The response of Escherichia coli to the alkylating agents Chloroacetaldehyde (cas 107-20-0) and styrene oxide
-
Add time:08/19/2019 Source:sciencedirect.com
DNA damage is ubiquitous and can arise from endogenous or exogenous sources. DNA-damaging alkylating agents are present in environmental toxicants as well as in cancer chemotherapy drugs and are a constant threat, which can lead to mutations or cell death. All organisms have multiple DNA repair and DNA damage tolerance pathways to resist the potentially negative effects of exposure to alkylating agents. In bacteria, many of the genes in these pathways are regulated as part of the SOS reponse or the adaptive response. In this work, we probed the cellular responses to the alkylating agents Chloroacetaldehyde (cas 107-20-0) (CAA), which is a metabolite of 1,2-dichloroethane used to produce polyvinyl chloride, and styrene oxide (SO), a major metabolite of styrene used in the production of polystyrene and other polymers. Vinyl chloride and styrene are produced on an industrial scale of billions of kilograms annually and thus have a high potential for environmental exposure. To identify stress response genes in E. coli that are responsible for tolerance to the reactive metabolites CAA and SO, we used libraries of transcriptional reporters and gene deletion strains. In response to both alkylating agents, genes associated with several different stress pathways were upregulated, including protein, membrane, and oxidative stress, as well as DNA damage. E. coli strains lacking genes involved in base excision repair and nucleotide excision repair were sensitive to SO, whereas strains lacking recA and the SOS gene ybfE were sensitive to both alkylating agents tested. This work indicates the varied systems involved in cellular responses to alkylating agents, and highlights the specific DNA repair genes involved in the responses.
We also recommend Trading Suppliers and Manufacturers of Chloroacetaldehyde (cas 107-20-0). Pls Click Website Link as below: cas 107-20-0 suppliers
Prev:Chloroacetaldehyde (cas 107-20-0) dehydrogenase from Ancylobacter aquaticus UV5: Cloning, expression, characterization and molecular modeling
Next:Targets of Chloroacetaldehyde (cas 107-20-0)-induced nephrotoxicity) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Mass and microwave spectroscopic studies of pyrolysis of Chloroacetaldehyde (cas 107-20-0) and its methyl derivatives08/26/2019
- DNA damage and mutations produced by Chloroacetaldehyde (cas 107-20-0) in a CpG-methylated target gene08/25/2019
- Schisandra chinensis extract decreases Chloroacetaldehyde (cas 107-20-0) production in rats and attenuates cyclophosphamide toxicity in liver, kidney and brain☆08/24/2019
- Evaluation of the mass transfers of caffeine and vitamin B12 in Chloroacetaldehyde (cas 107-20-0) treated renal barrier model using a microfluidic biochip08/23/2019
- Liquid chromatographic assay for the antiviral nucleotide analogue tenofovir in plasma using derivatization with Chloroacetaldehyde (cas 107-20-0)08/22/2019
- Acrolein and Chloroacetaldehyde (cas 107-20-0): An examination of the cell and cell-free biomarkers of toxicity08/21/2019
- Targets of Chloroacetaldehyde (cas 107-20-0)-induced nephrotoxicity08/20/2019
- Chloroacetaldehyde (cas 107-20-0) dehydrogenase from Ancylobacter aquaticus UV5: Cloning, expression, characterization and molecular modeling08/18/2019
-
Health and Chemical more >