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土壤中五氯苯酚的生物降解:对物理、化学和生物处理的响应

Biodegradation of pentachlorophenol in soil: the response to physical, chemical, and biological treatments.

作者信息

Seech A G, Trevors J T, Bulman T L

机构信息

Dearborn Environmental Consulting Group, Ltd., Mississauga, Ont., Canada L5A 3T5.

出版信息

Can J Microbiol. 1991 Jun;37(6):440-4. doi: 10.1139/m91-072.

Abstract

The effects of physical, chemical, and biological treatments on biodegradation of pentachlorophenol (PCP) were studied in a silt-loam soil contaminated with 175 mg PCP/kg and uniformly 14C-labelled PCP. Biodegradation of 14C-labelled PCP and technical-grade PCP were monitored over 210 days incubation. Mineralization of labelled PCP was significantly (p=0.05) influenced by soil treatments. Negligible biodegradation occurred in either the sterile control soil or the uninoculated control soil, with less than 1% of added 14C recovered as 14 CO2. Inoculation of unamended soil with a strain of Flavobacterium (ATCC 39723) known to degrade PCP increased biodegradation of PCP; approximately 60% of the [14C]PCP was recovered as 14CO2. Increased soil water content (60% versus 30% w/w) enhanced biodegradation (67% recovery of 14C as CO2), while increased chloride ion concentration and anoxic conditions were inhibitory (20 and 1% recoveries, respectively). Residual soil PCP concentrations were also influenced by various treatments. In the sterile control soil and noninoculated control, after 210 days incubation, concentrations of PCP were 143 and 1223 mg/kg, respectively, while the PCP concentration in the inoculated soil was 21 mg/kg. When soil organic matter was increased by adding finely ground red clover leaf and stem material, the residual PCP concentration was reduced to 6 mg/kg after 210 days. Increased soil water content resulted in a residual PCP concentration of 5 mg/kg. High-pressure liquid chromatography of soil extracts revealed no accumulation of partial PCP degradation products. The results indicated that biodegradation of PCP in soil was significantly influenced by various soil amendments.

摘要

在受175毫克五氯苯酚/千克污染且五氯苯酚统一用14C标记的粉质壤土中,研究了物理、化学和生物处理对五氯苯酚(PCP)生物降解的影响。在210天的培养期内监测了14C标记的五氯苯酚和工业级五氯苯酚的生物降解情况。标记的五氯苯酚的矿化受到土壤处理的显著影响(p = 0.05)。在无菌对照土壤或未接种的对照土壤中,生物降解可忽略不计,添加的14C中作为14CO2回收的不到1%。用已知能降解五氯苯酚的黄杆菌菌株(ATCC 39723)接种未改良的土壤,可提高五氯苯酚的生物降解;约60%的[14C]五氯苯酚作为14CO2回收。土壤含水量增加(60%对30% w/w)可增强生物降解(14C作为CO2的回收率为67%),而氯离子浓度增加和缺氧条件则具有抑制作用(分别为20%和1%的回收率)。残留土壤五氯苯酚浓度也受各种处理的影响。在无菌对照土壤和未接种对照中,培养210天后,五氯苯酚浓度分别为143和1223毫克/千克,而接种土壤中的五氯苯酚浓度为21毫克/千克。通过添加精细研磨的红三叶草叶和茎材料增加土壤有机质后,210天后残留五氯苯酚浓度降至6毫克/千克。土壤含水量增加导致残留五氯苯酚浓度为5毫克/千克。土壤提取物的高压液相色谱分析表明没有五氯苯酚部分降解产物的积累。结果表明,土壤中五氯苯酚的生物降解受到各种土壤改良措施的显著影响。

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