首页> 美国卫生研究院文献>DNA Research: An International Journal for Rapid Publication of Reports on Genes and Genomes >Comparison of the complete genome sequences of four γ-hexachlorocyclohexane-degrading bacterial strains: insights into the evolution of bacteria able to degrade a recalcitrant man-made pesticide
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Comparison of the complete genome sequences of four γ-hexachlorocyclohexane-degrading bacterial strains: insights into the evolution of bacteria able to degrade a recalcitrant man-made pesticide

机译:比较四种降解γ-六氯环己烷的细菌菌株的完整基因组序列:深入了解能够降解难降解的人造农药的细菌的进化

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摘要

γ-Hexachlorocyclohexane (γ-HCH) is a recalcitrant man-made chlorinated pesticide. Here, the complete genome sequences of four γ-HCH-degrading sphingomonad strains, which are most unlikely to have been derived from one ancestral γ-HCH degrader, were compared. Together with several experimental data, we showed that (i) all the four strains carry almost identical linA to linE genes for the conversion of γ-HCH to maleylacetate (designated “specific” lin genes), (ii) considerably different genes are used for the metabolism of maleylacetate in one of the four strains, and (iii) the linKLMN genes for the putative ABC transporter necessary for γ-HCH utilization exhibit structural divergence, which reflects the phylogenetic relationship of their hosts. Replicon organization and location of the lin genes in the four genomes are significantly different with one another, and that most of the specific lin genes are located on multiple sphingomonad-unique plasmids. Copies of IS6100, the most abundant insertion sequence in the four strains, are often located in close proximity to the specific lin genes. Analysis of the footprints of target duplication upon IS6100 transposition and the experimental detection of IS6100 transposition strongly suggested that the IS6100 transposition has caused dynamic genome rearrangements and the diversification of lin-flanking regions in the four strains.
机译:γ-六氯环己烷(γ-HCH)是顽固的人造氯化农药。在这里,比较了四种降解γ-HCH的鞘氨醇单胞菌菌株的完整基因组序列,这些菌株最不可能来自一个祖先的γ-HCH降解体。连同一些实验数据,我们表明(i)所有四个菌株均携带几乎相同的linA至linE基因,以将γ-HCH转化为顺丁烯二乙酸酯(指定为“特定” lin基因),(ii)使用了截然不同的基因四个菌株之一中的马来乙酸乙酸酯的代谢,以及(iii)γ-六氯环己烷利用所必需的推定ABC转运蛋白的linKLMN基因表现出结构差异,这反映了它们宿主的系统发育关系。 lin基因在四个基​​因组中的复制子组织和位置彼此之间存在显着差异,并且大多数特定的lin基因位于多个鞘磷脂独特质粒上。 IS6100的副本(这是四个菌株中最丰富的插入序列)通常紧邻特定的lin基因。对IS6100换位后靶标重复序列的足迹分析和对IS6100换位的实验检测强烈表明,IS6100换位已引起这四个菌株中的动态基因组重排和林侧翼区的多样化。

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