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Comparing Insertion Libraries in Two Pseudomonas aeruginosa Strains to Assess Gene Essentiality.

Comparing Insertion Libraries in Two Pseudomonas aeruginosa Strains to Assess Gene Essentiality. Research Abstract Details 

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  • Comparing Insertion Libraries in Two Pseudomonas aeruginosa Strains to Assess Gene Essentiality. Abstract Text:

    nicole t liberatiNicole T Liberati,jonathan m urbachJonathan M Urbach,tara k thurberTara K Thurber,gang wuGang Wu,frederick m ausubelFrederick M Ausubel,

    Putative essential genes can be identified by comparing orthologs not disrupted in multiple near-saturated transposon insertion mutation libraries in related strains of the same bacterial species. Methods for identifying all orthologs between two bacterial strains and putative essential orthologs are described. In addition, protocols detailing near-saturation transposon insertion mutagenesis of bacteria are presented, including (1) conjugation-mediated mutagenesis, (2) automated colony picking and liquid handling of mutant cultures, and (3) arbitrary polymerase chain reaction amplification and sequencing of genomic DNA adjacent to transposon insertion sites.

    Comparing Insertion Libraries in Two Pseudomonas aeruginosa Strains to Assess Gene Essentiality. Publishing Authors By Initials

    nt liberatiNT Liberati,jm urbachJM Urbach,tk thurberTK Thurber,g wuG Wu,fm ausubelFM Ausubel,

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    Comparing Insertion Libraries in Two Pseudomonas aeruginosa Strains to Assess Gene Essentiality. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Methods in molecular biology (Clifton, N.J.)

    VOLUME: 416

    Page Numbers: 153-70

    Journal Abbreviation: Methods Mol. Biol.

    ISSN: 1064-3745

    DAY: 21

    MONTH: 02

    YEAR: 2007

    Comparing Insertion Libraries in Two Pseudomonas aeruginosa Strains to Assess Gene Essentiality. Information

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    LANGUAGE: eng

    NlmUniqueID: 9214969

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    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Methods Mol Biol

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