# Davidson Missouri W/Traveling Salesperson Problem

*in vivo*| Mathematical Modeling | Gene Splitting | Controlling Expression |

**Traveling Salesperson Problem**| Backwards Promotion and Read-Through Transcription | Resources and Citations

Although our current project is to develop a bacterial computer that solves Hamiltonian path problems, in the future we would like to tackle the Traveling Salesman problem using similar methods. Given a directed graph where each edge has a cost associated with it, what is the cheapest, or shortest, path to take such that you end at your starting point and visit every node exactly once?

The graph above shows a modified complete graph with edges leaving the ending node (#4), returning to the start node (#1), and moving from the start to the stop node removed. If we wanted to solve this weighted and directed graph for the shortest path through all nodes, starting at node #1, ending at node #4, and passing through each node only once, we could use our current HPP *E. coli* computer construct with one slight modification.

Instead of putting each half-gene back to back along an edge, we could add in spacers of specified lengths that would allow us to model the various weights in the graph above. These weights would give edges different lengths (in base pairs). After performing PCR on all of the solved plasmids (with primers binding to the promoter and terminator), we would be able to find the shortest path through all of the nodes by running the PCR products on a gel. Because the total length of the genes in any Hamiltonian Path through the graph is a constant, the smallest solved fragment will have the lowest total spacer length and will, therefore, be the solution to the Traveling Salesperson Problem (shown above).

This image shows an alternate route through the graph. The length of this fragment is longer than the length of the solution to the TSP.

False positives can also come into play with this construct. However, certain rules can be put into place when choosing spacer lengths to avoid having false positive PCR products that are longer than the true solution.