Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Sulfur Compounds”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 145 records · Page 8Linked to original sources

Sulfurtransferase activity and sulfur compound content in Rana temporaria brain following hibernation.

The activity of rhodanese, 3-mercaptopyruvate sulfurtransferase and gamma-cystathionase and the content of glutathione and sulfane sulfur compounds were determined in Rana temporaria brain in April. The high sulfane sulfur level observed in the spring seems to be associated with protection against cellular oxidative stress after the period of hibernation with its minimal oxidative metabolism.

Animals↗

Effects of food materials on removal of Allium-specific volatile sulfur compounds.

Effects of food materials were investigated on removal of several kinds of thiols, sulfides, and disulfides, which arise from vegetables of Allium species during food preparation and eating. Methanethiol, propanethiol, and 2-propenethiol were captured by raw foods such as fruits, vegetables, and mushrooms or a mixture of their acetone powders and phenolic compounds. The odor of diallyl disulfide was remarkably reduced by kiwi fruit, spinach, cutting lettuce, parsley, basil, mushrooms, and, particularly, cow's milk, raw egg, boiled rice, and bovine serum albumin (BSA). This suggests that the removal of diallyl disulfide could be caused by a physical and chemical interaction between the disulfide and foods. Furthermore, milk and BSA captured propanethiol, 2-propenethiol, dipropyl sulfide, diallyl sulfide, dimethyl disulfide, and dipropyl disulfide very well. An enzymatic degradation of diallyl disulfide by spinach and asparagus was also observed. These results demonstrate that the deodorization with foods is achieved by multiple actions including physical and chemical interaction between volatile sulfur compounds and foods, enzymatic degradation of disulfides, and addition of thiols to polyphenolic compounds, catalyzed by polyphenol oxidases or peroxidases.

Acetone↗

Transformation of sulfur compounds by an abundant lineage of marine bacteria in the alpha-subclass of the class Proteobacteria.

Members of a group of marine bacteria that is numerically important in coastal seawater and sediments were characterized with respect to their ability to transform organic and inorganic sulfur compounds. Fifteen strains representing the Roseobacter group (a phylogenetic cluster of marine bacteria in the alpha-subclass of the class Proteobacteria) were isolated from seawater, primarily from the southeastern United States. Although more than one-half of the isolates were obtained without any selection for sulfur metabolism, all of the isolates were able to degrade the sulfur-containing osmolyte dimethyl sulfoniopropionate (DMSP) with production of dimethyl sulfide (DMS). Five isolates also degraded DMSP with production of methanethiol, indicating that both cleavage and demethylation pathways for DMSP occurred in the same organism, which is unusual. Five isolates were able to reduce dimethyl sulfoxide to DMS, and several isolates also degraded DMS and methanethiol. Sulfite oxygenase activity and methanesulfonic acid oxygenase activity were also present in some of the isolates. The ability to incorporate the reduced sulfur in DMSP and methanethiol into cellular material was studied with one of the isolates. A group-specific 16S rRNA probe indicated that the relative abundance of uncultured bacteria in the Roseobacter group increased in seawater enriched with DMSP or DMS. Because this group typically accounts for >10% of the 16S ribosomal DNA pool in coastal seawater and sediments of the southern United States, clues about its potential biogeochemical role are of particular interest. Studies of culturable representatives suggested that the group could mediate a number of steps in the cycling of both organic and inorganic forms of sulfur in marine environments.

Alphaproteobacteria↗

Polymorphisms of glutathione S-transferase M1 and T1 modulate blood pressure of individuals chronically exposed to natural sour gas containing sulfur compounds.

In order to find the effect of genetic polymorphisms of GSTM1 and GSTT1 on blood pressure of individuals chronically exposed to sulfur compounds, the present study was done. Study subjects (38 males, 38 females) were residents of contaminated areas of Masjid-i-Sulaiman (southwest of Iran). The GSTM1 and GSTT1 genotypes were determined using a polymerase chain reaction (PCR)-based method. The non-parametric Sign test was applied in order to detect differences between the GSTs genotypes of study subjects and the normal mean values according to the sex and age of subjects. From four combination of genotypes, systolic blood pressure significantly decreased in combination of null-GSTM1 and present-GSTT1 (Z=-2.41; P=0.016), and diastolic blood pressure significantly increased in combination of present-GSTM1 and null-GSTT1 (Z=+2.14; P=0.032). It is speculated about polymorphisms of GSTs in individuals chronically exposed to natural sour gas, which contains H2S, fulfilling a physiological role(s) in regulating blood pressure.

Blood Pressure↗

Removal of Sulfur Compounds from Coal by the Thermophilic Organism Sulfolobus acidocaldarius.

The thermophilic, reduced-sulfur, iron-oxidizing bacterium Sulfolobus acidocaldarius was used for the removal of sulfur compounds from coal. The inclusion of complex nutrients such as yeast extract and peptone, and chemical oxidizing agents, 0.01 M FeCl(3) into leaching medium, reduced the rate and the extent of sulfur removal from coal. The rate of sulfur removal by S. acidocaldarius was strongly dependent on the sulfur content of the coal and on the total external surface area of coal particles. Approximately 96% of inorganic sulfur was removed from a 5% slurry of coal which had an initial total sulfur content of 4% and an inorganic (pyritic S and sulfate) sulfur content of 2.1%. This resulted in removal of 50% of initial total sulfur present in coal.

Journal Article↗

Evaluation of volatile sulfur compounds in the expired alveolar gas in patients with liver cirrhosis.

Trace amounts of volatile sulfur compounds were determined in the expired alveolar gas by gas chromatography. Among these sulfur containing substances, methyl mercaptan and dimethyl sulfide were quantitatively analyzed in 116 subjects; 53 normal, 13 acute hepatitis, 11 chronic hepatitis, 20 hepatic cirrhosis, and 19 stomach ulcer and/or biopsy of gastric mucosa. Fasting level of dimethyl sulfide in cirrhotics was 4.05 +/- 1.06 ng/dl, significantly elevated by comparison with normal controls (1.54 +/- 0.09 ng/dl) (P less than 0.05). In contrast, methyl mercaptan did not show a statistically significant rise in this study. The implications of the significant increase in dimethyl sulfide concentration in liver cirrhosis are discussed.

Adult↗

Inhibition of orally produced volatile sulfur compounds by zinc, chlorhexidine or cetylpyridinium chloride--effect of concentration.

Zinc ions, chlorhexidine (CHX) and cetylpyridinium chloride (CPC) are all known to inhibit production of volatile sulfur compounds (VSCs). The objective was to examine the anti-VSC dose-response effects of each of the above agents. Oral malodor was induced in 13 test subjects using the cysteine challenge method. The oral VSC response to rinses with 6 mm l-cysteine (pH 7.2) before and 1, 2 and 3 h after rinsing with zinc ions (Zn2+: 0.1, 0.3 and 1.0%), CHX and CPC (0.025 and 0.2%) was measured. Mouth air was analysed for VSC by gas chromatography (GC) according to current methodology. Zinc had a marked dose- and time-dependent anti-VSC effect. Zinc at 1% concentration had a somewhat unpleasant taste, whereas the lowest concentration was found acceptable. Chlorhexidine maintained a moderate anti-VSC effect over time. At 3 h, 0.2% CHX was the most effective agent but tasted relatively unpleasant. Cetylpyridinium at a concentration of 0.2% was only marginally more effective than 0.025% CHX over the 3 h, while 0.025% CPC had no better anti-VSC effect than water at both 2 h and 3 h. It was concluded that the three test agents demonstrated different anti-VSC kinetics. Although Zn had the best anti-VSC effect at 1 h, 0.2% CHX was at least as effective as 1% Zn at 3 h, most likely as a result of its unique substantivity.

Adult↗

Marine acidophilic sulfur-oxidizing bacterium requiring salts for the oxidation of reduced inorganic sulfur compounds.

An acidophilic sulfur-oxidizing bacterium was isolated from seawater, and designated as strain SH. Strain SH was a Gram-negative, rod-shaped and motile bacterium, which had an optimum temperature and pH value for growth of 30 degrees C and 4.0, respectively. The mol% guanine plus cytosine of the DNA was 46.0. Chemolithotrophic growth was observed with elemental sulfur and tetrathionate at pH 4.0, and was not observed with ferrous ion. The isolate was able to utilize carbon dioxide as a carbon source, and was unable to grow heterotrophically with yeast extract or glucose. The growth of strain SH was activated in medium supplemented with NaCl. However, LiCl and KCl did not sustain the growth of strain SH. The results indicate that strain SH was an acidophilic, halophilic, and obligately chemolithotrophic sulfur-oxidizing bacterium. Phylogenetic analysis based on 16S rDNA sequences indicated that strain SH had a close relationship to Acidithiobacillus thiooxidans. The oxidizing activities of sulfur and sulfite with resting cells were stimulated not only by the addition of NaCl, but also by KCl and LiCl. The oxidation of sulfite was inhibited by ionophores, carbonyl cyanide- m-chlorophenylhydrazone (CCCP), and monensin, and respiratory inhibitors, KCN and 2-heptyl-4-hydroxy-quinoline-N-oxode (HQNO).

Acidithiobacillus thiooxidans↗

On the performance and inertness of different materials used for the enrichment of sulfur compounds from air and gaseous samples.

The performance of the sorbent polydimethylsiloxane (PDMS) is compared to that of the adsorbents Carbotrap and Tenax for the enrichment of volatile and reactive sulfur compounds. These included: 1- and 2-propanethiol, tetrahydrothiophene, 2-thioethanol and 2-ethylthioethanol. Several artifact-forming reactions were identified on both Tenax and Carbotrap including: H2S elimination and dimerization of thiols. Additionally, permanent adsorption was also observed for heavier solutes. These effects are absent when PDMS is applied. This superior performance is explained by the absence of catalytic or adsorptive activity on PDMS.

Adsorption↗

The loss patterns of reduced sulfur compounds in contact with different tubing materials.

To collect or transfer samples of airborne pollutants, tubings made of various materials are used. To analyze the reactive loss patterns of reduced sulfur compounds (RSC) in the use of tubing fittings, a series of laboratory experiments were conducted so that the concentration changes were induced by the physical contact between gas samples and tubing walls. For the purpose of this study, a total of five tubing materials were investigated in reference to silcosteel (S1) tubing: stainless steel (S2), silicone (S3), PTFE Teflon (T1), tygon (T2), and copper (C). This comparative experiment was made using gaseous standards containing equimolar concentrations of four RSCs (H(2)S, CH(3)SH, DMS, and DMDS). The loss patterns of RSC were then evaluated and compared in terms of their calibration slope values across different tubing materials. The results of this comparative analysis indicated that except for a few cases, a fairly good compatibility was seen consistently among different tubing types and different RSCs. The results generally showed that the magnitude of calibration slope values obtained from different tubing materials tend to increase with an increase in RSC molecular weights. If the results are compared between different tubing materials, a highly contrasting pattern was evident. For instance, C tubing shows significant losses of light RSCs (H(2)S and CH(3)SH), while S3 tubing experiences the large losses of DMS and DMDS. A line of evidence found in this study thus suggests that most tubing types have their unique loss mechanism for RSCs, when they contact RSCs in sample gas stream passing through the tubing walls.

Copper↗

The transformation of inorganic sulfur compounds and the assimilation of organic and inorganic carbon by the sulfur disproportionating bacterium Desulfocapsa sulfoexigens.

The physiology of the sulfur disproportionator Desulfocapsa sulfoexigens was investigated in batch cultures and in a pH-regulated continuously flushed fermentor system. It was shown that a sulphide scavanger in the form of ferric iron was not obligatory and that the control of pH allowed production of more biomass than was possible in carbonate buffered but unregulated batch cultures. Small amounts of sulphite were produced during disproportionation of elemental sulfur and thiosulphate. In addition, it was shown that in the presence of hydrogen, a respiratory type of process is favored before the disproportionation of sulphite, thiosulphate and elemental sulfur. Sulphate reduction was not observed. D. sulfoexigens assimilated inorganic carbon even in the presence of organic carbon sources. Inorganic carbon assimilation was probably catalyzed by the reverse CO-dehydrogenase pathway, which was supported by the constitutive expression of the gene encoding CO-dehydrogenase in cultures grown in the presence of acetate and by the high carbon fractionation values that are indicative of this pathway.

Acetates↗

Volatile sulfur compounds in mouth air from clinically healthy subjects and patients with periodontal disease.

Volatile sulfur compounds (VSC) in mouth air were estimated by gas chromatography. The amount of VSC and the methyl mercaptan/hydrogen sulfide ratio were significantly increased in patients with periodontal disease. These two parameters also increased in proportion to the bleeding index and probing depth. A study was also done on the effect of removal of tongue coating on VSC concentrations in mouth air from patients with periodontal involvement. VSC and the methyl mercaptan/hydrogen sulfide ratio were reduced to 49% and 35%, respectively, by removal of the tongue coating. The average amount of tongue coating removed from patients with periodontal disease was significantly higher than from controls (90.1 mg vs. 14.6 mg, p less than 0.01). Estimated production of VSC from tongue coating was 4 times higher than the control value, and the methyl mercaptan/hydrogen sulfide ratio was also markedly increased. However, a saliva putrefaction study suggested that saliva does not contribute to the elevated ratio of methyl mercaptan in mouth air. These results strongly suggest that, in addition to periodontal pockets, tongue coating has an important role in VSC production, in particular leading to an elevated concentration of methyl mercaptan, which is more pathogenic than hydrogen sulfide.

Adult↗

High-Pressure Iron-Sulfur Compound, Fe3S2, and Melting Relations in the Fe-FeS System

An iron-sulfur compound (Fe3S2) was synthesized at pressures greater than 14 gigapascals in the system Fe-FeS. The formation of Fe3S2 changed the melting relations from a simple binary eutectic system to a binary system with an intermediate compound that melted incongruently. The eutectic temperature in the system at 14 gigapascals was about 400°C lower than that extrapolated from Usselman's data, implying that previous thermal models of Fe-rich planetary cores could overestimate core temperature. If it is found in a meteorite, the Fe3S2 phase could also be used to infer the minimum size of a parent body.

Journal Article↗

Additional sulfur compounds from the anal glands of the striped polecat, Ictonyx striatus (Mustelidae, Mammalia).

Two sulfur compounds have been identified in the anal gland secretions of captive-raised adults of the striped polecat (Ictonyx striatus), an African mustelid. 3-Ethyl-1,2-pentanedithiolane was observed in the secretions of an adult male and an adult female. 1,3-Pentanedithiol was observed in the male; this compound has not previously been reported from mustelid anal glands.

Anal Canal↗

Synergistic fungicidal activity of Cu(2+) and allicin, an allyl sulfur compound from garlic, and its relation to the role of alkyl hydroperoxide reductase 1 as a cell surface defense in Saccharomyces cerevisiae.

Cu(2+) showed a dose-dependent fungicidal activity against Saccharomyces cerevisiae cells, and its lethal effect was extremely enhanced in the presence of allicin, an allyl sulfur compound from garlic. The fungicidal activity of Cu(2+) was unaffected or rather attenuated by other sulfur-containing compounds such as N-acetyl-cysteine, l-cysteine or dithiothreitol. Ca(2+) could absolutely protect against the lethal effect of Cu(2+) itself, but showed no protection against the fungicidal activity of Cu(2+) newly generated in combination with allicin. Cu(2+) accelerated an endogenous generation of reactive oxygen species (ROS) in S. cerevisiae cells at a lethal concentration, but such intracellular oxidative stress induction was not observed during cell death progression upon treatment with Cu(2+) and allicin. A surfactant, sodium N-lauroyl sarcosinate (SLS), enhanced the solubilization of a few proteins including alkyl hydroperoxide reductase 1 (AHP1) in intact cells, accounting for the absence of this protein in the extract from allicin-treated cells. Allicin-treated cells were rendered extremely sensitive to the subsequent Cu(2+) treatment as in the case of SLS-treated cells. Allicin-treated cells and SLS-treated cells similarly showed an increased sensitivity to exogenously added tert-butyl hydroperoxide (t-BOOH), an organic peroxide that is detoxified by the action of AHP1. Our study suggests that allicin influences the mode of cell surface localization or the related function of AHP1 as a defense against phospholipid peroxidation by the external action of Cu(2+).

Anti-Infective Agents↗

ACCUMULATION OF INORGANIC POLYPHOSPHATE IN AEROBACTER AEROGENES. II. ENVIRONMENTAL CONTROL AND THE ROLE OF SULFUR COMPOUNDS.

Harold, F. M. (National Jewish Hospital, Denver, Colo.) and Susan Sylvan. Accumulation of inorganic polyphosphate in Aerobacter aerogenes. II. Environmental control and the role of sulfur compounds. J. Bacteriol. 86:222-231. 1963.-The accumulation of inorganic polyphosphate in Aerobacter aerogenes was shown to be a function of the growth medium. In low-phosphate medium, polyphosphate accumulated whenever nucleic acid synthesis ceased due to a nutritional deficiency, regardless of its nature. In high-phosphate medium polyphosphate accumulation was induced only by sulfur starvation. Polyphosphate accumulation could thus be induced or suppressed at will by manipulation of the sulfur and phosphorus content of the medium. The specific requirement for sulfur starvation was traced to the presence of an intracellular inhibitor of polyphosphate accumulation. This was depleted during sulfur starvation and replenished when sulfate was restored. The inhibitor was identified as oxidized glutathione or a closely related compound. Suppression of polyphosphate accumulation required the simultaneous presence of a high exogenous phosphate concentration and a high intracellular glutathione level. Suppression of polyphosphate accumulation resulted in a constant polyphosphate level, due to a steady state of polyphosphate synthesis and degradation. The former continued at half the original rate while the latter was sharply accelerated. The synthetic and degradative phases of polyphosphate metabolism could be completely dissociated by inhibitors of energy generation. It is proposed that the primary effect of glutathione plus phosphate is the stimulation of polyphosphate degradation. Polyphosphate synthesis appears to be a general consequence of the inhibition of nucleic acid synthesis, but net accumulation may be obscured by concurrent degradation.

Culture Media↗