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Synthesis and bronchodilatory activity of some nitrogen bridgehead compounds.

A series of tricyclic nitrogen bridgehead compounds 7-22 have been synthesised and evaluated for their in vitro bronchodilatory activity using isolated guinea pig tracheal chain, precontracted with acetylcholine. The relaxant effect of 2,3,4,5-tetrahydroazepino[2,1-b]-8,9-dimethoxyquinazolin-11(1H)-one (7) (DPJ-386) was greater than that of theophylline, aminophylline and quinazoline derivative 3, which lacks methoxy groups at positions 8 and 9. Various nitrogen containing functionalities such as benzylamino, acetamido, benzamido and phthalimido were also introduced at 9 position of 3. This resulted in loss of relaxation activity in precontracted guinea pig tracheal chain. These results show that the better relaxation property possessed by compound 7 hydrochloride is due to methoxy groups at 8 and 9 positions.

Acetylcholine↗

Cytokinins in Vinca rosea L. Crown Gall Tumor Tissue as Influenced by Compounds Containing Reduced Nitrogen.

Several compounds containing reduced nitrogen markedly increased the yields of cell-division compounds extractable from an A6 Vinca rosea L. crown gall tumor tissue. Casein hydrolysate, several amino acids, and ammonium salts were effective. Both trans-zeatin and ribosyl-trans-zeatin were substantially increased in total amount per culture and in concentration. These two compounds have been identified by several criteria including mass spectra. The reduced nitrogen treatments also caused the appearance of a cytokinin not previously detected in this tissue; it has not yet been identified. The tumor tissue rapidly absorbed [8-(14)C]adenine from a liquid medium. Within 1 hour, the tissue converted some of the adenine to zeatin and ribosylzeatin, and greater degrees of conversion occurred in 2-, 4-, and 8-hour periods. The tissue grown on a medium containing ammonium chloride accumulated considerably greater quantities of the two cytokinins made from the labeled adenine during each incubation period.

Journal Article↗

Determination of N-chloramines in As-samra chlorinated wastewater and their effect on the disinfection process.

Chlorine is the most widely used disinfectant of wastewater due to its capacity to inactivate most pathogenic microorganisms quickly. However, chlorine reacts with natural organic compounds present in wastewater to produce some undesirable organic byproducts. One such class of compounds is the nitrogenous compounds. The reaction between chlorine and compounds containing a nitrogen atom with one or more hydrogen atoms attached to it will form chloramines which have lower disinfection efficiency. Eighty percent of the wastewater generated in Jordan is treated at the Khirbet As-Samra wastewater treatment plant for eventual use in agriculture. In this study efficiency of chlorination was studied by collecting samples from the effluent of the treatment plant. The yield concentration of N-chloramines upon chlorination was determined. Efficiency of disinfection process as a function of contact time, concentration of chlorine dosage, concentration of nitrogenous compound and pH were studied. In this study, it has been found that at a chlorine dosage of 15 mg/L and contact time of 15 min, the percentage total coliform kill in As-samra wastewater sample was 100%. After addition of histidine, glycine and phenylalanine (15 mg/L in each case) to the wastewater sample, the percentage of total coliform kill dropped to 58, 78 and 79% respectively. When chlorine dosage was increased to 24 mg/L the percentage total coliform kill reached 96, 99 and 100% in wastewater samples treated with 5 mg/L histidine, glycine and phenylalanine, respectively. The percentage total coliform kill dropped to zero in wastewater samples treated with histidine, glycine and phenylalanine at a concentration of 30 mg/L each. This work supports the theory that amino acids and ammonia preferentially react with chlorine to form N-chloramine which significantly reduces the disinfection efficiency of the chlorination process.

Ammonium Chloride↗

[Effect of nitrogen-containing compounds on hydrogen light emission and nitrogen fixation by purple bacteria].

The cells of Rhodospirillum rubrum and Thiocapsa roseopersicina grown in media containing glutamate and arginine, respectively, as well as under conditions of nitrogen fixation evolve H2 in the light. If the cultures were grown in media with NH4+, NO3-, urea, glutamine or asparagine, hydrogen photoevolution by the cells and acetylene reduction started after the lag-phase and proceeded at a low rate. Extracts of such cells did not display the activity of nitrogenase which could be assayed by the ATP-dependent evolution of H2 from dithionite. The data obtained confirm the fact that hydrogen photoevolution by purple bacteria involves nitrogenase whose synthesis is regulated (according to the action of glutamine) with the participation of glutamine synthetase. NH4+, glutamine and asparagine inhibit also hydrogen photoproduction by purple bacteria and acetylene photoreduction. However, they have no effect on hydrogen evolution in the dark by the cells of R. rubrum and T. roseopersicina in the presence of formiate or pyruvate, respectively, whereas carbon monoxide inhibits hydrogen production. Therefore, hydrogen production by purple bacteria in the dark must be catalyzed by hydrogenase.

Arginine↗

[Synthesis of the nitrogen-fixing enzyme system in oligonitrophilic bacteria].

Oligonitrophilic bacteria were cultivated on a medium containing only 2.5--10.0 mg/litre of nitrogen compounds. They assimilated elementary nitrogen only after utilization of these nitrogen compounds during growth and formation of nitrogen-fixing enzyme system. Their cells grown on a medium containing high concentrations of bound nitrogen did not fix nitrogen during further incubation in the atmosphere of 15N; therefore, the enzymes involved in nitrogen fixation were induced. These organisms are characterized by diauxia during their growth on media containing "start" doses of nitrogen. Enzymes catalysing nitrogen fixation in azotobacter are also induced. But, contrary to oligonitrophilic bacteria, the azotobacter does not require nitrogen compounds in the medium in order to adapt to molecular nitrogen, and its growth curve is not of a biphasal character. These data and the evidence of other authors suggest that all nitrogen-fixing microorganisms are characterized by the induced, not constitutive, enzymes involved in reduction of molecular nitrogen.

Bacillus↗

Ability to assimilate nitrogenous oxides is limited to a few species of yeasts.

Several species of yeasts, Saccharomyces cerevisiae, Debaryomyces hansenii, Candida utilis, C. albicans, C. pelliculosa and C. tropicalis, were tested for their ability to utilise different inorganic nitrogen compounds as sole sources of nitrogen, and the results are presented as a function of their growth. All of them grew well on reduced nitrogenous compounds such as ammonium sulphate (ammonia) and L-asparagine, while only C. utilis and C. pelliculosa grew, at a slower rate, on oxidised nitrogenous compounds, nitrate and nitrite. The differences observed in the ability of various yeasts to assimilate the inorganic nitrogen compounds are believed to reflect their individuals abilities to regulate the uptake rates of potentially toxic compounds and keep them in a bound/transient state until reduced to less toxic and more-readily assimilable forms.

Candida↗

Speciation of nitrogen-containing compounds in diesel fuel by comprehensive two-dimensional gas chromatography.

Nitrogen-containing compounds in diesel fuel have been speciated by comprehensive two-dimensional gas chromatography with nitrogen chemiluminescence detector (GC x GC-NCD). The speciation of nitrogen-containing compounds in diesel is difficult because of low concentration and complexity. The advantages of GC x GC are improved resolution and enhanced sensitivity. GC x GC-NCD can achieve the type and class separation of nitrogen-containing compounds with an appropriate separation column combination. Diesel contains both neutral (indoles and carbazoles) and basic (pyridines and quinolines) nitrogen-containing compounds. Relative concentrations of each class as well as each carbon number family can be quantified by integrating their peak volumes. This study demonstrates the capability of GC x GC-NCD for speciation of nitrogen-containing compound classes.

Journal Article↗

Utilization of carbon and nitrogen-containing compounds for neomycin production by Streptomyces fradiae.

A number of carbon and nitrogen compounds were tested for their effect on growth of Streptomyces fradiae 3535 and neomycin production. Dextrin, starch, and maltose were excellent carbon sources for neomycin production, and sodium nitrate, aspartic acid, and glutamic acid were adequate nitrogen sources. Studies on biochemical changes during fermentation in four typical media indicated that there was no direct relation between the growth of the organism and neomycin formation. The pH of the medium might be an important factor for neomycin synthesis. The quantitative formation of neomycin components depended on the variation of carbon and nitrogen sources. On the basis of this study, a suitable synthetic medium for neomycin production has been developed.

Alcohols↗

Identification of structures of nitrogen-containing compounds in crude oils in conjunction with chemometric resolution.

A universal method was established for the systematically structural identification of nitrogen-containing compounds in crude oils. Pre-fractionation of the non-hydrocarbons in a crude oil sample into 7 fractions was performed by di-adsorption column chromatography using neutral aluminum oxide and silica gel; subsequent high-resolution separation of individual components was achieved by using capillary column gas chromatography, and compound types were detected by mass spectrometer. The two-dimensional data from the compounds in the fractions were further resolved by a chemometric method to obtained the deconvoluted chromatogram and mass spectrum of every compound, and then, the nitrogen-containing compounds were identified in combination with the retention indices. This method could relieve the difficulty of classical analysis in identifying those species with very low contents or incompletely separation, particularly in the cases where the authentic standards were not available for addition into the unknown samples in order to reveal what indeed existed in them. The structures of 168 nitrogen-containing compounds in a crude oil sample were determined by this method with satisfactory results.

Aluminum Oxide↗

Novel tricyclic quinazolinimines and related tetracyclic nitrogen bridgehead compounds as cholinesterase inhibitors with selectivity towards butyrylcholinesterase.

Tetracyclic nitrogen bridgehead compounds, dibenzodiazecines and tricyclic quinazolinimines, in which the size of the alicyclic ring system and the length of the alkyl chain between the quinazolinimine moiety and a phenyl ring connected to the imine nitrogen atom were changed systematically, were synthesized and their ability to inhibit acetyl- and butyrylcholinesterase (AChE/BChE), respectively, was evaluated. Moderate and strong inhibitors of BChE--compared to galanthamine and rivastigmine--were identified, which show mixed affinities or are moderately or highly selective towards BChE, respectively.

Animals↗

Structure-dependent response of a chemiluminescence nitrogen detector for organic compounds with adjacent nitrogen atoms connected by a single bond.

High-throughput screening (HTS) of chemical libraries is indispensable for drug discovery research. However, the HTS data quality for lead discovery, lead optimization, and quantitative structure activity relationship studies has been severely compromised due to the uncertain compound concentrations in screening plates. In order to address this issue, we compared various high-throughput technologies for quantification of compounds in microtiter plate format without the need for authentic compounds as standards and identified the chemiluminescence nitrogen detector (CLND) as the method of choice at the present time. However, the structure dependence of this detector has not been well studied. A proposed rule suggested that the only exception to equimolar response is for compounds that contain adjacent nitrogen atoms. The response should be zero when the adjacent nitrogen atoms are connected by a double bond and 0.5 when they are connected by a single bond. In this investigation, we studied a broad range of compounds with isolated and adjacent nitrogen atoms. We confirmed that compounds with isolated nitrogen atoms produce an equimolar response with a 15-20% variation depending on structures and compounds with adjacent nitrogen atoms connected by a double bond giving nearly zero response. We discovered that the CLND response for compounds containing adjacent nitrogen atoms that are connected with a single bond is highly structure dependent. Substitutions on the nitrogen atoms or nearby in the molecule can increase the CLND response to approach a value higher than the predicted value 0.5 (maximal value 0.82/nitrogen atom). Without substitution, much lower values than predicted (minimal value 0.0-0.08/nitrogen atom) are obtained. Therefore, the prediction of response of 0.5/nitrogen atom for compounds with adjacent nitrogen atoms connected by a single bond should be abandoned. Compounds with similar structures should be used to generate calibration curves for quantification of this class of compounds.

Luminescence↗

Apparatus and method for interfacing capillary electrophoresis and chemiluminescence nitrogen detection for the analysis of nitrogen-containing compounds.

We have developed an interface that allows the specific detection of nitrogen-containing compounds by using a chemiluminescence nitrogen detector. The feasibility of using this interface was demonstrated by separating and detecting two nitrogen-containing compounds, p-aminosalicylic acid and L-phenylalanine. Although baseline separation was achieved, the theoretical plates were lower when compared to UV detection (25000 vs. approximately 85000). A sensitivity of 75 ng (approximately 500 pmol) per injection was achieved with this system which is adequate for pharmaceutical and biotech applications.

Aminosalicylic Acid↗

A role for the diazotrophic cyanobacterium, Cyanothece sp. strain ATCC 51142, in nitrogen cycling for CELSS applications.

Simple calculations show that fixed nitrogen regeneration in a CELSS may not be as efficient as stowage and resupply of fixed nitrogen compounds. However, fixed nitrogen regeneration may be important for the sustainability and safety of a deployed CELSS. Cyanothece sp. strain ATCC 51142, a unicellular, aerobic, diazotrophic cyanobacterium, with high growth rates and a robust metabolism, is a reasonable candidate organism for a biological, fixed nitrogen regeneration system. In addition, Cyanothece sp. cultures may be used to balance gas exchange ratio imparities between plants and humans. The regeneration of fixed nitrogen compounds by cyanobacterial cultures was examined in the context of a broad computer model/simulation (called CELSS-3D). When cyanothece sp. cultures were used to balance gas exchange imparities, the biomass harvested could supply as much as half of the total fixed nitrogen needed for plant biomass production.

Biomass↗

[Relationship between the chemical components in the meat of bulls].

During the chemical analysis of the meat of bullocks of different breeds (sample from Musc. long. dorsi), a negative relationship was found between free and bound water on the one hand and dry matter, nitrogen compounds, protein, and fat on the other, between nitrogen compounds and fat, and between protein and fat, and a positive relationship between the content of dry matter, nitrogen compounds, protein, and fat, between free and bound water, and nitrogen compounds and protein. The dependences were mostly significant to highly significant. No relationship was found between the content of ash and the studied chemical components of meat.

Animals↗