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  • 1
    ISSN: 1520-5851
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Environmental science & technology 22 (1988), S. 836-839 
    ISSN: 1520-5851
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Environmental science & technology 25 (1991), S. 302-305 
    ISSN: 1520-5851
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Microbial ecology 17 (1989), S. 263-274 
    ISSN: 1432-184X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract One hundred six strains of aerobic bacteria were isolated from the Fiora River which drains an area of cinnabar deposits in southern Tuscany, Italy. Thirty-seven of the strains grew on an agar medium containing 10μg/ml Hg (as HgCl2) with all of these strains producing elemental mercury. Seven of the 37 strains also degraded methylmercury. None of 106 sensitive and resistant strains produced detectable monomethylmercury although 15 strains produced a benzene-soluble mercury species. Two strains of alkylmercury (methyl-, ethyl- and phenylmercury) degrading bacteria were tested for the ability to degrade several other analogous organometals and organic compounds, but no activity was detected toward these compounds. Mercury methylation is not a mechanism of Hg resistance in aerobic bacteria from this environment. Growth of bacteria on the agar medium containing 10μg/ml HgCl2 was diagnostic for Hg detoxification based on reduction.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Water, air & soil pollution 56 (1991), S. 465-475 
    ISSN: 1573-2932
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract Bacteria are resistant to Hg compounds by virtue of two specific enzymes: mercuric reductase and organomercurial lyase. We investigate these specific enzyme systems 1) to determine McHg in biological samples by its enzymatic transformation to the respective hydrocarbon and 2) as an environmental index of Hg pollution in geothermal areas, by studying the distribution of the percentage of Hg-resistant bacteria. The first application is based on the enzymatic conversion of McHg to CH4. by whole cells of the Pseudomonas putida strain FBI. A 1 ml aliquot of 0.01N aqueous solution of thiosulphate containing MeHg, extracted from a biological sample by a conventional procedure was mixed with a dense (1 mg cells/mL dw) culture of FBI strain in a microreaction vessel. After a suitable period of incubation (from 4 to 18 hours), methane was assayed in the headspace by gas chromatograph equipped with flame ionization detector. In the second application, Hg-resistant bacteria (MRB) isolated from mosses collected in a geothermal area (Travale) in Tuscany showed almost the same distribution pattern as total Hg in briophytes. Mosses and MRB are both suitable bioindicators for mapping contaminated areas. The finding of Hg-resistant strains depends on the availability of the metal for cell accumulation and interaction at molecular level in the cytoplasm to produce mercuric reductase. MRB/g dw is therefore an indirect measure of the enzyme in this terrestrial geothermal environment.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Water, air & soil pollution 80 (1995), S. 805-815 
    ISSN: 1573-2932
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract The transformation of MeHg under anaerobic conditions in axenic cultures ofDesulfovibrio desulfuricans strain LS is compared to that in anoxic marine sediments contaminated by Hg of industrial origin. MeHg was added to cultures ofD. desulfuricans strain LS and incubated at 28°C for two weeks. Significant amounts of dimethylmercury and metacinnabar were produced. These two Hg compounds were formed from the slow decomposition of the intermediate dimethylmercury-sulfide. Other collateral compounds, such as methane and ionic Hg, were also detected during the MeHg degradation process. On the other hand a sample of fresh sediment (1.5 g d.w.) was spiked with 10 μg of MeHg and 2 mmoles.ml−1 of pyruvate, as carbon source for sulfate-reducing bacteria. After 9 days of incubation at 28°C, significant amounts of dimethylmercury were produced. A lower content of this volatile species was found in a subsample of sediment supplemented with sodium molybdate, which is a strong inhibitor of sulfatereducing activity. A kinetic study showed the disappearance of monomethylmercury from the sediment and the formation of dimethylmercury over the incubation period. The environmental significance of dimethylmercury and dimethylmercury-sulfide in the natural biogeochemical cycle of Hg is discussed.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 7 (1993), S. 487-493 
    ISSN: 0268-2605
    Keywords: Mercury ; methylation ; methylcobalamine ; Vitamin B12 ; Fourier transform IR spectroscopy ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new approach was used to determine the reaction products of methylcobalamin and ionic mercury: purge-and-trap gas chromatography in line with Fourier transform infrared spectroscopy (PT GC/FTIR). This technique simultaneously and specifically determines the spectrum of dimethylmercury (DMeHg) and methylmercury produced by the reaction. No interference from other known organic mercury species could be detected. The method is different from others because it does not require solvent extraction of the organomercurials from aqueous solution, but relies on immediate volatilization from the reaction vessel by addition of 100 μl of 10 mM NaBH4. The sample was purged with nitrogen for 10 min. The volatile species of mercury were trapped in a column at -120°C, injected into the gas chromatograph and detected by FTIR. The efficiency of DMeHg and MeHg formation depended on different parameters: pH, temperature, reaction time, and the methylcobalamin/ionic mercury ratio. The initial reaction product was MeHg which was further transformed to DMeHg. The first methylation rate was two times faster than the second. MeHg formed first, reaching a maximum at higher temperatures (28°C and 37°C) and later decreasing as DMeHg formed. At lower temperatures (20°C) the rate of MeHg formation was slower, being similar to the formation rate of DMeHg. Different species of inorganic mercury such as HgSO4, Hg(NO3)2, Hg(SCN)2, HgCl2 and Hgl2 were used to study differences in methylation by methylcobalamin under standard conditions of acidity, temperature and cofactor Hg(II) ratio.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 8 (1994), S. 687-691 
    ISSN: 0268-2605
    Keywords: Methylmercury ; dimethylmercury ; purge and trap GC-FTIR-AAS ; hydride generation ; fish ; water ; sediment ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A method of detecting methylmercury species (MeHg) and dimethylmercury (DMM) has been studied. MeHg was transformed prior to its determination as methylmercury hydride (MMH) by use of NaBH4. The two volatile forms of organic mercury were detected by a purge and trap (PT) unit in-line with a gas chromatograph (GC) connected with a Fourier transform infrared spectrometer (FTIR) which was also in-line with an atomic absorption spectrometer (AAS). Environmental samples were analyzed by this technique. MeHg was detected in thiosulfate extracts of fish and sediment, and MeHg and DMM directly in water samples. Picogram levels of sensitivity were obtained, the limit of detection being 100 pg for MeHg and 50 pg for DMM. The calibration graph was linear for both compounds up to 10 ng as Hg.
    Additional Material: 4 Ill.
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  • 10
    Publication Date: 1991-04-01
    Print ISSN: 0049-6979
    Electronic ISSN: 1573-2932
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Published by Springer
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