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石油污染土壤生物修复过程中氮循环功能基因的动态检测
摘要点击 2718  全文点击 1207  投稿时间:2011-08-29  修订日期:2011-10-24
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中文关键词  土壤修复  动态监测  功能基因  生态评估  实时定量PCR
英文关键词  soil remediation  dynamic monitoring  functional gene  ecological assessment  real-time PCR
作者单位E-mail
吴彬彬 清华大学化学工程系,北京 100084  
卢滇楠 清华大学化学工程系,北京 100084 ludiannan@tsinghua.edu.cn 
刘铮 清华大学化学工程系,北京 100084 liuzheng@tsinghua.edu.cn 
中文摘要
      氮循环相关功能微生物在土壤发挥其生态功能中起着重要的作用.为定量分析其中的固氮细菌、反硝化细菌和硝化细菌在石油污染土壤生物修复过程中的演变情况,采用了实时定量PCR技术对其相关功能基因nifHnarGamoA的拷贝数进行检测.结果表明,污染土壤中nifHnarGamoA基因拷贝数及其占总16S rRNA基因拷贝数的比例远低于正常土壤,修复后土壤中的同类分析结果与正常土壤接近.表明石油污染物破坏了氮循环相关菌落结构,而生物修复则使其得以恢复.进一步分析了不同修复方式下氮循环功能基因的恢复情况以及土壤中石油烃降解率.也表明同时添加秸秆和菌剂具有最好的修复效果,处理40 d后其nifHnarGamoA基因拷贝数(以干土计)分别恢复到2.68×106、 1.71×106和8.54×104 g-1,石油烃降解率达到48%.投加真菌-细菌复合菌剂的效果优于只投加细菌菌剂的效果.本研究结果表明氮循环功能基因的动态监测可以从基因和物种水平上反映土壤修复的效果,为土壤修复的监控和效果评估提供参考.
英文摘要
      Microorganisms in nitrogen cycle serve as an important part of the ecological function of soil. The aim of this research was to monitor the abundance of nitrogen-fixing, denitrifying and nitrifying bacteria during bioaugmentation of petroleum-contaminated soil using real-time polymerase chain reaction (real-time PCR) of nifH, narG and amoA genes which encode the key enzymes in nitrogen fixation, nitrification and ammoniation respectively. Three different kinds of soils, which are petroleum-contaminated soil, normal soil, and remediated soil, were monitored. It was shown that the amounts of functional microorganisms in petroleum-contaminated soil were far less than those in normal soil, while the amounts in remediated soil and normal soil were comparable. Results of this experimentdemonstrate that nitrogen circular functional bacteria are inhibited in petroleum-contaminated soil and can be recovered through bioremediation. Furthermore, copies of the three functional genes as well as total petroleum hydrocarbons (TPH) for soils with six different treatments were monitored. Among all treatments, the one, into which both E. cloacae as an inoculant and wheat straw as an additive were added, obtained the maximum copies of 2.68×106, 1.71×106 and 8.54×104 per gram dry soil for nifH, narG and amoA genes respectively, companying with the highest degradation rate (48% in 40 days) of TPH. The recovery of functional genes and removal of TPH were better in soil inoculated with E cloacae and C echinulata collectively than soil inoculated with E cloacae only. All above results suggest that the nitrogen circular functional genes could be applied to monitor and assess the bioremediation of petroleum-contaminated soil.

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