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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 5 (1991), S. 427-430 
    ISSN: 0268-2605
    Keywords: Arsenobetaine ; trimethylarsine oxide ; dimethylarsinic acid ; degradation ; bacteria ; micro-organisms ; chitons ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The intestinal micro-organisms of Liolophura japonica chitons converted arsenobetaine [(CH3)3As+CH2COO-] to trimethylarsine oxide [(CH3)3AsO] and dimethylarsinic acid [(CH3)2AsOOH] in the arsenobetaine-containing 1/5 ZoBell 2216E medium under aerobic conditions, no conversion being observed in an inorganic salt medium. This conversion pattern of arsenobetaine → trimethylarsine oxide ← dimethylarsinic acid was comparable with that shown by the microorganisms associated with marine macroalgae. On the other hand, no conversion was observed in either medium under anaerobic conditions.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 5 (1991), S. 435-438 
    ISSN: 0268-2605
    Keywords: Arsonobetaine ; dimethylarsinic acid ; degradation ; bacteria ; micro-organisms ; sediment ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Arsenobetain [(CH3)3As+CH2COO-]-containing growth media (1/5 ZoBell 2216E and solution of inorganic salts) were inoculated with two bacterial strains, which were isolated from a coastal sediment and identified as members of the Vibro-Aeromonas group, and incubated under aerobic and anaerobic conditions. Arsenobetaine was converted to a metabolite only under aerobic conditions. This arsenic metabolite was identified as dimethylarsinic acid [(CH3)2AsOOH] by hydride generation/cold trap/GC MS/SIM analysis and high-performance liquid-chromatographic behaviour. The conversion pattern shown by these arsenobetaine-decomposing bacteria (that is, arsenobetaine → dimethylarsinic acid) was fairly different from that shown by the addition of sediment itself as the source of arsenobetaine-decomposing micro-organisms (that is, arsenobetaine → trimethylarsine oxide → inorganic arsenic). This result suggests to us that various micro-organisms, including the arsenobetaine-decomposing bacteria isolated in this study, participate in the degradation of arsenobetaine in marine environments.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 6 (1992), S. 375-381 
    ISSN: 0268-2605
    Keywords: Arsenocholine ; arsenobetaine ; trimethylarsine oxide ; dimethylarsinic acid ; methanearsonic acid ; micro-organisms ; sediments ; arsenic metabolism ; marine ecosystems ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: As one of the experiments to pursue marine circulation of arsenic, we studied microbiological conversion of arsenocholine to arsenobetaine, because arsenocholine may be a precursor of arsenobetaine in these ecosystems. Two culture media, 1/5 ZoBell 2216E and an aqueous solution of inorganic salts, were used in this in vitro study. To each medium (25 cm3) were added synthetic arsenocholine (0.2%) and about 1 g of the sediment, and they were aerobically incubated at 25°C in the dark. These conversion experiments were performed in May and July 1990. In both seasons, two or three metabolites were derived in each mixture. These metabolites were purified using cation-exchange chromatography. Their structures were confirmed as arsenobetaine, trimethylarsine oxide and dimethylarsinic acid by high-performance liquid chromatography, thin-layer chromatography, FAB mass spectrometry and a combination of gas-chromatographic separation with hydride generation followed by a cold-trap technique and selected-ion monitoring mass spectrometric analysis. From this and other evidence it is concluded that, in the arsenic cycle in these marine ecosystems, as recently postulated by us, the pathway arsenocholine → arsenobetaine → trimethylarsine oxide → dimethylarsinic acid → methanearsonic acid → inorganic arsenic can be carried out by micro-organisms alone.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 2 (1988), S. 371-376 
    ISSN: 0268-2605
    Keywords: Arsenobetaine ; trimethylarsine oxide ; marine animals ; micro-organisms ; arsenic metabolism ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Arsenic compounds were extracted with chloroform/methanol/water from tissues of marine animals (four carnivores, five herbivores, five plankton feeders). The extracts were purified by cation and anion exchange chromatography. Arsenobetaine [(CH3)3As+CH2COO-], dimethylarsinic acid [(CH3)2AsOOH], trimethylarsine oxide [(CH3)3AsO] and arsenite, arsenate, and methylarsonic acid [(CH3)AsO(OH)2] as a group with the same retention time were identified by high-pressure liquid chromatography. Arsenic was determined in the collected fractions by graphite furnace atomic absorption spectrometry. Arsenobetaine found in all the animals was almost always the most abundant arsenic compound in the extracts. These results show that arsenobetaine is present in marine animals independently of their feeding habits and trophic levels.Arsenobetaine-containing growth media (ZoBell 2216E; solution of inorganic salts) were mixed with coastal marine sediments as the source of microorganisms. Arsenobetaine was converted in both media to trimethylarsine oxide and trimethylarsine oxide was converted to arsenite, arsenate or methylarsonic acid but not to dimethylarsinic acid. The conversion rates in the inorganic medium were faster than in the ZoBell medium. Two dominant bacterial strains isolated from the inorganic medium and identified as members of the Vibro-Aeromonas group were incapable of degrading arsenobetaine.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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