2002
DOI: 10.1023/a:1014951524286
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Cited by 214 publications
(30 citation statements)
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References 57 publications
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“…All the reports claim that increased activities of POD, CAT and APX were observed. Antioxidants of POD, CAT and APX are H 2 O 2 -scavengers in plants (Foyer & Noctor 2000, Pereira et al 2002. The greater activities of these three enzymes in the fronds of fern PCA, than the other plants, suggested that fern PCA was more capable of elimination of excess H 2 O 2 and of remaining in homeostasis (Fig.…”
Section: Antioxidative Responses To Sb In Fern Plantsmentioning
confidence: 96%
See 1 more Smart Citation
“…All the reports claim that increased activities of POD, CAT and APX were observed. Antioxidants of POD, CAT and APX are H 2 O 2 -scavengers in plants (Foyer & Noctor 2000, Pereira et al 2002. The greater activities of these three enzymes in the fronds of fern PCA, than the other plants, suggested that fern PCA was more capable of elimination of excess H 2 O 2 and of remaining in homeostasis (Fig.…”
Section: Antioxidative Responses To Sb In Fern Plantsmentioning
confidence: 96%
“…However, peroxidase (POD), catalase (CAT) and ascorbate peroxidase (APX) are important intrinsic antioxidative enzymes in plant cells. They control the H 2 O 2 levels through degradation of unnecessary H 2 O 2 to harmless H 2 O (Foyer & Noctor 2000, Pereira et al 2002. Whether the exposure of Sb may induce oxidative stress in Asaccumulating plants, and whether such plants are equipped with a more efficient ROS-scavenging system than found in non-As-accumulating plants, are important subjects for further investigation.…”
Section: Introductionmentioning
confidence: 99%
“…The homogenate was centrifuged (16,000g) at 4°C for 15 min (Pereira et al 2002). The supernatant was used for the analysis of superoxide dismutase (SOD), catalase (CAT), guaiacol peroxidase (GPX), ascorbate peroxidase (APX) and glutathione reductase (GR).…”
Section: Determination Of Mda and H 2 O 2 Contentmentioning
confidence: 99%
“…Superoxide dismutase activity was determined on the gel as described by [42]. The gels were rinsed in water and incubated in the dark for 30 min at room temperature in an assay mixture containing 50 mM potassium phosphate buffer (pH 7.8), 1 mM EDTA, 0.05 mM riboflavin, 0.1 mM nitroblue tetrazolium and 0.3% N,N,N 0 ,N 0 -tetramethylethylenediamine (TEMED).…”
Section: Gel Electrophoresismentioning
confidence: 99%