DNA sequence analysis for the promoter of pyruvate oxidase gene from Streptococcus oralis / 华西口腔医学杂志
West China Journal of Stomatology
;
(6): 350-352, 2003.
Article
in Chinese
| WPRIM
| ID: wpr-283583
ABSTRACT
<p><b>OBJECTIVE</b>To elucidate the molecular structure of pyruvate oxidase gene promoter.</p><p><b>METHODS</b>The 1.30 kb fragment with promoter activity, amplified from upstream of Streptococcus oralis pyruvate oxidase gene (Sopox), was cloned into vector PBK-CMV. The positive transformed E. coli JM109 clone was selected, the recombinant plasmid was further identified with restriction mapping analysis. The positive recombinant plasmid was studied with sequence analysis.</p><p><b>RESULTS</b>After digesting the recombinant plasmid with Hind III, 1% agarose electrophoresis showed 1.30 kb fragment, which was consistent with predicted size. Sequence analysis revealed 1,350 bp.</p><p><b>CONCLUSION</b>The Sopox promoter region is sequenced. Further characterization of the Sopox promoter region will elucidate the molecular mechanism of H2O2 production of streptococcus oralis.</p>
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Plasmids
/
Pyruvate Oxidase
/
Molecular Sequence Data
/
Base Sequence
/
Promoter Regions, Genetic
/
Cloning, Molecular
/
Sequence Analysis, DNA
/
Streptococcus oralis
/
Escherichia coli
/
Genes, Bacterial
Limits:
Humans
Language:
Chinese
Journal:
West China Journal of Stomatology
Year:
2003
Type:
Article
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