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Comprehensive transposon mutant library of Pseudomonas aeruginosa

机译:铜绿假单胞菌的综合转座子突变体文库

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摘要

We have developed technologies for creating saturating libraries of sequence-defined transposon insertion mutants in which each strain is maintained. Phenotypic analysis of such libraries should provide a virtually complete identification of nonessential genes required for any process for which a suitable screen can be devised. The approach was applied to Pseudomonas aeruginosa. an opportunistic pathogen with a 6.3-Mbp genome. The library that was generated consists of 30,100 sequence-defined mutants, corresponding to an average of five insertions per gene. About 12% of the predicted genes of this organism lacked insertions; many of these genes are likely to be essential for growth on rich media. Based on statistical analyses and bioinformatic comparison to known essential genes in E. coli, we estimate that the actual number of essential genes is 300-400. Screening the collection for strains defective in two defined multigenic processes (twitching motility and prototrophic growth) identified mutants corresponding to nearly all genes expected from earlier studies. Thus, phe-notypic analysis of the collection may produce essentially complete lists of genes required for diverse biological activities. The trans-posons used to generate the mutant collection have added features that should facilitate downstream studies of gene expression, protein localization, epistasis, and chromosome engineering.
机译:我们已经开发出用于创建序列定义的转座子插入突变体的饱和文库的技术,其中每个菌株都在其中维持。此类文库的表型分析应能提供对可以设计合适筛选的任何过程所需的非必需基因的几乎完整鉴定。该方法被应用于铜绿假单胞菌。具有6.3 Mbp基因组的机会病原体。生成的文库由30,100个序列定义的突变体组成,对应于每个基因平均5个插入片段。该生物的大约12%的预测基因缺少插入;这些基因中的许多可能对于在富媒体上生长至关重要。基于统计分析和与大肠杆菌中已知必需基因的生物信息学比较,我们估计必需基因的实际数量为300-400。在两个确定的多基因过程(抽动运动和原养生长)中筛选有缺陷的菌株的集合,鉴定出与早期研究预期几乎所有基因相对应的突变体。因此,该集合的phe-nottypic分析可能会产生各种生物学活动所需的基因的基本完整清单。用于产生突变体集合的转座子具有增加的功能,这些功能应有助于基因表达,蛋白质定位,上位性和染色体工程的下游研究。

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