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1株筛自柴油污染土壤的铜绿假单胞菌对萘的降解特性研究
摘要点击 1758  全文点击 1121  投稿时间:2014-07-31  修订日期:2014-09-02
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中文关键词  微生物  生物修复    土壤  污染  降解    定量PCR
英文关键词  microorganism  bioremediation  naphthalene  soil  pollution  degradation  enzyme  real-time PCR
作者单位E-mail
刘文超 辽宁石油化工大学石油化工学院, 抚顺 113001 406911387@qq.com 
吴彬彬 清华大学化学工程系, 北京 100084  
李晓森 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 
刘永民 辽宁石油化工大学石油化工学院, 抚顺 113001 liu79ym@tom.com 
中文摘要
      从柴油污染土壤中筛选分离出1株萘降解菌HD-5,经16S rDNA序列分析鉴定为铜绿假单胞菌(Pseudomonas aeruginosa),对功能基因进行PCR扩增证实该菌株中含有萘双加氧酶基因nah. 采用生物强化、生物刺激以及二者相结合的方式修复萘含量为0.5%的自配污染土壤,综合比较了在不同修复方式下土壤中萘的降解率,修复过程中土壤FDA水解酶活和脱氢酶活的变化,以及运用定量PCR的方法动态分析了总细菌基因拷贝数和nah基因拷贝数. 结果表明,在生物强化(B)、生物刺激(S)以及生物强化与生物刺激相结合(BS)这3种修复方式下,31 d后萘去除率分别为71.94%、62.22%和83.14%,BS组在修复过程中土壤FDA水解酶活和脱氢酶活明显高于另外两组,31 d后BS组土壤中总细菌基因拷贝数和nah基因拷贝数分别增长了约2.67×1011 g-1和8.67×108 g-1. 上述研究结果表明筛选得到的萘降解菌株在土壤中具有良好的定植特性,在生物刺激与该降解菌株的共同作用下,可以有效地实现土壤中萘降解,这对此类污染生物修复过程研究具有一定的指导意义.
英文摘要
      A naphthalene-degrading bacterium (referred as HD-5) was isolated from the diesel-contaminated soil and was assigned to Pseudomonas aeruginosa according to 16S rDNA sequences analysis. Gene nah, which encodes naphthalene dioxygenase, was identified from strain HD-5 by PCR amplification. Different bioremediation approaches, including nature attenuation, bioaugmentation with strain Pseudomonas aeruginosa, biostimulation, and an integrated degradation by bioaugmentation and biostimulation, were evaluated for their effectiveness in the remediating soil containing 5% naphthalene. The degradation rates of naphthalene in the soil were compared among the different bioremediation approaches, the FDA and dehydrogenase activity in bioremediation process were measured, and the gene copy number of 16S rRNA and nah in soil were dynamically monitored using real-time PCR. It was shown that the naphthalene removal rate reached 71.94%, 62.22% and 83.14% in approaches of bioaugmentation (B), biostimulation(S) and integrated degradation composed of bioaugmentation and biostimulation (BS), respectively. The highest removal rate of naphthalene was achieved by using BS protocol, which also gives the highest FDA and dehydrogenase activity. The gene copy number of 16S rRNA and nah in soil increased by about 2.67×1011 g-1 and 8.67×108 g-1 after 31 days treatment using BS protocol. Above-mentioned results also demonstrated that the screened bacterium, Pseudomonas aeruginosa, could grow well in naphthalene-contaminated soil and effectively degrade naphthalene, which is of fundamental importance for bioremediation of naphthalene-contaminated soil.

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