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Microbiology (Reading) ; 155(Pt 8): 2683-2693, 2009 Aug.
Article in English | MEDLINE | ID: mdl-19443545

ABSTRACT

There are barriers to cross-expression of genes between Bacteroides spp. and Escherichia coli. In this study, a lux-based reporter system was developed for Bacteroides and used to compare the promoter structure and function of a Bacteroides thetaiotaomicron 4001 (BT4001) 16S rRNA promoter with those of E. coli in vivo. Analysis of the BT4001 sequences upstream of the 16S rRNA gene revealed the same overall structure known for E. coli 16S rRNA promoters in that there were two promoters separated by approximately 150 bp. However, the BT4001 16S rRNA promoter contains the proposed Bacteroides -7 and -33 consensus sequences instead of the E. coli -10 and -35 consensus sequences. The biological activity of various configurations of the BT4001 16S rRNA promoter was analysed. Experiments pairing the BT4001 16S rRNA promoter with an E. coli RBS, and vice-versa, confirmed that gene expression between the two species is restricted at the level of transcription. In Bacteroides, a difference in translation initiation also appears to limit expression of foreign genes.


Subject(s)
Bacteroides , Escherichia coli , Gene Expression , Genes, rRNA , RNA, Ribosomal, 16S/metabolism , Bacteroides/genetics , Bacteroides/metabolism , Base Sequence , Consensus Sequence , DNA, Bacterial/analysis , DNA, Bacterial/genetics , Escherichia coli/genetics , Escherichia coli/metabolism , Genes, Reporter , Luminescent Measurements/methods , Molecular Sequence Data , Photorhabdus/genetics , Promoter Regions, Genetic , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA
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