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朱涛, 欧阳荟, 金士威, 徐盈, 宋碧玉, 徐旭东. Janibacter sp.对活性污泥反应器中二苯并呋喃降解的强化作用及其遗传学分析[J]. 水生生物学报, 2007, 31(4): 499-502.
引用本文: 朱涛, 欧阳荟, 金士威, 徐盈, 宋碧玉, 徐旭东. Janibacter sp.对活性污泥反应器中二苯并呋喃降解的强化作用及其遗传学分析[J]. 水生生物学报, 2007, 31(4): 499-502.
ZHU Tao, OUYANG Hui, JIN Shi-Wei, XU Ying, SONG Bi-Yu, XU Xu-Dong. ENHANCEMENT OF DIBENZOFURAN DEGRADATION BY JANIBACTER SP. IN AN ACTIVATED SLUDGE REACTOR AND GENETIC ANALYSES OF THE DEGRADING CAPABILITY[J]. ACTA HYDROBIOLOGICA SINICA, 2007, 31(4): 499-502.
Citation: ZHU Tao, OUYANG Hui, JIN Shi-Wei, XU Ying, SONG Bi-Yu, XU Xu-Dong. ENHANCEMENT OF DIBENZOFURAN DEGRADATION BY JANIBACTER SP. IN AN ACTIVATED SLUDGE REACTOR AND GENETIC ANALYSES OF THE DEGRADING CAPABILITY[J]. ACTA HYDROBIOLOGICA SINICA, 2007, 31(4): 499-502.

Janibacter sp.对活性污泥反应器中二苯并呋喃降解的强化作用及其遗传学分析

ENHANCEMENT OF DIBENZOFURAN DEGRADATION BY JANIBACTER SP. IN AN ACTIVATED SLUDGE REACTOR AND GENETIC ANALYSES OF THE DEGRADING CAPABILITY

  • 摘要: 二苯并呋喃(DF)是研究二英类化合物生物降解的模式化合物之一。本文报道了一种降解菌Janibacter sp.对活性污泥降解二苯并呋喃的强化作用,以及对其降解基因的分析结果。向反应器中添加5%的降解菌,与活性污泥共同作用,可在48h内将约56mg/L剂量的DF几乎完全降解,提高降解率28%以上。利用PCR方法,克隆和测序分析证明有DF降解基因丛的存在,并且发现以丰富培养基在高温下培养可去除该基因丛;丢失该基因丛的突变株同时失去利用DF作为唯一碳源进行生长的能力,显示其很可能位于一个大质粒上。

     

    Abstract: Dibenzofuran (DF) is one of the model compounds for the study of biodegradation of dioxin-like pollutants. This paper presents studies of the enhancing effect of a Janibacter strain on the degradation of DF by activated sludge and analyses of its DF-degrading genes. When 1% or 5 % Janibacter cells were added to the activated sludge reactor, DF of 56 mg/L was almost completely degraded after d8h or 24h, while in the control reactor, 38 % of the DF remained after 48h. A stretch of 4018-bp DNA region containing dfdA1A2A3A4 cluster was cloned with PCR and sequenced and found to be almost identical to that from Janibacter strain YK3, except 5 sbustitutions. To test whether the dfdA cluster is located on a large plasmid, we examined 27 single colonies grown on rich medium plates at 37℃ with PCR and found all tested colonies lost the dfdA cluster at high temperature. This result indicated that the gene cluster was readily cured from the cells, hence it must be located on an extra-chromosomal genetic element. Mutants abolished of the gene cluster were unable to grow in medium with DF as the sole carbon source. The implications of these results to the application of DF-degrading strains in activated sludge reactors are discussed.

     

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