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首页> 外文期刊>Journal of bacteriology >Identification and Characterization of IS1411, a New Insertion Sequence Which Causes Transcriptional Activation of the Phenol Degradation Genes inPseudomonas putida
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Identification and Characterization of IS1411, a New Insertion Sequence Which Causes Transcriptional Activation of the Phenol Degradation Genes inPseudomonas putida

机译:IS1411的鉴定和表征,IS1411是一种新的插入序列,可导致恶臭假单胞菌中苯酚降解基因的转录激活。

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A new insertion sequence (IS element), IS1411, was identified downstream of the phenol degradation genes pheBAthat originated from plasmid DNA of Pseudomonas sp. strain EST1001. According to sequence analysis, IS1411 belongs to a new family of IS elements that has recently been named the ISL3 family (J. Mahillon and M. Chandler, Microbiol. Mol. Biol. Rev. 62:725–774, 1998). IS1411 generates 8-bp duplication of the target DNA and carries 24-bp inverted repeats (IRs), highly homologous to the IRs of other IS elements belonging to this family. IS1411 was discovered as a result of insertional activation of promoterless pheBA genes in Pseudomonas putida due to the presence of outward-directed promoters at the left end of IS1411. Both promoters located on the IS element have sequences that are similar to the consensus sequence ofEscherichia coli ?70. IS1411 can produce IS circles, and the circle formation is enhanced when two copies of the element are present in the same plasmid.
机译:在来自假单胞菌 sp质粒DNA的酚降解基因 pheBA 的下游鉴定了一个新的插入序列(IS元件)IS 1411 。 。菌株EST1001。根据序列分析,IS 1411 属于一个新的IS元素家族,该家族最近被称为ISL 3 家族(J. Mahillon和M. Chandler,Microbiol。Mol (《生物化学评论》 62:725-774,1998)。 IS 1411 产生目标DNA的8 bp复制,并带有24 bp的反向重复序列(IR),与该家族其他IS元件的IR高度同源。 IS 1411 被发现是由于在左侧的 Pseudomonas putida 中无启动子的 pheBA 基因的插入激活导致的,这是因为左侧存在向外定向的启动子IS 1411 的结尾。位于IS元件上的两个启动子具有与大肠杆菌? 70 的共有序列相似的序列。 IS 1411 可以产生IS环,并且当同一质粒中存在两个元素的拷贝时,环的形成就会增强。

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