2015
DOI: 10.1002/jssc.201400925
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Determination of metal content in superoxide dismutase enzymes by capillary electrophoresis†

Abstract: Superoxide dismutases are antioxidant scavenger enzymes that contain a metal cofactor (copper, zinc, iron, and manganese) in their active site. Metal content measurement is one of the essential steps to characterize enzyme biological activity. We have developed a capillary electrophoretic protocol for the determination of the metal content in superoxide dismutase enzymes. The background electrolyte containing 10 mM pyridine-2,6-dicarboxylic acid and 1 mM 1-methyl-3-tetradecylimidazolium chloride at pH 3.8 was … Show more

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Cited by 8 publications
(9 citation statements)
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References 21 publications
(27 reference statements)
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“…The co‐factor of enzymatic antioxidants is a metallic core that participates in the redox reactions. Methods such as capillary electrophoresis have been developed to characterize the enzymatic activity of antioxidants through the measurement of metal content in the enzyme . Nitroblue tetrazolium (NBT) reduction is used to assess O 2 ●− production by xanthine oxidase .…”
Section: Measuring Cellular Oxidative Stressmentioning
confidence: 99%
“…The co‐factor of enzymatic antioxidants is a metallic core that participates in the redox reactions. Methods such as capillary electrophoresis have been developed to characterize the enzymatic activity of antioxidants through the measurement of metal content in the enzyme . Nitroblue tetrazolium (NBT) reduction is used to assess O 2 ●− production by xanthine oxidase .…”
Section: Measuring Cellular Oxidative Stressmentioning
confidence: 99%
“…Catalase activity was determined by the decomposition of hydrogen peroxide [15][16]. Activity superoxide dismutase (SOD) determined in the system nitro-blue tetrazoliumphenazinemethosulfate-nicotinamidedinucleotide (NBT-PMS-NADN).…”
Section: Methodsmentioning
confidence: 99%
“…Анализ ферментативной активности (ед./ мг белка) осуществляли на двулучевом спектрофотометре UV-1800 (Shimadzu, Япония), длина волны λ=480 нм и λ=347 нм, при комнатной температуре, учитывая тот факт, что исследовали пойкилотермных организмов в физиологически адекватных условиях. Активность каталазы определяли по реакции разложения перекиси водорода [9][10][11]. Активность супероксиддисмутазы (СОД) определялась спектрофотометрическим методом в системе нитро-синий тетразолиевый-феназинметасульфат-никотинамиддинуклеотид (НСТ-ФМС-НАДН).…”
Section: объекты и методы исследованийunclassified