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1株氟氯氰菊酯降解菌GZ-3的分离和鉴定
引用本文:张建云,崔树军,武秀琴,宋海军. 1株氟氯氰菊酯降解菌GZ-3的分离和鉴定[J]. 安徽农业科学, 2010, 38(13): 6635-6636,6640. DOI: 10.3969/j.issn.0517-6611.2010.13.005
作者姓名:张建云  崔树军  武秀琴  宋海军
作者单位:河南工程学院资源与环境工程系,河南郑州,451191;河南工程学院资源与环境工程系,河南郑州,451191;河南工程学院资源与环境工程系,河南郑州,451191;河南工程学院资源与环境工程系,河南郑州,451191
基金项目:河南工程学院青年基金,河南省教育厅自然科学研究项目 
摘    要:[目的]研究氟氯氰菊酯降解菌GZ-3的分类鉴定和降解性能。[方法]通过富集筛选的方法,从农药污染的土壤中筛选到1株氟氯氰菊酯的高效降解菌GZ-3,观察其菌落及菌体形态特征,通过培养观测其对氟氯氰菊酯的降解率,并对其进行16S rDNA同源性序列分析和生理生化特征分析,还利用Biolog生态板就氟氯氰菊酯降解菌对31种碳源利用情况进行初步研究。[结果]氟氯氰菊酯降解菌GZ-3在37℃和220r/min培养条件下培养72h后对初始浓度为50mg/L的氟氯氰菊酯的降解效率可达80%以上。同源性分析结果表明,该菌株的16S rDNA序列与多数铜绿假单胞菌的序列同源性均在99%以上,结合生理生化特性,初步鉴定该菌株属于铜绿假单胞菌。[结论]该研究为进一步利用该菌对氟氯氢菊酯农药污染的治理奠定基础。

关 键 词:氯氟氰菊酯  生物降解  16S  rDNA  铜绿假单胞菌

Isolation and Identification of A Cyfluthrin-degradation Bacteria GZ-3
Abstract:[Objective]The study aimed to research the classification identification and the degradation performance of cyfluthrin-degrading bacteria GZ-3. [Method]A high-efficiency cyfluthrin-degrading bacteria GZ-3 was screened from pesticide-contaminated soil through the enrichment and screening method,its the bacterial colony morphology were observed,its degradation rate on the cypermethrin was observed and its 16S rDNA sequencing homology analysis and the physiological and biochemical characteristics analysis were made out. The utilization status of cyfluthrin-degrading bacteria on 31 kinds of carbon source was studied preliminarily by using Biolog eco-boards.[Result]Cyfluthrin-degrading bacterium GZ-3 showed the degradation rate of over 80% on the cypermethrin at the initial concentration of 50 mg/L under the culture conditions at 37 ℃ and 220 r/min for 72 h. Homology analysis showed that the 16S rDNA sequences of the strain had the sequence homology of more than 99%with the majority of Pseudomonas aeruginosa,and combined with its physiological and biochemical characteristics,it was identified preliminarily that the strain belonged to P. aeruginosa. [Conclusion]The study laidA the foundation for the governance of HCFC pyrethroid pesticide contamination by further using the bacteria.
Keywords:16S  rDNA
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