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Query: UNIPROT:P04040 (Catalase)
 3,577 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Chlorine dioxide (Cl02) has been proposed as an alternative disinfectant to chlorine to avoid formation of organohalides. Cl02 and metabolites, chlorite (Cl0-2) and chlorate (Cl0-3) in drinking water produced decreases in rat and chicken blood GSH. The GSH dependent system was studied in rat and chicken blood after chronic treatment for 6 months with CL02 (0, 1, 10, 100, 1000 MG/L), Cl0-2 or Cl0-3 (10, 100 mg/l) in drinking water. There was a 60% increase in GSH reductase in the Cl02 treatment groups of rats and chickens. A similar increase was shown in rats treated with Cl0-2 but with Cl0-3 no change was observed. GSH peroxidase was without change in rat but chickens drinking 1000 mg/l Cl02 had decreased activity. Catalase was significantly higher than control in rat and chicken in the 1000 mg/l groups. However, catalase activity was decreased in rat treated with Cl0-2 and at the same time that GSH was decreased. These studies support the view that catalase is the first line of defense against the oxidative stress of Cl02 in rat and chicken erythrocytes.
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PMID:Effect of chlorine dioxide and metabolites on glutathione dependent system in rat, mouse and chicken blood. 54 25

The peroxidase-supported N-demethylations catalyzed by chloroperoxidase, a heme protein isolated from Caldariomyces fumago, have been investigated as models for cytochrome P-450-catalyzed N-dealkylations. The turnover number for the ethyl hydrogen peroxide-supported dealkylation of N,N-dimethylaniline by chloroperoxidase (1476) was much greater than that for cytochrome P-450-catalyzed dealkylations. The dealkylations of N,N-dimethylaniline by chloroperoxidase yielded N-methylaniline and formaldehyde in equimolar amounts with no other products detectable by high pressure liquid chromatography analysis of the reaction mixture. Ethyl hydrogen peroxidase could be replaced by other hydroperoxides, peroxides, or peracids. Chloride ions stimulated the reaction at low pH. The dealkylation reaction exhibited normal Michaelis-Menten saturation kinetics with respect to N,N-dimethylaniline (Km = 0.08 mM) and ethyl hydrogen peroxide (Km = 0.8 mM) at low substrate concentrations. However, substrate inhibition occurred at higher concentrations of N,N-dimethylaniline. The chloroperoxidase-catalyzed demethylations were inhibited by inhibitors of cytochrome P-450 such as azide or n-propyl gallate, but not by metyrapone, SKF-525A, or piperonyl butoxide. Although tiron and DL-epinephrine, trapping agents for the superoxide anion, inhibited the demethylation reactions, superoxide dismutase had no effect. There was no significant inhibition by alpha-phenyl-t-butyl-nitrone or 5,5-dimethyl-pyrroline-N-oxide, which react with free radicals. Diphenylfuran and DL-histidine, which react with singlet oxygen, did not inhibit the reaction. Substitution of D2O for H2O resulted in a marked inhibition with a solvent isotope effect (VH/VD) of 3.6. Chloroperoxidase did not catalyze the demethylation of N,N-dimethylaniline-N-oxide, indicating that the reaction does not proceed via an N-oxide intermediate.
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PMID:N-Demethylation reactions catalyzed by chloroperoxidase. 719 53

The results of studies on producing the biocatalyst based on catalase immobilized in the fibers from triacetate are presented. The catalase producer is Penicillium fungus. Catalase was produced by precipitation with the use of ethyl alcohol from the cultural fluid with separate and unseparate mycelium. The highest activity of catalase in the cultural fluid is seen on the nutrient medium containing 4% of carbon source. For immobilization the water solution of enzyme was concentrated in the vacuum-rotor evaporator at temperature of 25 degrees C. The enzyme was included in the structure of fibers during the process of their formation. Of the fiber-producing polymers (cellulose triacetate, chlorine, polysulphone) the most enzymatic activity has the catalase-containing fibers derived from the cellulose triacetate, in this case, the fine fibers of biocatalyst have the higher specific activity. It is established that the fibers obtained by using catalase of microbiological origin possess high stability and their activity does not practically change in the aqueous environment. The unpurified catalase is one and a half higher than at purified catalase. Under laboratory conditions there turned out the experimental batches of fibers and there conducted their endurance tests. Catalase included in cellulase triacetate has effectively functioned during a period of 2 years purifying the distilled water containing 50 mg/l of hydrogen peroxide.
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PMID:[Immobilized catalase in water purification systems]. 985 84

In this paper, the quenching of hydrogen peroxide by catalase, sodium hypochlorite, sodium thiosulfate and sodium sulfite, prior to UFC testing, was investigated. Sodium hypochlorite, sodium thiosulfate and sodium sulfite were found to be unsuitable for quenching H2O2 residuals because the procedures are time-consuming and complicated in that they require potentially multiple measurements of the peroxide and chlorine residuals. In contrast, quenching of peroxide with catalase is a simple procedure. Catalase doses of less than 0.2 mg/L were found to have no impact on DBP (TTHM, HAA and aldehyde) formation in the UFC test, and the time that was needed to quench 100 mg/L peroxide (room temperature, pH 8.3) was less than 10 min. In addition, peroxide was found to react with DPD reagents that are used to measure chlorine residuals, a phenomenon that may lead to falsely high chlorine residuals in the UFC test.
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PMID:Optimal methods for quenching H2O2 residuals prior to UFC testing. 1286 37

Screening and confirmatory methods for detecting abnormal milk, mastitic milk, or milk of high somatic cell count are reviewed. Those procedures reviewed in some detail include the Catalase Test. Brabant Mastitis Reaction, pH and chlorine analysis, Ruakura Rolling Ball Viscometer method. California Mastitis Test (CMT), Wisconsin Mastitis Test (WMT), Optical Somatic Cell Count (OSCC). Direct Microscopic Somatic Cell Count (DMSCC), and Electronic Somatic Cell count (ESCC). Other detection methods are tabulated.
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PMID:Methods to Detect Abnormal Milk - A Review. 3082 25