首页> 外文期刊>Plasmid: An International Journal Devoted to Extrachromosomal Gene Systems >Identification of the plasmid-mobilization potential of the strain Klebsiella pneumoniae ozenae KIIIA isolated from a polluted aquatic environment.
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Identification of the plasmid-mobilization potential of the strain Klebsiella pneumoniae ozenae KIIIA isolated from a polluted aquatic environment.

机译:从污染的水生环境中分离出的肺炎克雷伯菌肺炎克雷伯菌KIIIA的质粒动员潜力的鉴定。

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The Klebsiella pneumoniae ozenae KIIIA strain was isolated from the River Rhine soon after a serious mercury pollution episode and was selected for mercury resistance as well as for intergeneric DNA mobilization helper potential. This transfer helper capacity was shown to be related to the presence of a Tn3-like transposable element, Tn5403. Because transposon-mediated fusion was found to be involved in the mobilization potential of KIIIA, the visualization and the identification of the conjugative element, responsible for the transfer, were necessary. Our results show that, in addition to the four nonconjugative plasmids visualized in a previous study, K. pneumoniae ozenae KIIIA harbors two other plasmids, pK130 and pK45, of respective sizes of 130 and 45 kb, but none of these plasmids is involved in the mobilization mechanism. The presence of yet another extrachromosomal element pK225, with a size of 225 kb, was established by indirect methods, since yields of pK225 isolated from KIIIA were low and the plasmid was difficult to visualize directly. However, the integration of this plasmid into the chromosome was not detected. The present paper highlights the problem of detecting some plasmids in bacteria which have been isolated from the environment. For these plasmids, indirect approaches, that detect conjugative functions, constitute a feasible alternative for the investigation of the plasmid content of bacteria, if the direct approach fails. An analysis of the different types of transconjugants indicated that the mercury-resistance marker as well as the mobilization potentials, expressed by KIIIA, are linked to pK225. This plasmid could not be assigned to a described Inc group either by DNA hybridization or by PCR amplification. Copyright 1999 Academic Press.
机译:严重的汞污染事件发生后不久,从莱茵河中分离出肺炎克雷伯氏菌(Klebsiella ozenae ozenae)KIIIA菌株,并被选作耐汞性和跨基因DNA动员的辅助剂。已表明这种转移辅助能力与Tn3样转座因子Tn5403的存在有关。由于发现转座子介导的融合与KIIIA的动员潜力有关,因此有必要对负责转移的结合元件进行可视化和鉴定。我们的结果表明,除了先前研究中显示的四个非结合质粒外,肺炎克雷伯氏菌KIIIA还包含另外两个质粒pK130和pK45,分别大小分别为130和45 kb,但这些质粒均不参与动员机制。通过间接方法建立了另一种大小为225 kb的染色体外元件pK225的存在,因为从KIIIA分离出的pK225的产量很低,并且质粒很难直接可视化。但是,未检测到该质粒整合入染色体。本论文着重指出了从环境中分离出细菌中检测某些质粒的问题。对于这些质粒,如果直接方法失败,则检测缀合功能的间接方法将构成研究细菌质粒含量的可行替代方法。对不同类型的共轭结合物的分析表明,由KIIIA表达的耐汞标记以及迁移潜力与pK225相关。不能通过DNA杂交或PCR扩增将该质粒分配给所述的Inc组。版权所有1999 Academic Press。

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