Reductive biodegradation of 1,2-dichloroethane by methanogenic granular sludge:: perspectives for in situ remediation

被引:5
作者
De Wildeman, S
Nollet, H
Van Langenhove, H
Diekert, G
Verstraete, W
机构
[1] Ghent Univ, Fac Agr & Appl Biol Sci, Lab Microbial Ecol & Technol, LabMET, B-9000 Ghent, Belgium
[2] Ghent Univ, Fac Agr & Appl Biol Sci, Organ Chem Lab, B-9000 Ghent, Belgium
[3] Univ Jena, Fac Biol & Pharmaceut, Lab Appl & Environm Microbiol, D-07743 Jena, Germany
关键词
Acetobacterium sp; anaerobic dechlorination; 1,2-dichloroethane; in situ bioremediation;
D O I
10.2166/wst.2002.0284
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Granular methanogenic sludge was able to dechlorinate 1,2-dichloroethane (1,2-DCA) to ethene in UASB reactors. Ethanol served as the sole carbon and energy source. The average dechlorination rate measured on the basis of ethene production varied between 1.7 and 2.1 mumol 1,2-DCA/(h.gVSS) (46.7 and 57.4 mg/L.d). In order to elucidate the microbial origin of this bioconversion, enrichment cultures of the methanogenic sludge were prepared with different carbon and electron sources: pyruvate, lactate, H-2/CO2, ethanol and formate. Dithiothreitol (DTT) was the strong reductant in order to increase the negative redox potential in the media. A homo-acetogenic gram-positive strain could be isolated in the presence of formate. 16S rRNA of the isolated strain showed that the bacterium was closely related (99.7%) to Acetobacterium wieringae. The strain also grew on pyruvate, lactate, H-2/CO2 and ethanol, although dechlorination rates of 1,2-DCA were at least 5 times higher when formate was the (only) electron source. Average conversion rates reached 3 mumol/(h.g(dry cells)) and appeared to relate to cometabolic biocatalysis on the corrinoid centers of the homo-acetogenic strain. Some perspectives of anaerobic in situ bioremediation of groundwater polluted with chloroethanes are presented.
引用
收藏
页码:43 / 48
页数:6
相关论文
共 15 条
[1]   ABIOTIC DEHALOGENATION OF 1,2-DICHLOROETHANE AND 1,2-DIBROMOETHANE IN AQUEOUS-SOLUTION CONTAINING HYDROGEN-SULFIDE [J].
BARBASH, JE ;
REINHARD, M .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1989, 23 (11) :1349-1358
[2]   HIGH-RATE CONTINUOUS BIODEGRADATION OF CONCENTRATED CHLORINATED ALIPHATICS BY A DURABLE ENRICHMENT OF METHANOGENIC ORIGIN UNDER CARRIER-DEPENDENT CONDITIONS [J].
BOUCQUEY, JB ;
RENARD, P ;
AMERLYNCK, P ;
MODESTO, P ;
AGATHOS, SN ;
NAVEAU, H ;
NYNS, EJ .
BIOTECHNOLOGY AND BIOENGINEERING, 1995, 47 (03) :298-307
[3]   TRANSFORMATIONS OF 1-CARBON AND 2-CARBON HALOGENATED ALIPHATIC ORGANIC-COMPOUNDS UNDER METHANOGENIC CONDITIONS [J].
BOUWER, EJ ;
MCCARTY, PL .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1983, 45 (04) :1286-1294
[4]  
BRAUN M, 1982, ZBL BAKT MIK HYG I C, V3, P368
[5]  
CALAHAN MA, 1979, PUBLICATION US EPA
[6]   Transformations of 1,1,2,2-tetrachloroethane under methanogenic conditions [J].
Chen, C ;
Puhakka, JA ;
Ferguson, JF .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1996, 30 (02) :542-547
[7]   METABOLISM OF HOMOACETOGENS [J].
DIEKERT, G ;
WOHLFARTH, G .
ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY, 1994, 66 (1-3) :209-221
[8]   REDUCTIVE DECHLORINATION CATALYZED BY BACTERIAL TRANSITION-METAL COENZYMES [J].
GANTZER, CJ ;
WACKETT, LP .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1991, 25 (04) :715-722
[9]   Corrinoid-mediated reduction of tetrachloroethene, trichloroethene, and trichlorofluoroethene in homogeneous aqueous solution: Reaction kinetics and reaction mechanisms [J].
Glod, G ;
Angst, W ;
Holliger, C ;
Schwarzenbach, RP .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1997, 31 (01) :253-260
[10]   Reductive dehalogenation of trichloroethylene using zero-valent iron [J].
Gotpagar, J ;
Grulke, E ;
Tsang, T ;
Bhattacharyya, D .
ENVIRONMENTAL PROGRESS, 1997, 16 (02) :137-143