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1.
Antonie Van Leeuwenhoek ; 96(2): 161-70, 2009 Aug.
Article in English | MEDLINE | ID: mdl-19238575

ABSTRACT

The Cupriavidus metallidurans CH34 arsR gene, which is part of the arsRIC(2)BC(1)HP operon, and its putative arsenic-resistance regulatory protein were identified and characterized. The arsenic-induced transcriptome of C. metallidurans CH34 showed that the genes most upregulated in the presence of arsenate were all located within the ars operon, with none of the other numerous heavy metal resistance systems present in CH34 being induced. A transcriptional fusion between the luxCDABE operon and the arsR promoter/operator (P/O) region was used to confirm the in vivo induction of the ars operon by arsenite and arsenate. The arsR gene was cloned into expression vectors allowing for the overexpression of the ArsR protein as either his-tagged or untagged protein. The ability of the purified ArsR proteins to bind to the ars P/O region was analyzed in vitro by gel mobility shift assays. ArsR showed an affinity almost exclusively to its own ars P/O region. Dissociation of ArsR and its P/O region was metal dependent, and based on decreasing degrees of dissociation three groups of heavy metals could be distinguished: As(III), Bi(III), Co(II), Cu(II), Ni(II); Cd(II); Pb(II) and Zn(II), while no dissociation was observed in the presence of As(V).


Subject(s)
Arsenic/pharmacology , Bacterial Proteins/metabolism , Cupriavidus , Drug Resistance, Bacterial , Gene Expression Profiling , Gene Expression Regulation, Bacterial , Trans-Activators/metabolism , Arsenates/pharmacology , Arsenic/metabolism , Arsenites/pharmacology , Bacterial Proteins/genetics , Cupriavidus/drug effects , Cupriavidus/genetics , Cupriavidus/growth & development , Cupriavidus/metabolism , Molecular Sequence Data , Oligonucleotide Array Sequence Analysis , Operon/drug effects , Trans-Activators/genetics , Up-Regulation
2.
Appl Environ Microbiol ; 71(12): 8500-5, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16332840

ABSTRACT

Poplar, a plant species frequently used for phytoremediation of groundwater contaminated with organic solvents, was inoculated with the endophyte Burkholderia cepacia VM1468. This strain, whose natural host is yellow lupine, contains the pTOM-Bu61 plasmid coding for constitutively expressed toluene degradation. Noninoculated plants or plants inoculated with the soil bacterium B. cepacia Bu61(pTOM-Bu61) were used as controls. Inoculation of poplar had a positive effect on plant growth in the presence of toluene and reduced the amount of toluene released via evapotranspiration. These effects were more dramatic for VM1468, the endophytic strain, than for Bu61. Remarkably, none of the strains became established at detectable levels in the endophytic community, but there was horizontal gene transfer of pTOM-Bu61 to different members of the endogenous endophytic community, both in the presence and in the absence of toluene. This work is the first report of in planta horizontal gene transfer among plant-associated endophytic bacteria and demonstrates that such transfer could be used to change natural endophytic microbial communities in order to improve the remediation of environmental insults.


Subject(s)
Biodegradation, Environmental , Burkholderia cepacia/genetics , Gene Transfer, Horizontal , Populus/microbiology , Toluene/pharmacokinetics , Burkholderia cepacia/metabolism , DNA Primers , Plant Leaves/microbiology , Plant Roots/microbiology , Plant Stems/microbiology , Polymerase Chain Reaction , Populus/growth & development , Soil Microbiology
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