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Bio-electric interface
Bio-electric interface BioBricks cloning
Methods
- Bacteria used: Escherichia coli JM109 and Shewanella oneidensis MR-1. Both organisms were obtained from cultures in Chris French’s lab at the University of Edinburgh. S. oneidensis cultures were grown on LB agar at room temperature not exceeding 30°C. Plates were subcultured each week. E. coli cultures were grown on LB agar in a 37 degree incubator overnight and then left to grow at room temperature and subcultured by lab staff when needed.
- PCR: most PCR reactions were performed using the following OpenWetWare protocol CFrench: KodPCR. Optimal annealing temperature for S. oneidensis genes was found to be around 50-52°C while E. coli genes showed good results with annealing temperatures in the range of 50-55°C. S. oneidensis cell suspension in sterile water was used as template for mtrA, MtrCAB, S. oneidensis ccmA-E and ccmF-H genes. E. coli cell suspension in sterile water was used as template for napC and E. coli ccmA-H genes.
- PolyA tailing: for several genes polyA tailing was performed using Taq polymerase and the following protocol: 20 minutes denaturation at 95°C, followed by addition of Taq polymerase, followed by 15 minutes extension at 72°C.
- Gel electrophoresis: gel analysis was used following OpenWetWare CFrench: AGE protocol except 0,5 TAE buffer was used rather that 1x TAE. Gel staining was done using the SYBR-Safe staining solution.
- Gel purification and DNA purification: for ccm and several ligation attempts for other genes the PCR samples were run on the gel then the appropriate bands were cut out and purified using standardised QIAquick Gel Extraction Kits. For pure PCR products OpenWetWare protocol CFrench: DNAPurification1 was used.
- Vectors used: For most reaction the standard BioBrick vector pSB1C3 (provided by the Registry) was used, except for samples that were subjected to polyA tailing which were then ligated into the pGEM vector (Promega)
- Restriction digestions: Restriction digests were performed for PCR products along with vector digestion following the OpenWetWare CFrench:restriction1 protocol. For enhanced efficiency, varying ratios of insert to vector were used with the optimum ratio reached at about 3:1 to 5:1 ratio of insert digest to vector digest. Analytical restriction digests were also performed for miniprep samples using the original protocol.
- Ligations: Digested samples were mixed with 1 ul T4 ligase buffer and 1 ul T4 ligase and mixed with water to reach the final volume of 20 ul if necessary. Alternatively, polyA tailed PCR sampels were mixed with pGEM vector and used directly for ligation.
- Fusion PCR: following the ligation the samples were used as template for fusion PCR, following KodPCR protocol using forward primer for the gene and reverse primer for the vector. Extension time was adjusted to suit the length of the vector with insert.
- Transformation: Ligation and fusion PCR products were used to transform E coli JM109 competent cells using the OpenWetWare protocol Cfrench:compcellprep1 for preparation of competent cells and cell transformation).
- Transformed cell selection: Transformed cells were spread on LB agar with chloramphenicol (when using pSB1C3 vector) or LB agar with carbenicillin, Xgal and IPTG. Following overnight incubation at 37°C white colonies were chosen (rather than red colonies from pSB1C3-RFP vector or blue colonies from pGEM vector) and subcultured on plates containing the same medium.
- Miniprepping: Subcultures were used to set up overnight liquid cultures in 2,5 ml of LB. Miniprepping was performed using either the OpenWetWare protocol Cfrench:minipreps1 or standarised QIAprep Spin MiniPrep Kit. Minipreps were then restriction digested and run on a gel.
- Sequencing: size confirmed minipreps were then sent for sequencing at the University of Edinburgh GenePool.
Results
NapC
- Throughout the summer we have managed to clone the napC gene from E coli (BBa_K917003). We have inserted the gene into the standard BioBrick vector pSB1C3 and submitted it to the parts Registry. We have then linked the napC gene to the lac promoter (BBa_K917012) to characterise its functionality.
Figure 1: napC PCR
Figure 2: napC miniprep
Figure 3: pLac-napC construct analytical digestion with XbaI and PstI
Lanes 3, 4 = pSB1C3-Plac-lacZ'-napC, clones 1 and 2, digested with XbaI-PstI. Clone 2 looks as expected, clone 1 has an unexpected band around 0.6 kb.
MtrA
- We also managed to obtain the mtrA gene (BBa_K917008) of S. oneidensis and cloned it into the pSB1C3 plasmid.
Figure 4: MtrA PCR
Figure 5: mtrA transformation
Figure 6: mtrA miniprep
The obtained mtrA gene contains an internal PstI site which needs to be mutated out prior to submission and use.
CymA
We have managed to clone the cymA gene (BBa_K917009) from S. oneidensis. We have tested the gene for internal restriction sites and linked the cymA gene to the lac promoter (BBa_K917014) to characterise its functionality.
Figure 7: lanes 3, 4 = pSB1C3-cymA clones 1 and 2, analytically digested with EcoRI. Band has size correct for linearised plasmid with the gene(3kb)
lanes 5, 6 = pSB1C3-cymA clones 1 and 2, double digested with EcoRI/SpeI.
Figure 8: pSB1C3-cymA clones 1 and 2, testing internal restriction sites.
Lanes 1, 2 = clones 1 and 2, NdeI.
Lanes 3, 4 = clone 1, XbaI and XbaI/HindIII.
Lanes 5, 6 = clone 2, XbaI and XbaI/HindIII.
Gel results appear as expected
Figure 9: Lanes 4 to 6, pSB1C3-Plac-lacZ'-cymA clones 1-3, analytically digested with XbaI-PStI.
Clones 1 and 2 show bands of appropriate sizes.
ccm cytochrome maturation cluster of E. coli
We have cloned the E. coli ccm gene cluster (BBa_K917006), analysed its internal restriction sites and linked it with the lac promoter (BBa_K917013).
Figure 10: E coli ccm genes PCR (right lanes)
Figure 11: pSB1C3-ccm clones 1-6, digested with EcoRI.
Clones 1 and 5 show bands of expected size, the other clones are too small
Figure 12: pSB1C3-ccm clones 1 and 5, testing internal restriction sites.
Lanes 1, 2 = EcoRI/SpeI digestion.
Lanes 3, 4 = BamHI digestion.
Lanes 5, 6 = ClaI digestion.
Results appear as expected assuming 2 of the 3 ClaI sites are uncuttable due to overlapping dam methylation
Figure 13: Lanes 1, 2 = pSB1C3-Plac-lacZ'-ccm, clones 1 and 2, digested with XbaI-PstI.
Clone 2 looks as expected, clone 1 has an unexpected band around 0.6 kb.
MtrCAB and S. oneidensis ccm
We have also obtained good quality pure PCR products of mtrCAB and ccm genes from S. oneidensis
Figure 14: MtrCAB PCR
Figure 15: ccm genes from S. oneidensis and E. coli
Discussion and conclusions
We managed to obtain the napC, cymA, ccm and mtrA genes which are now ready for testing, using haem staining and half fuel cells. The mtrA gene still contains an internal PstI site which has to be mutated out prior to submission. We have linked napC, ccm and cymA to the lac promoter to test these new BioBricks using haem staining and half fuel cells, using our current results as reference. However, it is possible that the transformed cells will require multiple genes to function properly. Ccm genes are responsible for cytochrome maturation, which is necessary for the proper folding of multihaem cytochromes such as NapC, CymA and especially the decahaem cytochrome MtrA.
We had some success in cloning the mtrCAB and S. oneidensis ccm genes which may enhance the efficiency of the system. We intend to clone these genes into the pSB1C3 vector (BBa_K917007), link them to a promoter and test them together in order to assess the efficiency of the system.
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 (polyA tailing, fusion PCR).
The complete electron export conduit should be able to reliably export electrons in response to an external stimulus. This system can be used to enhance current biosensor systems.
One possible application would be to link our system to the arsenic promoter and construct a reliable, cheap arsenic biosensor which would generate easy to interpret data that can be stored on a computer.
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