Part:BBa_K2573000
MetE Coding Device
Usage and Biology
Methionine is an essential amino acid for E.coli growth, and the MetE gene is essential for methionine synthesis. It encodes for an enzyme that catalyzes the final step of de novo methionine biosynthesis without using an intermediate methyl carrier. For optimal MetE function, vitamin B12 should not be present, as it functions as a MetE repressor.
This part is the MetE gene cassette under the inducible LacI promoter, designed to be a MetE coding device.
A 2.4kb fragment containing the MetE gene from plasmid pSKA397 was cloned into Bba_J04450 via PCR and NEBuilder HiFi DNA Assembly.
REFERENCES:
Pejchal, Robert, and Martha L Ludwig. “Cobalamin-Independent Methionine Synthase (MetE): A Face-to-Face Double Barrel That Evolved by Gene Duplication.” PLOS ONE, Public Library of Science, journals.plos.org/plosbiology/article?id=10.1371%2Fjournal.pbio.0030031.
“Escherichia Coli K-12 Substr. MG1655 MetE.” MetaCyc Parathion Hydrolase, biocyc.org/gene?orgid=ECOLI&id=EG10584.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 1864
- 1000COMPATIBLE WITH RFC[1000]
Characterization of MetE Coding Device
We transformed this BioBrick (BBa_K2573000) into E. coli strain JT2. JT2 has MetE in its genome, under the CcaS/R promoter. However, this strain does not contain genes encoding CcaS/R, meaning it is unable to express MetE.
BBa_K2573000 in JT2 was grown in M9 medium with and without methionine. Since methionine is essential for bacterial growth, and JT2 is a methionine knockout, growth of JT2 in a methionine deficient medium indicates that the MetE BioBrick functions as intended. Empty JT2 cells were also grown in M9 with and without methionine, to confirm that the MetE gene in the JT2 genome is non-functional. BBa_J04450 in E. coli DH5a cells, which contain MetE in the genome, were also grown in the same media as a control to show that bacteria are able to grow in the M9 prepared.
Figure 1: BioBrick in JT2, empty JT2, and DH5a cells were grown in LB. Overnight cultures of BioBrick in JT2, empty JT2, and DH5a were rinsed 3x with M9 to remove residual LB.
Figure 2: Each strain (BioBrick in JT2, empty JT2, DH5a) was inoculated in M9 with and without methionine.
OD 600 after inoculation
- 20ul of overnight culture (washed of LB) inoculated into 5ml M9 (with or without methionine) and appropriate antibiotics:
| Sample | OD 600nm |
|---|---|
| JT2 Empty (+ meth) | 0.011 |
| JT2 Empty | 0.012 |
| BBa_K2573000 (+meth) | 0.011 |
| BBa_K2573000 | 0.010 |
| BBa_J04450 (+meth) | 0.005 |
| BBa_J04450 | 0.006 |
Figure 3: Growth of each strain in M9 with or without methionine
OD 600 after 10h of growth in 37 degree incubator
| Sample | OD 600nm | Growth |
|---|---|---|
| JT2 Empty (+ meth) | 1.262 | Positive |
| JT2 Empty | 0.0752 | Negative |
| BBa_K2573000 (+meth) | 1.237 | Positive |
| BBa_K2573000 | 1.311 | Positive |
| BBa_J04450 (+meth) | 1.420 | Positive |
| BBa_J04450 | 1.506 | Positive |
RESULTS
The empty JT2 was able to grow in M9 with methionine, but not able to grow in M9 without methionine, showing that JT2 is unable to grow in methionine deficient media. However, when transformed with this BioBrick, (BBa_K2573000) JT2 was then able to grow in M9 without methionine.
Part Improvement
Group: iGEM19_Waterloo (2019-10-21)
Author: Michael Lam, Katie Walker
Summary
The MetE coding device was designed to be implemented in an auxotrophic strain of E.coli for methionine, or a strain that is incapable of biosynthesizing methionine on its own. The system does not function within a plasmid, and must be integrated into the genome [1]. The integration of this device allows methionine, an essential amino acid for E. coli growth, to be synthesized endogenously. The coding device was comprised of the MetE gene cassette under the LacI promoter. However, the LacI promoter originally used was not inducible in... Therefore, two improvements upon the MetE Coding Device were made:
1. The LacI promoter was swapped out for the optogenetically controllable CcaS/R promoter.
The new MetE coding device has the inducible CcaS/R promoter in place of the LacI promoter, allowing for the expression of methionine to be controlled optogenetically. With the CcaS/R promoter, exposure to green wavelengths of light activate gene expression, while exposure to red wavelengths of light turn off gene expression.
2. Homology arms were added to the sequence to facilitate the replacement of an existing MetE gene, allowing for the device's integration into prototrophic strains for methionine.
The new MetE coding device has homology arms added to each end of the sequence, allowing the device to remove any MetE genes already existing in prototrophic strains during integration. Although prototrophic strains can biosynthesize methionine endogenously, methionine expression can now be optogenetically controlled by the CcaS/R promoter.
REFERENCES:
[1] Milias-Argeitis A, Rullan M, Aoki SK, Buchmann P, Khammash M. Automated optogenetic feedback control for precise and robust regulation of gene expression and cell growth. Nat Commun. 2016;7:12546. Published 2016 Aug 26. doi:10.1038/ncomms12546
[2] CcaS/CcaR. OptoBase. https://www.optobase.org/switches/Cyanobacteriochromes/CcaS-CcaR/.
Characterization of Improved MetE Coding Device
Similar to the characterization done for the original BioBrick (BBa_K2573000), treatments of the E. coli strain JT2 were grown in M9 medium with and without methionine, and under exposure to either red or green light. The growth of JT2 in methionine deficient medium indicated the expression of methionine and thus the function of a BioBrick, since methionine is essential for bacterial growth and JT2 is a methionine knockout. As well, the growth of JT2 in methionine deficient medium when exposed to green light but not when exposed to red light characterized the function of the inducible CcaS/R promoter in the improved Biobrick (BBa_K2995002). Growing JT2 in M9 medium with methionine acted as a positive control for JT2 growth in each treatment.
Three treatments of JT2 were tested in order to characterize the function of the new BioBrick (BBa_K2995002):
1. Transformed the new BioBrick (BBa_K2995002) into JT2.
This treatment was tested in order to confirm the function of the improved BioBrick BBa_K2995002. The growth of JT2 in M9 medium without methionine under exposure to green light, in combination with the absence of growth under exposure to red light would yield a positive result. The absence of growth in either condition or growth in both conditions would yield a negative result.
2. Transformed the original BioBrick (BBa_K2573000) containing the LacI promoter into JT2.
This treatment acted as a negative control for MetE gene inducibility, as JT2 transformed with BioBrick BBa_K2573000 would express methionine regardless of being exposed to green or red light.
3. Empty JT2 without transformation.
Empty JT2 cells were also grown in M9 with and without methionine as a negative control for MetE gene expression.
RESULTS
//plasmid
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