Part:BBa_K1701000

GolB

Gold-specific binding protein (GolB) is a gold-binding chaperon discovered in S. Typhimurium which has been verified that the display of GolB on E.coli cell surface permitted selective enrichment of gold ions from media containing various metal ions.

Sequence and Features

Assembly Compatibility:

• 10
  COMPATIBLE WITH RFC[10]
• 12
  COMPATIBLE WITH RFC[12]
• 21
  COMPATIBLE WITH RFC[21]
• 23
  COMPATIBLE WITH RFC[23]
• 25
  COMPATIBLE WITH RFC[25]
• 1000
  COMPATIBLE WITH RFC[1000]

Background

Certain living organisms usually have mechanisms for maintaining homeostasis and resistance to heavy metal ions including gold. This offered an opportunity for genetically engineered microorganisms applied to gold detection and absorption. The MerR family is such a group of bacterial transcriptional regulators that respond to environmental stimuli such as heavy metals. GolS, a member of the MerR family presented in S. typhimurium, which shows sequence similarity with the E. coli and Salmonella CueR, had been demonstrated to be with high specificity for recognition of Au salts without cross-detection and helps the bacteria adapt to survive in Au-rich environments. And golB, a small neighbouring gene which codes for a putative gold-chaperone that is induced by GolS in the presence of Au ions, had also been verified.

Biology

Gold-specific binding protein (GolB) is a gold-binding chaperon discovered in S. typhimurium which is less than seventy amino acids in length. It has been verified that the display of GolB on E.coli cell surface permitted selective enrichment of gold ions from media containing various metal ions. The following figure shows the genetic organization of the gol locus in the S. typhimurium LT2 genome.

a)

Figure 1(a).Genetic organization of the gol locus in the S. typhimurium LT2 genome.

b)

Figure 1 (b).Genetic organization of the gold inductive RFP expression plasmid in E. coli.

c)

Figure 1 (c). Fluorescence measurement of E. coli cells containing the gold induced RFP expression plasmid after gradient concentrations of HAuCl4 (Au3+) induction and re-suspended in PBS buffer (pH 7.4).

Part uses

we heterologously expressed the gold-binding chaperon GolB gene from S. Typhimurium into Bacillus subtilis. Hence, we displayed GolB on Bacillus subtilis biofilm or its spore surface to construct a whole-cell absorption specific for gold, which is able to be easily recovered and therefore is good for application outside of laboratory settings. What’s more, it can adsorb gold under both benign conditions and adverse circumstances.

We used TasA, the major protein of the biofilm matrix component in B. subtilis, and CotC, the B.subtilis spore component, as fusion partner to display GolB.

When nutrition is sufficient, we can use plant polysaccharides to induce the formation of biofilm, on which protein TasA can be simultaneously expressed with GolB. Besides, when conditions get adverse for the growth of cells, B. subtilis produce spores to survive. If we express the GolB along with the coat protein CotC, spores will be capable of gold adsorption. Therefore, B. subtilis can adsorb gold under both benign conditions and adverse circumstances, which tremendously improve the efficiency of gold adsorption.

To realize this goal, we have designed four pathways shown in Figure 2, which are used in our project. In order to improve the efficiency of the expression of the two former pathways, we utilized a constitutive promoter Pveg, a biobrick part in the biological parts of iGEM used by us to replace the promoter Ptas and Pcot, which is involved in the two latter payways.

Figure 2. Four pathways designed by our group involving GolB part.

We will construct our plasmid in E.coli first and affirm the feasibility of the pathways, after which we will transform the plasmid into B.subtilis. After linearization of the plasmid, we can integrate the target genes into the chromosomes of B.subtilis utilizing homologous recombination. The process and shuttle plasmid can be shown as follows.

Figure 3. The process to integrate the target genes into the chromosomes of B.subtilis utilizing homologous recombination.

Figure 4. The shuttle plasmid designed by our project including the preceding pathways.

To further improve the selectivity of gold adsorption, we had a plan to design a pathway as follows. With the gol specific promoter pGolB, the heavy metal-binding biofilm protein/coat protein can be expressed only when there is specific gold in the solution. In addition, we could do a pre-test to demonstrate the feasibility of the pathway by replacing GolB with the reporter protein GFP.

Figure 5. The designed pathway to improve the selectivity of gold adsorption.

Results

Homologous recombination

After we constructed the 16 kits in E.coli, we inserted them into the shuttle plasmid pDG1730 which can transfer from E.coli to B. subtilis. We insert our fusion genes between two sequences of the amylase genes on the plasmid. By homologous recombination, our fusion genes will replace the amylase gene on the genome of B. subtilis. In order to test and verify whether homologous recombination is successful, we built the following three steps. Antibiotic selection, bacterial PCR analysis and amylase activity analysis. After a series of test and verification experiments, we have successfully inserted the 16 kits into the genome of B. subtilis. The following figure shows the result of the amylase activity analysis. The picture on the right is the control group while the pictures on the left are the experiment groups. When we applied iodine on the plate with starch, there would be hydrolysis cycles on the plate because the α-amylase gene wasn’t replaced. However, there wouldn’t be hydrolysis cycles on the plate if homologous recombination was successful.

Figure 6. Result of homologous recombination.

Bio-adsorption

As shown in Fig. 7, B. subtilis bacteria with the TasA-dependent surface displayed GolB with promoter Pveg were able to adsorb gold ions with a capacity of about 5.2 μmol g-1cells, which is 26-fold higher than un-displayed samples. While bacteria with promoter Ptas were able to adsorb gold ions with a capacity of about 3.5 μmol g-1cells, which is 18-fold higher than un-displayed samples.

Figure 7. Adsorption of gold ions by B. subtilis TasA-dependent surface-displayed GolB protein.

As shown in Fig. 8, B. subtilis endospores with the CotC-dependent surface displayed GolB with promoter Pveg were able to adsorb gold ions with a capacity of about 4.4 μmol g-1cells, which is 22-fold higher than un-displayed samples. While bacteria with promoter Pcot were able to adsorb gold ions with a capacity of about 3.85 μmol g-1cells, which is 19-fold higher than un-displayed samples.

Figure 8. Adsorption of gold ions by B. subtilis endospore CotC dependent surface-displayed GolB protein.

In conclusion, the engineered B. subtilis as well as the endospores worked well in heavy metal adsorption. Besides, it is proved by us that Pveg is a more efficient promoter than Ptas and Pcot, so maybe we can utilize promoter Pveg when engineering B. sublitis.

References

[1].Wei, W.; Zhu, T.; Wang, Y.; Yang, H.; Hao, Z.; Chen, P.*; Zhao, J.*. “Engineering a Gold-specific Regulon for Cell-based Visual Detection and Recovery of Gold”, Chem. Sci., 2012, 3, 1780-1784.

[2].Cerminati, S., F.C. Soncini and S.K. Checa, Selective detection of gold using genetically engineered bacterial reporters. Biotechnol Bioeng, 2011. 108(11): p. 2553-60.