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1.
Appl Microbiol Biotechnol ; 100(11): 4761-71, 2016 Jun.
Article in English | MEDLINE | ID: mdl-27087527

ABSTRACT

Millimeter waves (MMW) or electromagnetic fields of extremely high frequencies at low intensity is a new environmental factor, the level of which is increased as technology advance. It is of interest that bacteria and other cells might communicate with each other by electromagnetic field of sub-extremely high frequency range. These MMW affected Escherichia coli and many other bacteria, mainly depressing their growth and changing properties and activity. These effects were non-thermal and depended on different factors. The significant cellular targets for MMW effects could be water, cell plasma membrane, and genome. The model for the MMW interaction with bacteria is suggested; a role of the membrane-associated proton FOF1-ATPase, key enzyme of bioenergetic relevance, is proposed. The consequences of MMW interaction with bacteria are the changes in their sensitivity to different biologically active chemicals, including antibiotics. Novel data on MMW effects on bacteria and their sensitivity to different antibiotics are presented and discussed; the combined action of MMW and antibiotics resulted with more strong effects. These effects are of significance for understanding changed metabolic pathways and distinguish role of bacteria in environment; they might be leading to antibiotic resistance in bacteria. The effects might have applications in the development of technique, therapeutic practices, and food protection technology.


Subject(s)
Bacteria/radiation effects , Electromagnetic Fields , Escherichia coli/radiation effects , Adenosine Triphosphatases/metabolism , Anti-Bacterial Agents/pharmacology , Bacteria/drug effects , Cell Membrane/drug effects , Cell Membrane/radiation effects , Drug Resistance, Bacterial , Electromagnetic Radiation , Escherichia coli/drug effects , Microbial Sensitivity Tests , Water/chemistry
2.
Cell Biochem Biophys ; 67(3): 829-35, 2013.
Article in English | MEDLINE | ID: mdl-23516095

ABSTRACT

The effects of low-intensity electromagnetic irradiation (EMI) with the frequencies of 51.8 and 53 GHz on Lactobacillus acidophilus growth and survival were revealed. These effects were compared with antibacterial effects of antibiotic ceftazidime. Decrease in bacterial growth rate by EMI was comparable with the inhibitory effect of ceftazidime (minimal inhibitory concentration-16 µM) and no enhanced action was observed with combined effects of EMI and the antibiotic. However, EMI-enhanced antibiotic inhibitory effect on bacterial survival. The kinetics of the bacterial suspension oxidation-reduction potential up to 24 h of the growth was changed by EMI and ceftazidime. The changes were more strongly expressed by combined effects of EMI and antibiotic especially up to 12 h. Moreover, EMI did not change overall energy (glucose)-dependent H(+) efflux across the membrane but it increased N,N'-dicyclohexylcarbodiimide (DCCD)-inhibited H(+) efflux. In contrast, this EMI in combination with ceftazidime decreased DCCD-sensitive H(+) efflux. Low-intensity EMI had inhibitory effect on L. acidophilus bacterial growth and survival. The effect on bacterial survival was more significant in the combination with ceftazidime. The H(+)-translocating F 0 F 1-ATPase, for which DCCD is specific inhibitor, might be a target for EMI and ceftazidime. The revealed bactericide effects on L. acidophilus can be applied in biotechnology, food producing and safety technology.


Subject(s)
Anti-Bacterial Agents/pharmacology , Ceftazidime/pharmacology , Electromagnetic Radiation , Lactobacillus acidophilus/drug effects , Lactobacillus acidophilus/radiation effects , Bacterial Proteins/antagonists & inhibitors , Bacterial Proteins/metabolism , Cell Membrane/drug effects , Cell Membrane/metabolism , Cell Membrane/radiation effects , Dicyclohexylcarbodiimide/chemistry , Dicyclohexylcarbodiimide/pharmacology , Hydrogen/metabolism , Kinetics , Lactobacillus acidophilus/growth & development , Microbial Viability/drug effects , Oxidation-Reduction , Proton-Translocating ATPases/antagonists & inhibitors , Proton-Translocating ATPases/metabolism
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