Genotoxic Effect of Dicyclopropanated 5-Vinyl-2-Norbornene.
Uliana S NovoyatlovaAndrei G KessenikhOlga V KononchukSergey V BazhenovAlexander A FomkinAnna A KudryavtsevaSergey V ShorunovMaxim V BermeshevIlya V ManukhovPublished in: Biosensors (2022)
Dicyclopropanated 5-vinyl-2-norbornene (dcpVNB) is a strained polycyclic hydrocarbon compound with a high energy content, which makes it promising for the development of propellant components based on it. In this work, the genotoxic properties of dcpVNB were studied using whole-cell lux -biosensors based on Escherichia coli and Bacillus subtilis . It was shown that the addition of dcpVNB to bacterial cells leads to the appearance of DNA damage inducing the SOS response and Dps expression with slight activation of the OxyR-mediated response to oxidative stress. The highest toxic effect of dcpVNB is detected by the following lux -biosensors: E. coli pColD-lux, E. coli pDps, B. subtilis pNK-DinC, and B. subtilis pNK-MrgA, in which the genes of bacterial luciferases are transcriptionally fused to the corresponding promoters: P cda , P dps , P dinC , and P mrgA . It was shown that lux -biosensors based on B. subtilis, and E. coli are almost equally sensitive to dcpVNB, which indicates the same permeability to this compound of cell wall of Gram-positive and Gram-negative bacteria. The activation of P dps after dcpVNB addition maintains even in oxyR mutant E. coli strains, which means that the P dps induction is only partially determined by the OxyR/S regulon. Comparison of specific stress effects caused by dcpVNB and 2-ethyl(bicyclo[2.2.1]heptane) (EBH), characterized by the absence of cyclopropanated groups, shows that structural changes in hydrocarbons could significantly change the mode of toxicity.
Keyphrases
- escherichia coli
- oxidative stress
- dna damage
- induced apoptosis
- bacillus subtilis
- cell wall
- klebsiella pneumoniae
- biofilm formation
- poor prognosis
- gram negative
- cell cycle arrest
- genome wide
- endothelial cells
- single cell
- stem cells
- ischemia reperfusion injury
- mesenchymal stem cells
- ionic liquid
- cell therapy
- diabetic rats
- gene expression
- pseudomonas aeruginosa
- transcription factor
- dna methylation
- wild type
- bone marrow