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J Appl Microbiol ; 113(5): 1130-8, 2012 Nov.
Article in English | MEDLINE | ID: mdl-22816429

ABSTRACT

AIMS: Arabidopsis thaliana l- and d-cysteine desulfhydrases (AtLCD and AtDCD) are two important H(2) S-generating enzymes. This study determined the effects of H(2) S derived from AtLCD and AtDCD on cadmium (Cd) toxicity in Escherichia coli. METHODS AND RESULTS: AtLCD and AtDCD were cloned into pET28a vectors and transformed into wild-type E. coli strain BL21(DE3), named BL21(LCD) and BL21(DCD). In the induced BL21(LCD) and BL21(DCD) compared with wild type, significantly higher H(2) S generation rates were observed. Additionally, higher survival rates, reduced contents of malondialdehyde (MDA) and hydrogen peroxide (H(2) O(2)), decreased activities of superoxide dismutase and catalase under 220 µmol l(-1) Cd stress were noted. We obtained similar results in the wild type treated with NaHS, a H(2) S donor. The above changes were substantially counteracted by the mixture of ammonia and pyruvic acid potassium (NH(3) + C(3) H(3) KO(3)), a synthetic inhibitor of H(2) S. CONCLUSIONS: AtLCD and AtDCD catalyse the H(2) S production, generating an ameliorating effect against Cd-induced oxidative stress and resulting in E. coli resistance to Cd toxicity. SIGNIFICANCE AND IMPACT OF THE STUDY: H(2) S as a gasotransmitter is certified to have an ameliorating effect against Cd toxicity, thus providing information for further research regarding the role of H(2) S in regulating resistance to the heavy metal stress in organisms.


Subject(s)
Arabidopsis/enzymology , Cadmium/pharmacology , Cystathionine gamma-Lyase/metabolism , Escherichia coli/drug effects , Hydrogen Sulfide/metabolism , Arabidopsis/genetics , Arabidopsis Proteins/genetics , Arabidopsis Proteins/metabolism , Catalase/metabolism , Cloning, Molecular , Cystathionine gamma-Lyase/genetics , Escherichia coli/growth & development , Escherichia coli/metabolism , Genetic Vectors , Hydrogen Peroxide/analysis , Malondialdehyde/analysis , Oxidative Stress/drug effects , Recombinant Proteins/genetics , Recombinant Proteins/metabolism , Sulfides , Superoxide Dismutase/metabolism
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