首页> 外文期刊>Environmental microbiology >Isolation and characterization of Tn-Dha1, a transposon containing the tetrachloroethene reductive dehalogenase of Desulfitobacterium hafniense strain TCE1
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Isolation and characterization of Tn-Dha1, a transposon containing the tetrachloroethene reductive dehalogenase of Desulfitobacterium hafniense strain TCE1

机译:Tn-Dha1的分离和鉴定,转座子含有哈弗脱硫杆菌TCE1的四氯乙烯还原性脱卤素酶

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摘要

A new 9.9 kb catabolic transposon, Tn-Dha1, containing the gene responsible for tetrachloroethene (PCE) reductive dechlorination activity, was isolated from Desulfitobacterium hafniense strain TCE1. Two fully identical copies of the insertion sequence ISDha1, a new member of the IS256 family, surround the gene cluster pceABCT, a truncated gene for another transposase and a short open reading frame with homology to a member of the twin-arginine transport system (tatA). Evidence was obtained by Southern blot for an alternative form of the transposon element as a circular molecule containing only one copy of ISDha1. This latter structure most probably represents a dead-end product of the transposition of Tn-Dha1. Strong indications for the transposition activity of ISDha1 were given by polymerase chain reaction (PCR) amplification and sequencing of the intervening sequence located between both inverted repeats (IR) of ISDha1 (IR junction). A stable genomic ISDha1 tandem was excluded by quantitative real-time PCR. Promoter mapping of the pceA gene, encoding the reductive dehalogenase, revealed the presence of a strong promoter partially encoded in the right inverted repeat of ISDha1. A sequence comparison with pce gene clusters from Desulfitobacterium sp. strains PCE-S and Y51 and from Dehalobacter restrictus, all of which show 100% identity for the pceAB genes, indicated that both Desulfitobacterium strains seem to possess the same transposon structure, whereas only the pceABCT gene cluster is conserved in D. restrictus.
机译:一个新的9.9 kb分解代谢转座子,Tn-Dha1,包含负责四氯乙烯(PCE)还原性脱氯活性的基因,从哈弗脱硫杆菌TCE1中分离出来。插入序列ISDha1的两个完全相同的副本(IS256家族的一个新成员)围绕着基因簇pceABCT,另一个转座酶的截短基因以及与双精氨酸转运系统(tatA)同源的短开放阅读框)。通过DNA印迹获得的证据表明,转座子元件的另一种形式是仅包含一个ISDha1拷贝的环状分子。后一种结构很可能代表了Tn-Dha1转座的最终产物。通过聚合酶链反应(PCR)扩增和对位于ISDha1的两个反向重复序列(IR)之间的插入序列(IR连接)进行测序,可以强烈指示ISDha1的转座活性。定量实时PCR排除了稳定的基因组ISDha1串联。 pceA基因的启动子作图,编码还原性脱卤素酶,揭示了在ISDha1的右反向重复序列中部分编码的强启动子的存在。与来自Desulfitobacterium sp。的pce基因簇的序列比较。 PCE-S和Y51菌株以及限制性嗜盐杆菌均与pceAB基因表现出100%的同一性,表明这两个脱硫杆菌菌株似乎都具有相同的转座子结构,而在限制性嗜血杆菌中只有pceABCT基因簇是保守的。

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