Comparison of response of six different luminescent bacterial bioassays to bioremediation of five contrasting oils

被引:30
作者
Bundy, JG
Campbell, CD
Paton, GI
机构
[1] Univ Aberdeen, Dept Plant & Soil Sci, Aberdeen AB24 3UU, Scotland
[2] Macaulay Land Use Res Inst, Aberdeen AB15 8QH, Scotland
来源
JOURNAL OF ENVIRONMENTAL MONITORING | 2001年 / 3卷 / 04期
关键词
D O I
10.1039/b103104j
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The performance of six different bioluminescent bacteria for the assessment of oil bioremediation was compared. Three contained lux genes linked to promoters from hydrocarbon degradation pathways: Pseudomonas fluorescens HK44 (pUTK21), Escherichia coli HMS174 (pOS25) and E. coli DH5 alpha (pGEc74, pJAMA7), responding to naphthalene, isopropylbenzene and octane, respectively. The other three expressed lux constitutively: E. coli HB101 (pUCD607) and P. putida F1 (pUCD607) are genetically engineered, while Vibrio fischeri is naturally bioluminescent and was included to facilitate comparison with previous work. Five different oils (four crude oils plus diesel) were spiked into soil, and the progress of remediation was followed over a period of 119 d by monitoring both hydrocarbon disappearance and changes in the microbial response to soil extracts. The octane bioassay was the only one of the hydrocarbon-responsive bacterial assays to show any appreciable response, with up to 20-fold induction by light crude oils. Heavy crude oil and diesel elicited a much weaker response. The metabolic (lux constitutively expressed) bioassays showed that there was a general increase in toxicity over the course of the experiment, although toxicity to E. coli HB101 (pUCD607) appeared to be decreasing by the final sampling point. The metabolic bioassay response was much less variable between the different oils than for the first three, catabolic, strains.
引用
收藏
页码:404 / 410
页数:7
相关论文
共 41 条
[21]  
Rus V, 1996, CHEMOSPHERE, V32, P1435, DOI 10.1016/0045-6535(96)00052-5
[22]   Crude oil hydrocarbon bioremediation and soil ecotoxicity assessment [J].
Salanitro, JP ;
Dorn, PB ;
Huesemann, MH ;
Moore, KO ;
Rhodes, IA ;
Jackson, LMR ;
Vipond, TE ;
Western, MM ;
Wisniewski, HL .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1997, 31 (06) :1769-1776
[23]  
Sanseverino J., 1993, Biodegradation, V4, P303, DOI 10.1007/BF00695976
[24]  
Saterbak A, 2000, ENVIRON TOXICOL CHEM, V19, P2643, DOI [10.1002/etc.5620191105, 10.1897/1551-5028(2000)019&lt
[25]  
2643:EAAAOE&gt
[26]  
2.0.CO
[27]  
2]
[28]   Use of an ipb-lux fusion to study regulation of the isopropylbenzene catabolism operon of Pseudomonas putida RE204 and to detect hydrophobic pollutants in the environment? [J].
Selifonova, OV ;
Eaton, RW .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (03) :778-783
[29]   Re-inoculation of autoclaved soil as a non-sterile treatment for xenobiotic sorption and biodegradation studies [J].
Shaw, LJ ;
Beaton, Y ;
Glover, LA ;
Killham, K ;
Meharg, AA .
APPLIED SOIL ECOLOGY, 1999, 11 (2-3) :217-226
[30]  
SHEN J, 1994, INT BIODETER BIODEGR, V33, P61, DOI 10.1016/0964-8305(94)90055-8