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At least 19 recordsLinked to original sources
PubMed1984

Possibility of diacetyl and related compounds as the 4-carbon compound necessary for the formation of riboflavin in Ashbya gossypii.

The effects of various compounds (0.5%) involved in the butanediol and the glycolytic pathways on riboflavin formation in whole cells of Ashbya gossypii at rest were examined. The addition of acetate, glycerol and diacetyl inhibited riboflavin formation, while the addition of acetoin had no effect on it, and the addition of ethanol, 2,3-butanediol, pyruvic acid and glucose accelerated it. The relation of diacetyl and acetoin to riboflavin formation during resting cell incubation in the presence of 0.5% ethanol and various concentrations of 2,3-butanediol was examined. The results quantitatively revealed a precursor-product relation between riboflavin formation and the formation of diacetyl and acetoin. The results obtained provide evidence that a high flavinogenic agent, ethanol, was converted to acetaldehyde, pyruvic acid, acetoin and diacetyl in this order, that a week flavinogenic agent, 2,3-butanediol, was transferred to diacetyl through acetoin, and that the diacetyl produced can be utilized as the 4-carbon compound for riboflavin formation in the flavinogenic mold, Ashbya gossypii. It remains obscure whether diacetyl is enzymatically involved in riboflavin formation.

Acetaldehyde↗
PubMed1979

Mutagenicity of halogenated and oxygenated three-carbon compounds.

Four structurally related three-carbon compounds, known for their antifertility activity in the male, and the brominated derivatives of two of these compounds were tested for mutagenic activity by the Salmonella typhimurium test of Ames et al. In the presence of strain TA-100, a base-pair substituion detector strain, 1,2-dibromo-3-chloropropane (DBCP), was the most active compound tested but required enzymatic conversion by 59 microsomal preparation to an active mutagen. Three of these compounds containing an epoxide group-epichlorohydrin, epibromohydrin, and glycidol-were highly active direct mutagens, not requiring 59 for activation, alpha-Chlorohydrin was the least active compound tested; alpha-bromohydrin was 40 times more active than its chlorinated analog. Epibromohydrin was only slightly more active than epichlorohydrin, but both were highly active. With both of the halogenated epoxides, 59 preparation caused a substantial decrease in mutagenic activity at every concentration tested. All six compounds showed dose-related responsiveness for the base-pair substitution detector strains used. However, they were relatively inactive against the frameshift detector strain of S. typhimurium, TA-98. Glycerol, propylene glycol, and n-propanol, which are also three-carbon compounds containing one or more hydroxy groups, were inactive when trested at high concentrations with strain TA-100.

Alcohols↗
PubMed1984

Effects of cyclic 12-, 8-, and 6-carbon compounds on glutathione S-transferase activity.

The effects of feeding ICR/Ha mice cyclic 12-, 8-, and 6-carbon compounds on glutathione S-transferase (GST) activity in the liver, intestinal mucosa, and the forestomach were determined. The compounds used for this study were 1,5,9-trans,trans,cis- cyclododecatriene , 1,2-trans-5,6-trans-9,10-cis- cyclododecatriene -1,2-oxide, cyclododecanol , cyclododecene oxide, cyclododecane , 1,5- cyclooctadiene , cyclooctene oxide, cyclohexene, and cyclohexene oxide. The unsaturated cyclic 12-carbon compounds elicited the greatest increase in GST activity. Thus, feeding 1,5,9-trans,trans,cis- cyclododecatriene increased this activity almost 4-fold in the livers and the intestinal mucosa of experimental animals. Cyclic 8-carbon compounds were less effective and feeding the cyclic 6-carbon compounds did not result in any significant increase in GST activity. None of the compounds elicited increased GST activity in the fore-stomach. Previous studies have shown that compounds inducing increased GST activity can protect against chemical carcinogens. It remains to be determined whether the compounds identified in the present investigation as inducers of this enzyme system will have such protective capacities.

Animals↗
PubMed1975

Effect of the concentration of available carbon compounds on the microbial reduction of sulphates.

A change of the concentration of available carbon compounds in the reaction medium affecting the carbon to sulphur ratio (C/S) affects the reduction degree of sulphates. The time interval between the initial and the log phase of the process (to) also varies depending on the concentration of carbon compounds. It was demonstrated that optimal reduction conditions for the strain Desulfovibrio desulphuricans used exist in media of C/S = 1.84 +/- 0.2. Kinetic data for the reduction process are presented.

Carbon↗
PubMed1964

EFFECT OF SUGARS AND OTHER CARBON COMPOUNDS ON GERMINATION AND POSTGERMINATIVE DEVELOPMENT OF BACILLUS MEGATERIUM SPORES.

Hyatt, Mildred T. (Pioneering Research Division. U.S. Army Natick Laboratories, Natick, Mass.), and Hillel S. Levinson. Effect of sugars and other carbon compounds on germination and postgerminative development of Bacillus megaterium spores. J. Bacteriol. 88:1403-1415. 1964.-A total of 77 carbon-containing compounds were tested for their ability to support germination and postgerminative development of Bacillus megaterium spores. The only effective germination agents were certain of the hexose sugars and their derivatives. With unheated spores, only d-glucose, d-mannose, 2-deoxy-d-glucose, d-glucosamine, and N-acetyl-d-glucosamine (all at 25 mm) supported appreciable germination (ca. 25%). Heat-shock at 60 C for 10 min increased germination and decreased the concentration of sugar required for germination, so that these compounds, at 2.5 mm, supported 40 to 60% germination. Higher concentrations (25 mm) of other compounds, d-fructose, l-sorbose, d-allose, d-altrose, 2-hydroxyethyl-d-glucose, and beta-methyl-d-glucoside, were required for appreciable germination of heated spores. Glucose or mannose contamination accounted for the germination apparently induced by certain other sugars. Ionic contamination did not appear to contribute to the germination induced by d-glucose, d-fructose, 2-deoxy-d-glucose, or l-sorbose. There was no clear-cut evidence for a multiplicity of metabolic pathways in the triggering of B. megaterium spore germination by various sugars. Postgerminative development of germinated spores was supported by a wider variety of carbon compounds, including some pentoses and hexoses, many oligosaccharides, sugar derivatives, some alcohols, and some of the tricarboxylic acid cycle intermediates. Compounds effective for germination were not necessarily utilizable for growth, and vice versa. Oxygen consumption rates reflected the progress and extent of postgerminative development on the various carbon compounds. Utilization of glucose during postgerminative development was followed, and the concentration requirements were determined.

Acetylglucosamine↗
PubMed1996

Inhibition of regain in body weight and fat with addition of 3-carbon compounds to the diet with hyperenergetic refeeding after weight reduction.

OBJECTIVE: To investigate the efficacy of the 3-carbon compounds pyruvate and dihydroxyacetone (PD) in inhibiting reaccumulation of body weight and fat with refeeding after weight loss. DESIGN: Longitudinal, in Clinical Research Center. After weight loss induced by hypoenergetic diet (1.3 MJ/d) for 3 weeks, refeeding with hyperenergetic diet (1.5 x resting energy expenditure) for 3 weeks. Refeeding diet randomized to contain PD or placebo (PL, polyglucose) as approximately 20% of energy intake. SUBJECTS: 17 obese healthy women (n = 8 in PL group, n = 9 in PD group) (age: 22-60 y, weight: 72.5-139.7 kg). MEASUREMENTS: Resting energy expenditure (REE), body composition (by bioelectrical impedance), nitrogen balance, serum proteins, biochemical profile, thyroid hormones, and insulin, before and after refeeding and weight and fat gain. RESULTS: Refeeding with a hyperenergetic diet, weight gain was significantly less in patients receiving PD compared to placebo (1.8 + 0.2 kg vs 2.9 +/- 0.1 kg, P < 0.01). Body fat regain was also less with feeding of PD (0.8 +/- 0.2 kg vs 1.8 +/- 0.2 kg, P < 0.01). Body protein metabolism, as measured by nitrogen balance, serum protein concentrations and fat free mass, was similar in subjects consuming either PD or PL. CONCLUSIONS: We conclude that 3-carbon compounds decrease weight gain and reaccumulation of body fat, without decreasing body protein gain, in obese subjects with hyperenergetic refeeding subsequent to weight loss.

Adipose Tissue↗
PubMedDate not supplied

[The intensification of biological nitrogen fixation by using ammonium carbonate compounds and the routes of their action on microorganisms and plants].

The intensification of activity of associative and symbiotic nitrogen fixation while using low amounts of ammonium-carbonate compounds, carbonic-ammonium salts, in particular, has been established. The main ways and mechanisms of the action of ammonium-carbonate salts as a new and perspective agrochemical on physiological and biochemical processes of microorganisms and agricultural plants were presented on the basis of the analysis of literary information and the author's investigations.

Agrochemicals↗
PubMed1985

Isolation and characterization of Paracoccus denitrificans mutants with defects in the metabolism of one-carbon compounds.

Mutants deficient in the metabolism of one-carbon compounds have been obtained by treating Paracoccus denitrificans with the mutagen N-methyl-N'-nitro-N-nitrosoguanidine. Mutants were selected without enrichment procedures by newly developed plate screening tests. The obtained mutants were characterized by their growth responses, cytochrome composition, enzyme activities, and immunogenic reaction with antisera against methanol dehydrogenase. By these criteria five mutant classes could be distinguished. Class I mutants are involved in the expression of methanol dehydrogenase. Three mutants of this class have a defect in the structural gene. A double mutant was found with defects in the expression of both methanol dehydrogenase and hydrogenase. Class II mutants have a defect in a regulatory gene involved in the regulation of both methanol dehydrogenase and methylamine dehydrogenase. Class III mutants are deficient in formaldehyde metabolism. A defect may exist in the expression of a second non-NAD-linked formaldehyde dehydrogenase which was postulated to be involved in C1 metabolism. Class IV mutants are deficient in cytochrome c. Mutants of class V have a defect in synthesis of the molybdenum cofactor essential for the function of formate dehydrogenase.

Alcohol Oxidoreductases↗
PubMed2003

Linear free-energy relationship analysis of the fate of chlorinated 1- and 2-carbon compounds by redox-manipulated smectite clay minerals.

This paper expands on earlier work on the effect of molecular structure on the fate of a series of chlorinated 1- and 2-carbon compounds (RCl), including carbon tetrachloride, 1,1,1-trichloroethane, 1,1,2,2-tetrachloroethane, pentachloroethane, hexachloroethane, trichloroethene, tetrachloroethene, trichloronitromethane, and trichloroacetonitrile, in the presence of unaltered (SWa-U) and reduced (SWa-R) ferruginous smectite. A linear free-energy relationships (LFERs) analysis was conducted to explain kinetic data for RCl adsorption and dechlorination. Correlation analyses based on RCl hydration energies, hydrolysis rate constants, or bond dissociation energies were significant (r2 > 0.87) for RCl adsorption by SWa-R but not so for RCl adsorption by SWa-U (r2 < 0.5). The most statistically significant relationships describing RCl kinetic data were achieved using multivariable regression analysis including RCl hydration energies (or hydrolysis rate constant) and bond dissociation energies for RCl heterolysis. The outcome of this study indicates that the oxidation state of structural Fe in the clay strongly influences RCl hydration. A mechanism consistent with the present LFERs analysis corresponds to RCl hydration as the limiting step for adsorption and dechlorination by redox-manipulated smectites.

Adsorption↗
PubMed2003

Reconstructed mass-spectrometric pattern for characterization of carbon compounds in smoker's lung in situ.

BACKGROUND: Cigarette smoke is a major anthropogenic pollutant and contributes to the permanent load of ambient particulate matter in the air, particularly indoors. It is the leading risk factor for premature loss of life due to chronic bronchitis, emphysema and lung cancer. Smoker's lung and graphite pneumoconiosis are pathological states characterized by the deposition of carbonaceous particles. METHODS: Mass spectrometry was used to evaluate unstained lung sections obtained in vivo from a heavy smoker and a patient with occupationally acquired graphite pneumoconiosis. RESULTS AND DISCUSSION: The composition of carbon compounds deposited in lung tissue samples is demonstrated here for the first time. Thirty carbonaceous-containing microareas from ten biopsies (three areas per biopsy) of lung tissues were analyzed mass-spectrometrically. In each case, the samples were taken from a smoker's lung or those demonstrating a graphite pneumoconiosis. The lung-tissue samples were selected by light microscopy before they were evaporated for mass spectrometry. First-order criteria were anionic and cationic mass peaks which occur within the mass patterns in lung tissues of smoker's lung, although not in graphite pneumoconiosis. Second-order criteria were mass peaks from smoker's lung with standard deviations SD < or = 14% of the mean value. First and second-order mass peaks matched the mass peaks of experimental cigarette-smoke condensate in 9 out of 11 peaks. A software program was developed that enabled fast, automated recognition of the typical mass peaks, and thereby confirmed the histological diagnosis of smoker's lung. CONCLUSIONS: The analysis of carbonaceous particles within lung biopsies from a heavy smoker corresponded to the spectra of tobacco condensate and not to the investigated biopsies of graphite peneumoconiosis. RECOMMENDATION AND OUTLOOK: The analyses were performed in order to find out whether mass-spectrometric criteria exist for the differentiation of carbonaceous lung-tissue deposits. Mass spectrometry may be a valuable tool in determining the composition of carbon compounds deposited in human lung tissue. So far, qualitative assessment of the composition of deposits in lung tissue is only possible after the patient is deceased (autopsy).

Aged↗
PubMed2002

Different Mg to Fe ratios in the mixed metal MgFe hydroxy-carbonate compounds and the effect on phosphate binding compared with established phosphate binders.

Due to the side effects of the current oral phosphate binders, there is a need for effective alternatives. A number of mixed metal hydroxy-carbonate compounds (MMHCs) based on Mg and Fe have recently been established as effective phosphate binders. We have now carried out further studies on the MMHCs with different ratios of Mg(2+):Fe(3+) in different forms to assess for phosphate binding efficacy and ionic release in aqueous solution and food slurries. The compounds that provide the most promise are those with Mg(2+):Fe(3+) ratios of 2:1 and 4:1 in the unaged/dry form. Their phosphate binding efficacy was compared with a wide range of established phosphate binders, such as aluminum hydroxide [Al(OH)(3)], calcium carbonate (CaCO(3)), calcium acetate (CaAc(2)), magnesium hydroxide [Mg(OH)(2)], and lanthanum carbonate [La(2)(CO(3))(3)] in various food slurries. The results showed that the MgFe compounds were much more effective (on a weight for weight basis) than the established binders, and their properties were relatively pH independent. Calcium compounds (CaCO(3) and CaAc(2)) were ineffective under the experimental conditions. Mg(OH)(2) was effective at low pH but not at pHs greater than 5.0, and also released two- to threefold more magnesium than the MgFe compounds. Al(OH)(3) showed some degree of efficacy, but the binding capacity was, at best, less than 50% of the MMHCs. La(2)(CO(3))(3) required at least a 10-fold increase in weight to give comparable binding to the MMHCs. In conclusion, MgFe hydroxy-carbonate compounds are effective phosphate binders and may provide a better alternative to both existing and emerging binders for combating hyperphosphataemia.

Binding Sites↗
PubMed1985

Studies on the 4-carbon compound needed for the formation of the O-xylene ring of riboflavin.

The 4-carbon compound necessary for the formation of the o-xylene ring of riboflavin, was examined using labeled glucose and diacetyl in resting cells of Eremothecium ashbyii. The specific activity-time curves of riboflavin and lumichrome in the tracer experiments with [U-14C] glucose indicated that the specific activity of riboflavin during the incubation is much higher than that of its photolytic product, lumichrome. It is far above the level expected if the ribityl moiety of an intermediate, 4-ribitylamino-5-amino-2,6-dihydroxy-pyrimidine (RAADP), was to be utilized as the source of the 4-carbon unit on the o-xylene ring of riboflavin. It was further demonstrated that the specific activities of diacetyl and lumichrome at 10.5 h of the incubation and those of crystalline riboflavin and lumichrome at the later stage (20 h) of the incubation were identical respectively. Radioactive diacetyl furthermore proved to be likewise incorporated with a two fold dilution into riboflavin and lumichrome at 17 h of the incubation. The results reveal that it is not the ribityl fragment of RAADP bu the diacetyl that is the 4-carbon unit for the formation of the pyrazine ring of 6,7-dimethyl-8-ribityllumazine, that is, the o-xylene ring of riboflavin in the mold of Eremothecium ashbyii, although we still do not know whether the diketone requiring reaction is enzymatic or non-enzymatic.

Acetoin↗
PubMed1987

Additional characteristics of one-carbon-compound utilization by Eubacterium limosum and Acetobacterium woodii.

Growth characteristics of Eubacterium limosum and Acetobacterium woodii during one-carbon-compound utilization were investigated. E. limosum RF grew with formate as the sole energy source. Formate also replaced a requirement for CO2 during growth with methanol. Growth with methanol required either rumen fluid, yeast extract, or acetate, but their effects were not additive. Cultures were adapted to grow in concentrations of methanol of up to 494 mM. Growth occurred with methanol in the presence of elevated levels of Na+ (576 mM). The pH optima for growth with methanol, H2-CO2, and carbon monoxide were similar (7.0 to 7.2). Growth occurred with glucose at a pH of 4.7, but not at 4.0. The apparent Km values for methanol and hydrogen were 2.7 and 0.34 mM, respectively. The apparent Vmax values for methanol and hydrogen were 1.7 and 0.11 mumol/mg of protein X min-1, respectively. The Ks value for CO was estimated to be less than 75 microM. Cellular growth yields were 70.5, 7.1, 3.38, and 0.84 g (dry weight) per mol utilized for glucose, methanol, CO, and hydrogen (in H2-CO2), respectively. E. limosum was also able to grow with methoxylated aromatic compounds as energy sources. Glucose apparently repressed the ability of E. limosum to use methanol, hydrogen, or isoleucine but not CO. Growth with mixtures of methanol, H2, CO, or isoleucine was not diauxic. The results, especially the relatively high apparent Km values for H2 and methanol, may indicate why E. limosum does not usually compete with rumen methanogens for these energy sources.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1981

Variable assimilation of carbon compounds by Candida albicans.

A total of 215 typical strains of Candida albicans were studied for their ability to assimilate 11 carbon compounds. All isolates assimilated lactic acid, ribitol, succinic acid, methyl alpha-D-glucopyranoside. None of the isolates assimilated cellobiose and salicin; 1.9% of the isolates assimilated L-arabinose. Citric acid, glycerol, and L-sorbose were assimilated by greater than 97% of the isolates, whereas melezitose was assimilated by 81% of the isolates. Assimilation results depended on duration of incubation, temperature, and methodology.

Candida albicans↗
PubMed1998

Biodegradation and metabolism of unusual carbon compounds by anoxygenic phototrophic bacteria.

Anoxygenic phototrophic bacteria play an important role in anaerobic nutritional cycles. The most readily used and widely studied carbon sources for growth of these bacteria are organic acids and a few carbohydrates. In this review we survey the growing knowledge on the metabolism of a number of other carbon sources, particularly polymers (starch, poly(3-hydroxyalkanoates)), aromatic compounds (natural and xenobiotic), one-carbon compounds, alcohols, aliphatic hydrocarbons and higher fatty acids, and their influence on various cellular activities of purple non-sulfur bacteria. We also discuss the possible exploitations in various biotechnological processes of this group of microorganisms while metabolizing unusual carbon compounds.

Acyl Coenzyme A↗
PubMed1965

Carbon compounds in terrestrial samples and the Orgueil meteorite.

Meteorites contain extraterrestrial carbonaceous materials. The Alais, Orgueil, Tonk, and Ivuna meteorites resemble in their carbon, free sulfur, and non-metamorphosed mineral contents, densities, and general appearances certain organic-rich terrestrial sediments. Structural and isotopic determinations of carbon compounds in the Orgueil chondrite indicate that these compounds are primarily indigenous. Benzene extractable carbonaceous materials from Orgueil fragments and terrestrial sediments have similar chromatographic properties. Infrared and ultraviolet spectra show that they contain compounds of the same functional types. Mass spectrometric analyses of the alkanes from the Orgueil meteorite, sediments and organisms are statistically indistinguishable at the 95 per cent confidence level. Theoretical considerations and experimental data are presented which support the view that alkanes are well constituted to serve as indicators of former life. Complex alkanes in living things are structurally and isotopically analogous to hydrocarbons in petroleum. Pristane and phytane are constituents of a crude oil that is more than a billion years old. The structures and abundances of many alkanes in various sedimentary environments attest to the source and stability of these compounds. Based on the characteristics and distributions of organic substances on Earth, alkanes may provide the clearest insight into the origin of some carbonaceous substances in chondrites.

Alkanes↗