Difference between revisions of "Part:BBa K3470021"
| Line 1: | Line 1: | ||
==Circuit== | ==Circuit== | ||
| − | Constitutive Promoter - RBS - MerE - RBS - Double Terminator | + | '''Constitutive Promoter - RBS - MerE - RBS - Double Terminator''' |
==Usage and Biology== | ==Usage and Biology== | ||
| Line 9: | Line 9: | ||
==Proposed Experimentation== | ==Proposed Experimentation== | ||
| − | To determine the final transport design, | + | To determine the final transport design, three circuits consisting of a combination of genes among MerP, MerC, MerT and MerE have been proposed. The circuit showing the most effective results must be chosen as the bio-brick for the transport system for our first plasmid. |
| − | + | Circuits we test for the final transport design system: | |
| − | 1. | + | <p> 1. '''MerP - MerT - MerC - MerE''' </p> |
| + | <p> 2. '''MerC - MerE''' </p> | ||
| + | <p> 3. '''MerP - MerT – MerE''' </p> | ||
| − | |||
| − | + | To test the efficiency and characterize each of the 4 parts separately, experiments must be carried out with each of the parts making use of 2 test circuits and 2 controls. | |
| − | + | '''Circuits:''' | |
| − | 2. Wild type Escherichia coli DH5alpha. | + | <p> 1. The final transport design system </p> |
| + | <p> 2. Constitutive Promoter- RBS – (The part to be tested, i.e. MerP, MerC, MerT or MerE) -RBS-Double Terminator </p> | ||
| + | |||
| + | '''Controls:''' | ||
| + | |||
| + | <p> 1. Final circuit design without the part to be tested </p> | ||
| + | <p> 2. Wild type ''Escherichia coli DH5alpha'' </p> | ||
| + | |||
| + | E. coli cells inoculated with methylmercury chloride must be grown for the required amount of time according to the results of the preliminary experiment respectively for the 2 circuits to be tested and 2 controls. The cell suspension must be centrifuged and the mercury concentration in the supernatant for each set should be determined with gas chromatography. Plots of concentration vs time for each of the sets must analyzed to understand the efficiency of the parts in transporting methylmercury. | ||
| + | |||
| + | |||
| + | '''Expected result:''' | ||
| + | |||
| + | The most efficient transport system is the final transport circuit design. | ||
| + | |||
| + | If there are two transport system circuits are of similar efficiency, the one with the least expected genetic burden (smaller length) must be selected. The expected result should show the efficiency of MerP, MerT, MerE, MerC all together in transporting methylmercury, which should be higher than the natural transport (without mer operon transporters). | ||
| − | |||
==References== | ==References== | ||
1. Sone, Y., Nakamura, R., Pan-Hou, H., Itoh, T., & Kiyono, M. (2013). Role of MerC, MerE, MerF, MerT, and/or MerP in resistance to mercurials and the transport of mercurials in escherichia coli. Biological and Pharmaceutical Bulletin, 36(11), 1835–1841. https://doi.org/10.1248/bpb.b13-00554 | 1. Sone, Y., Nakamura, R., Pan-Hou, H., Itoh, T., & Kiyono, M. (2013). Role of MerC, MerE, MerF, MerT, and/or MerP in resistance to mercurials and the transport of mercurials in escherichia coli. Biological and Pharmaceutical Bulletin, 36(11), 1835–1841. https://doi.org/10.1248/bpb.b13-00554 | ||
Revision as of 02:55, 22 October 2020
Circuit
Constitutive Promoter - RBS - MerE - RBS - Double Terminator
Usage and Biology
MerE is a transmembrane component of the mer transport system which helps in the uptake of mercury inside the cell. It helps in the transport of organo-mercury compounds. (Sone et al., 2013)
Proposed Experimentation
To determine the final transport design, three circuits consisting of a combination of genes among MerP, MerC, MerT and MerE have been proposed. The circuit showing the most effective results must be chosen as the bio-brick for the transport system for our first plasmid.
Circuits we test for the final transport design system:
1. MerP - MerT - MerC - MerE
2. MerC - MerE
3. MerP - MerT – MerE
To test the efficiency and characterize each of the 4 parts separately, experiments must be carried out with each of the parts making use of 2 test circuits and 2 controls.
Circuits:
1. The final transport design system
2. Constitutive Promoter- RBS – (The part to be tested, i.e. MerP, MerC, MerT or MerE) -RBS-Double Terminator
Controls:
1. Final circuit design without the part to be tested
2. Wild type Escherichia coli DH5alpha
E. coli cells inoculated with methylmercury chloride must be grown for the required amount of time according to the results of the preliminary experiment respectively for the 2 circuits to be tested and 2 controls. The cell suspension must be centrifuged and the mercury concentration in the supernatant for each set should be determined with gas chromatography. Plots of concentration vs time for each of the sets must analyzed to understand the efficiency of the parts in transporting methylmercury.
Expected result:
The most efficient transport system is the final transport circuit design.
If there are two transport system circuits are of similar efficiency, the one with the least expected genetic burden (smaller length) must be selected. The expected result should show the efficiency of MerP, MerT, MerE, MerC all together in transporting methylmercury, which should be higher than the natural transport (without mer operon transporters).
References
1. Sone, Y., Nakamura, R., Pan-Hou, H., Itoh, T., & Kiyono, M. (2013). Role of MerC, MerE, MerF, MerT, and/or MerP in resistance to mercurials and the transport of mercurials in escherichia coli. Biological and Pharmaceutical Bulletin, 36(11), 1835–1841. https://doi.org/10.1248/bpb.b13-00554