
Most phytoremediation studies utilize merA or merB genes to modify plants via the nuclear or chloroplast genome, expressing organomercurial lyase and/or mercuric ion reductase in the cytoplasm, endoplasmic reticulum or within plastids. Several plant species including Arabidopsis, tobacco, poplar, rice, Eastern cottonwood, peanut, salt marsh grass and Chlorella have been transformed with these genes. Transgenic plants grew exceedingly well in soil contaminated with organic (approximately 400 microM PMA) or inorganic mercury (approximately 500 microM HgCl(2)), accumulating Hg in roots surpassing the concentration in soil (approximately 2000 microg/g). However, none of these plants were tested in the field to demonstrate real potential of this approach. Availability of metal transporters, translocators, chelators and the ability to express membrane proteins could further enhance mercury phytoremediation capabilities.
TRANSPORT PROTEIN, COMPLETE NUCLEOTIDE-SEQUENCE, POLLUTED SOILS, Mercury, BACTERIAL MERA GENE, ION REDUCTASE, Plants, Genetically Modified, Biochemical Research Methods, CHLOROPLAST GENOME, Biodegradation, Environmental, PHOTOSYSTEM-II, Biotechnology & Applied Microbiology, Dentistry, ARABIDOPSIS-THALIANA, PLANTS, Genetic Engineering, RESISTANCE
TRANSPORT PROTEIN, COMPLETE NUCLEOTIDE-SEQUENCE, POLLUTED SOILS, Mercury, BACTERIAL MERA GENE, ION REDUCTASE, Plants, Genetically Modified, Biochemical Research Methods, CHLOROPLAST GENOME, Biodegradation, Environmental, PHOTOSYSTEM-II, Biotechnology & Applied Microbiology, Dentistry, ARABIDOPSIS-THALIANA, PLANTS, Genetic Engineering, RESISTANCE
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