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. 2015 Oct 1;6(19):3911-4.
doi: 10.1021/acs.jpclett.5b01585. Epub 2015 Sep 17.

Electron Resonance Decay into a Biological Function: Decrease in Viability of E. coli Transformed by Plasmid DNA Irradiated with 0.5-18 eV Electrons

Affiliations

Electron Resonance Decay into a Biological Function: Decrease in Viability of E. coli Transformed by Plasmid DNA Irradiated with 0.5-18 eV Electrons

S Kouass Sahbani et al. J Phys Chem Lett. .

Abstract

Transient negative ions (TNIs) are ubiquitous in electron-molecule scattering at low electron impact energies (0-20 eV) and are particularly effective in damaging large biomolecules. Because ionizing radiation generates mostly 0-20 eV electrons, TNIs are expected to play important roles in cell mutagenesis and death during radiotherapeutic cancer treatment, although this hypothesis has never been directly verified. Here, we measure the efficiency of transforming E. coli bacteria by inserting into the cells, pGEM-3ZfL(-) plasmid DNA that confers resistance to the antibiotic ampicillin. Before transformation, plasmids are irradiated with electrons of specific energies between 0.5 and 18 eV. The loss of transformation efficiency plotted as a function of irradiation energy reveals TNIs at 5.5 and 9.5 eV, corresponding to similar states observed in the yields of DNA double strand breaks. We show that TNIs are detectable in the electron-energy dependence of a biological process and can decrease cell viability.

Keywords: DNA; cell transformation efficiency; low-energy electrons; radiation damage; transient anions.

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Conflict of interest statement

The authors declare no competing financial interest.

Figures

Figure 1
Figure 1
Variation of transformation efficiency of JM109 E. coli cells by pGEM 3Zf(−) plasmids, with incident electron fluence at 10 eV. The data is taken from ref . Each point is the average of three identical measurements. At each fluence, the error bars represent the standard deviation. The solid line is a fit to the data using the parametric model described in ref .
Figure 2
Figure 2
(a) Variation of transformation efficiency of JM109 E. coli cells by pGEM 3Zf(−) plasmids irradiated by 0.5 to 18 eV electrons at a fluence of 27 × 1013 electrons/cm2. The y axis is inverted. Effective yield functions for (b) single strand breaks (SSBs), (c) double strand breaks (DSBs) and (d) DNA cross-links, from ref .

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