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Incorporation of chlorophenols and humic monomer into soils by metal oxides and a fungal laccase.

机译:通过金属氧化物和真菌漆酶将氯酚和腐殖质单体掺入土壤中。

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In this series of studies, Trametes villosa laccase as a model enzyme, birnessite, ferrihydrite and aluminum hydroxide as model metal oxides, 2,4-dichlorophenol (2,4-DCP) as a model xenobiotic, and catechol as a model humic precursor were used for this study.; The capacity of biotic and abiotic catalysts to incorporate chlorophenols and the potential of both catalysts to remediate soil polluted with chlorophenols were also determined. Two soils from Pennsylvania with 2.8 or 7.4% organic matter contents (Soils 1 and 2, respectively) were amended with 14 C-labeled 2,4-DCP and 4-chlorophenol (4-CP) incubated with a laccase (free or immobilized on montmoriilonite), or three poorly crystalline metal oxides. After treatment with laccases, 2,4-DCP was either transformed to methanol-soluble polymeric products (11--32%) or covalently bound to soil organic matter (53--85%); unaltered 2,4-DCP could be recovered from soil by methanol extraction (0--38%) at the completion of a 14-day incubation period. In Soil 1, both free and immobilized laccase removed 100% of 2,4-DCP without regard for moisture conditions. In Soil 2, immobilized laccase removed more 2,4-DCP than free enzyme. Binding of 2,4-DCP in the humin fraction was nearly the same for free and immobilized laccase. In general, immobilized laccase performed better than free laccase.; After a 3-d incubation with birnessite, up to 77% of 4-CP was transformed and covalently bound to Soil 1, while up to 71% of 2,4-DCP was disappeared from Soil 1. There was no significant difference in bound residue of 2,4-DCP between Soil 1 and 2. Binding of both chlorophenols in soil occurred on the humin fraction. Ferrihydrite and aluminum hydroxide showed significantly less ability to remove both chlorophenols from Soil 1 and 2 than birnessite.; To investigate the interaction between Trametes villosa laccase, poorly crystalline metal oxides, and a naturally occurring phenolic compound (catechol), these three components were monitored during incubation period. Birnessite had an inhibitory effect on the disappearance (transformation and adsorption) of catechol from solutions in the presence of laccase, while aluminum hydroxide and ferrihydrite had additive effects. (Abstract shortened by UMI.)
机译:在这一系列研究中,分别以Trametes villosa漆酶为模型酶,水钠锰矿,三水铝石和氢氧化铝为模型金属氧化物,将2,4-二氯苯酚(2,4-DCP)作为模型异生物源,将儿茶酚作为模型腐殖质前体。用于这项研究。还确定了生物和非生物催化剂掺入氯酚的能力,以及两种催化剂修复被氯酚污染的土壤的潜力。宾夕法尼亚州的两种土壤中有机物含量分别为2.8%或7.4%的土壤(土壤1和2)分别用14 C标记的2,4-DCP和4-氯苯酚(4-CP)与漆酶(游离的或固定化的)孵育蒙脱石)或三种结晶度较差的金属氧化物。用漆酶处理后,将2,4-DCP转化为可溶于甲醇的聚合物产品(11--32%)或与土壤有机物共价结合(53--85%);在14天的孵育期结束后,可以通过甲醇萃取(0--38%)从土壤中回收未改变的2,4-DCP。在土壤1中,游离的和固定的漆酶都去除了100%的2,4-DCP,而不考虑湿度条件。在土壤2中,固定化的漆酶比游离酶去除了更多的2,4-DCP。对于游离的和固定的漆酶,在人红素部分中的2,4-DCP的结合几乎相同。通常,固定化漆酶的性能要优于游离漆酶。与水钠锰矿孵育3天后,多达77%的4-CP转化并与土壤1共价结合,而高达71%的2,4-DCP从土壤1中消失。结合中无显着差异土壤1和2之间的2,4-DCP残基。腐殖质部分上土壤中的两种氯酚都发生了结合。水铁矿和氢氧化铝显示出从土壤1和2中除去两种氯酚的能力明显低于水钠锰矿。为了研究绒毛漆酶,结晶性较差的金属氧化物与天然存在的酚类化合物(邻苯二酚)之间的相互作用,在孵育期间对这三个成分进行了监测。在漆酶存在下,水钠锰矿对溶液中邻苯二酚的消失(转化和吸附)具有抑制作用,而氢氧化铝和三水铝石则具有累加效应。 (摘要由UMI缩短。)

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