JOUR
  - Fang, F,Flynn, S,Li, Y,Claesson, MJ,van Pijkeren, JP,Collins, JK,van Sinderen, D,O'Toole, PW
  - 2008
  - May
  - Applied and Environmental Microbiology
  - Characterization of endogenous plasmids from Lactobacillus salivarius UCC118
  - Validated
  - ()
  - LACTIC-ACID BACTERIA GRAM-POSITIVE BACTERIA PROGRAMMED CELL-DEATH GENE-EXPRESSION SEQUENCE-ANALYSIS CLONING VECTOR HOST-RANGE IN-VITRO MOLECULAR CHARACTERIZATION ENTEROCOCCUS-FAECALIS
  - 74
  - 3216
  - 3228
  - The genome of Lactobacillus salivarius UCC118 comprises a 1.83-Mb chromosome, a 242-kb megaplasmid (pMP118), and two smaller plasmids of 20 kb (pSF118-20) and 44 kb (pSF118-44). Annotation and bioinformatic analyses suggest that both of the smaller plasmids replicate by a theta replication mechanism. Furthermore, it appears that they are transmissible, although neither possesses a complete set of conjugation genes. Plasmid pSF118-20 encodes a toxin-antitoxin system composed of pemI and pemK homologs, and this plasmid could be cured when PemI was produced in trans. The minimal replicon of pSF118-20 was determined by deletion analysis. Shuttle vector derivatives of pSF118-20 were generated that included the replication region (pLS203) and the replication region plus mobilization genes (pLS208). The plasmid pLS203 was stably maintained without selection in Lactobacillus plantarum, Lactobacillus fermentum, and the pSF118-20-cured derivative strain of L. salivarius UCC118 (strain LS201). Cloning in pLS203 of genes encoding luciferase and green fluorescent protein, and expression from a constitutive L. salivarius promoter, demonstrated the utility of this vector for the expression of heterologous genes in Lactobacillus. This study thus expands the knowledge base and vector repertoire of probiotic lactobacilli.
  - DOI 10.1128/AEM.02631-07
DA  - 2008/05
ER  - 
@article{V43335579,
   = {Fang,  F and Flynn,  S and Li,  Y and Claesson,  MJ and van Pijkeren,  JP and Collins,  JK and van Sinderen,  D and O'Toole,  PW },
   = {2008},
   = {May},
   = {Applied and Environmental Microbiology},
   = {Characterization of endogenous plasmids from Lactobacillus salivarius UCC118},
   = {Validated},
   = {()},
   = {LACTIC-ACID BACTERIA GRAM-POSITIVE BACTERIA PROGRAMMED CELL-DEATH GENE-EXPRESSION SEQUENCE-ANALYSIS CLONING VECTOR HOST-RANGE IN-VITRO MOLECULAR CHARACTERIZATION ENTEROCOCCUS-FAECALIS},
   = {74},
  pages = {3216--3228},
   = {{The genome of Lactobacillus salivarius UCC118 comprises a 1.83-Mb chromosome, a 242-kb megaplasmid (pMP118), and two smaller plasmids of 20 kb (pSF118-20) and 44 kb (pSF118-44). Annotation and bioinformatic analyses suggest that both of the smaller plasmids replicate by a theta replication mechanism. Furthermore, it appears that they are transmissible, although neither possesses a complete set of conjugation genes. Plasmid pSF118-20 encodes a toxin-antitoxin system composed of pemI and pemK homologs, and this plasmid could be cured when PemI was produced in trans. The minimal replicon of pSF118-20 was determined by deletion analysis. Shuttle vector derivatives of pSF118-20 were generated that included the replication region (pLS203) and the replication region plus mobilization genes (pLS208). The plasmid pLS203 was stably maintained without selection in Lactobacillus plantarum, Lactobacillus fermentum, and the pSF118-20-cured derivative strain of L. salivarius UCC118 (strain LS201). Cloning in pLS203 of genes encoding luciferase and green fluorescent protein, and expression from a constitutive L. salivarius promoter, demonstrated the utility of this vector for the expression of heterologous genes in Lactobacillus. This study thus expands the knowledge base and vector repertoire of probiotic lactobacilli.}},
   = {DOI 10.1128/AEM.02631-07},
  source = {IRIS}
}
AUTHORSFang, F,Flynn, S,Li, Y,Claesson, MJ,van Pijkeren, JP,Collins, JK,van Sinderen, D,O'Toole, PW
YEAR2008
MONTHMay
JOURNAL_CODEApplied and Environmental Microbiology
TITLECharacterization of endogenous plasmids from Lactobacillus salivarius UCC118
STATUSValidated
TIMES_CITED()
SEARCH_KEYWORDLACTIC-ACID BACTERIA GRAM-POSITIVE BACTERIA PROGRAMMED CELL-DEATH GENE-EXPRESSION SEQUENCE-ANALYSIS CLONING VECTOR HOST-RANGE IN-VITRO MOLECULAR CHARACTERIZATION ENTEROCOCCUS-FAECALIS
VOLUME74
ISSUE
START_PAGE3216
END_PAGE3228
ABSTRACTThe genome of Lactobacillus salivarius UCC118 comprises a 1.83-Mb chromosome, a 242-kb megaplasmid (pMP118), and two smaller plasmids of 20 kb (pSF118-20) and 44 kb (pSF118-44). Annotation and bioinformatic analyses suggest that both of the smaller plasmids replicate by a theta replication mechanism. Furthermore, it appears that they are transmissible, although neither possesses a complete set of conjugation genes. Plasmid pSF118-20 encodes a toxin-antitoxin system composed of pemI and pemK homologs, and this plasmid could be cured when PemI was produced in trans. The minimal replicon of pSF118-20 was determined by deletion analysis. Shuttle vector derivatives of pSF118-20 were generated that included the replication region (pLS203) and the replication region plus mobilization genes (pLS208). The plasmid pLS203 was stably maintained without selection in Lactobacillus plantarum, Lactobacillus fermentum, and the pSF118-20-cured derivative strain of L. salivarius UCC118 (strain LS201). Cloning in pLS203 of genes encoding luciferase and green fluorescent protein, and expression from a constitutive L. salivarius promoter, demonstrated the utility of this vector for the expression of heterologous genes in Lactobacillus. This study thus expands the knowledge base and vector repertoire of probiotic lactobacilli.
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DOI_LINKDOI 10.1128/AEM.02631-07
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