Difference between revisions of "Part:BBa K3470010"
 
(One intermediate revision by the same user not shown)
Line 1: Line 1:
−
Constitutive Promoter - RBS – MerP – RBS – Double Terminator
+
<partinfo>BBa_K3470010 short</partinfo>
  
 +
==Circuit==
  
−
MerP is the periplasmic component of the mer transport system which helps in the uptake of mercury inside the cell. It binds to a single Hg (II) ion using its two conserved cysteine residues, which define its metal-binding motif. It removes any attached ligands before passing the Hg (II) on to MerT transmembrane protein. It is the most abundantly synthesized protein in the mer operon due to its role in scavenging of Hg (II) in the periplasm. (Steele, R. A., & Opella, S. J.1997)
+
'''Constitutive Promoter - RBS – MerP – RBS – Double Terminator'''
−
To determine the final transport design, we test three circuits consisting of a combination of genes among MerP, MerC, MerT and MerE. The circuit showing the most effective results can be chosen as the bio-brick for the transport system for our first plasmid. Circuits we test for the final transport design system: MerP-MerT-MerC-MerE, MerC-MerE, MerP-MerT –MerE. To test the efficiency and characterize each of the 4 parts separately we carry out experiments with each of the parts making use of 2 test circuits and 2 controls. Circuits: The final transport design system, Constitutive Promoter- RBS – (The part to be tested, i.e. MerP, MerC, MerT or MerE) -RBS-Double Terminator. Controls: Final circuit design without the part to be tested, Wild type Escherichia coli DH5alpha. 
+
−
E. coli cells inoculated with methylmercury chloride are 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 is centrifuged and the mercury concentration in the supernatant for each set is determined with gas chromatography. Plots of concentration vs time for each of the sets are analysed to understand the efficiency of the parts in transporting methylmercury.
+
−
Expected result: The most efficient transport system is the final transport circuit design. What is unecpected is if there are two transport system circuits with similar efficiency, the one with the least genetic burden will 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).
+
  
 +
==Usage and Biology==
  
 +
MerP is the periplasmic component of the mer transport system which helps in the uptake of mercury inside the cell. It binds to a single Hg (II) ion using its two conserved cysteine residues, which define its metal-binding motif. It removes any attached ligands before passing the Hg (II) on to MerT transmembrane protein. It is the most abundantly synthesized protein in the mer operon due to its role in scavenging of Hg (II) in the periplasm. (Steele, R. A., & Opella, S. J.1997).
  
−
References:  
+
==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:  
 +
 
 +
<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:'''
 +
 
 +
<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).
 +
 
 +
==Sequence and features==
 +
 
 +
<partinfo>BBa_K3470010 SequenceAndFeatures</partinfo>
 +
 
 +
==References==
  
  
 
Steele, R. A., & Opella, S. J. (1997). Structures of the reduced and mercury- bound forms of merP, the periplasmic protein from the bacterial mercury detoxification system. Biochemistry, 36(23), 6885–6895. https://doi.org/10.1021/bi9631632
 
Steele, R. A., & Opella, S. J. (1997). Structures of the reduced and mercury- bound forms of merP, the periplasmic protein from the bacterial mercury detoxification system. Biochemistry, 36(23), 6885–6895. https://doi.org/10.1021/bi9631632

Latest revision as of 13:53, 23 October 2020

Methylmercury Transport system - merP (Without MerR)

Circuit

Constitutive Promoter - RBS – MerP – RBS – Double Terminator

Usage and Biology

MerP is the periplasmic component of the mer transport system which helps in the uptake of mercury inside the cell. It binds to a single Hg (II) ion using its two conserved cysteine residues, which define its metal-binding motif. It removes any attached ligands before passing the Hg (II) on to MerT transmembrane protein. It is the most abundantly synthesized protein in the mer operon due to its role in scavenging of Hg (II) in the periplasm. (Steele, R. A., & Opella, S. J.1997).

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).

Sequence and features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]

References

Steele, R. A., & Opella, S. J. (1997). Structures of the reduced and mercury- bound forms of merP, the periplasmic protein from the bacterial mercury detoxification system. Biochemistry, 36(23), 6885–6895. https://doi.org/10.1021/bi9631632