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Complete Nucleotide Sequence of an Exogenously Isolated Plasmid, pLB1, Involved in γ-Hexachlorocyclohexane Degradation

机译:涉及γ-六氯环己烷降解的外源分离质粒pLB1的完整核苷酸序列

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The α-proteobacterial strain Sphingobium japonicum UT26 utilizes a highly chlorinated pesticide, γ-hexachlorocyclohexane (γ-HCH), as a sole source of carbon and energy, and haloalkane dehalogenase LinB catalyzes the second step of γ-HCH degradation in UT26. Functional complementation of a linB mutant of UT26, UT26DB, was performed by the exogenous plasmid isolation technique using HCH-contaminated soil, leading to our successful identification of a plasmid, pLB1, carrying the linB gene. Complete sequencing analysis of pLB1, with a size of 65,998 bp, revealed that it carries (i) 50 totally annotated coding sequences, (ii) an IS6100 composite transposon containing two copies of linB, and (iii) potential genes for replication, maintenance, and conjugative transfer with low levels of similarity to other homologues. A minireplicon assay demonstrated that a 2-kb region containing the predicted repA gene and its upstream region of pLB1 functions as an autonomously replicating unit in UT26. Furthermore, pLB1 was conjugally transferred from UT26DB to other α-proteobacterial strains but not to any of the β- or γ-proteobacterial strains examined to date. These results suggest that this exogenously isolated novel plasmid contributes to the dissemination of at least some genes for γ-HCH degradation in the natural environment. To the best of our knowledge, this is the first detailed report of a plasmid involved in γ-HCH degradation.
机译:α变形杆菌日本血吸虫UT26利用高度氯化的农药γ-六氯环己烷(γ-HCH)作为碳和能量的唯一来源,卤代烷脱卤酶LinB催化了UT26中γ-HCH降解的第二步。 UT26的linB突变体UT26DB的功能互补是通过使用HCH污染的土壤通过外源质粒分离技术完成的,从而成功鉴定了携带linB基因的质粒pLB1。对pLB1的完整测序分析(大小为65,998 bp)显示,它带有(i)50个完全注释的编码序列,(ii)包含两个linB拷贝的IS6100复合转座子,以及(iii)复制,维持,与其他同源物相似程度较低的共轭转移。微型复制子测定法证明,包含预测的repA基因的2 KB区域及其pLB1的上游区域在UT26中充当自主复制单位。此外,pLB1从UT26DB共轭转移到其他α-细菌菌株,但没有转移到迄今检查的任何β-或γ-细菌菌株。这些结果表明,该外源分离的新质粒有助于在自然环境中传播至少一些用于γ-HCH降解的基因。据我们所知,这是涉及γ-六氯环己烷降解的质粒的第一个详细报告。

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