Difference between revisions of "Team:Tec-Monterrey/Description"

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iGEM 2016 - Tec de Monterrey

Bioleaching Experiments

Our first microorganism, A. ferrooxidans is currently used in a few mining companies for the recovery of Zn, Ni and Cu from the residual dirt and rocks of their processes. A. ferrooxidans can recover these metals thanks to its extracellular matrix, which has an environment that facilitates electron interchange. The enzyme tetrathionate hydrolase (TetH), which is produced inside the bacteria and then taken out to the external matrix, constantly converts tetrathionate to two molecules: thiosulfate and elemental sulfur.
The reaction that takes place is illustrated in the following figure:

Figure 1. TetH is involved in the electron transfer for A. ferrooxidans. The reaction increases the acidity of the media and releases sulfates, which chelate metals.

For the bioleaching process, e-waste was washed three times with distilled water to diminish the natural basic pH of the metals. The protocol for the bioleaching experiments consisted in adding 1 g of slag per liter of medium in a flask containing A. ferrooxidans in a set exponential phase. The flasks were incubated for 15 days, taking aliquotes the days 3, 6, 9, 12 and 15 to analyze the metal content with ICP-OES, then the data would be compared to the original ewaste and the metals solubilized were calculated.

After being washed three times with distilled water, the solid residues of the bioleach treatment or the acid medium treatment were transferred to the Chromobacterium violaceum alkaline bioleaching phase of our MetalEca process.

A. Ferrooxidans is an acidophilic bacteria that turns its own culture media into a more acidic environment to satisfy its growing conditions. We added bromocresol green (0.5% V/V) on the petri dishes in order to identify the colonies and calculate the colony-forming unit of each experimental group.

Tetrathionate is a key intermediate during RISC oxidation, hydrolyzed by tetrathionate hydrolase (TetH), and used as sole energy source. The overexpression of TetH in A. ferrooxidans leads to have a high expression of sulfates in the culture media, with more activity, more protons are released to the media and leads to a greater solubilization of metal ions.

FUR/FURBOX

Although iron is the most abundant transition metal on Earth, its solubility is very low at neutral pH in aerobic environments. In such environments, Fe(II) is generally not available because it rapidly oxidizes to Fe(III), which precipitates as insoluble ferric ion complexes. (Quatrini, 2005). Thanks to the acidic conditions of A. ferrooxidans Fe(II) is stable and Fe(III) is more soluble than at standard pH (7.0)

Notes
Phase I: Acidithiobacillus ferrooxidans was obtained from the Geomicrobiology Laboratory of the Autonomous University of San Luis Potosí, which was isolated from a mine in Durango, Mexico. The medium contained the following ingredients (g/L): 0.2 - ammonium sulfate, 0.5 - magnesium sulfate, 0.25 - calcium chloride, 3 - dipotassium hydrogen phosphate and 0.005 - iron sulfate. The agar medium was made with the same concentrations, only 12.5 g/L was added. Both mediums were adjusted to a pH of 4.0 and autoclaved at 121 Celsius for 15 min.

A first experiment was carried to evaluate the growth of the bacteria in liquid medium with elemental sulfur and sodium thiosulfate. Group 1 had 10 g/L of elemental sulfur, group 2 had 10 g/L of sodium thiosulfate and group 3 had 5 g/L of elemental sulfur + 5 g/L of sodium thiosulfate.

The groups of the experiment consisted in: (1) Control medium without bacteria, (2) Control medium with bacteria without genetic modifications, (3) Bacteria with tetH overexpression. It was expected that the curve of the group 3 had the biggest slope value.

Unfortunately three weeks after our first inoculum we lost our strain due to a failure in the pH measurements, when we tried to inoculate them again to fresh media cells would not grow. It was found that the pH of the original strain had come down to a pH of 0.63, thus all organic material was dissolved despite A. ferrooxidans being an acidophile.

Aim of the module: gold & silver solubilization

With the acid oxidation process used in Module I, metals such as copper, zinc and nickel are solubilized by A. ferrooxidans, but valuable metals like gold and silver are not. However, the recovery of these last two metals is vital in making the process economically viable, due to their high market value and relative scarcity. An effective way to solubilize them is by bioleaching with a cyanide-producing organism such as C. violaceum.

Process description

Why Chromobacterium violaceium

How will we improve the process?

In order to improve the efficiency of the process, we will modify C. violaceum using two basic constructs:

A gold/copper-sensitive cyanide producing system
- Though C. violaceum is a native cyanide producer, this basal production is relatively low and regulated by quorum sensing.
  - In a previous study, cyanide production was successfully uncoupled from quorum sensing regulation by transformation with hydrogen cyanide synthase (hcnABC) under pARA regulation (Tay et al, 2013).
- pGolS is a promoter that… (sensitive to gold)
- Our construct is constituted by the pgolS promoter and the coding sequence of CueR. As the pgolS promoter has a basal transcription level, some CueR would be constantly expressed. CueR is a transcription factor that stimulates the transcription at the pgolS promoter when bound to copper or gold, as was described by the iGEM York 2013. Thus, this construct increases its own expression through positive feedback in the presence of gold or copper through the production of a copper/gold sensitive protein. Its organism of origin is Salmonella typhimurium.
Proton Pump
- Hydrogen cyanide synthase generates HCN, not free CN- ions. Since free CN- ions are responsible for the reaction that solubilizes gold, we must take into account the dissociation of HCN. As HCN is a weak acid (pKa = 9.22[source?]), it requires a basic pH in order to dissociate. In the mining industry, it has been established that a pH > 9.4 is ideal (Marsden & House, 2006), as at lower pH values not enough HCN is dissociated; and at higher pH values other factors (such as salinity) become more important. [source?]
- As shown in the modelling section, the overall gold solubilizing reaction generates H+. Thus, in order to mantain a pH = 9.5, a base has to be continously added to the reactor.
- In order to improve the efficiency of C. violaceum’s activity under these alkaline conditions, we will introduce a proton pump. [explicación de por qué creemos que esto funcionaría, referenciada al paper de Suria]. Specifically, we will use the intermembrane protein Na(+)/H(+) antiporter NhaA, which is a proton pump from E. coli. It excretes one Na(+) ion in exchange for two H(+) external protons. This protein is active at alkaline pH.
- Within our construct, the proton pump is regulated by a weak constitutive promoter from the Anderson collection, and the coding sequence is optimized for its expression in C. violaceum. We will also test it as a potential selectivity marker for C. violaceum under these alkaline conditions (pH=9.5).

Safety Considerations

Post-processing:cyanide degradation module

After gold is recovered in the third module, we will degrade the remaining cyanide, as it is too toxic to be released to the environment without previous treatment.

We will use a different transformant of C. violaceum that will overexpress cyanide hydratase, a cyanide degrading enzyme. This enzyme has been found in different cyanide-degrading fungi such as Aspergillus niger and Fusarium lateritium.

Cyanide hydratase has been successfully expressed in E. coli, where it retains its original activity. In fact, Brown, Turner, and O'reilly (1995) reported that a modified E. coli reached 5.5 times the cyanide degrading activity compared to that observed in the native F. lateritium.

References

Broetto, L., Cecagno, R., Sant'anna, F. H., Weber, S., & Schrank, I. S. (2005). Stable transformation of Chromobacterium violaceum with a broad-host-range plasmid. Appl Microbiol Biotechnol Applied Microbiology and Biotechnology, 71(4), 450-454. doi:10.1007/s00253-005-0140-5
Pham, V., & Ting, Y. P. (2009). Gold Bioleaching of Electronic Waste by Cyanogenic Bacteria and its Enhancement with Bio-Oxidation. AMR Advanced Materials Research, 71-73, 661-664. doi:10.4028/www.scientific.net/amr.71-73.661
Niven, D. F., Collins, P. A., & Knowles, C. J. (1975). The Respiratory System of Chromobacterium violaceum Grown under Conditions of High and Low Cyanide Evolution. Journal of General Microbiology,90(2), 271-285. doi:10.1099/00221287-90-2-271
Tay, S. B., Natarajan, G., Rahim, M. N., Tan, H. T., Chung, M. C., Ting, Y. P., & Yew, W. S. (2013). Enhancing gold recovery from electronic waste via lixiviant metabolic engineering in Chromobacterium violaceum. Scientific Reports, 3. doi:10.1038/srep02236
Marsden, J. O., & House, C. I. (2006). The chemistry of gold extraction. Littleton: Society of Mining Metallurgy and Exploration.
Perky, R., Browner, R., Dunnei, R., & Stoitis, N. (1999). Low pH cyanidation of gold. Minerals Engineering, 12(12), 1431-1440. doi:10.1016/s0892-6875(99)00132-6
Brown, D. T., Turner, P. D., & O'reilly, C. (1995). Expression of the cyanide hydratase enzyme from Fusarium lateritium in Escherichia coli and identification of an essential cysteine residue. FEMS Microbiology Letters, 134(2-3), 143-146. doi:10.1111/j.1574-6968.1995.tb07928
Brazilian National Genome Project Consortium (2003). The complete genome sequence of Chromobacterium violaceum reveals remarkable and exploitable bacterial adaptability. Proceedings of the National Academy of Sciences, 100(20), 11660-11665. doi:10.1073/pnas.1832124100
Rinágelová, A., Kaplan, O., Veselá, A. B., Chmátal, M., Křenková, A., Plíhal, O., … Martínková, L. (2014). Cyanide hydratase from Aspergillus niger K10: Overproduction in Escherichia coli, purification, characterization and use in continuous cyanide degradation. Process Biochemistry, 49(3), 445–450. http://doi.org/10.1016/j.procbio.2013.12.008

References

Centers for disease control and prevention. (2009). Biosafety in Microbiological and Biomedical Laboratories. (5th Edition ed.). United States: HHS Publication.

Norma Oficial Mexicana NOM-157-SEMARNAT-2009. Diario Oficial de la Federación, 30 de agosto de 2011.

Norma Mexicana NMX-AA-058-SCFI-2001. Diario Oficial de la Federación, 09 de julio de 2009.