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Article Dans Une Revue Nucleic Acids Research Année : 2010

The synthetic integron: an in vivo genetic shuffling device

Résumé

As the field of synthetic biology expands, strategies and tools for the rapid construction of new biochemical pathways will become increasingly valuable. Purely rational design of complex biological pathways is inherently limited by the current state of our knowledge. Selection of optimal arrangements of genetic elements from randomized libraries may well be a useful approach for successful engineering. Here, we propose the construction and optimization of metabolic pathways using the inherent gene shuffling activity of a natural bacterial site-specific recombination system, the integron. As a proof of principle, we constructed and optimized a functional tryptophan biosynthetic operon in Escherichia coli. The trpA-E genes along with 'regulatory' elements were delivered as individual recombination cassettes in a synthetic integron platform. Integrase-mediated recombination generated thousands of genetic combinations overnight. We were able to isolate a large number of arrangements displaying varying fitness and tryptophan production capacities. Several assemblages required as many as six recombination events and produced as much as 11-fold more tryptophan than the natural gene order in the same context.
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Dates et versions

hal-01876815 , version 1 (18-09-2018)

Licence

Paternité - Pas d'utilisation commerciale

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David Bikard, Stéphane Julié-Galau, Guillaume Cambray, Didier Mazel. The synthetic integron: an in vivo genetic shuffling device. Nucleic Acids Research, 2010, 38 (15), ⟨10.1093/nar/gkq511⟩. ⟨hal-01876815⟩

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