Markerless Escherichia coli rrn Deletion Strains for Genetic Determination of Ribosomal Binding Sites

Author:

Quan Selwyn1,Skovgaard Ole2,McLaughlin Robert E3,Buurman Ed T13,Squires Catherine L4

Affiliation:

1. Department of Biology, Stanford University, Stanford, California 094305

2. Department of Science, Systems and Models, Roskilde University, DK-4000 Roskilde, Denmark

3. Department of Biosciences, Infection Innovative Medicines Unit, AstraZeneca R&D Boston, Waltham, Massachusetts 02451

4. Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts 02111

Abstract

Abstract Single-copy rrn strains facilitate genetic ribosomal studies in Escherichia coli. Consecutive markerless deletion of rrn operons resulted in slower growth upon inactivation of the fourth copy, which was reversed by supplying transfer RNA genes encoded in rrn operons in trans. Removal of the sixth, penultimate rrn copy led to a reduced growth rate due to limited rrn gene dosage. Whole-genome sequencing of variants of single-copy rrn strains revealed duplications of large stretches of genomic DNA. The combination of selective pressure, resulting from the decreased growth rate, and the six identical remaining scar sequences, facilitating homologous recombination events, presumably leads to elevated genomic instability.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology

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