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首页> 外文期刊>Radiation Research: Official Organ of the Radiation Research Society >Effects of XeClUV308 (nm) laser radiation on survival and mutability of recA-proficient and recA-defective Escherichia coli strains
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Effects of XeClUV308 (nm) laser radiation on survival and mutability of recA-proficient and recA-defective Escherichia coli strains

机译:XeClUV308(nm)激光辐射对recA高效和recA缺陷型大肠杆菌菌株的存活和变异性的影响

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摘要

recA1, recA13 and recA56 are considered null alleles of the Escherichia coli recA gene because they were shown to have essentially no activity in vivo. In this study, we used strains harboring the recA null alleles and their recA-proficient congenic counterpart to assess the lethal and the mutagenic effects elicited by near-UV308nm coherent radiation generated by a XeCl excimer laser. We compared these effects with those produced by a conventional far-UV254nm germicidal lamp. Compared to the germicidal lamp, the excimer laser was able to better discriminate the different recA-defective strains on the basis of their UV-radiation sensitivity, which was progressively higher in the strains with the alleles in the order recA1, recA56 and recA13. This finding was consistent with previous data on residual biochemical activities of the respective mutated RecA proteins in vitro. The discrepancy between the results obtained with the lamp and laser irradiation suggested that the biological response to the two radiations involves distinct mechanisms. This hypothesis was supported by the evidence that exposure to near-UV308nm radiation induced mutagenesis in recA-defective strains at an extent considerably greater than in recA-proficient strains. In contrast, far-UV254nm-radiation-induced mutagenesis was reported to be largely dependent on a functional recA allele. (c) 2006 by Radiation Research Society.
机译:recA1,recA13和recA56被认为是大肠杆菌recA基因的无效等位基因,因为它们在体内基本上没有活性。在这项研究中,我们使用了带有recA无效等位基因及其recA熟练的同基因对应物的菌株,以评估XeCl准分子激光产生的近UV308nm相干辐射引起的致死和诱变效应。我们将这些效果与传统的远紫外线254nm杀菌灯产生的效果进行了比较。与杀菌灯相比,准分子激光能够根据其紫外线辐射敏感性更好地区分不同的recA缺陷菌株,在等位基因的菌株中,recA1,recA56和recA13的顺序逐渐提高。这一发现与先前关于体外各个突变的RecA蛋白的残留生化活性的先前数据一致。灯和激光照射的结果之间的差异表明,对两种辐射的生物学反应涉及不同的机制。该假设得到以下证据的支持:在recA缺陷菌株中暴露于近UV308nm辐射会引起诱变,其程度远大于在recA熟练菌株中。相反,据报道,远紫外线254nm辐射诱导的诱变很大程度上取决于功能性recA等位基因。 (c)辐射研究学会,2006年。

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