Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:3.1.3.1 (alkaline phosphatase)
 47,916 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

beta-Glucosidase released by the phytoflagellate Ochromonas danica was the result of secretion; this was adduced from the following: (1) The enzyme was released during growth, including early log phase. (2) The amount released was calculated to be much more than could be attributed to cell lysis. (3) beta-Glucosidase was released by cells during short term incubation in a dilute salt solution; this release was nearly linear for at least 24 h. (4) Release occurred while cell counts remained nearly constant and cells remained viable. (5) Control experiments excluded cell damage resulting from incubation and cell manipulation as a source of the exoenzyme. (6) No alkaline phosphatase was released and 5 times less phosphoglucose isomerase than glucosidase was released while the cells contained 7 times more phosphoglucose isomerase. (7) The kinetics of release of nonspecific protein and UV absorbing material was markedly different from glucosidase release. (8) Glucosidase release was temperature and energy dependent; anerobiosis decreased enzyme release. (9) Release was inhibited by cycloheximide. (10) Cells incubated with 3H-leucine synthesized labeled protein which was secreted linearly for at least 24 h. Cycloheximide inhibited incorporation of 3H-leucine into protein and the secretion of the labeled protein.
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PMID:Secretion of beta-glucosidase by Ochromonas danica. 98 14

Ethanol feeding to rats for 40 days enhanced (p < 0.001) the activities of alkaline phosphatase, sucrase, gamma-glutamyltransferase (GTP), and p-nitrophenyl (PNP)-beta-D-galactosidase (p < 0.05) with no change in leucine amino peptidase (LAP) and PNP-beta-D-glucosidase activities in intestine compared with control rats. The activities of alkaline phosphatase, sucrase, and GTP were diminished (p < 0.01) in ethanol-fed malnourished rats. There was no change in LAP activity, but the levels of glucosidase and galactosidase were elevated under these conditions. Brush-border sialic acid, fucose, hexose, and hexosamine contents were elevated in ethanol-fed protein-deficient animals. Ethanol administration to normally fed rats elevated the membrane sialic acid and hexose contents, reduced fucose content, and had no effect on brush-border hexosamine content compared with the control group. These results are in agreement with data on lectin binding to brush borders under these conditions. Alcohol ingestion reduced the incorporation of [14C]-glucosamine into brush borders in rats maintained on an 18% protein diet but augmented the incorporation of [14C]-glucosamine and [14C]-mannose in protein-malnourished membranes. These observations suggest that nutrition status influences the sensitivity of microvillus membrane glycosylation to ethanol feeding in rat intestine.
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PMID:Chronic ethanol feeding and microvillus membrane glycosylation in normal and protein-malnourished rat intestine. 142 85

The effects of hydrocortisone and insulin on the intestinal brush border membrane enzymatic activities in an anuran amphibian, Alytes obstetricans, were investigated at the end of spontaneous metamorphosis and 2 weeks after its completion. At the end of metamorphosis, the brush border is differentiating in the apical region of a developing neoformed epithelium. Two weeks after the completion of metamorphosis, this epithelium is entirely formed. The animals received one hormone injection per day for 2 or 3 days running (hydrocortisone: 1, 5, or 25 micrograms/g body wt/day; insulin: 0.5, 1, or 5 mU/g body wt/day). The hydrolases studied were three glucosidases (maltase, glucoamylase, trehalase), gamma-glutamyl-transferase and alkaline phosphatase. In animals reaching the end of metamorphosis, hormonal treatments rarely modify the three glucosidase activities. Two weeks after metamorphosis, a 5 microgram/g body wt/day hydrocortisone injection usually results in a significant increase of the three glucosidase activities. Conversely, a 0.5 mU/g body wt/day insulin injection induced a marked decrease in these activities. At the end of metamorphosis, hydrocortisone has variable effects on gamma-glutamyl-transferase activity; insulin, however, does not significantly modify this activity. Two weeks later, insulin and sometimes hydrocortisone inhibit gamma-glutamyl-transferase activity. Whatever the developmental stage is, hydrocortisone is able to stimulate alkaline phosphatase activity. At the end of metamorphosis, insulin has no influence on this activity, but 2 weeks after metamorphosis, low doses of the hormone (0.5 mU/g body wt/day) significantly reduce it. These results emphasize the possibility that after spontaneous metamorphosis the enzymatic activities of the new intestinal brush border are hormone controlled. This control could be related to the development of the interrenal and pancreatic islet functions.
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PMID:Hormonal control of the intestinal brush border enzyme activities in developing anuran amphibians. I. Effects of hydrocortisone and insulin during and after spontaneous metamorphosis. 286 4

Miglitol (Bay m 1099), a deoxynojirimycin derivative, is a new glucosidase inhibitor. The possible hypoglycemic effect of this new product was tested in 12 volunteer noninsulin-dependent diabetics (NIDDs) in a double-blind crossover acute study. The patients twice received a test meal (1554 kJ including 34 g carbohydrates), once with placebo and on another day with a 50-mg tablet of Bay m 1099. A wash-out period of 2 to 7 days separated the test days. Venous blood samples were collected before and every 30 min for a total of 3 h after the drug administration. Mean blood sugar values were in general lower after the meal + Bay m 1099 than the meal + placebo. The differences were statistically significant at the 60- and 90-min time intervals (8.43 versus 11.17 and 9.24 versus 11.59 mmol/l, respectively, p less than 0.05). No flatulence, diarrhea or other untoward effects were observed. Furthermore no changes in serum glutamic oxaloacetic transaminase, serum glutamic pyruvic transaminase, creatinine, alkaline phosphatase, bilirubin, haemoglobin, white blood count and differential counts were noted. Thus, in a one-day study 50 mg of Bay m 1099 reduced the postprandial hyperglycemia in NIDDs. No signs of any acute renal, liver and blood toxicity were observed.
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PMID:A double-blind study on the efficacy and tolerance of a new alpha-glucosidase inhibitor in type-2 diabetics. 353 89

The enzymatic profiles of 109 clinical isolates of Acinetobacter calcoaceticus subsp. anitratus and lwoffi were determined with conventional plate tests and the rapid API ZYM system (Analytab Products, Plainview, N.Y.). The majority of strains tested lacked DNase, hemolysin, protease, elastase and gelatinase. Strong enzymatic activities of butyrate esterase (C4), caprylate esterase (C8) and leucine arylamidase were detected in all isolates. No trypsin, chymotrypsin, alkaline phosphatase or glucosidase activities were present. This profile was characteristic of all isolates examined by the API ZYM system and could serve as a useful diagnostic feature of Acinetobacter calcoaceticus subsp. anitratus and subsp. lwoffi.
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PMID:Enzymatic profile of clinical isolates of Acinetobacter calcoaceticus. 400 64

Urinary levels of L-, Y-glutamyl transferase, alkaline phosphatase, L-leucine arylaminidase, lactate dehydrogenase, N-acetyl-beta-D-glucose aminidase, pseudocholine esterase, neutral L-glucosidase were examined in 76 urolithiasis patients. The activity of the above enzymes was found enhanced. This may be due to dysfunction of the tubular system. The content of L-leucine arylaminidase, N-acetyl-beta-D-glucose aminidase, L-glucosidase provide the most complete diagnostic information compared to the other enzyme tests.
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PMID:[The diagnostic significance of enzymuria in assessing kidney function in patients with urolithiasis]. 912 69

Biofilm-produced and commercially-purified a- and b-glucosidase and alkaline phosphatase were subjected to different spectral portions of natural and artificial light and exposed to various humic substances to elucidate their impact on enzyme activities. Photochemical degradation of all enzymes occurred under different portions of the light spectrum. UVB irradiance produced the greatest overall photochemical degradation of enzymes, with significant rates occurring with UVA and PAR irradiance. The complexation of enzymes with humic substances resulted in inhibition, stabilization, and photochemical protection of the enzyme. Inhibition of enzyme activity occurred via reductions in overall enzyme activity in the presence of humic substances. However, humic-enzyme complexation also resulted in stabilization by restricting enzyme degradation while retaining high activities. Enzymes exposed to natural and artificial light sources had significantly lower reductions in enzyme activities in the presence of humic substances, which indicates that humic-enzyme complexes may protect enzymes from light-induced photochemical degradation. Bacterial surface-bound a- and b-glucosidase activities were significantly reduced in the presence of humic substances. Photosynthetically induced pH changes within biofilm communities can cause large reductions in a- and b-glucosidase activities while enhancing the hydrolytic activity of alkaline phosphatase.
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PMID:Complexation, Stabilization, and UV Photolysis of Extracellular and Surface-Bound Glucosidase and Alkaline Phosphatase: Implications for Biofilm Microbiota. 1202 40

As secretion of the middle (MHBs) glycoprotein of hepatitis B virus is highly dependent upon the action of the host oligosaccharide processing enzymes glucosidase I and II, drugs that inhibit this enzyme have been proposed as potential antiviral agents. To facilitate the identification of new, more effective inhibitors of MHBs secretion, an assay has been developed based on the expression of this glycoprotein alone by transfection of Huh7 hepatoma cells. The data clearly demonstrate that both mono- and di-glycosylated forms of MHBs are produced in this system and both forms are equally dependent upon glucosidase processing for secretion. In addition, inclusion of a co-transfected reporter construct that encodes secreted alkaline phosphatase (SEAP) to permit normalization of transfection revealed that the SEAP gene product was itself sensitive to glucosidase inhibition. This sensitivity also was observed in HepG2 human hepatoma cells. Thus, measuring SEAP secretion may be another method for evaluating glucosidase inhibition. In addition, this finding has important implications for the use of a SEAP reporter in screens of potential antiviral agents.
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PMID:Assays for glucosidase inhibitors with potential antiviral activities: secreted alkaline phosphatase as a surrogate marker. 1566 65

Multiple biochemical assays of microbial mass and activities were applied to the estuarine detrital microbiota colonizing morphologically similar polyvinyl chloride needles and needles from slash pine (Pinus elliottii). Biodegradable pine needles consistently showed 2- to 10-fold higher values of extractable adenosine 5'-triphosphate, rates of oxygen utilization, activities of alkaline phosphatase and phosphodiesterase, and the mucopeptide cell wall component muramic acid than did the polyvinyl chloride needles, during a 14-week incubation in a semitropical estuary. The higher activities by the microbiota of the biodegradable substrate correlated with estimates of the microbial density from scanning electron microscopy. The microbial community associated with the nondegradable substrate showed minimal activity of beta-d-galactosidase, beta-d-glucosidase, and alpha-d-mannosidase in contrast to the biota of the degradable substrate, which showed 10- to 100-fold higher activities of these glycoesterases. These enzymes logically could be involved in catabolism of the carbohydrate polymers of the detritus. Assuming equivalent rates of predation, a surface that is also a utilizable substrate supports a three- to fivefold more active microbial population.
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PMID:Effects of substrate biodegradability on the mass and activity of the associated estuarine microbiota. 1634 62

The recovery of a degraded soil was assayed in greenhouse conditions by applying organic amendments and revegetation with grasses. Two types of organic residues were used: sewage sludge composted with pruning waste (CPW), at 8.5 and 85 Mg ha(-1) and sewage sludge treated by thermal drying (TD), at 22 and 46 Mg ha(-1). The vegetal cover was established by sowing different herbaceous species commonly used in the revegetation of degraded alkaline soils (100 and 200 Kg of seeds ha(-1)). The chemical soil parameters and enzymatic activities (alkaline phosphatase, urease, and beta-glucosidase) and the vegetal biomass were evaluated. The type of amendment and the doses applied had different effects on the soil characteristics. However sowing dose did not have a significant effect on the parameters analysed. Organic matter was the only soil parameter affected by the interaction between the sowing rate and the amendment dose. The phosphatase and glucosidase activities showed significant correlation with the percentage of N in the leaves and stems, furthermore the phosphate activity was significantly related to the dry weight of leaves and stems.
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PMID:Evaluation of the soil biological activity in a remediation soil assay using organic amendments and vegetal cover. 1730 65


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