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Quantification of ultraviolet-C irradiation induced cyclobutane pyrimidine dimers and their removal in Beauveria bassiana conidiospore DNA

机译:紫外-C辐射诱导的环丁烷嘧啶二聚体的定量及其在球孢白僵菌分生孢子DNA中的去除

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Ultraviolet (UV) radiation-induced DNA damage leading to entomopathogenic fungal inactivation is commonly measured by viability counts. Here we report the first quantification of UV-induced cyclobutane pyrimidine dimers (CPD) in DNA of the entomopathogenic fungus, Beauveria bassiana. Changes in the mobility of-UV-C irradiated DNA were resolved with CPD specific bacteriophage T4 endonuclease V and alkaline agarose gel electrophoresis. The maximum number of CPD formed in B. bassiana DNA in vitro by UV-C irradiation was 28 CPD/ 10 kb after 720 J/m(2) dose. The maximum number of CPDs formed in B. bassiana conidiospore DNA irradiated in vivo was 15 CPD/10 kb after 480 J/m(2) dose and was quantified from conidiospores that were incubated to allow photoreactivation and nucleotide excision repair. The conidiospores incubated for photoreactivation and nucleotide excision repair showed decreased number of CPD/10 kb DNA and a higher percent survival of conidiospore populations than conidiospores not allowed to repair.
机译:紫外线(UV)辐射引起的导致致病性真菌失活的DNA损伤通常通过生存力计数来衡量。在这里,我们报告昆虫致病性真菌球孢白僵菌的DNA中的紫外线诱导的环丁烷嘧啶二聚体(CPD)的首次定量。用CPD特异性噬菌体T4核酸内切酶V和碱性琼脂糖凝胶电泳解决了UV-C辐照DNA迁移率的变化。 720 J / m(2)剂量后,通过UV-C辐射在体外球孢杆菌DNA中形成的CPD的最大数量为28 CPD / 10 kb。在480 J / m(2)剂量后,在体内照射的球孢白僵菌分生孢子DNA中形成的CPD的最大数量为15 CPD / 10 kb,并从孵育的分生孢子中进行定量,以进行光激活和核苷酸切除修复。与不允许修复的分生孢子相比,为光激活和核苷酸切除修复而孵育的分生孢子显示出CPD / 10 kb DNA数量减少,分生孢子种群的存活率更高。

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