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Properties of Mitomycin C-sensitive Mutants of Escherichia coli K-12

机译:大肠杆菌K-12丝裂霉素C敏感突变体的性质

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摘要

Strains hypersensitive to mitomycin C (MC) were isolated from Escherichia coli K-12 after treatment with nitrosoguanidine. Of 43 MC-sensitive strains tested for their ultraviolet light (UV) sensitivity and for their ability to reactivate UV-inactivated λ phage, 38 were found to be insensitive to UV irradiation and to be able to reactivate UV-irradiated bacteriophage λ. Some properties of the MC-sensitive, uvr+ mutants were analyzed. Synthesis of deoxyribonucleic acid (DNA) in MC-sensitive, uvr+ mutants was inhibited at a lower concentration of MC than in the wild-type strain. Mutant cells, labeled with 3H-thymidine and then exposed to MC, released radioactivity as low molecular weight compounds. The amount of radioactivity released was the same as that from the wild-type strain. MC-sensitive, uvr+ mutants, as well as the corresponding wild-type strain, were equally susceptible to induction of prophage φ80 by UV irradiation. However, MC induction of prophage was achieved in MC-sensitive, uvr+ mutants at a lower concentration of the antibiotic than in the wild-type strain. Genetic experiments indicated that a gene controlling MC sensitivity is located close to that determining lactose fermentation of E. coli. It is situated on episome F′13, and the wild type is dominant to the MC-sensitive allele.
机译:在用亚硝基胍处理后,从大肠杆菌K-12中分离出对丝裂霉素C(MC)高度敏感的菌株。在43个对MC敏感的菌株进行了紫外线(UV)敏感性检测和它们重新激活UV灭活的λ噬菌体的能力测试中,发现38个对UV辐射不敏感并且能够重新激活UV照射的噬菌体λ。分析了MC敏感的uvr + 突变体的一些特性。 MC敏感的uvr + 突变体中脱氧核糖核酸(DNA)的合成在MC浓度低于野生型菌株时受到抑制。用 3 H-胸苷标记的突变细胞,然后暴露于MC,以低分子量化合物的形式释放放射性。释放的放射性量与野生型菌株释放的放射性量相同。对MC敏感的uvr + 突变体以及相应的野生型菌株同样容易受到紫外线辐射诱导的噬菌体φ80的影响。然而,在MC敏感的uvr + 突变体中,在抗生素浓度低于野生型菌株的情况下,MC可以实现对噬菌体的诱导。遗传实验表明,控制MC敏感性的基因位于决定大肠杆菌乳糖发酵的基因附近。它位于附加体F'13上,野生型占MC敏感等位基因的主导。

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