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首页> 外文期刊>Microbes and Environments >Phylogenetic and Transcriptional Analyses of a Tetrachloroethene- Dechlorinating 'Dehalococcoides' Enrichment Culture TUT2264 and Its Reductive-Dehalogenase Genes
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Phylogenetic and Transcriptional Analyses of a Tetrachloroethene- Dechlorinating 'Dehalococcoides' Enrichment Culture TUT2264 and Its Reductive-Dehalogenase Genes

机译:四氯乙烯脱氯“ Dehalococcoides”富集培养TUT2264及其还原性脱卤酶基因的系统发生和转录分析。

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A dechlorinating microbial enrichment culture designated TUT2264 was cultured with tetrachloroethene and then characterized for tetrachloroethene- dechlorination by culture-dependent and -independent methods. The fourth- transferred TUT2264 culture completely dechlorinated tetrachloroethene and trichloroethene, and accumulated more trans-1,2-dichloroethene than cis-1,2- dichloroethene. A real-time PCR analysis revealed that "Dehalococcoides" cells made up only 0.3% of the total. Eight distinct reductive-dehalogenase- homologous genes (rdh) were detected with degenerate primers. Phylogenetic analyses revealed 5 of the 8 RdhAs to be very similar to RdhAs reported previously but not to share 100% identity. Transcriptional levels were quantified as the number of transcripts per rdhA by combining the reverse transcription real-time PCR and exogenous internal reference mRNA methods. TUT2264 responded to all the chloroethenes tested. rdhA4 was transcribed with all chloroethenes except vinyl chloride, whereas rdhA8 was only transcribed on tetrachloroethene. Furthermore, multiple rdhAs were induced to express by a single chloroethene as a growth-supporting or non-supporting substrate. These results suggested that Rdhs are multi-functional and rdhAs are a powerful tool to evaluate the potential of contaminated sites and isolates to dechlorinate chloroethenes.
机译:将脱氯微生物富集培养物(称为TUT2264)与四氯乙烯一起培养,然后通过依赖于培养物和不依赖于培养物的方法对四氯乙烯进行脱氯处理进行表征。第四次转移的TUT2264培养物将四氯乙烯和三氯乙烯完全脱氯,并且比顺式1,2-二氯乙烯积累更多的反式1,2-二氯乙烯。实时PCR分析显示“脱卤球菌”细胞仅占总数的0.3%。用简并引物检测到八个不同的还原-脱卤素酶同源基因(rdh)。系统发育分析表明,在8个RdhA中,有5个与以前报道的RdhA非常相似,但没有100%的同一性。通过结合逆转录实时荧光定量PCR和外源内部参考mRNA方法,将转录水平量化为每rdhA的转录数量。 TUT2264响应了所有测试的氯乙烯。 rdhA4与除氯乙烯外的所有氯乙烯一起转录,而rdhA8仅在四氯乙烯上转录。此外,多种rdhA被单个氯乙烯诱导表达为生长支持或非支持底物。这些结果表明,Rdhs具有多功能性,rdhA是评估污染位点和分离物对氯乙烯进行脱氯的潜力的强大工具。

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