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耐热石油烃降解混合菌的筛选及其群落结构分析
引用本文:刘其友,宗明月,张云波,赵东风,赵朝成.耐热石油烃降解混合菌的筛选及其群落结构分析[J].生态环境,2012(8):1468-1472.
作者姓名:刘其友  宗明月  张云波  赵东风  赵朝成
作者单位:1. 中国石油大学华东化学工程学院, 山东 青岛 266580
2. 中国石油工程设计有限责任公司新疆石油勘察设计研究院 有限公司,新疆 克拉玛依 834000
基金项目:中央高校基本科研业务费专项资金资助(No.27R1204018A)
摘    要:对克拉玛依采集的部分石油污染土壤进行了筛选,得到了5组石油烃高效降解混合菌,其中混合菌KL9-1在45℃的条件下,通过7 d的降解,稀油的降解率达到43.27%,稠油的降解率达到20.09%。混合菌KL9-1经过多次分离纯化后,获得3株具有石油烃降解能力的优势单菌,3株单菌对稀油的降解率都在30%以上。结合分离单菌株的形态、生理生化特征和16S rDNA基因序列的分析结果,初步鉴定KL9-1-1为Pseudomonas putida,KL9-1-2和KL9-1-3为Pseudomonas sp.。

关 键 词:石油污染土壤  耐热降解菌  筛选  降解  16SrDNA

Screening of a hydrocarbon-degrading bacterial group of heat-resistant and analysis of its community structure
LIU Qiyou,ZONG Mingyue,ZHANG Yunbo,ZHAO Dongfeng,ZHAO Chaocheng.Screening of a hydrocarbon-degrading bacterial group of heat-resistant and analysis of its community structure[J].Ecology and Environmnet,2012(8):1468-1472.
Authors:LIU Qiyou  ZONG Mingyue  ZHANG Yunbo  ZHAO Dongfeng  ZHAO Chaocheng
Institution:1(1. College of Chemical Engineering, China University of Petroleum (Huadong), Qingdao 266580, China; 2. Xinjiang Petrol Surveying and Design Institute, Engineering Co. Ltd., CNPC, Karamay 834000, China)
Abstract:5 highly efficient hydrocarbon-degrading mixed bacteria were obtained from the petroleum-contaminated soil samples of Karamay by the traditional method of enrichment and acclimation. The KL9-1 group has a wide temperature tolerance range and higher hydrocarbon degrading ability. The degradation rate of thin oil and heavy oil was up to 43.27% and 20.09% respectively through 7 d at 45 ℃. After several times of isolation and purification, three dominant strains with the capability of hydrocarbon-degrading were obtained, and their petroleum degradation rates were all over 30%. According to its morphological, physiological, biochemical, and 16S rDNA sequence characteristics, the KL9-1-1 strain was identified as Pseudomonas putida, the KL9-1-2 strain and KL9-1-3 strain were identified as Pseudomonas sp.
Keywords:petroleum polluted soil  heat-resistant bacteria  screening  degrading  16S rDNA
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