Nishimura Minoru, Ebisawa Maiko, Sakihara Sakari, Kobayashi Ai, Nakama Tetsushi, Okochi Mina, Yohda Masafumi
Department of Biotechnology and Life Science, Tokyo University of Agriculture and Technology, 2-24-16, Naka-cho, Koganei, Tokyo 184-8588, Japan.
Biotechnol Appl Biochem. 2008 Sep;51(Pt 1):1-7. doi: 10.1042/BA20070171.
Previous studies have shown that Dehalococcoides species are responsible for the anaerobic bioremediation of chloroethene pollution. It has been thought that co-operation of several species is required for complete dechlorination to ethene. In the present study, we used quantitative PCR of 16 S rRNA and RDase (reductive dehalogenase) genes to examine species changes and the population of Dehalococcoides species in ground water in which the dechlorination of TCE (trichloroethene) to ethene was enhanced by delivery of hydrogen-releasing compounds. The results have shown that at least two different Dehalococcoides species co-operate in the dechlorination of TCE to ethene. Initially, the number of strains equipped with TCE RDase increased approx. 10(5)-fold. This was followed by a decrease to the original level, according to the exhaustion of TCE. Subsequently, another strain appeared, which had a VC (vinyl chloride) RDase gene similar to bvcA of Dehalococcoides sp. BAV1 and is probably responsible for the dechlorination of VC to ethene. Analysis of several genes has suggested that the former strain is like Dehalococcoides sp. FMC-TCE, and the latter strain is similar to the Dehalococcoides sp. strain that exists in the Dehalococcoides-containing mixed culture KB1. These results support the notion that monitoring Dehalococcoides species by the presence of RDase genes as genetic markers provides detailed information on the progress of bioremediation of chloroethenes, which will be useful to improve the efficiency of bioremediation.
以往的研究表明,脱卤球菌属物种负责氯乙烯污染的厌氧生物修复。人们一直认为,完全脱氯生成乙烯需要几种物种的协同作用。在本研究中,我们使用16S rRNA和RDase(还原脱卤酶)基因的定量PCR来检测通过添加释氢化合物增强三氯乙烯(TCE)向乙烯脱氯的地下水中脱卤球菌属物种的变化和数量。结果表明,至少有两种不同的脱卤球菌属物种协同参与TCE向乙烯的脱氯过程。最初,配备TCE RDase的菌株数量增加了约10^5倍。随后,随着TCE的耗尽,数量降至原始水平。随后,出现了另一种菌株,其具有与脱卤球菌属BAV1的bvcA相似的氯乙烯(VC)RDase基因,可能负责将VC脱氯生成乙烯。对几个基因的分析表明,前一种菌株类似于脱卤球菌属FMC-TCE,后一种菌株类似于存在于含脱卤球菌属混合培养物KB1中的脱卤球菌属菌株。这些结果支持了这样一种观点,即通过将RDase基因作为遗传标记来监测脱卤球菌属物种,可以提供有关氯乙烯生物修复进展的详细信息,这将有助于提高生物修复的效率。