Difference between revisions of "Team:British Columbia/Proof"

Revision as of 02:43, 20 October 2016

As a part of our design, we have developed a functional prototype of the proposed consortium. In the prototype co-culture, cellulases expressed on C.crescentus surface degrade cellulose to serve as the substrate for E.coli which is producing β-carotene. Due to the slow rate of cellulose degradation by expressed cellulases, shown in our modelling section, culture lengths for the prototype experiment were three days or longer. E.coli and C.crescentus containing the recombinant plasmids were inoculated in M2 media with 0.2% cellulose as the sole carbon source. C.crescentus strains expressing Endo5A and Gluc1C cellulase enzymes were cultured alongside E.coli to determine the best candidates for a consortium. As a control, C.crescentus without cellulase expression genes were seeded with E.coli using it as a negative control for cellulose degradation. Over the course of three days, samples were taken and plated. These plated cultures can be identified based on either species unique morphology.

A measurement of OD600 indicates that the growth has occurred in several conditions with cellulose as the only substrate. Cultures containing C.crescentus expressing Endo5A cellulases seem to be most prolific. For these cultures, based on plate count data, E.coli growth has increased compared to cultures grown without cellulase expressing cells. In the cultures containing C.crescentus expressing Gluc1C, the ratio of E.coli to C.crescentus is nearly equal to the control, while in cultures containing C.crescentus expressing Endo5A, have a dominant C.crescentus population. This result likely indicates that there are diffusion limitations for glucose in the conditions with Endo5A expressing C.crescentus. A culture with mixed Endo5A and Gluc1C expressing C.crescentus seems to have increased C.crescentus growth, possibly due to the Endo5A expressing cells proliferating more rapidly. A marked increase in E.coli growth relative to the control cultures without expressed cellulases indicate the potential for our system.

To confirm that the E.coli densities were higher in the co-cultures containing Endo5A and Gluc1C cellulases, samples from each culture were plated after 6 days of growth on PYE and culture at 37 degrees Celsius. These conditions do not permit C.crescentus growth, and as a result, the relative cell density grown from each sample is directly proportional to the E.coli density in each culture. When the colony forming units were counted, there was nearly a four-fold increase in the number of E.coli existing in cultures containing C.crescentus with Endo5A expression. In the cultures containing C.crescentus only expressing Gluc1C, there was no clear difference in E.coli growth compared to the control cultures. The densities of E.coli in each culture can be seen in Figure 3.

Figure 3: E.coli densities in the different mixed culture systems

This experiment validates the design, showing the possibility for E.coli growth and product formation supported by cheap cellulose feed stock. Caulobacter is able to transforming raw biomass into fermentable sugars to sustain its own growth and the growth E.coli partner.

Check out other parts of our project below!