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« Previous AbstractSequence analysis of Enterococcus faecalis aggregation substance encoded by the sex pheromone plasmid pAD1    Next Abstract"Time since discharge of 9mm cartridges by headspace analysis, part 1: Comprehensive optimisation and validation of a headspace sorptive extraction (HSSE) method" »

Mol Microbiol


Title:Transcriptional control of sex-pheromone-inducible genes on plasmid pAD1 of Enterococcus faecalis and sequence analysis of a third structural gene for (pPD1-encoded) aggregation substance
Author(s):Galli D; Friesenegger A; Wirth R;
Address:"Lehrstuhl fur Mikrobiologie, Universitat Munchen, Germany"
Journal Title:Mol Microbiol
Year:1992
Volume:6
Issue:10
Page Number:1297 - 1308
DOI: 10.1111/j.1365-2958.1992.tb00851.x
ISSN/ISBN:0950-382X (Print) 0950-382X (Linking)
Abstract:"The expression of several neighbouring genes on plasmid pAD1 that are necessary for conjugation depend on induction with sex pheromone cAD1. Analyses of transcripts by Northern blot hybridization demonstrated that the genes sea1 (encoding surface exclusion protein) and asa1 (encoding aggregation substance) are transcribed independently. Both genes are organized in different operons together with neighbouring open reading frames of unknown function. Several transcripts could be identified for sea1 and asa1. Their transcriptional start sites were determined by primer extension experiments, confirming the results of the Northern blot experiments. We also could identify sea1- and iad- (encoding an inhibitory peptide counteracting sex pheromone cAD1) specific transcripts which are expressed constitutively, but to a lower extent relative to induced conditions. In addition, we localized the asp1 gene coding for aggregation substance of sex pheromone plasmid pPD1 and determined its DNA sequence, which was found to be highly homologous to asa1 (aggregation substance gene of pAD1) and prgB (aggregation substance gene of pCF10). The structural genes were found to be organized more or less identically on the three sex-pheromone plasmids pAD1, pCF10, and pPD1, and to be highly conserved. Regions supposed to be of crucial importance for regulatory functions, however, were found to differ. We also could identify some conserved DNA motifs which might be potential target sites for transcriptional regulators. In combination these data allowed us to formulate a model for the regulation of sex-pheromone-inducible genes of plasmid pAD1. Its main statement is that only in the presence of cAD1 can the gene traE1 be transcribed. The positive regulatory factor TraE1 then can trigger expression of the structural genes sea1 and asa1"
Keywords:"Amino Acid Sequence Bacterial Adhesion Bacterial Proteins/*genetics Base Sequence Conjugation, Genetic/genetics Enterococcus faecalis/*genetics *Gene Expression Regulation, Bacterial *Genes, Bacterial Molecular Sequence Data Oligopeptides/*genetics Open R;"
Notes:"MedlineGalli, D Friesenegger, A Wirth, R eng Research Support, Non-U.S. Gov't England 1992/05/01 Mol Microbiol. 1992 May; 6(10):1297-308. doi: 10.1111/j.1365-2958.1992.tb00851.x"

 
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