Real-time monitoring of physiological parameters in the study of Escherichia coli early response to peroxide stress
DOI:
https://doi.org/10.17072/1994-9952-2022-1-35-41Keywords:
рhysiological parameters, integral parameters of bacterial culture, electrochemical sensors, real-time monitoring, Escherichia coli, peroxide stressAbstract
The response of aerobically growing Escherichia coli cultures to peroxide stress was studied using synchronous real-time monitoring of parameters pO2 (oxygen partial pressure), pH, Eh (redox potential of the culture), extracellular levels of K+ and S2-, in combination with traditional physiological, biochemical and genetic methods. A sharp increase in pO2 level in the medium caused by the destruction of H2O2 by endogenous catalases was observed in the early response to peroxide stress. The addition of 100 µM H2O2 provoked a reversible decrease in the specific growth rate, accompanied by an increase of extra- and intracellular glutathione and a short-term increase in sulfide production. Treatment with a high dose of H2O2 (10 mM) led to growth inhibition and a CFU loss, most pronounced in glutathione synthesis mutants. Simultaneously, in 8% of cells, the membrane potential decreased, a part of potassium was released into the medium, and the expression of the sulA gene, which is part of the SOS-regulon, increased. Application of an integrated approach to the study of stress revealed a close relationship between growth parameters (specific growth rate and survival), respiratory activity, sulfide production, and the ability of E. coli cells to maintain the membrane potential and K+ gradient.References
Baba T. et al. Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection // Mol. Syst. Biol. 2006. Vol. 2. P. 1–11. DOI:10.1038/msb4100050
Miller J.H. Experiments in molecular genetics // Cold Spring Harbor: Cold Spring Harbor Laboratory Press. 1972. 466 p.
Oktyabrskii O.N., Smirnova G.V. Redox potential changes in bacterial cultures under stress conditions // Microbiology (Moscow). 2012. Vol. 81, № 2. P. 131–142. DOI:10.1134/s0026261712020099
Owens R.A., Hartman P.E. Export of glutathione by some widely used Salmonella typhimurium and Esch-erichia coli strains // J. Bacteriol. 1986. Vol. 168. P. 109–114. DOI:10.1128/jb.168.1.109-114.1986
Smirnova G.V. et al. Transmembrane glutathione cycling in growing Escherichia coli cells // Microbiol. Res. 2012. Vol. 167. P. 166–172. DOI:10.1016/j.micres.2011.05.005
Smirnova G.V. et al. Ciprofloxacin provokes SOS-dependent changes in respiration and membrane poten-tial and causes alterations in redox status of Escherichia coli. // Res. Microbiol. 2017. Vol. 168. P. 64–73. DOI:10.1016/j.resmic.2016.07.008.
Smirnova G.V. et al. The sharp phase of respiratory inhibition during amino acid starvation in Escherichia coli is RelA-dependent and associated with the regulation of ATP synthase activity. // Res. Microbiol. 2018. Vol. 169. P. 157–165. DOI:10.1016/j.resmic.2018.02.003
Smirnova G.V. et al. Cysteine homeostasis under inhibition of protein synthesis in Escherichia coli cells. // Amino Acids. 2019. Vol. 51. P. 1577–1592. DOI:10.1007/s00726-019-02795-2
Tietze F. Enzymic method for quantitative determination of nanogram amounts of total and oxidized glu-tathione: applications to mammalian blood and other tissues // Anal. Biochem. 1969. Vol. 27. P. 502–522. DOI: 10.1016/0003-2697(69)90064-5
Tyulenev A.V. et al. The role of sulfides in stress-induced changes of Eh in Escherichia coli cultures. // Bioelectrochemistry. 2018. Vol. 121. P. 11–17. DOI: 10.1016/j.bioelechem.2017.12.012
Zhao X. et al. Moving forward with reactive oxygen species involvement in antimicrobial lethality. // J. Antimicrob. Chemother. 2015. Vol. 70. P. 639–642. DOI:10.1093/jac/dku463