Part:BBa_K3282007
PbrD and pbrT under Tac promoter
The part consists of Tac promoter (BBa_K3282006), two Anderson RBS (Part:BBa_J61109), separating two coding regions of lead binding protein (BBa_K3282002) and lead transport protein (BBa_K3282001), followed by a TE terminator (Part:BBa_B0012).
The pbrD gene encodes a Pb(II)-binding protein which is essential for functional lead sequestration whereas the expression of pbrT leads to uptake of lead into the cytoplasm to reduce interaction of free Pb(II) with side chains of membrane and periplasmic proteins, which would cause extensive cellular damage [1].
Experiment
This part was ligated into pUC19 and transformed into Escherichia coli Nissle. The expression of pbrD and pbrT was demonstrated by performing sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analysis. The cells were cultured in enriched media (containing peptone, yeast extract, phosphates, chlorides and sulphates) at 37 °C. The cells were grown overnight followed by cell harvesting to normalize the OD values to 2. After normalization, the cells were resuspended in fresh enriched medium containing 10 µM, 50 µM and 200 µM of Pb(NO3)2. As a negative control, the experiment was also performed with the non engineered EcN in growth medium containing 50 µM Pb(NO3)2. Samples were collected every hour for OD measurement. For investigating the lead accumulation by engineered bacteria, samples were collected at 0 hour, 2.5 hour and 5 hour after the addition of Pb(NO3)2.
Results
The SDS-PAGE analysis result can be seen in Figure 1. The pbrD is a 26.7 kDa and pbrT 68.3 kDa protein. Therefore the bands were expected just above the 25 kDa band and just below 70 kDa band for pbrD and pbrT respectively. The gel shows that the engineered bacteria as well as the control have bands with the expected molecular weight. Thus, we cannot confirm that the bands corresponds to the desired proteins. It is possible that there are other proteins expressed in E. coli of the same molecular weight, masking the expression of pbrD and pbrT.
Figure 1: Bioaccumulation of Lead. Samples were harvested at different time points, and the total cellular proteins were analyzed by SDS-PAGE. Image with protein bands of EcN after induction with IPTG, showing pbrD at 26.7 kDa and pbrT at 68.3 kDa. The control shown is wild type EcN without pbrD and pbrT.
Figure 2: Comparison of lead uptake by engineered EcN with wild type control of EcN.
Figure 3: Comparison of growth rate of engineered EcN with wild type control of EcN.
A significant difference in the lead concentration can be seen between the engineered EcN cells containing lead uptake and transport proteins, and the wild type EcN cells without the proteins. The initial lead concentration added was 41.44 mg/L, maintained at pH 3 and the concentration at 0 hour was 6 mg/L, showcasing 85.52 % decrease. The culture maintained at pH 5 with an initial lead concentration of 10.36 mg/L also showed a 89.38 % decrease in lead concentration at time 0 hour. In comparison, the control shows no lead accumulation. This rapid decrease proves that the engineered cells are capable of accumulating lead and can survive under conditions simulating gut. However, a certain percentage of the total reduction in lead concentration can be attributed to the use of borosilicate glass Erlenmayer flasks since it has been shown that borosilicate glass can adsorb lead ions [2]. However, the study also mentions that adsorption of lead by borosilicate glass is time dependent and adsorption was found to be only 17.2% over a period of 20 hours. This concludes that not all the lead adsorption was by borosilicate glass but also by the bacterial strains, proving that the engineered EcN cells can accumulate lead and can survive under adverse conditions such as pH 3 and pH 5, as is evident from Figure 3. The overall lead accumulation was calculated to be 41 % by the engineered EcN.
Future Improvements
Since there was no visible protein expression at the expected position, one could try to add a histidine tag, making purification of protein possible and one would be able to assess the protein expression. Another solution would be to use a stronger promoter, which would give a higher expression of protein, and might be visible on the SDS-PAGE. Another improvement could be to make sure the protein is not stuck in the wells of the gel. Further, fluorescent protein reporters such as GFP and RFP can be used for more convenient protein detection and stronger output signals as shown by Xiaoqiang, J et al [3].
References
1. Borremans, B., Hobman, J. L., Provoost, A., Brown, N. L., & van Der Lelie, D. (2001). Cloning and functional analysis of the pbr lead resistance determinant of Ralstonia metallidurans CH34. Journal of bacteriology, 183(19), 5651–5658. doi:10.1128/JB.183.19.5651-5658.2001
2. Kim, N. D., & Hill, S. J. (1993). Sorption of lead and thallium on borosilicate glass and polypropylene: Implications for analytical chemistry and soil science. Environ Technol, 14(11), 1015-1026. doi:10.1080/09593339309385378
3. Xiaoqiang Jia, Tingting Zhao, Yilin Liu, Rongrong Bu, Kang Wu, Gene circuit engineering to improve the performance of a whole-cell lead biosensor, FEMS Microbiology Letters, Volume 365, Issue 16, August 2018, fny157, https://doi.org/10.1093/femsle/fny157
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 1450
Illegal NheI site found at 1648 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1398
Illegal NgoMIV site found at 1861 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 2005
Illegal SapI.rc site found at 2235
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