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Solvent Tolerance Mechanisms in Shewanella putrefaciens IBBPo6

机译:腐烂希瓦氏菌IBBPo6的耐溶剂性机理

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Shewanella putrefaciens IBBPo6 (KM405339) showed good tolerance to 5 % organic solvents. The growth was higher when S. putrefaciens IBBPo6 cells were exposed to n-decane, as compared with the growth of cells exposed to toluene, o-xylene, ethylbenzene, cyclohexane, or n-hexane. Thus, n-decane was less toxic for S. putrefaciens IBBPo6 cells, while toluene, o-xylene, ethylbenzene, cyclohexane, and n-hexane were more toxic for this bacterium. The release of nucleic acids was higher when S. putrefaciens IBBPo6 cells were exposed to toluene, o-xylene, ethylbenzene, cyclohexane, or n-hexane, as compared with the release of nucleic acids from control cells and n-decane exposed cells. The cell surface hydrophobicity increased when S. putrefaciens IBBPo6 cells were exposed to n-decane, while in the presence of toluene, o-xylene, ethylbenzene, cyclohexane, and n-hexane, a decrease in the cell surface hydrophobicity was acquired. The exposure of S. putrefaciens IBBPo6 cells to 5 % organic solvents had induced biofilms formation, and their structure differs according to the nature of the hydrophobic substrate. Two secondary metabolites (i.e., biosurfactants, carotenoids) were produced by S. putrefaciens IBBPo6 control cells, as well as by the cells exposed to 5 % organic solvents. S. putrefaciens IBBPo6 possesses alkB1 and alkM1 catabolic genes and HAE1 transporter gene. A homologue of otsA1 gene was also detected in this bacterium. Some differences between the polymerase chain reaction (PCR) patterns of S. putrefaciens IBBPo6 control cells and cells exposed to 5 % organic solvents were observed. Distinct repetitive sequence-based PCR (rep-PCR), random amplification of DNA fragments (RAPD), and amplified ribosomal DNA restriction analysis (ARDRA) patterns were also acquired in S. putrefaciens IBBPo6 cells exposed to 5 % organic solvents, compared with the control cells.
机译:腐臭希瓦氏菌IBBPo6(KM405339)显示出对5%有机溶剂的良好耐受性。与暴露于甲苯,邻二甲苯,乙苯,环己烷或正己烷的细胞相比,腐烂链球菌IBBPo6细胞暴露于正癸烷的生长更高。因此,正癸烷对腐烂链球菌IBBBo6细胞的毒性较小,而甲苯,邻二甲苯,乙苯,环己烷和正己烷对这种细菌的毒性更大。与从对照细胞和正癸烷暴露的细胞中释放出的核酸相比,腐烂链球菌IBBBo6细胞暴露于甲苯,邻二甲苯,乙苯,环己烷或正己烷时,核酸的释放更高。当腐乳链霉菌IBBPo6细胞暴露于正癸烷时,细胞表面疏水性增加,而在甲苯,邻二甲苯,乙苯,环己烷和正己烷的存在下,细胞表面疏水性得到降低。腐链霉菌IBBPo6细胞暴露于5%的有机溶剂中会诱导生物膜形成,并且其结构会根据疏水性底物的性质而有所不同。腐烂链球菌IBBBo6对照细胞以及暴露于5%有机溶剂的细胞会产生两种次级代谢产物(即生物表面活性剂,类胡萝卜素)。腐烂链球菌IBBBo6具有alkB1和alkM1分解代谢基因以及HAE1转运蛋白基因。在该细菌中也检测到otsA1基因的同源物。观察到腐烂链球菌IBBBo6对照细胞与暴露于5%有机溶剂的细胞的聚合酶链反应(PCR)模式之间存在一些差异。与暴露于5%有机溶剂的腐烂链球菌IBBPo6细胞相比,还获得了基于重复序列的独特PCR(rep-PCR),DNA片段随机扩增(RAPD)和核糖体DNA限制性酶切分析(ARDRA)模式。控制细胞。

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