Bardiya Nirmala, Bae Jae-Ho
Department of Civil and Environmental Engineering and Geosystem Engineering, Inha University, 253 Yonghyun-Dong, Nam-Gu, Inchon 402-751, South Korea.
Chemosphere. 2005 Jan;58(1):83-90. doi: 10.1016/j.chemosphere.2004.09.001.
The purpose of this work was to explore the reductive bioremediation potential of a perchlorate-enriched facultative anaerobic consortium. Rapid perchlorate reduction and bacterial growth were observed up to 1.84 g l(-1) of perchlorate, but not at 3.82 g l(-1) due to the toxicity. The specific growth rate of the mixed consortium was 0.1 h(-1). The consortium co-reduced perchlorate and nitrate with acetate as e- donor and carbon source. The presence of nitrate slowed down the perchlorate reduction rate. The other e- acceptors utilized include oxygen, chlorate, Cr(VI), and selenate. Over 95% of the 16 mg l(-1) of added Cr(VI) was reduced within 24 h of incubation with a high-density perchlorate-grown consortium. However, the consortium failed to couple growth with reduction of nitrite, sulfate, thiosulfate, and sulfite. During the search for autotrophic perchlorate reduction, many consortia from very diverse natural sources could not use sulfur compounds such as thiosulfate as e- donor.
本研究旨在探索富含高氯酸盐的兼性厌氧菌群的还原生物修复潜力。观察到在高氯酸盐浓度高达1.84 g l(-1)时,高氯酸盐能快速还原且细菌能生长,但在3.82 g l(-1)时由于毒性作用则不然。混合菌群的比生长速率为0.1 h(-1)。该菌群以乙酸盐作为电子供体和碳源,共同还原高氯酸盐和硝酸盐。硝酸盐的存在减缓了高氯酸盐的还原速率。利用的其他电子受体包括氧气、氯酸盐、Cr(VI)和硒酸盐。在与高密度高氯酸盐生长菌群孵育24小时内,添加的16 mg l(-1) Cr(VI)中有超过95%被还原。然而,该菌群未能将生长与亚硝酸盐、硫酸盐、硫代硫酸盐和亚硫酸盐的还原相耦合。在寻找自养型高氯酸盐还原过程中,许多来自非常不同自然来源的菌群无法使用硫代硫酸盐等硫化合物作为电子供体。