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Bio-electric Interface:
Discussion and conclusions
For the fuel cell experiment we have obtained a series of interesting results. In our half fuel cells, E. coli seemed to exhibit properties similar to S. oneidensis. E. coli generates potential which closely relates to S. oneidensis outputs and the results repeat throughout multiple media, except for the final experiment using M9 with sodium acetate, which limited the growth of E. coli altogether as well as limiting the electrogenicity of other bacteria. However, S. oneidensis electrogenicity remains superior in all experiments, most likely because of its electron export system proteins. We hope that transferring S. oneidensis genes (especially mtrA or mtrCAB)into E. coli would improve its response.
It seems that electrogenicity can be linked to the growth of cultures, at least in the minimal media. This shows a great potential for using microbial half fuel cells in combination with different promoters and selectable markers. To test this concept we have tested J33203 (arsenic promoter) + lacZ construct in our half fuel cells as a growth-based biosensor. We have obtained encouraging results, where transformed cells show faster voltage change compared to controls, showing a good potential for our system to serve as a reliable bio-detector generating data which would be easy to obtain and link to a computer system. With its potential for automation and miniaturisation this system offers a potential advancement in the field of biosensors. We are intending to further test this idea by using cells with arsenic promoter linked to the sucrose hydrolase gene. In such a system, detection of arsenic would induce expression of sucrose hydrolase, necessary for growth in media containing sucrose as the sole carbon source.
We managed to obtained, BioBricked and submitted the napC, cymA, ccm and mtrA genes. We have tested ccm, cymA and napC using haem staining procedure and obtained positive results. We have mutagenised the internal PstI side in mtrA. We had some success in cloning the mtrCAB and S. oneidensis ccm genes which may enhance the efficiency of the system. We would like to clone these genes into the pSB1C3 vector to create a functional BioBrick (BBa_K917007). However, the longer products (mtrCAB and ccm genes) seem to be more problematic to clone, with the digestion/ligation step being the limiting factor, despite using several alternative techniques (A-tailing with Taq and TA cloning, fusion PCR).
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