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« Previous AbstractCloning and genetic analyses of the bacteriocin 41 determinant encoded on the Enterococcus faecalis pheromone-responsive conjugative plasmid pYI14: a novel bacteriocin complemented by two extracellular components (lysin and activator)    Next Abstract[Highly conjugative plasmids in enterococci] »

J Bacteriol


Title:"Genetic analysis of the Enterococcus vancomycin resistance conjugative plasmid pHTbeta: identification of the region involved in cell aggregation and traB, a key regulator gene for plasmid transfer and cell aggregation"
Author(s):Tomita H; Ike Y;
Address:"Department of Bacteriology, Gunma University Graduate School of Medicine, Maebashi, Gunma 371-8511, Japan. tomitaha@med.gunma-u.ac.jp"
Journal Title:J Bacteriol
Year:2008
Volume:20081003
Issue:23
Page Number:7739 - 7753
DOI: 10.1128/JB.00361-08
ISSN/ISBN:1098-5530 (Electronic) 0021-9193 (Print) 0021-9193 (Linking)
Abstract:"The Enterococcus plasmid pHTbeta (63.7 kbp) is a pheromone-independent, highly conjugative pMG1-like plasmid that carries a Tn1546-like transposon encoding vancomycin resistance. The transfer-related regions (Tra I, Tra II, and Tra III) containing oriT and a putative nickase gene (traI) have previously been identified in pHTbeta, and in this study, we found that the plasmid conferred the ability to self-aggregate on the host strain Enterococcus faecalis FA2-2. A region where mutation resulted in the impairment of aggregation was identified and mapped to a point upstream of the transfer-related Tra I region. This region consisted of an approximately 6-kbp segment that contained the five open reading frames (ORFs) ORF9 to ORF13. These ORFs are considered to encode the aggregation function, although the precise mode of action of each ORF has not yet been elucidated. An in-frame deletion mutant of ORF10 resulted in reduced aggregation and decreased transfer frequency in broth mating. Transcription analysis of the aggregation region showed that the five ORFs from ORF9 to ORF13 form an operon structure, and a long transcript that started from a promoter region located upstream of ORF9 was identified. Tra II spans a 1.7-kbp region containing ORF56 and ORF57. Tn917-lac insertions into or an in-frame deletion mutant of ORF56 (187 amino acids) resulted in impaired transfer and aggregation. The cloned ORF56 complemented these functions in trans. The transcription levels of ORF10 and ORF13 were reduced in the in-frame mutants of ORF56, but this reduction was complemented by a cloned ORF56 in trans. The results indicated that ORF56 positively regulated the aggregation and plasmid transfer in the host strain, and ORF56 was designated traB"
Keywords:"Anti-Bacterial Agents/pharmacology Bacterial Proteins/*metabolism Bacteriological Techniques Cell Aggregation Cloning, Molecular Enterococcus faecalis/*drug effects/*genetics Gene Deletion Gene Expression Regulation, Bacterial/physiology Mutagenesis, Inse;"
Notes:"MedlineTomita, Haruyoshi Ike, Yasuyoshi eng Research Support, Non-U.S. Gov't 2008/10/07 J Bacteriol. 2008 Dec; 190(23):7739-53. doi: 10.1128/JB.00361-08. Epub 2008 Oct 3"

 
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