Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:6.3.4.6 (urease)
 7,490 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The residual activity of enzymes immobilized in the membrane on the basis on 1-vinyl-2-pyrrolidinone as photopolymerizable composition is studied. It is established, that under conditions of the immobilization at 20 degrees C the residual activity glucoseoxidase is about 35% from a initial level, horseredish peroxidase and urease from Jeack beans--42% and 20%, respectively. In case of an immobilization of beta-glucoseoxidase -50 degrees C it reaches almost 50% from a initial level. It was investigated the influence of different sources of UV-radiation and different substances on stability of the enzymes in the composition and in the immobilization matrix at storage. Dynamic of changes of enzyme activity at the photoimmobilization was characterized, and also the requirements for providing of its maximal storage was selected.
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PMID:[Optimization of the conditions of immobilization of enzymes in a photopolymeric membrane]. 1291 41

Studies on the soil microbes, soil enzyme activity and soil biochemical intensity in copper mining wasteland indicated that the total quantity of major soil microbes declined by 68.43%-80.32%, compared with that of the non-minig soil. The proportion of bacteria and actinomyces decreased, while that of fungi did not changed obviously. The amount of major physiological groups including ammonifiers, nitrogen fixing bacteria, cellulose decomposing bacteria, aerobic nitrogen fixing bacteria and anaerobic nitrogen fixing bacteria all decreased, and soil basic respiration descended, compared with the control. The activity of soil enzymes weakened, which included urease, sucrase, proteinase, acid phosphtase, peroxidase, polyphenol oxidase and dehydrogenase. Soil biochemical intensity including ammonification, nitrification, nitrogen fixation and cellulose decomposition descended, and the circulation of C and N in mining soil inhibited. All the results showed that the weakening of microbial activity was one of major characteristics in reclaimed mining soil.
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PMID:[Microbial eco-characteristics of reclaimed mining wasteland in red soil area of southern China. I. Effects on soil microbial activity]. 1499 48

Hydroxyurea has emerged as a new therapy for sickle cell disease but a complete mechanistic description of its beneficial actions does not exist. Patients taking hydroxyurea show evidence for the in vivo conversion of hydroxyurea to nitric oxide (NO), which also has drawn interest as a sickle cell disease treatment. While the chemical oxidation of hydroxyurea produces NO or NO-related products, NO formation from the reactions of hydroxyurea and hemoglobin do not occur fast enough to account for the observed increases in patients taking hydroxyurea. Both horseradish peroxidase and catalase catalyze the rapid formation of nitric oxide and nitroxyl (HNO) from hydroxyurea. In these reactions, hydroxyurea is converted to an acyl nitroso species that hydrolyzes to form HNO. The ferric heme protein then oxidizes HNO to NO that combines with the heme iron to form a ferrous-NO complex that may act as an NO donor. In general, acyl nitroso compounds, regardless of the method of their preparation, hydrolyze to form HNO and the corresponding carboxylic acid derivative. Similarly, the incubation of blood and hydroxyurea with urease rapidly form NO-related species suggesting the initial urease-mediated hydrolysis of hydroxyurea to hydroxylamine, which then reacts quickly with hemoglobin to form these products. These studies present two NO releasing mechanisms from hydroxyurea that are kinetically competent with clinical observations.
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PMID:N-hydroxyurea and acyl nitroso compounds as nitroxyl (HNO) and nitric oxide (NO) donors. 1610 27

Paracoccidioides brasiliensis, the etiologic agent of paracoccidioidomycosis, is a dimorphic fungus, which is found as mycelia at 22-26 degrees C and as yeasts at 37 degrees C. A remarkable feature common to several pathogenic fungi is their ability to differentiate from mycelium to yeast morphologies, or vice-versa. Although P. brasiliensis is a recognized pathogen for humans, little is known about its virulence genes. In this sense, we performed a search for putative virulence genes in the P. brasiliensis transcriptome. BLAST comparative analyses were done among P. brasilienses assembled expressed sequence tags (PbAESTs) and the sequences deposited in GenBank. As a result, the putative virulence PbAESTs were grouped into five classes, metabolism-, cell wall-, detoxification-related, secreted factors, and other determinants. Among these, we have identified orthologs of the glyoxylate cycle enzymes, a metabolic pathway involved in the virulence of bacteria and fungi. Besides the previously described alpha- and beta-glucan synthases, orthologs to chitin synthase and mannosyl transferases, also important in cell wall synthesis and stabilization, were identified. With respect to the enzymes involved in the intracellular survival of P. brasiliensis, orthologs to superoxide dismutase, thiol peroxidase and an alternative oxidase were also found. Among the secreted factors, we were able to find phospholipase and urease orthologs in P. brasiliensis transcriptome. Collectively, our results suggest that this organism may possess a vast arsenal of putative virulence genes, allowing the survival in the different host environments.
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PMID:Virulence insights from the Paracoccidioides brasiliensis transcriptome. 1611 Apr 52

A pot experiment with rice under submerged condition showed that with the increase of Cd concentration, soil microbial biomass carbon (Cmic) and nitrogen (Nmic) increased initially but decreased at a certain concentration, and the turning points varied with different soil types. Soil enzyme activities had the similar variation trend with soil Cmic and Nmic, and the turning points varied with different soil types and soil enzymes. The variation coefficients were in order of dehydrogenase activity > acid phophatase activity > urease activity. Soil respiration rate and metabolic quotient increased tardily with increasing cadmium concentration. The chlorophyll content of rice increased initially but decreased then with the increase of Cd contamination, and the turning points differed with different soil types. Rice proline content and peroxidase activity were enhanced gradually with increasing cadmium concentration. The variation coefficients of rice physiological indices on paddy soils derived from silty loam and clayed red earth were in order of peroxidase activity > chlorophyll content > proline content, and peroxidase activity > proline content > chlorophyll content, respectively. Correlation analysis indicated that there was a close correlation between the variations of soil microbial biomass and enzymatic activities and rice physiological indices under Cd contamination.
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PMID:[Effects of Cd contamination on paddy soil microbial biomass and enzyme activities and rice physiological indices]. 1647 60

The aim of this study was determination and comparison of the levels of myeloperoxidase (MPO), xanthine oxidase (XO), and superoxide dismutase (SOD) in gastric mucosa of children who were infected and noninfected with Helicobacter pylori (HP). The MPO, and XO enzyme activities were detected via kinetic measurement, and the MPO, XO and SOD enzyme protein levels were detected via Western blot, in antral mucosa specimens of 43 patients who underwent upper gastrointestinal endoscopy with various indications. The diagnosis of HP infection was made with a positive rapid urease test and histopathologic detection. MPO activity and enzyme protein levels were measured in 14 [8 HP (+) and 6 HP (-)], and in 9 [5 HP (+) and 4 HP (-)] while XO activity and enzyme protein levels were measured in 16 [10 HP (+) and 6 HP (-)] and in 9 [5 HP (+) and 4 HP (-)] patients, respectively. SOD protein level was detected in 13 [7 HP (+) and 6 HP (-)] patients. Of 43 patients 25 were HP (+) and 18 were HP (-). MPO activities were 75.6 +/- 40.5 and 98.8 +/- 44.1 U/g. protein (p = 0.302) while XO activities were 0.5 +/- 0.3 and 0.4 +/- 0.2 U/g. protein in HP (+) and HP (-) patients, respectively (p = 0.625). Measured enzyme protein levels of MPO, XO and SOD were found statistically indifferent in HP (+) and HP (-) patients (p = 0.327, p = 0.086, and p = 0.775, respectively). The results of this study revealed that, MPO, XO and SOD conditions in gastric mucosa alone were not affected from HP presence. That's why MPO, XO, and SOD may not have important roles in the pathogenesis of HP related gastric disease in children.
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PMID:Myeloperoxidase, xanthine oxidase and superoxide dismutase in the gastric mucosa of Helicobacter pylori positive and negative pediatric patients. 1675 2

A pot experiment with 3 levels of elemental sulfur (0, 30, and 60 mg S x kg(-1)) showed that sulfur fertilization on soybean increased the side roots number by 8.6% - 33.2%, root dry weight by 6.6% - 34.3%, root nodules number by 2.7% - 35.9% and dry weight by 13.0% - 75.7%, chlorophyll content by 0.4 - 3.9 unit, and yield per plant by 7.3% - 12.8%. Sulfur fertilization also increased the amount of soil bacteria, fungi and actinomycetes and the activities of peroxidase, urease, neutral phosphatase and polyphenoloxidase significantly. The effects of sulfur supply differed with its application rate, and 30 mg S x kg(-1) was more appropriate for getting high soybean yield.
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PMID:[Physiological and ecological effects of sulfur fertilization on soybean]. 1733 Apr 83

Series of liquid photopolymerizable compositions (LPhPC) based on oligouretanemetacrylate (OUM-1000T and OUM-2000T) and oligocarbonatemetacrylate (OCM-2), monomethacrylic ether of ethylene glycol and vinylpyrrolidone (VP) were tested. It was shown that the LPhPC, which contained VP (as basic hydrophylic matrix), OCM-2 (cross-linking agent) and OUM-2000T (to increase adsorption of polymer) was the most optimal. The blend contained 3 g/100 ml of enzyme. ISFET based biosensors for analysis of glucose and urea had the following characteristics: linear response in the range of concentrations 0.1-10 mmol/l, 0.05-20 mmol/l, angle of slope of concentration curve--30 mV/pC, 38 mV/pC, and response time of approximately 10-15, 5-10 min, correspondingly. The value of Km for immobilized urease and beta-glucose oxidase (GOD) achieved 0.85 and 3.1 mmol/l, respectively. It was established that under immobilization conditions at 20 degrees C the residual activity of GOD was about 35% from the initial level, the residual activity of horseradish peroxidase (HRP) and urease was 42% and 20%, respectively. In case of an immobilization of GOD at -50 degrees C its residual activity reached almost 50% from the initial level. It was investigated how different sources of UV radiation and different substances (including specific and non-specific substrates) influenced stability of the enzymes in the LPhPC and in the prepared membrane at storage. Dynamics of changes of enzyme activity at the process of photo immobilization was characterized, and requirements for enzyme maximal storage were selected. The proposed LPhPC may be prepared in advance since enzymes do not lose their activity during 2 months. Therefore, two processes, i.e. manufacturing of a transducer and preparation of a biological membrane on its surface, can be combined in one. In order to achieve this, approaches of modern electronics, such as for example photolithography, can be used. The developed LPhPC is homogenous, non-active to biological substances, permeable for the analyzed sample, can be prepared using a simple immobilization procedure, and has a defined hydrophobic-hydrophilic balance and sufficient level of adhesion to transducer surfaces. These all cover the requirements to modern biosensors.
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PMID:Liquid photopolymerizable compositions as immobilized matrix of biosensors. 1738 43

Conjugation of enzymes to antibodies involves the formation of a stable, covalent linkage between an enzyme [e.g., horseradish peroxidase (HRPO), urease, or alkaline phosphatase] and an antigen-specific monoclonal or polyclonal antibody in which neither the antigen-combining site of the antibody nor the active site of the enzyme is functionally altered. This unit describes procedures for cross-linking HRPO, urease or alkaline phosphatase to immunoaffinity-purified monoclonal or polyclonal antibodies (IgG).
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PMID:Conjugation of enzymes to antibodies. 1826 67

Many chitosan biological activities depend on the interaction with biomembranes, but so far it has not been possible to obtain molecular-level evidence of chitosan action. In this article, we employ Langmuir phospholipid monolayers as cell membrane models and show that chitosan is able to remove beta-lactoglobulin (BLG) from negatively charged dimyristoyl phosphatidic acid (DMPA) and dipalmitoyl phosphatidyl glycerol (DPPG). This was shown with surface pressure isotherms and elasticity and PM-IRRAS measurements in the Langmuir monolayers, in addition to quartz crystal microbalance and fluorescence spectroscopy measurements for Langmuir-Blodgett (LB) films transferred onto solid substrates. Some specificity was noted in the removal action because chitosan was unable to remove BLG incorporated into neutral dipalmitoyl phosphatidyl choline (DPPC) and cholesterol monolayers and had no effect on horseradish peroxidase and urease interacting with DMPA. An obvious biological implication of these findings is to offer reasons that chitosan can remove BLG from lipophilic environments, as reported in the recent literature.
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PMID:Chitosan as a removing agent of beta-lactoglobulin from membrane models. 1830 43


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