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. 2017 Aug 16;7:8325. doi: 10.1038/s41598-017-08449-1

Figure 3.

Figure 3

Measurement of oxidative stress experienced by bacteria by the select treatments. (a) Detection of reactive oxidative species (ROS) within E. coli O157:H7 using CellROX® Reagent Green upon treatment by GA (15 mM), PG (10 mM), HCl (pH 3.1), water, or hydrogen peroxide (HP, 1.5%), in the absence or presence of UV-A light for 30 or 5 min. Absolute fluorescence values were corrected by subtracting the fluorescence values for samples incubated in water and in dark. *Indicates that corrected fluorescence value was zero. (b) Fluorescent microscopy images (×100) of bacteria incubated with CellROX® Reagent Green and (1) 15 mM GA + UV-A, (2) 15 mM GA in dark, (3) HCl (pH = 3.1) + UV-A, (4) HCl (pH = 3.1) in dark, (5) DI water in dark. (c) Average maximum fluorescence intensity within the bacteria imaged using fluorescence microscopy. (d) Measurement of free thiols content from E. coli O157:H7 suspensions treated by GA (15 mM), PG (10 mM), HCl (pH 3.1), or water, with the presence or absence of UV-A light for 30 or 5 min. Hydrogen peroxide (HP, 1.5%), was used as a positive control. (e) Logarithmic reduction of E. coli O157:H7 by 15 mM GA + UV-A light, with or without 5% DMSO. Mean ± SD.