Selection and optimization of gene targets for the metabolic engineering of E. coli

[摘要] (cont.) The clostridial genes ptb and buk were capable of producing S-3-hydroxybutyric acid from the butyrate pathway intermediate metabolite S-3-hydroxybutyryl-CoA. In parallel, the intracellular concentrations of pathway metabolites was measured for a set of strains expressing the clostridial butanol biosynthesis pathway in various configurations. Comparison of measured pool sizes and pool sizes for thermodynamic equilibrium pinpointed the butyryl-CoA dehydrogenase step, encoded by bcd, as a bottleneck enzyme. Thus, points for genetic intervention are ptb, buk, and bcd. The second case is tyrosine overproduction in E. coli. Constraints-based models of E. coli metabolism proved incapable of predicting gene knockout targets. Therefore, to understand factors underlying tyrosine overproduction, the intracellular concentrations of amino acids were measured. In tyrosine overproducers, the intracellular concentrations of most proteinogenic amino acids were vastly perturbed relative to non-producing strains. This fact and thermodynamic considerations suggested that the transamination of p-hydroxyphenylpyruvate to tyrosine was near equilibrium, and thus that nitrogen supply may be limiting tyrosine production. Culture media amended with glutamate or glutamine, but not with a-ketoglutarate or other organic acids, increased tyrosine production in these strains more than 8-fold, showing that interventions which affect nitrogen supply are attractive targets for engineering tyrosine overproduction in E. coli. The last case addresses the question of what types of intervention are best. A series of 22 promoters with well-characterized, variable strengths was created by mutagenesis. This library was used to replace promoters for key genes in the biosynthesis of lycopene or biomass from glucose. These metabolic phenotypes exhibited strain-dependent optima with respect to the expression levels of the key rate-controlling genes genes. Promoter engineering thus shows that subtle genetic interventions can have profound effects on pathway function.

[发布机构] Massachusetts Institute of Technology