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Biometals ; 13(4): 273-80, 2000 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-11247032

RESUMO

A marine bacterial strain putatively identified as Bacillus thuringiensis strain DM55, showed multiple heavy metal resistance and biosorption phenotypes. Electron microscopic studies revealed that DM55 cells are encased in anionic cell wall polymers that can immobilize discrete aggregates of cations. Factors affecting cell surface affinity for metal cations, monitored by means of Cd2+ binding capability, are investigated. The mechanisms of cadmium resistance and Cd2+ biosorption by the bacterium appeared to be inducible and coincident. Medium components affecting metal removal under cadmium-stressed growth conditions were explored based on the application of two sequential multi-factorial statistical designs. Concentrations of potassium phosphates and peptone were the most significant variables. Optimized culture conditions allowed DM55 cells grown in the presence of 0.25 mM CdCl2 to remove about 79% of the metal ions within 24 h with a specific biosorption capacity of 21.57 mg g(-1) of biomass. Both fresh and dry cells of DM55 prepared under cadmium-free optimal nutrient condition were also able to biosorb Cd2+. In addition to the concentration of phosphate in the medium, KinA, a major phosphate provider in the phosphorelay of Bacillus cells, was also demonstrated to regulate the magnitude of cell surface affinity for cadmium ions.


Assuntos
Bacillus thuringiensis/metabolismo , Cádmio/farmacocinética , Absorção , Bacillus thuringiensis/efeitos dos fármacos , Bacillus thuringiensis/genética , Bacillus thuringiensis/crescimento & desenvolvimento , Proteínas de Bactérias/genética , Proteínas de Bactérias/metabolismo , Cádmio/farmacologia , Cátions Bivalentes/farmacocinética , Cátions Bivalentes/farmacologia , Divisão Celular/efeitos dos fármacos , Membrana Celular/metabolismo , Parede Celular/metabolismo , Resistência Microbiana a Medicamentos , Microscopia Eletrônica , Concentração Osmolar , Fenótipo , Fosfatos/metabolismo , Proteínas Quinases/genética , Proteínas Quinases/metabolismo , Esporos Bacterianos/efeitos dos fármacos
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