| Literature DB >> 26083904 |
Tsz Wai Ng1, Taicheng An2, Guiying Li3, Wing Kei Ho4, Ho Yin Yip1, Huijun Zhao5, Po Keung Wong6.
Abstract
Inactivation of Escherichia coli K-12 was conducted by applying a continuous supplying of commercial H2O2 to mimic the H2O2 production in a photocatalytic system, and the contribution of H2O2 in photocatalytic inactivation was investigated using a modified "partition system" and five E. coli mutants. The concentration of exogenous H2O2 required for complete inactivation of bacterial cells was much higher than that produced in-situ in common photocatalytic system, indicating that H2O2 alone plays a minor role in photocatalytic inactivation. However, the concentration of exogenously produced H2O2 required for effective inactivation of E. coli K-12 was much lower when the light irradiation was applied. To further investigate the possible physiological changes, inactivation of E. coli BW25113 (the parental strain), and its corresponding isogenic single-gene deletion mutants with light pretreatment was compared. The results indicate that light irradiation increases the bacterial intracellular Fe(2+) level and favors hydroxyl radical (OH) production via the catalytic reaction of Fe(2+), leading to increase in DNA damage. Moreover, the results indicate that the properties of light source, such as intensity and major emission wavelength, may alter the physiology of bacterial cells and affect the susceptibility to in-situ resultant H2O2 in the photocatalytic inactivation processes, leading to significant influence on the photocatalytic inactivation efficiencies of E. coli K-12.Entities:
Keywords: Escherichia coli; Photocatalytic inactivation mechanism; Reactive oxidative species; Single-gene deletion mutant
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Year: 2015 PMID: 26083904 DOI: 10.1016/j.jphotobiol.2015.06.007
Source DB: PubMed Journal: J Photochem Photobiol B ISSN: 1011-1344 Impact factor: 6.252