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At least 811 records · Page 45Linked to original sources

PubMed2000

Cytochrome c oxidase rapidly metabolises nitric oxide to nitrite.

Previous studies have shown that the addition of nitric oxide to cytochrome c oxidase rapidly generates spectral changes compatible with the formation of nitrite at the binuclear haem:copper centre. Here we directly demonstrate nitrite release following nitric oxide addition to the enzyme. The nitrite complex is kinetically inactive and the off rate for nitrite was found to be slow (0.024 min(-1)). However, the presence of reductants enhances the off rate and enables cytochrome oxidase to catalyse the rapid oxidation of nitric oxide to nitrite free in solution. This may play a major role in the mitochondrial metabolism of nitric oxide.

Electron Transport Complex IV↗

PubMed1999

Omeprazole and dietary nitrate independently affect levels of vitamin C and nitrite in gastric juice.

BACKGROUND & AIMS: Hypochlorhydria is associated with an increased risk of gastric cancer. We have studied the effect of pharmacologically induced hypochlorhydria on the gastric juice ascorbate/nitrite ratio, which regulates the synthesis of potentially carcinogenic N-nitroso compounds. METHODS: Saliva, gastric juice, and serum from 20 healthy volunteers (9 positive for Helicobacter pylori), with a mean age of 30 years (range, 20-47 years), were analyzed for nitrite, ascorbic acid, and total vitamin C before and for 2 hours after ingestion of 2 mmol [corrected] nitrate (nitrate content of a standard salad meal). This was repeated after 4 weeks of treatment with omeprazole, 40 mg daily. RESULTS: Before omeprazole treatment, the nitrate meal lowered gastric ascorbic acid levels from 3.8 to 0.9 microg/mL (P < 0.05) and increased median salivary nitrite levels from 44 to 262 micromol/L (P < 0.001); gastric nitrite concentration remained undetected in 10 subjects. Omeprazole increased median fasting gastric nitrite levels from 0 to 13 micromol/L (P = 0.001) and decreased fasting gastric ascorbic acid levels from 3.8 to 0.7 microg/mL (P < 0.001). With omeprazole treatment, gastric nitrite levels after the nitrate meal were markedly increased at 154 micromol/L (range, 49-384 micromol/L; P < 0.001). In H. pylori-infected subjects, omeprazole also decreased total vitamin C levels in both gastric juice and serum. CONCLUSIONS: Omeprazole and dietary nitrate independently decrease the ascorbate/nitrite ratio. This may lead to an increased risk of gastric cancer.

Adult↗

PubMed1980

Gas chromatographic determination of nitrite in foods as trimethylsilyl derivative of 1H-benzotriazole.

1,2-Diaminobenzene reacts with nitrite in acidic solution to form 1H-benzotriazole, which can be extracted into ethyl acetate. After evaporation of the ethyl acetate, 1H-benzotriazole is determined as its trimethylsilyl derivative by gas--liquid chromatography on a column of 15% SE-30 on chromosorb G HP at 200 degrees C with flame-ionization detection. The nitrite concentration is calculated from the peak height. Amounts of 0.5--10 microgram of nitrite-nitrogen can be determined. For the determintion of nitrite in foods, clean-up of the crude extracts by ion-exchange column chromatography allows the satisfactory elimination of interferents and permits concentrations down to 0.41 ppm to be determined. The recovery of the nitrite added to foods at the 4.1 ppm level ranges from 94.6 to 98.7% and at the 8.2 ppm level it ranges from 95.2 to 98.8%. The trimethylsilyl derivative of 1H-benzotriazole was identified as 1-trimethylsilylbenzotriazole by combined gas chromatographic--mass spectrometric examination and nuclear magnetic resonance spectrometry.

Food Analysis↗

PubMed2002

Rapid ion chromatography of L-ascorbic acid, nitrite, sulfite, oxalate, iodide and thiosulfate by isocratic elution utilizing a postcolumn reaction with cerium(IV) and fluorescence detection.

Rapid separation and determination of mixtures of L-ascorbic acid, nitrite, sulfite, oxalate, iodide and thiosulfate by conventional ion chromatography is often difficult due to incomplete separation of L-ascorbic acid and nitrite from the water peak when using eluents giving short elution times for iodide and thiosulfate. Separation of the six species within about 15 min has been achieved by isocratic elution using a resin-based ion-exchange column with a carbonate eluent containing a trace amount of 1,3,5-benzenetricarboxylic acid (BTA) and fluorescence measurement of cerium(III) formed via postcolumn reactions of the separated sample species with cerium(IV). Calibration plots of peak height versus concentration were linear up to 10.0 microM (1.76 ppm) for L-ascorbic acid, 8.0 microM (0.37 ppm) for nitrite, 8.0 microM (0.70 ppm) for oxalate, 80.0 microM (10.2 ppm) for iodide and 25.0 microM (2.80 ppm) for thiosulfate, whilst the sulfite calibration was linear up to 25.0 microM (2.00 ppm) when peak area was plotted against concentration. Detection limits (defined as S/N = 3) were 18 ppb for L-ascorbic acid, 4 ppb for nitrite, 16 ppb for sulfite, 7 ppb for oxalate, 72 ppb for iodide and 37 ppb for thiosulfate. The proposed method was applied successfully to the determination of L-ascorbic acid, nitrite, sulfite, oxalate, iodide or thiosulfate in water samples.

Anions↗

PubMed2003

Highly sensitive capillary zone electrophoresis with artificial seawater as the background electrolyte and transient isotachophoresis as the on-line concentration procedure for simultaneous determination of nitrite and nitrate in seawater.

Transient isotachophoresis-capillary zone electrophoresis with artificial seawater as the background electrolyte (BGE) was improved to further lower the limit of detection (LOD) for determination of nitrite and nitrate in seawater. By lowering the pH of BGE, the difference between effective mobility of nitrite and that of nitrate increased, thereby permitting increased sample volumes to be tolerated and their LOD values to decrease. Artificial seawater with pH adjusted to 3.0 using phosphate buffer was adopted as the BGE. To reverse electroosmotic flow (EOF), a capillary was flushed with 0.1 mM dilauryldimethylammonium bromide for 3 min before the capillary was filled with the BGE. Limits of detection (LODs) for nitrite and nitrate were 2.7 and 3.0 microg/l (as nitrogen), respectively. The LODs were obtained at a signal-to-noise ratio of 3. Values of the relative standard deviation (RSD) of peak area for these ions were 2.0 and 0.75%, respectively, when nitrite concentration was 0.05 mg/l and that of nitrate was 0.5 mg/l. The RSDs of peak height were 4.4 and 2.3%. The RSD values of migration time for these ions were 0.19 and 0.17%. The proposed method was applied to determination of nitrite and nitrate in a proposed certified reference material for nutrients in seawater, MOOS-1, distributed by the National Research Council of Canada. Results agreed with the assigned tolerance interval. This method was also applied to determination of these ions in seawater collected around Osaka Bay. Results nearly agreed with those obtained by a conventional spectrophotometric method.

Buffers↗

PubMed2003

New method for analyzing the nitrite level in PC12 cells using capillary electrophoresis.

Nitric oxide (NO) is a gaseous molecule shown to have signal transmitter properties in organisms. Direct measurement of NO in physiological conditions has been difficult due to its short lifetime and low concentration. Nitrite has been used as a marker for NO formation in biological systems. Capillary electrophoresis (CE) has been recently used to measure nitrite in biological fluids. The purpose of this study is to analyze nitrite in PC12 cells (pheochromocytoma cell line) using CE. Optimal CE performance was employed with 150 mM Tris-phosphate, 6 microM hexadecyltrimethyammonium chloride buffer at pH 7.0 and a fused-silica column of 57 cm x 75 microm I.D. The signal was measured with a UV detector at 214-nm wavelength and negative potential of 10 kV was applied for nitrite analysis. Under the optimum conditions, we monitored the changes in the concentration of the nitrite levels through synergistic stimulation of tumor necrosis factor alpha plus gamma-interferon in PC12 cells.

Animals↗

PubMed2002

Influence of aeration and sludge retention time on ammonium oxidation to nitrite and nitrate.

Partial nitrification to nitrite was reported to be technically feasible and economically favourable, especially when wastewater with high ammonium concentrations or low C/N ratios are treated. Nitritation can be obtained by selectively inhibiting nitrite oxidizing microrganisms through appropriate regulation of the system's pH, temperature, and sludge retention time. In addition to already known methods, the work showed that aeration patterns may play a relevant role too. Nitrification tests were performed in two lab-scale reactors operated under continuous and intermittent aeration, respectively. In both plants, temperature was maintained at 32 degrees C and pH was regulated at 7.2 by providing external buffer capacity when needed. The results showed that partial nitrification to nitrite was steadily obtained under oxygen limitation, independent of the sludge age. Therefore, the aeration pattern is proposed as an alternative parameter to the sludge retention time for controlling ammonium oxidation to nitrite.

Bacteria↗

PubMed2003

Nitrification with high nitrite accumulation for the treatment of wastewater with high ammonia concentration.

The objective of this paper was to determine the best conditions for partial nitrification with nitrite accumulation of simulated industrial wastewater with high ammonia concentration, lowering the total oxygen needed in the nitrification step, which may mean great saving in aeration. Dissolved oxygen (DO) concentration and pH were selected as operational parameters to study the possibility of nitrite accumulation not affecting overall ammonia removal. A 2.5L activated sludge reactor was operated in nitrification mode, feeding a synthetic wastewater simulating an industrial wastewater with high ammonia concentration. During the start-up a pH of 7.85 and a DO of 5.5mg/L were used. The reactor was operated until stable operation was achieved at final nitrogen loading rate (NLR) of 3.3kgN- NH(4)(+)/m(3)d with an influent ammonia concentration of 610mg N-NH(4)(+)/L. The influence of pH was studied in continuous operation in the range of 6.15-9.05, changing the reactor pH in steps until ammonia accumulation (complete nitrification inhibition) took place. The influence of DO was studied in the same mode, changing the DO in steps from 5.5 to 0.5mg/L. The pH was not a useful operational parameter in order to accumulate nitrite, because in the range of pH 6.45-8.95 complete nitrification to nitrate occurs. At pH lower than 6.45 and higher than 8.95 complete inhibition of nitrification takes place. Setting DO concentration in the reactor at 0.7mg/L, it was possible to accumulate more than 65% of the loaded ammonia nitrogen as nitrite with a 98% ammonia conversion. Below 0.5mg/L of DO ammonia was accumulated and over a DO of 1.7mg/L complete nitrification to nitrate was achieved. In conclusion, it is possible under the conditions of this study, to treat high ammonia synthetic wastewater achieving an accumulation of at least 65% of the loaded nitrogen as nitrite, operating at a DO around 0.7mg/L. This represents a reduction close to 20% in the oxygen necessary, and therefore a considerable saving in aeration.

Ammonia↗

PubMed2003

Impact of hydrogen peroxide on nitrite formation during UV disinfection.

One concern with UV disinfection of water is the production of nitrite when polychromatic UV sources are utilized. Based on previous work, it was hypothesized that a small addition of hydrogen peroxide (H(2)O(2)) may be useful in controlling nitrite during UV disinfection. However, it was found that H(2)O(2) addition (5 or 10mg/L) during polychromatic UV irradiation of drinking water at doses used for disinfection significantly increases the levels of nitrite produced relative to solutions without H(2)O(2). Enhancement rates ranged from approximately 15% to 40% depending upon pH and H(2)O(2) concentration; the relative increase in the NO(2)(-) yield was greater at pH 6.5 than at pH 8.3. The observed effects are tentatively ascribed to a combination of enhanced superoxide production and increased hydroxyl radical scavenging when H(2)O(2) is added. These results indicate that H(2)O(2) cannot be used to control nitrite production during UV disinfection and that enhanced nitrite formation will occur if H(2)O(2) is added during UV water treatment to achieve advanced oxidation of contaminants.

Disinfection↗

PubMed2004

Catalytic generation of nitric oxide from nitrite at the interface of polymeric films doped with lipophilic CuII-complex: a potential route to the preparation of thromboresistant coatings.

A novel approach potentially useful for the development of more thromboresistant polymeric materials is examined. The method is based on the catalytic generation of nitric oxide (NO) via Cu(I) mediated reduction of nitrite ions. Preliminary solution phase studies demonstrate that ascorbate or thiolate anions can generate Cu(I) from Cu(II) with subsequent catalytic conversion of any nitrite ions present to NO by the unstable Cu(I) species. Incorporation of this same chemistry within a hydrophobic polymeric material requires immobilizing Cu(II) ions into a polymeric phase via use of a lipophilic Cu(II) chelating ligand (dibenzo [e,k]-2,3,8,9-tetraphenyl-1,4,7,10-tetraaza-cyclododeca-1,3,7,9-tetraene (DTTCT)). It is shown that this complex can be reduced to its Cu(I) form by appropriate reducing equivalents present in the bathing solution. The resulting Cu(I) complex can then reduce nitrite to NO with the NO generation occurring at the polymer/solution interface at physiological pH. Data from chemiluminescence experiments indicate that the flux of NO at the polymer surface is comparable to that of endothelial cells (>/=1x10(-10)mol/cm(2)min) when 0.5mM nitrite/1mM ascorbate are present in the bathing solution. Potentially more useful NO generation can be achieved by doping the polymer film with the Cu(II) complex along with a lipophilic quaternary ammonium nitrite salt. In this case reducing equivalents within the aqueous phase enable the nitrite derived from the polymer to be converted into NO by the Cu(II/I) ligand complex. Films of this type are shown to generate NO for at least 6h in PBS buffer with fluxes on the order of 1.5x10(-10)mol/cm(2)min. Physiologically relevant levels of NO release are also shown to exist at the polymer interface when films are soaked in fresh plasma as well as undiluted whole blood, indicating that endogenous reducing equivalents present in blood can efficiently reduce the Cu(II)-ligand within the polymer film. The prospects of using these new NO releasing films to devise more biocompatible polymeric coatings for biomedical applications are discussed.

Ascorbic Acid↗

PubMed2002

Spectroscopic and functional characterization of Cu-containing nitrite reductase from Hyphomicrobium denitrificans A3151.

The Cu-containing nitrite reductase from Hyphomicrobium denitrificans (HydNIR) has been spectroscopically and functionally characterized. The visible absorption spectrum implies that the enzyme has two type 1 Cu ions in one subunit (ca. 50 kDa). The electron paramagnetic resonance (EPR) spectrum of HydNIR is simulated assuming the sum of three distinct S = 1/2 systems: two type 1 Cu signals (axial and rhombic symmetries) and one type 2 Cu signal. The intramolecular electron transfer reaction from the type 1 Cu to the type 2 Cu at pH 6.0 does not occur in the absence of nitrite, but a very slow electron transfer reaction is observed in the presence of nitrite. The apparent first-order rate constants for the intramolecular electron transfer reactions (k(ET(intra))) in the presence of nitrite and also the apparent catalytic rate constants (k(cat)) of HydNIR decrease gradually with increasing pH in the range of pH 4.5-7.5. These pH profiles are substantially similar to each other, suggesting that the intramolecular electron transfer process is linked to the subsequent nitrite reduction process.

Bacterial Proteins↗

PubMed2002

Study on the oxyhemocyanin, deoxyhemocyanin, oxygen affinity and acid-base balance of Marsupenaeus japonicus following exposure to combined elevated nitrite and nitrate.

Marsupenaeus japonicus (11.47+/-0.71 g) exposed individually to six different nitrite and nitrate regimes [(0.002 (control), 0.359 and 1.456 mM nitrite combined with 0.005 (control) and 7.458 mM nitrate)] in salinity of 30 ppt (parts per thousand) were examined for hemocyanin oxygen affinity, the fractionation of oxyhemocyanin and deoxyhemocyanin, and the acid-base balance after 24 h. Ambient nitrite at concentration of 0.359 mM caused reduction of oxyhemocyanin and protein by 27 and 11%, respectively, whereas ambient nitrate as high as 7.458 mM caused reduction of oxyhemocyanin and protein by 10 and 7%. Ambient nitrite at concentration of 1.456 mM caused increases of P(50) (indicating reduced oxygen affinity) and pO(2), but caused reduction in hemolymph pCO(2), pH, HCO(3)(-) and TCO(2). Following exposure to combined solutions of 1.456 mM nitrite and 7.458 mM nitrate there were no further changes in oxyhemocyanin, protein, hemolymph P(50), pO(2), pCO(2), HCO(3)(-) and TCO(2), but there was a significant reduction of pH.

Acid-Base Equilibrium↗

PubMed2000

Characterization of a heme c nitrite reductase from a non-ammonifying microorganism, Desulfovibrio vulgaris Hildenborough.

A cytochrome c nitrite reductase (NiR) was purified for the first time from a microorganism not capable of growing on nitrate, the sulfate-reducing bacterium Desulfovibrio vulgaris Hildenborough. It was isolated from the membranes as a large heterooligomeric complex of 760 kDa, containing two cytochrome c subunits of 56 and 18 kDa. This complex has nitrite and sulfite reductase activities of 685 micromol NH(4)(+)/min/mg and 1.0 micromol H(2)/min/mg. The enzyme was studied by UV-visible and electron paramagnetic resonance (EPR) spectroscopies. The overall redox behavior was determined through a visible redox titration. The data were analyzed with a set of four redox transitions, with an E(0)' of +160 mV (12% of total absorption), -5 mV (38% of total absorption), -110 mV (38% of total absorption) and -210 mV (12% of total absorption) at pH 7.6. The EPR spectra of oxidized and partially reduced NiR show a complex pattern, indicative of multiple heme-heme magnetic interactions. It was found that D. vulgaris Hildenborough is not capable of using nitrite as a terminal electron acceptor. These results indicate that in this organism the NiR is not involved in the dissimilative reduction of nitrite, as is the case with the other similar enzymes isolated so far. The possible role of this enzyme in the detoxification of nitrite and/or in the reduction of sulfite is discussed.

Amino Acid Sequence↗

PubMed1986

Nitrite reduction related to serogroups in Neisseria meningitidis.

Among meningococci, nitrite reducing and non-reducing strains occur. From 1319 strains isolated between 1978 and 1984, all serogroup A, D and X isolates reduced nitrite. In strains belonging to the remaining serogroups, nitrite reduction was a variable characteristic. In group B strains isolated in 1978 and 1979 and possibly in group Z' (29 E) strains, sulfadiazine resistance seemed to be coupled to nitrite reduction. Differing from gonococci, N. meningitidis grew well under anaerobic conditions; its growth in the absence of atmospheric oxygen was not stimulated in the presence of nitrite.

Anaerobiosis↗

PubMed1982

Nitrate reductase activity and nitrite levels in the saliva of habitual users of various tobacco products.

Nitrite found in human saliva is the product of the microbial reduction of nitrate circulating through the salivary glands. Saliva samples were collected under controlled conditions from volunteers who were habitual users of different types of tobacco products (tobacco chewers, cigarette smokers, bidi smokers and masheri users) and from controls. The saliva samples were analysed for nitrite levels and for nitrate reductase activity spectrophotometrically. Samples were collected from two different areas, Bombay (urban) and Ghodegaon (rural). Salivary nitrite levels in the control groups ranged from 1.6 ppm in Ghodegaon to 11 ppm in Bombay. The nitrite levels of the masheri-using groups from both locations and of the tobacco-chewing group from Bombay were significantly higher than those of the controls. A number of volunteers showed undetectable levels of salivary nitrate reductase. Volunteers who chewed tobacco or used masheri had higher levels of nitrate reductase activity than the controls. However, there did not seem to be any clear correlation between nitrite levels and nitrate reductase activity in the saliva.

Adult↗

PubMed2002

Dietary vitamin E and selenium and toxicity of nitrite and nitrate.

Nitrites and nitrates are important antimicrobial and flavoring/coloring agents in meat and fish products. However, nitrites and nitrates may cause methemoglobinemia and other illness, and may react with certain amines to form carcinogenic nitrosamines. The nutritional status of vitamin E and selenium has long been associated with nitrite and nitrate toxicity, although the mechanism involved is not yet clear. Information available recently shows that nitrites and nitrates are both oxidation products and ready sources of nitric oxide (NO*), that NO* reacts rapidly with superoxide to form highly reactive peroxynitrite (ONOO-), and that vitamin E may mediate the generation and availability of superoxide and NO*. Increased formation of ONOO- resulting from nitrite treatment and low intake of vitamin E and selenium may thus be the critical event leading to tissue damage and animal mortality observed previously. The protection against the adverse effects of nitrites/nitrates by vitamin E is attributed to its ability to reduce ONOO- formation, while selenium exerts its protective effects via seleno-enzymes/compounds, which reduce ONOO- formed.

Animals↗

PubMed1999

Nitrite determination in human plasma and synovial fluid using reactions of nitric oxide with 3, 5-dibromo-4-nitrosobenzenesulphonate (DBNBS).

DBNBS (3,5-dibromo-4-nitrosobenzenesulphonate) reacts with nitric oxide (NO) produced from nitrite ions in acid solution to give a radical with a characteristic electron spin resonance spectrum, attributable to a 'DBNBS-NO' product, and comprising a triplet with alphaN=0.96 mT. This is identical with the spectrum obtained when NO, introduced from the gas phase, reacts with DBNBS. Under certain conditions, an additional signal is observed, attributable to oxidation of DBNBS to the radical cation, DBNBS*+ (a triplet with alphaN=1.32 mT). Conditions are described for the determination of nitrite, which avoid this DBNBS oxidation. The height of the low-field signal from the DBNBS-NO product is directly proportional to the nitrite concentration up to about 0.08 mM nitrite. The method has been applied to the measurement of nitrite concentrations in whole blood, plasma and synovial fluid taken from rheumatoid arthritis patients. In order to avoid the oxidation of DBNBS when analysing biological samples of this type, it is necessary to treat the specimen by ultrafiltration as soon as possible after collection and before addition of DBNBS.

Arthritis, Rheumatoid↗

PubMed2001

Capillary electrophoresis analysis of nitrite and nitrate in sub-microliter quantities of airway surface liquid.

We developed a simple capillary electrophoresis (CE) method to measure nitrite and nitrate concentrations in submicroliter samples of rat airway surface liquid (ASL), a thin (10-30 microm) layer of liquid covering the epithelial cells lining the airways of the lung. The composition of ASL has been poorly defined, in large part because of the small sample volume (approximately 1-3 microl per cm2 of epithelium) and difficulty of harvesting ASL. We have used capillary tubes for ASL sample collection, with microanalysis by CE using a 50 mM phosphate buffer (pH 3), with 0.5 mM spermine as a dynamic flow modifier, and direct UV detection at 214 nm. The limit of detections (LODs), under conditions used, for ASL analysis were 10 microM for nitrate and 30 microM for nitrite (SIN= 3). Nitrate and nitrite were also measured in rat plasma. The concentration of nitrate was 102+/-12 microM in rat ASL and 70+/-1.0 microM in rat plasma, whereas nitrite was 83+/-28 microM in rat ASL and below the LOD in rat plasma. After instilling lipopolysaccharide intratracheally to induce increased NO production, the nitrate concentration in ASL increased to 387+/-16 microM, and to 377+/-88 microM in plasma. The concentration of nitrite increased to 103+/-7.0 microM for ASL and 138+/-17 microM for plasma.

Animals↗