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Multiple Reductive-Dehalogenase-Homologous Genes Are Simultaneously Transcribed during Dechlorination by Dehalococcoides-Containing Cultures

机译:含Dehaloccocoides的培养物在脱氯过程中同时转录多个还原-脱卤素酶同源基因。

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摘要

Degenerate primers were used to amplify 14 distinct reductive-dehalogenase-homologous (RDH) genes from the Dehalococcoides-containing mixed culture KB1. Most of the corresponding predicted proteins were highly similar (97 to >99% amino acid identity) to previously reported Dehalococcoides reductive dehalogenases. To examine the differential transcription of these RDH genes, KB1 was split into five subcultures amended with either trichloroethene, cis-1,2-dichloroethene, vinyl chloride, 1,2-dichlorethane, or no chlorinated electron acceptor. Total RNA was extracted following the onset of reductive dechlorination, and RDH transcripts were reverse transcribed and amplified using degenerate primers. The results indicate that the transcription of RDH genes requires the presence of a chlorinated electron acceptor, and for all treatments, multiple RDH genes were simultaneously transcribed, with transcripts of two of the genes being present under all four electron-accepting conditions. Two of the transcribed sequences were highly similar to reported vinyl chloride reductase genes, namely, vcrA from Dehalococcoides sp. strain VS and bvcA from Dehalococcoides sp. strain BAV1. These findings suggest that multiple RDH genes are induced by a single chlorinated substrate and that multiple reductive dehalogenases contribute to chloroethene degradation in KB1.
机译:简并引物用于扩增来自含Dehaloccocoides的混合培养物KB1的14个不同的还原-脱卤化酶同源(RDH)基因。大多数相应的预测蛋白质与先前报道的Dehalococcoides还原性脱卤酶高度相似(97至> 99%氨基酸同一性)。为了检查这些RDH基因的差异转录,将KB1分为五个亚培养,分别用三氯乙烯,顺式1,2-二氯乙烯,氯乙烯,1,2-二氯乙烷或不使用氯化电子受体进行修饰。在还原性脱氯反应开始后提取总RNA,并使用简并引物逆转录RDH转录本并进行扩增。结果表明RDH基因的转录需要存在一个氯化的电子受体,并且对于所有处理,多个RDH基因都被同时转录,其中两个基因的转录本在所有四个电子接受条件下均存在。转录的两个序列与报道的氯乙烯还原酶基因高度相似,即来自Dehalococcoides的vcrA。 Dehalococcoides菌株VS和bvcA菌株。 BAV1株。这些发现表明,一个单一的氯化底物可以诱导多个RDH基因,并且多个还原性脱卤酶会导致KB1中的氯乙烯降解。

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