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首页> 外文期刊>Journal of bacteriology >Presence of DNA, encoding parts of bacteriophage tail fiber genes, in the chromosome of Escherichia coli K-12.
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Presence of DNA, encoding parts of bacteriophage tail fiber genes, in the chromosome of Escherichia coli K-12.

机译:在大肠杆菌K-12的染色体中,DNA的存在,噬菌体尾纤维基因部分的编码部分。

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The classical T-even bacteriophages recognize host cells with their long tail fibers. Gene products 35, 36, and 37 constitute the distal moiety of these fibers. The free ends of the tail fibers, which are formed by the CO2H terminus of gene product 37, possess the host range determinants. It was found that 4 out of 10 different strains of Escherichia coli K-12 contained regions of chromosomal DNA which hybridized with a probe consisting of genes 35, 36, and 37 of the T-even phage K3. From one strain this homologous DNA, which was associated with an EcoRI fragment of about 5 kilobases, was cloned into plasmid pUC8. Two independently recovered hybrid plasmids had undergone a peculiar rearrangement which resulted in the loss of about 3 kilobases of cloned DNA and a duplication of both the vector and the remaining chromosomal DNA. The mechanisms causing this duplication-deletion may be related to that of transposases. The cloned DNA was capable of recombination with phage T4 gene 36 and a phage T2 gene 37 amber mutant. DNA sequencing revealed the existence of regions of identity between the cloned DNA and genes 36 and 37 of phage T2. In addition, after growth of a derivative of phage K3 on a strain harboring T2 DNA, it was found that this phage contained the same parts of the T2 tail fiber genes which had been recovered from the bacterial chromosome. There appears to be little doubt that the phage had picked up this DNA from the host. The possibility is considered that a repertoire of parts of genes 36 and 37 of various T-even-type phages is present in their hosts, allowing the former to change their host ranges.
机译:典型的T-甚至噬菌体用它们的长尾纤维识别宿主细胞。基因产物35,36和37构成这些纤维的远端部分。由基因产物37的CO2H末端形成的尾纤维的自由端具有宿主范围的决定簇。发现10种不同的大肠杆菌C大肠杆菌K-12菌株中的4种含有染色体DNA的区域,其与由T-甚至噬菌体K3的基因35,36和37组成的探针杂交。从一个菌株,该同源DNA与约5千碱基的EcoRI片段相关联,克隆到质粒pUC8中。两个独立回收的杂交质粒经历了特殊的重排,导致克隆DNA的损失和载体和剩余染色体DNA的重复。导致这种复制缺失的机制可能与转座酶的机制有关。克隆的DNA能够用噬菌体T4基因36和噬菌体T2基因37琥珀突变体重组。 DNA测序显示克隆DNA和噬菌体T2的克隆DNA和基因37和37之间的身份区域存在。另外,在患有T2 DNA的菌株上噬菌体K3的衍生物的生长后,发现该噬菌体含有从细菌染色体中回收的T2尾纤维基因的相同部分。似乎毫无疑问,噬菌体从宿主挑选了这种DNA。认为可能性认为各种T型偶数噬菌体的基因部分36和37的部分存在于其宿主中,允许前者改变其宿主范围。

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