首页> 外文期刊>Journal of bacteriology >fii, a bacterial locus required for filamentous phage infection and its relation to colicin-tolerant tolA and tolB.
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fii, a bacterial locus required for filamentous phage infection and its relation to colicin-tolerant tolA and tolB.

机译:fii,丝状噬菌体感染所需的细菌基因座,及其与耐大肠菌素的tolA和tolB的关系。

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We describe mutations in a new bacterial locus, designated fii, which do not allow the filamentous bacteriophage f1 to infect bacteria harboring the F plasmid. Mutations at this locus do not affect the ability of F plasmid-containing bacteria to undergo conjugation or be infected by the F plasmid-specific RNA phage f2. The filamentous phage can still adsorb to the F sex pilus, but the DNA is unable to enter the bacteria. All fii mutants become tolerant to colicins E1, E2, and E3. Strains with amber mutations in fii also are unable to plaque P1, even though they can be infected with this phage. Mutations in fii also prevent infection of bacteria harboring the N plasmid by the filamentous bacteriophage IKe. The fii locus maps adjacent to tolA, mutants of which demonstrate tolerance to high levels of the E and K colicins. The three genes tolA, tolB, and fii are shown to reside on a 4.3-kilobase fragment of the Escherichia coli chromosome. Each gene has been cloned into a chimeric plasmid and shown to complement, in trans, mutations at the corresponding chromosomal locus. Studies in maxicells show that the product of fii appears to be a 24-kilodalton protein which copurifies with the cell envelope. The product of tolA has been identified tentatively as a 51-kilodalton protein. Data from cloning, Tn5 mutagenesis, and P1 transduction studies are consistent with the gene order sucA-fii-tolA-tolB-aroG near 17 min on the E. coli map.
机译:我们描述了一个新的细菌基因座,称为fii中的突变,它不允许丝状噬菌体f1感染带有F质粒的细菌。该基因座处的突变不会影响含F质粒的细菌发生结合或被F质粒特异性RNA噬菌体f2感染的能力。丝状噬菌体仍然可以吸附到F性菌毛上,但是DNA无法进入细菌。所有的fii突变体都耐受大肠菌素E1,E2和E3。 fii中具有琥珀色突变的菌株也无法噬菌斑P1,即使它们可以被该噬菌体感染。 fii中的突变还可以防止带有N质粒的细菌被丝状噬菌体IKe感染。 fil基因座图与tolA相邻,其tolA突变体表现出对高水平的E和K大肠杆菌素的耐受性。已显示三个基因tolA,tolB和fii驻留在大肠杆菌染色体的4.3碱基对的片段上。每个基因已被克隆到一个嵌合质粒中,并显示出在相应的染色体基因座处反式互补突变。对maxicells的研究表明,fii的产物似乎是与细胞被膜共纯化的24千达尔顿蛋白。 tolA的产品已被初步鉴定为51-千达尔顿蛋白。来自克隆,Tn5诱变和P1转导研究的数据与大肠杆菌图谱上接近17分钟的sucA-fii-tolA-tolB-aroG的基因顺序一致。

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