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Foimation and Fate of Bound Residues from Microbial Biomass during 2,4-D Degradation in Soil

机译:土壤中2,4-D降解过程中微生物生物质结合残留的形成和归宿

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摘要

During organic contaminant degradation in soil, bound or nonextractable residues (NER) are formed. Part of these residues may be biogenic, because degrading microorganisms assimilate carbon derived from the pollutant and mineralized CO_2 to form cellular components for example, [fatty acids (FA) and amino acids (AA)], which are subsequently stabilized within soil organic matter (SOM). We investigated the formation and fate of FA and AA from biodegradation of ~(13)Ce-2,4-D in soil and the incorporation of the ~(13)C-label into living biomass via ~(13)CO_2 fixation. After 64 days of incubation, ~(13)C-AA in SOM indicated that 44% of the initially applied ~(13)C_6-2,4-D equivalents had been converted to microbial biomass and finally to biogenic residues. The intermediate maximum of ~(13)C-FA in SOM indicated a 20% conversion of ~(13)C_6-2,4-0 to biomass, but'~(13)C-FA decreased to 50% of that value whereas ~(13)C-AA in the SOM remained stable. We provide the first evidence that nearly all bound residues from 2,4-D are biogenic, containing natural microbial residues stabilized in SOM. Because of biogenic residue formation, the potential risk of bound residues from readily metabolized xenobiotics in soils is highly overestimated. Hence, the formation of biogenic residues must be considered in general when performing mass balances of pollutant biodegradation in soils.
机译:在土壤中的有机污染物降解过程中,会形成结合的或不可提取的残留物(NER)。这些残基的一部分可能是生物残基,因为降解的微生物会吸收污染物和矿化的CO_2中的碳,形成细胞成分,例如[脂肪酸(FA)和氨基酸(AA)],这些成分随后稳定在土壤有机质中( SOM)。我们调查了〜(13)Ce-2,4-D在土壤中的生物降解以及〜(13)C-标签通过〜(13)CO_2固定到活生物质中的过程中FA和AA的形成和命运。孵育64天后,SOM中的〜(13)C-AA表明最初应用的〜(13)C_6-2,4-D当量的44%已转化为微生物生物质,最后转化为生物残基。 SOM中〜(13)C-FA的中间最大值表明〜(13)C_6-2,4-0转化为生物质20%,但'〜(13)C-FA降至该值的50%,而SOM中的〜(13)C-AA保持稳定。我们提供的第一个证据是,几乎所有来自2,4-D的结合残基都是生物基因,包含在SOM中稳定的天然微生物残基。由于形成了生物残留物,因此高估了土壤中容易代谢的异源生物结合残留物的潜在风险。因此,在土壤中进行污染物生物降解的质量平衡时,通常必须考虑生物残留物的形成。

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  • 来源
    《Environmental Science & Technology》 |2011年第3期|p.999-1006|共8页
  • 作者单位

    UFZ - Helmholtz Centre for Environmental Research, Departments of Environmental Biotechnology, Permoserstrasse 15, 04318 Leipzig, Germany;

    rnUFZ - Helmholtz Centre for Environmental Research, Departments of Environmental Biotechnology, Permoserstrasse 15, 04318 Leipzig, Germany;

    rnUFZ - Helmholtz Centre for Environmental Research, Departments of Isotope Biogeochemistry, Permoserstrasse 15, 04318 Leipzig, Germany;

    rnDepartment of Environmental Biology and Chemodynamics, RWTH Aachen University, Worringerweg 1, 52074 Aachen, Germany;

    rnUFZ - Helmholtz Centre for Environmental Research, Departments of Environmental Biotechnology, Permoserstrasse 15, 04318 Leipzig, Germany;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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