Cytochromes

Overview

Figure 1: Extracellular electron transfer via cytochromes in E. coli with a minimal set of genes with a minimal set of genes from Shewanella oneidensins MR-1.

To enable transfer of electrons from the general metabolism to the outside of the cell the mtrCAB gene cluster from Shewanella oneidensis MR-1 was heterologously expressed in E. coli. The cluster encodes for three genes that form a electron shuttle pathway via different c-type cytochromes an a β -barrel membrane protein. These genes represent a minimal set of genes for a working pathway.For correct heme insertion the cytochrome c maturation machinery is required. The corresponding genes are naturally expressed in E.coli under anaerobic cultivation, for aerobic expression they have to be expressed via plasmid. The mtrCAB cluster contains two illegal restriction sites, which where removed by a silent mutation via overlap-extension-PCR. The resulting three fragments were combined and ligated with pSB1C3 via Gibson assembly. Subsequently this gene cluster was combined with three promotors and ribosome binding sites of varying strength form the parts registry. Furthermore it was attempted to clone the ccmAH cluster as well was unsuccesfull. This is, however a minor issue, since the microbial fuel cell will work under anareobic conditions. The proteins could not be functional characterized via SDS-PAGE and absorption spectrometry.

Theory

Cell membranes work as a natural insulator and prevent the flow from electrons out of the cell. To enable transfer of electrons from the general metabolism to the outside of the cell we had to alter the membrane of our organism E. coli without disturbing cell growth, stability and metabolism. Some species from the genera Shewanella and Geobacter have developed different mechanisms to allow extracellular electron transfer. In Shewanella oneidensis MR-1 this is achieved via different c-type cytochromes, which shuttle the electrons along a defined molecular route from the cytoplasma and the inner membrane to the outside of the cell during anaerobic respiration. This pathway is very well understood and characterized.

Genetic Approach

Previous work suggests that a working electron transfer chain can be achieved by a minimal set of three genes, the periplasmatic decaheme MtrA, the outer membrane β -barrel protein mtrB and the outer membrane cytochromes MtrC. MtrA interacts with at least one native redox protein, f.e. CymA and can therefore start the transfer of electrons.
Additionally another set of genes, the cytochrome c maturation genes (ccmABCDEFGH), is required for correct protein localization and heme insertion into MtrA and MtrC. Under anaerobic conditions these genes are naturally expressed in E. coli, whereas under aerobic conditions we had to co-express them. For aerobic growth the cells were transformed with both plasmids, containing the cytochrome-cluster, as well as the ccm-cluster . By this approach extracellular electron transfer should be possible in E.coli and allow the use of this genetically engineered strain in a microbial fuel cell.

Protein Overview

• MtrA
  • Size:32 kD
  • periplamatic decaheme type c cytochrome
  • needs ccm machinery for heme insertion

• MtrB
  • Size:72 kD
  • 2 strand β-barrel membrane protein
  • needs MtrA for stability

• mtrC
  • Size:69 kD
  • outer membrane decaheme tyoe c cytochrome
  • needs ccm machinery for heme insertion
  • needs MtrB for correct localisation

• ccmAH
  • cytochrome c maturation cluster
  • loads heme to apocytochromes

Localisation

• The genes mtrA, mtrB and mtrC are organized in an operon (Beliaev et al. 1998, 2001) in the genome of Shewanella oneidensis MR-1 and could therefore expressed in one piece. However, because of two illegal PstI restriction sites at 1793bp and 2078bp, we used overlap extension pcr with primers suitable for Gibson assembly to amplify three individual fragments, where the restriction site in question was deleted by a silent mutation. The fragments were joined back together and ligated into the pSB1C3 vector via Gibson assembly in one step.

Mechanism

• mtrCAB and ccmAH are expressed in the cytosol. The proteins are translocated into the periplasma via the sec secretion system.
• The ccm proteins form a large complex and accomplish the maturation of the decaheme proteins MtrA and MtrC. The system first loads the heme into the periplasm and catalizes the formation of thioester bonds that link the heme to two cystein residues in the apocytochrome. Afterwards the axial ligands are located towards the heme and the holocytochrome is folded.(Sanders et al. 2010).
• In the following MtrB is transfered into the membrane, whereas mtrC is translocated at the outer membrane. MtrA remains in the periplasm.

Difficulties

• MtrA seems to be necessary for the stability of MtrB (Schicklberger et al. 2011)
• MtrB itself is required for the correct location and incorporation of MtrC (Meyer CR, Meyer JM, 2002) and is involved in the interaction between MtrC and MtrA (Beliaev AS, Saffarini DA1, 1998).
• Furthermore extensive postranslational processing is required for correct incorporation of all hemes, folding and localisation of the cytochromes. Considering these difficulties the expression of even a single cytochrome is a major challenge (Jensen et al. 2010).

Results

Genetics

• The isolation of the mtrCAB cluster from the genome of Shewanella and the deletion of illegal restriction sites could be accomplished
• The gene cluster was succesfully ligated into the shipping vector pSB1C3 forming the biobrick <bbpart>BBa_K1172401</bbpart>
• The gene cluster was ligated into three different expression vectors forming the following devices
  • <bbpart>BBa_K1172403</bbpart>
  • <bbpart>BBa_K1172404</bbpart>
  • <bbpart>BBa_K1172405</bbpart>

Characterisation

• A SDS-PAGE of periplasmatic and membrane fractions did not yield postive results
• The redox activity of MtrA and MtrC was probed via absorption spectroscopy and did not show any activity

Conclusion

• The electrone transfer system from Shewanella oneidensis MR-1 is known to be suitable for the usage in a microbial fuel cell.
• The expression, heme-loading, correct folding and localisation of the cytochromes is very complex and hard to achieve.

References

• Beliaev, A. S., D. A. Saffarini, J. L. McLaughlin, and D. Hunnicutt. 2001. MtrC, an outer membrane decahaem c cytochrome required for metal reduction in Shewanella putrefaciens MR-1. Mol. Microbiol. 39:722-730.

• Jensen HM, Albers AE, Malley KR, Londer YY, Cohen BE, et al. (2010) Engineering of a synthetic electron conduit in living cells. Proc Natl Acad Sci USA. 10.1073/pnas.1009645107.

• Grove, J., Tanapongpipat, S., Thomas, G., Griffiths, L., Crooke,

H., and Cole, J. (1996)Escherichia coliK-12 genes essential for the synthesis of c-type cytochromes and a third nitrate reductase located in the periplasm. Mol. Microbiol. 19, 467−481

• Sanders, C., Turkarslan, S., Lee, D.-W., and Daldal, F. (2010)

Cytochromecbiogenesis: the Ccm system.Trends Microbiol. 18, 266− 274.

• Schicklberger, M., Bucking, C., Schuetz, B., Heide, H., and

Gescher, J. (2011) Involvement of theShewanella oneidensisdecaheme cytochrome MtrA in the periplasmic stability of the beta-barrel protein MtrB.Appl. Environ. Microbiol. 77, 1520−1523.

• Myers CR, Myers JM (2002) MtrB is required for proper incorporation of the cytochromes OmcA and OmcB into the outer membrane of Shewanella putrefaciens

MR-1.Appl Environ Microbiol68:5585–5594.

• Beliaev AS, Saffarini DA (1998)Shewanella putrefaciensmtrB encodes an outer membrane protein required for Fe(III) and Mn(IV) reduction.J Bacteriol180:6292–6297.