首页> 美国卫生研究院文献>Journal of Bacteriology >Silent Mischief: Bacteriophage Mu Insertions Contaminate Products of Escherichia coli Random Mutagenesis Performed Using Suicidal Transposon Delivery Plasmids Mobilized by Broad-Host-Range RP4 Conjugative Machinery
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Silent Mischief: Bacteriophage Mu Insertions Contaminate Products of Escherichia coli Random Mutagenesis Performed Using Suicidal Transposon Delivery Plasmids Mobilized by Broad-Host-Range RP4 Conjugative Machinery

机译:沉默的恶作剧:噬菌体Mu插入污染的大肠杆菌随机诱变的产品使用宽宿主范围RP4结合机器动员的自杀转座子传递质粒。

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摘要

Random transposon mutagenesis is the strategy of choice for associating a phenotype with its unknown genetic determinants. It is generally performed by mobilization of a conditionally replicating vector delivering transposons to recipient cells using broad-host-range RP4 conjugative machinery carried by the donor strain. In the present study, we demonstrate that bacteriophage Mu, which was deliberately introduced during the original construction of the widely used donor strains SM10 λpir and S17-1 λpir, is silently transferred to Escherichia coli recipient cells at high frequency, both by hfr and by release of Mu particles by the donor strain. Our findings suggest that bacteriophage Mu could have contaminated many random-mutagenesis experiments performed on Mu-sensitive species with these popular donor strains, leading to potential misinterpretation of the transposon mutant phenotype and therefore perturbing analysis of mutant screens. To circumvent this problem, we precisely mapped Mu insertions in SM10 λpir and S17-1 λpir and constructed a new Mu-free donor strain, MFDpir, harboring stable hfr-deficient RP4 conjugative functions and sustaining replication of Π-dependent suicide vectors. This strain can therefore be used with most of the available transposon-delivering plasmids and should enable more efficient and easy-to-analyze mutant hunts in E. coli and other Mu-sensitive RP4 host bacteria.
机译:随机转座子诱变是将表型与其未知遗传决定因素相关联的选择策略。通常通过使用供体菌株携带的宽宿主范围的RP4结合机器,动员条件转移载体将转座子传递至受体细胞来进行。在本研究中,我们证明了在广泛使用的供体菌株SM10λpir和S17-1λpir的原始构建过程中有意引入的噬菌体Mu,通过hfr和通过hfr被高频无声地转移到大肠杆菌受体细胞中。供体菌株释放出Mu颗粒。我们的发现表明,噬菌体Mu可能已经用这些流行的供体菌株污染了对Mu敏感物种进行的许多随机诱变实验,从而导致对转座子突变体表型的潜在误解,从而干扰了突变体筛选的分析。为了解决这个问题,我们精确地绘制了在SM10λpir和S17-1λpir中的Mu插入片段,并构建了一个新的无Mu供体菌株MFDpir,它具有稳定的hfr缺陷型RP4结合功能,并维持Π依赖性自杀载体的复制。因此,该菌株可与大多数可用的转座子传递质粒一起使用,并应能够在大肠杆菌和其他对Mu敏感的RP4宿主细菌中进行更有效且易于分析的突变寻源。

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