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苯酚降解菌的分离、鉴定及降解特性
引用本文:张楠,陈波水,杨致邦,余瑛,黄伟九,方建华.苯酚降解菌的分离、鉴定及降解特性[J].后勤工程学院学报,2010,26(1):22-26,37.
作者姓名:张楠  陈波水  杨致邦  余瑛  黄伟九  方建华
作者单位:1. 后勤工程学院,军事油料应用与管理工程系,重庆,401311
2. 重庆医科大学,病原生物学与免疫学实验室,重庆,400016
3. 重庆理工大学,化学与生物工程学院,重庆,400050
4. 重庆理工大学,材料科学与工程学院,重庆,400050
基金项目:国家自然科学基金资助项目(50975282);;重庆市杰出青年科学基金资助项目(CSCT,2008BA4037);;重庆市高校创新团队建设计划资助项目
摘    要:以苯酚为唯一碳源进行选择性富集培养,从油污染土壤中筛选出2株菌,命名为Phe0901和Phe0902。在32℃、pH值为7.0、200r/min摇床振荡培养72h,用4-氨基安替比林分光光度法测定2菌株培养液中苯酚含量,结果表明2株菌均能彻底降解初始质量浓度为1000mg/L的苯酚培养液,即Phe0901和Phe0902为苯酚降解菌。经形态学观察、生理生化实验及16SrDNA基因序列比对分析,初步确定Phe0901为假单胞菌属(Pseudomonas)成员;Phe902为芽孢杆菌属(Bacillus)成员。在不同温度下用比浊法探讨降解菌株的生长情况,在不同pH值下用4-氨基安替比林分光光度法测定苯酚降解率,结果表明在32℃、pH值为7.0~7.8时适宜Phe0901的降解,Phe0901培养44h能彻底降解1000mg/L的苯酚;在32℃、pH值为7.0时适宜Phe0902的降解,Phe0902培养70h能彻底降解1000mg/L的苯酚。

关 键 词:生物降解  降解菌  基因序列比对  苯酚

Isolation, Identification and Characteristics of Bacterial Strains for Biodegradation of Phenol
ZHANG Nan,CHEN Bo-shui,YANG Zhi-bang,YU Ying,HUANG Wei-jiu,FANG Jian-hua.Isolation, Identification and Characteristics of Bacterial Strains for Biodegradation of Phenol[J].Journal of Logistical Engineering University,2010,26(1):22-26,37.
Authors:ZHANG Nan  CHEN Bo-shui  YANG Zhi-bang  YU Ying  HUANG Wei-jiu  FANG Jian-hua
Institution:1.Dept.of Oil Application & Management Engineering;LEU;Chongqing 401311;China;2.Laboratory of Pathobiology and Immunology;Chongqing University of Medical Sciences;Chongqing 400016;3.College of Chemical and Biological Technology;Chongqing University of Science and Technology;Chongqing 400050;4.College of Material Science and Engineering;China
Abstract:Utilizing phenol as sole carbon source, two bacterial strains, named as Phe0901 and Phe0902, were isolated from the oil-contaminated soil through selective enriched culture. The phenol concentrations of the culture fluids of the two strains were determined by the 4-amino-antipyrine spectrophotometric method. Results showed that initial phenol mass concentration 1 000 mg/L could be thoroughly degraded within 72 h of shake cultivation in swing bed at 200 r/min under 32 ℃ and pH = 7.0, indicating that the two strains were phenol degrading bacteria. The two degrading strains were preliminarily identified as genus Pseudomonas and Bacillus respectively through morphological observations, physiological and biochemical tests and 16S rDNA sequencing analysis. The impacts of the two strains under different temperatures and pH values on biodegradability of phenol were evaluated by the turbidimetric method and the 4-amino-antipyrine spectrophotometric method, respectively. The optimum biode- grading conditions of temperature and pH values for each strain were obtained, namely,32 ℃ and pH = 7.0 - 7.8 for Phe0901,32 ℃ and pH = 7.0 for Phe0902, under which initial phenol mass concentration 1 000 mg/L could be completely degraded with- in 44 h for Phe0901and within 70 h for Phe0902.
Keywords:biodegradation  degrading bacterium  gene sequencing  phenol  
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