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Episome-mediated Transfer of Drug Resistance in Enterobacteriaceae X. Restriction and Modification of Phages by fi? R Factors

机译:附加体介导的肠杆菌科细菌耐药性转移X.噬菌体对噬菌体的限制和修饰R因素

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Watanabe, Tsutomu (Keio University, Tokyo, Japan), Toshiya Takano, Toshihiko Arai, Hiroshi Nishida, and Sachiko Sato. Episome-mediated transfer of drug resistance in Enterobacteriaceae. X. Restriction and modification of phages by fi? R factors. J. Bacteriol. >92:477–486. 1966.—An fi? R factor, which restricts phages λ, T1, and T7 without modifying them, was found to restrict and not to modify an F?-specific phage, W-31, in Escherichia coli K-12, but not to restrict phage P-22 in Salmonella typhimurium LT-2, whereas other fi? R factors restricted and modified P-22 but not W-31; fi+ R factors did not restrict these phages. Transduction and lysogenization with phages λ and P-22 were reduced by these fi? R factors in K-12 and LT-2, respectively, and the transducing phages λ and P-22 were modified by these fi? R factors. Spontaneous as well as ultraviolet-induced production of phage P-22 and zygotic induction of phage λ were not significantly affected by any R factor. Injection of the nucleic acids of phages T1 and λ was not affected by R factors, but the injected phage nucleic acids were rapidly broken down in the bacteria carrying fi? R factors. The nucleic acids of the modified phages were not broken down in these bacteria. It was assumed from these results that the mechanism of restriction of phages by fi? R factors is due to the breakdown of the injected phage nucleic acids by a deoxyribonuclease(s), presumably located near the cell surface in the cells carrying fi? R factors. The deoxyribonuclease(s), formed in the cells carrying the nonmodifying fi? R factor, is considered to be different from that synthesized in the cells carrying the modifying fi? R factors. It was further shown that the average burst sizes of the unmodified as well as modified phages are slightly reduced by the presence of the fi? R factors.
机译:渡边,勉(日本东京庆应大学),高野敏也,新井俊彦,西田宏和佐藤幸子。附加体介导的肠杆菌科耐药性转移。 X. fi R因子对噬菌体的限制和修饰。 J.细菌。 > 92: 477-486。 1966年。发现一个 fi R因子限制了噬菌体λ,T1和T7,而没有对其进行修饰,从而限制了而不是对F 进行了修饰。 特异性噬菌体,W-31,在大肠杆菌 K-12中,但不限制鼠伤寒沙门氏菌 LT-2中的噬菌体P-22,而其他 fi R因子限制和修改了P-22,但未限制W-31; fi + R因子并不限制这些噬菌体。噬菌体λ和P-22的转导和溶菌作用分别被K-12和LT-2中的这些 fi R因子以及转导噬菌体λ和P减少这些 fi R因子对-22进行了修饰。自发以及紫外线诱导的噬菌体P-22的产生和合子诱导的噬菌体λ不受任何R因子的影响。噬菌体T1和λ的核酸的注入不受R因子的影响,但是所注入的噬菌体核酸在带有 fi R因子的细菌中迅速分解。在这些细菌中没有修饰的噬菌体的核酸被分解。从这些结果推测, fi R因子限制噬菌体的机制是由于脱氧核糖核酸酶破坏了注入的噬菌体核酸,大概位于携带 fi R因子的细胞的细胞表面附近。带有非修饰 fi R因子的细胞中形成的脱氧核糖核酸酶被认为与带有修饰的 fi的细胞中合成的脱氧核糖核酸酶不同。 R因素。进一步表明,由于存在 fi R因子,未修饰噬菌体和修饰噬菌体的平均爆发大小略有降低。

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