1953
DOI: 10.1021/j150504a007
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Kinetics and Thermodynamics of the Steady State System of Catalase with Hydrogen Peroxide

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Cited by 67 publications
(59 citation statements)
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(2 reference statements)
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“…This conclusion is supported by the lack of effect of SOD and Trolox. Of interest, we also observed that the endogenous SOD and catalase levels in neutrophils measured by standard methods [36,37], was significantly increased under hypoxic culture conditions (SOD activity after 20 h culture in 21% 02 was 10.05 + 0.287 U/mg protein and in 0% O2 was 18.68 + 3.32 U/mg protein (P < 0.05). Catalase activity after 20 h culture in 21% 02 was 125 + 13.83 U/rag protein and in 0% 02 was 263 + 32.71 U/protein (P < 0.05)).…”
Section: Resultsmentioning
confidence: 74%
“…This conclusion is supported by the lack of effect of SOD and Trolox. Of interest, we also observed that the endogenous SOD and catalase levels in neutrophils measured by standard methods [36,37], was significantly increased under hypoxic culture conditions (SOD activity after 20 h culture in 21% 02 was 10.05 + 0.287 U/mg protein and in 0% O2 was 18.68 + 3.32 U/mg protein (P < 0.05). Catalase activity after 20 h culture in 21% 02 was 125 + 13.83 U/rag protein and in 0% 02 was 263 + 32.71 U/protein (P < 0.05)).…”
Section: Resultsmentioning
confidence: 74%
“…CuZnSOD activity was calculated by subtracting MnSOD activity from total SOD activity. CAT activity in solution was measured by directly monitoring the decomposition of H 2 O 2 as described previously (Beers and Sizer, 1952). GPx activity was measured by an indirect assay that monitors the disappearance of NADPH (Lawrence and Burk, 1976).…”
Section: Antioxidant Enzyme Activity (Spectrophotometric) Assaysmentioning
confidence: 99%
“…The calibration proteins were Pseudomonas putida catabolic ornithine carbamoyltransferase ( M , = 420 000) [22], catalase ( M , = 240000), E. coli W ornithine carbamoyltransferase ( M , = 140000) [23], alkaline phosphatase ( M , = 78000) and hexokinase ( M , = 48000) which were assayed, respectively, according to Stalon et al [24], Beers and Sizer [25], Legrain et al [23], Garen and Levinthal [26] and Darrow and Colowick [27]. The column was equilibrated and eluted at 0 -4 "C with 60 mM potassium phosphate buffer, pH 7.5, 0.5 mM EDTA and 0.5 mM dithiothreitol.…”
Section: Molecular Weight Determination By Gel Sievingmentioning
confidence: 99%