Insertions of mini-Tn10 transposon T-POP in Salmonella enterica sv. typhi

Alejandro A. Hidalgo, A. Nicole Trombert, J. C. Castro-Alonso, Carlos A. Santiviago, Bruno R. Tesser, Philip Youderian, Guido C. Mora

Resultado de la investigación: Contribución a una revistaArtículorevisión exhaustiva

13 Citas (Scopus)

Resumen

We have mutagenized a clinical strain of Salmonella enterica sv. typhi with mini-transposon Tn10dTet (T-POP) to obtain conditional lethal (tetracycline-dependent) mutants with T-POP insertions upstream of essential genes. Generalized transducing phage P22 was used to introduce T-POP from a S. typhimurium donor into a S. typhi recipient. Chromosomal DNA was purified from the mutagenized donor strains, fragmented, and then electroporated into S. typhi to backcross the original T-POP insertions. Four tetracycline-dependent mutants with two distinct terminal phenotypes were found among 1700 mutants with T-POP insertions. When grown in the absence of tetracycline, two of the four tetracycline-dependent mutants arrest at a late stage in the cell cycle, can be rescued by outgrowth in media with tetracycline, and define a reversible checkpoint late in the cell cycle. One of these insertions creates an operon fusion with a gene, yqgF, that is conserved among gram-negative bacteria and likely encodes an essential Holliday junction resolvase. T-POP insertions can be used not only to identify essential S. typhi genes but also to reveal novel phenotypes resulting from the depletion of their products.

Idioma originalInglés
Páginas (desde-hasta)1069-1077
Número de páginas9
PublicaciónGenetics
Volumen167
N.º3
DOI
EstadoPublicada - jul 2004

Áreas temáticas de ASJC Scopus

  • Genética

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