首页> 外文期刊>Applied and Environmental Microbiology >Characterization of the Replication, Maintenance, and Transfer Features of the IncP-7 Plasmid pCAR1, Which Carries Genes Involved in Carbazole and Dioxin Degradation
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Characterization of the Replication, Maintenance, and Transfer Features of the IncP-7 Plasmid pCAR1, Which Carries Genes Involved in Carbazole and Dioxin Degradation

机译:IncP-7质粒pCAR1的复制,维持和转移特性的表征,该质粒携带涉及咔唑和二恶英降解的基因

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Isolated from Pseudomonas resinovorans CA10, pCAR1 is a 199-kb plasmid that carries genes involved in the degradation of carbazole and dioxin. The nucleotide sequence of pCAR1 has been determined previously. In this study, we characterized pCAR1 in terms of its replication, maintenance, and conjugation. By constructing miniplasmids of pCAR1 and testing their establishment in Pseudomonas putida DS1, we show that pCAR1 replication is due to the repA gene and its upstream DNA region. The repA gene and putative oriV region could be separated in P. putida DS1, and the oriV region was determined to be located within the 345-bp region between the repA and parW genes. Incompatibility testing using the minireplicon of pCAR1 and IncP plasmids indicated that pCAR1 belongs to the IncP-7 group. Monitoring of the maintenance properties of serial miniplasmids in nonselective medium, and mutation and complementation analyses of the parWABC genes, showed that the stability of pCAR1 is attributable to the products of the parWAB genes. In mating assays, the transfer of pCAR1 from CA10 was detected in a CA10 derivative that was cured of pCAR1 (CA10dm4) and in P. putida KT2440 at frequencies of 3 × 10?1 and 3 × 10?3 per donor strain, respectively. This is the first report of the characterization of this completely sequenced IncP-7 plasmid.
机译:pCAR1是从树脂假单胞菌CA10中分离的一个199-kb质粒,带有与咔唑和二恶英降解有关的基因。先前已经确定了pCAR1的核苷酸序列。在这项研究中,我们就pCAR1的复制,维持和结合进行了表征。通过构建pCAR1的微质粒并测试其在恶臭假单胞菌DS1中的建立,我们显示pCAR1复制是由于repA基因及其上游DNA区域引起的。可以在恶臭假单胞菌DS1中分离repA基因和推定的oriV区,并确定oriV区位于repA和parW基因之间的345 bp区域内。使用pCAR1和IncP质粒的微型复制子进行的不相容性测试表明,pCAR1属于IncP-7组。监测连续小质粒在非选择性培养基中的维持特性以及对parWABC基因的突变和互补分析表明,pCAR1的稳定性可归因于parWAB基因的产物。在交配试验中,在每个供体菌株分别以3×10?1和3×10?3的频率固化了pCAR1(CA10dm4)和恶臭假单胞菌KT2440的CA10衍生物中检测到pCAR1从CA10的转移。这是对该完全测序的IncP-7质粒进行表征的第一个报告。

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