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Formation of Bound Residues during Microbial Degradation of 14CAnthracene in Soil

机译:14C蒽在土壤中微生物降解过程中结合残留物的形成

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摘要

Carbon partitioning and residue formation during microbial degradation of polycyclic aromatic hydrocarbons (PAH) in soil and soil-compost mixtures were examined by using [14C]anthracenes labeled at different positions. In native soil 43.8% of [9-14C]anthracene was mineralized by the autochthonous microflora and 45.4% was transformed into bound residues within 176 days. Addition of compost increased the metabolism (67.2% of the anthracene was mineralized) and decreased the residue formation (20.7% of the anthracene was transformed). Thus, the higher organic carbon content after compost was added did not increase the level of residue formation. [14C]anthracene labeled at position 1,2,3,4,4a,5a was metabolized more rapidly and resulted in formation of higher levels of residues (28.5%) by the soil-compost mixture than [14C]anthracene radiolabeled at position C-9 (20.7%). Two phases of residue formation were observed in the experiments. In the first phase the original compound was sequestered in the soil, as indicated by its limited extractability. In the second phase metabolites were incorporated into humic substances after microbial degradation of the PAH (biogenic residue formation). PAH metabolites undergo oxidative coupling to phenolic compounds to form nonhydrolyzable humic substance-like macromolecules. We found indications that monomeric educts are coupled by C-C- or either bonds. Hydrolyzable ester bonds or sorption of the parent compounds plays a minor role in residue formation. Moreover, experiments performed with 14CO2 revealed that residues may arise from CO2 in the soil in amounts typical for anthracene biodegradation. The extent of residue formation depends on the metabolic capacity of the soil microflora and the characteristics of the soil. The position of the 14C label is another important factor which controls mineralization and residue formation from metabolized compounds.
机译:通过在不同位置标记的[ 14 C]蒽,研究了土壤和土壤-粪便混合物中微生物降解多环芳烃(PAH)时的碳分配和残留形成。在原生土壤中,[9- 14 C]蒽中有43.8%的土生微生物被矿化,有45.4%的土在176天内转化为结合残基。堆肥的添加增加了新陈代谢(67.2%的蒽被矿化)并减少了残留物的形成(20.7%的蒽被转化了)。因此,添加堆肥后较高的有机碳含量不会增加残留物形成的水平。 1,2,3,4,4a,5a位置标记的[ 14 C]蒽代谢较快,与土壤混合后形成的残渣含量更高(28.5%)。 [ 14 C]蒽被放射性标记在C-9位(20.7%)。在实验中观察到残留物形成的两个阶段。在第一阶段,原始化合物被螯合在土壤中,这表明其提取能力有限。在第二阶段,代谢物在PAH微生物降解(生物残留形成)后被掺入腐殖质中。 PAH代谢产物与酚类化合物发生氧化偶联,形成不可水解的腐殖质样大分子。我们发现有迹象表明单体离析物通过C-C-或任一键耦合。母体化合物的可水解酯键或吸附在残基形成中起较小作用。此外,对 14 CO2进行的实验表明,土壤中的CO2可能以蒽生物降解的典型量残留。残留物形成的程度取决于土壤微生物区系的代谢能力和土壤特性。 14 C标签的位置是另一个重要因素,它控制代谢化合物的矿化和残留物形成。

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