首页> 外文期刊>Journal of Food Science >DNA damage-inducible gene expression and formation of 5-fluorouracil-resistant mutants in Escherichia coli exposed to 2-dodecylcyclobutanone
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DNA damage-inducible gene expression and formation of 5-fluorouracil-resistant mutants in Escherichia coli exposed to 2-dodecylcyclobutanone

机译:暴露于2-十二烷基环丁酮的大肠杆菌中的DNA损伤诱导基因表达和5-氟尿嘧啶抗性突变体的形成

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摘要

2-Dodecylcyclobutanone (2-DCB) is formed by the radiolysis of palmitic acid and is present at low part-per-million (approximately 0.1 μ g/g) levels in irradiated meat products. Recently, equivocal results obtained using a DNA strand breakage test, the Comet Assay, raised the possibility that 2-DCB could be a weak genotoxin. To more accurately assess 2-DCB's potential genotoxicity, it was tested for the ability to increase expression of the DNA damage-inducible genes dinD, nfo, recA, and umuDC using Escherichia coli that contained promoter/β-galactosidase reporter constructs, and for the ability to increase the formation of 5-fluorouracil (5-FU)-resistant mutants. When E. coli was exposed to 125, 250, 500, and 1000 μ g/mL 2-DCB, with and without exogenous metabolic activation, no increase in dinD, nfo, recA, or umuDC gene expression, as measured by an increase in P-galactosidase activity, was observed. In addition, 2-DCB did not increase the formation of 5-FU-resistant mutants in E. coli, with and without exogenous metabolic activation, at the same concentrations. No evidence of 2-DCB-associated genotoxic activity was detected in this study.
机译:2-十二烷基环丁酮(2-DCB)是由棕榈酸经放射分解形成的,在辐照的肉制品中的含量低至百万分之几(约0.1μg / g)。最近,使用DNA链断裂测试(彗星分析)获得的模棱两可的结果增加了2-DCB可能是一种弱基因毒素的可能性。为了更准确地评估2-DCB的潜在遗传毒性,测试了使用含有启动子/β-半乳糖苷酶报告基因构建体的大肠杆菌提高DNA损伤诱导基因dinD,nfo,recA和umuDC表达的能力,增强5-氟尿嘧啶(5-FU)抗性突变体形成的能力。当大肠杆菌暴露于125、250、500和1000μg / mL的2-DCB时,无论是否有外源性代谢激活,如dinD,nfo,recA或umuDC基因表达的增加(通过增加观察到P-半乳糖苷酶活性。另外,在有和没有外源代谢激活的情况下,在相同浓度下,2-DCB不会增加大肠杆菌中对5-FU耐药的突变体的形成。在该研究中未发现2-DCB相关的遗传毒性活性的证据。

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