Genetics

We plan to use a single metabolic pathway for the conversion of glucose to aromatic chemicals. We are currently engineering a Pseudomonas putida strain containing a “switch” system enabling the manufacture of either shikimic acid (SA) or cinnamic acid (CA) as a major product. Future embodiments of this strain will contain additional directing mechanisms whereby a multitude of derivative chemicals can be favored.

Our metabolic engineering strategy is based on the invention of Dr. John Frost (US Patent No. 5168056, 6613552). The enzymatic activities leading to the production of SA will be enhanced by the addition of extra-chromosomal copies of endogenous genes modified such that expression is constitutive . Where necessary, these genes will be further modified through site-directed mutagenesis to abolish feedback regulation. Enzymatic activities which lead from SA to phenylalanine will be abolished by removing the underlying endogenous genes. These endogenous genes, in addition to a codon-optimized Rhodosporidium toruloides gene encoding for a phenylalanine ammonia-lysase (PAL) enzyme, will be re-introduced at an extra-chromosomal locus as will modified genes containing inducible promoter/repressor “switches” allowing us to direct metabolism toward CA at will. To further enhance the yield of our desired products, two additional categories of changes will be made to our host strain: (1) Enzymatic activities which direct metabolites away from the desired pathway will be abolished by removing the underlying endogenous genes and (2) transporter proteins responsible for re-uptake of SA or CA from the medium will be removed in the same manner. We are confident that this metabolic engineering strategy will enable us to improve product yield at least five-fold over currently reported values (CITATION).

Our genetic switch mechanism will be designed to tightly regulate gene expression. This will be accomplished by using both an inducer module and a repressor module so that strong expression of the regulated gene is only possible when a dual signal is given. One signal will cause an “inducer protein” to bind a cis regulatory element upstream of the promoter, where it can recruit cell machinery to initiate transcription. This signal alone, however, would be insufficient to allow expression. A repressor cis element located between the inducer cis element and the promoter is normally bound by a “repressor protein” which prevents movement of the transcription machinery down the gene. A second signal will cause the “repressor protein” to dissociate from its cis element, thus clearing the path of transcription machinery and allowing expression. The exact details of this regulatory system are still under investigation – the design of this system may become a focus of next year's Alberta North iGEM team.