Team:TU Delft/InterLab

InterLab Study

The Second International InterLab Measurement Study in Synthetic Biology.

Among 81 other teams from all over the world, our team decided to participate in this year’s iGEM Interlab Study of 2015.

Results

For this study, three devices needed to be constructed consisting of a constitutive Anderson promoter with low (J23117), medium (J23106) and high (J23101) promoter strengths expressing GFP (I13504) as reporter. Using the Biobrick distribution, the required promoters and GFP were cloned in E.coli top10 cells, restricted and ligated to afford the final devices. Fluorescence was measured from overnight cultures using FACS (fluorescence-activated cell sorting) to compare the individual promoter strengths in relative units.

To measure fluorescence, the cells were excited at a wavelength of 488 nm and emitted light was measured at 530 ± 30 nm and a total of 30’000 events were recorded. The data was shown in clouds of fluorescence on the x axis and fluorescent side scattering on the y axis.

In order to compare the three different promoters described above, a histogram showing the fluorescence intensity at 530 nm versus the number of cells is made (figure 1.). In the figure, it is clear how J23101 leads to a better GFP expression in average, while J23106 and J23117 show a lower performance in that order.

Interlab table
Figure 1. Histogram of fluorescence intensity at 530 nm per number of cells, comparing the reporter GFP intensity after J23101, J23106 and J23117 promoters.

Plasmids containing only the promoter without GFP were used as negative controls to calibrate the FACS machine. The Biobrick I20270 (containing J23151 as constitutive promoter, obtained from the distribution) was used as a positive control. x label: fluorescence (relative units); y label: FSC fluorescence side scattering (cell size)

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J23101_I13504 was grown in biological triplicate (hi clone 1,2,3) and was measured in technical triplicate (a,b,c). x label: fluorescence (relative units); y label: FSC fluorescence side scattering (cell size)

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J23106_I13504 was grown in biological triplicate (med clone 1,2,3) and was measured in technical triplicate (a,b,c). x label: fluorescence (relative units); y label: FSC fluorescence side scattering (cell size)

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J23106_I13504 was grown in biological triplicate (low clone 1,2,3) and was measured in technical triplicate (a,b,c). x label: fluorescence; y label: FSC fluorescence side scattering (cell size)

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To process our data, the relative fluorescence of the corresponding negative controls was subtracted from the measured samples to get relative data for our three constructs.

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As expected, high, medium and low levels of fluorescence were measured in accordance with the promoters used in our constructs. The weak promoter J23117 however was much weaker than was expected with only approximately 15 relative units higher than the negative controls. In contrast, the medium and high promoters lead to a significant increase in measured fluorescence. J23106 is approximately 70 times stronger than J23117, and J23101 approximately 170 times stronger than J23117. The high promoter J23101 thus is approximately 2.3 times stronger than the medium promoter J23106.

Statistical analysis of our data using standard deviations showed that differences among the biological triplicates are larger than instrument fluctuations (biological SD is roughly 5 to 15 times larger than techical SD). Thus, repeated measurement of the same sample generates a statistically more significant result than measuring several biological samples once. Based on standard deviations of roughly 10% for biological triplicates and 5% for technical triplicates, we recommend to increase the data set in order to improve statistical relevance.

Protocols

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  1. Plate Top10 cells and incubate at 37ºC overnight

  2. Pick one colony, inoculate in LB media and incubate overnight while shaking at 37ºC

  3. Dilute the culture in fresh medium, and continue the incubation until the OD600= 0.4-0.6

  4. Centrifugation 5 min. at 4000 rpm.

  5. Pellet cells and resuspend in 100mM of CaCl2 solution

  6. Incubate on ice for 20 min

  7. Centrifugation 5 min at 3000 rpm

  8. Pellet cells and suspend again in 100mM CaCl2 solution

  9. Incubate on ice for 60 min

  10. Centrifugation 5 min at 3000 rpm

  11. Add a solution of 100mM CaCl2 + 40% glycerol

  12. Store immediately at -80ºC

  1. Take the competent cells from the storage at -80ºC and leave them on ice for 10-15 min

  2. Add 1-2 µL of plasmid solution to the 50 µL cell tube

  3. Incubate on ice for 30 min

  4. Heat-shock the cells at 42ºC for 45s

  5. Incubate on ice for 2 min

  6. Add 500 µL of LB media and incubate 60 min at 37ºC

  7. Plate the cultures on agar plate

  1. Pick a single colony from a plate or cryostock

  2. Put the colony in a 50 mL sterile tube and add 5-10 mL of LB fresh medium

  3. Put the tube to incubate for at least 16 h, at 37ºC and 200 rpm

Gel making

  1. Prepare 200 mL of TAE buffer

  2. Mix the TAE solution with 2g of agarose (for 1%)

  3. Heat the solution to boiling, and then cool it to 50ºC aprox.

  4. Add 5 µL of Ethidium bromide to the solution

  5. Pour the solution in the electrophoresis vessel. Apply the combs.

  6. Let it polymerize, and then cover it with TAE

Gel running

  1. Add 1/6 of total volume of Loading buffer to every DNA sample.

  2. Remove the combs from the gel, and pipette DNA samples and DNA ladder

  3. Run at 100-130V for 30-60 min (depends on the fragments)

  1. Add 20-100 ng of vector DNA (can be calculated from the DNA concentration in the sample)

  2. Add X ng of insert DNA. X is calculated using the length of both vector and insert and the molar ratio desired.

  3. Add 2µL of ligation buffer

  4. Add MQ water to set the final volume to 15-20

  5. Add 1 µL of T4 ligase (always at the end to keep the enzyme in optimal conditions)

  6. Incubate for at least 3 hours at 16ºC

  1. Take 1.5 mL from a freshly grown culture and put it in a 1.5 mL tube

  2. Spin the tube for 10 min at 2000 rpm

  3. Decant the supernatant without disturbing the pellet

  4. Add 0.5 mL of LB media and 0.5 mL of glycerol 80% solution

  5. Mix by vortexing

  6. Save in the -80ºC freezer

  1. Add 1 µg of DNA (can be calculated from concentration in the sample)

  2. Add 5 µL of NEB buffer

  3. Add 1 µL of restriction enzyme 1

  4. Add 1 µL of restriction enzyme 2

  5. Add MQ water to set the final volume at 50 µL

  6. Mix the solution by flicking the tube

  7. Spin-down in a microcentrifuge for 15 s

  8. Incubate at 37ºC for 1-2 hours

  1. Add 1.5 mL of bacterial culture in LB medium to a 1.5 mL micro-centrifuge tube. Centrifuge that tube at max speed for 3 min

  2. Remove the supernatant, and add 600 µL of MQ water to the pellet

  3. Add 100 µL of Cell Lysis Buffer, and mix by inverting 6 times. The color change to blue indicates complete lysis

  4. Add 350 µL of cold (4-8ºC) Neutralization Buffer, and mix by inverting the tube. The color change to yellow indicates total neutralization

  5. Centrifugate at maximum speed for 3 minutes, and transfer the supernatant to a PureYield Minicolumn

  6. Place the minicolumn into a PureYield Collection Tube and centrifuge at maximum speed for 15 seconds

  7. Discard the flowthrough and place the minicolumn again into the same PureYield Collection tube

  8. Add 200 µL of Endotoxin Removal Wash to the minicolumn. Centrifuge at maximum speed for 15 seconds. Do not empty the Collection Tube now

  9. Add 400 µL of Column Wash Solution to the minicolumn, and centrifuge at maximum speed for 30 seconds

  10. Transfer the minicolumn to a clean 1.5 mL tube, and 30 µL of hot (50ºC, pre-warmed) MQ water directly to the minicolumn matrix. Let stand for 5 minutes at room temperature

  11. Centrifuge at maximum speed in a microcentrifuge for 15 seconds to elute plasmidic DNA. Cap the tube, and store the DNA solution at -20 ºC (or use it directly for cloning experiments)

  1. Weigh a 1.5 mL microcentrifuge tube for each DNA fragment to be isolated, and record the weight

  2. Visualize the DNA in the agarose gel using a long-wavelength UV lamp and an intercalating dye (Ethidium bromide). Irradiate the gel the minimum possible time to reduce nicking

  3. Excise the DNA fragment of interest in a minimal volume of agarose using a clean scalpel or razor blade. Transfer the gel slice to a weighted 1.5 mL tube and record the weight, again. Subtract the previously measured tube weight to obtain the weight of the gel slice containing the DNA fragment

  4. Add Membrane Binding Solution at a ratio of 10 µL of solution per 10 mg of agarose gel slice

  5. Vortex the mixture and incubate at 50-65ºC for 10 minutes, or until the gel slice is completely dissolve in the liquid. You can vortex the tube every few minutes to increase the rate of agarose melting

  6. Centrifuge the tube briefly at room temperature to ensure the contents are at the bottom of the tube. Once the agarose gel is melted, the gel will not re-solidify at room temperature

  7. Place one SV Minicolumn in a Collection Tube for each dissolved gel slice

  8. Transfer the dissolved gel mixture to the SV minicolumn assembly and incubate for 1 minute at room temperature

  9. Centrifuge the SV Minicolumn assembly in a microcentrifuge at max speed for 1 minute. Remove the SV Minicolumn from the Spin Column assembly and discard the liquid in the Collection Tube. Return the SV Minicolumn to the Collection Tube afterwards

  10. Wash the column by adding 700 µL of Membrane Wash Solution, previously diluted with 95% ethanol to the SV Minicolumn. Centrifuge the SV Minicolumn assembly for 1 minute at maximum speed

  11. Empty the Collection Tube as before, and place the SV Minicolumn back in the Collection Tube. Repeat the wash with 500 µL of Membrane Wash Solution, and centrifuge the SV Minicolumn assembly for 5 minutes at maximum speed

  12. Remove the SV Minicolumn assembly from the centrifuge (not wetting the bottom of the column with the supernatant). Empty the Collection Tube and centrifuge the assembly for 1 minute with the microcentrifuge lid open (or off) to allow ethanol evaporation

  13. Carefully transfer the SV Minicolumn to a clean 1.5 mL tube. Apply 50 µL of Nuclease-Free Water (at 50ºC) directly to the center of the column, without touching the membrane with the pipette. Incubate at room temperature for 5 minutes

  14. Centrifuge for 1 minute at 14000 rpm. Discard the SV Minicolumn, and store the tube containing the eluted DNA at 4ºC or -20ºC

  1. Add an equal volume of Membrane Binding Solution to the restriction product tube

  2. Place one SV Minicolumn in a Collection Tube for each restriction product solution

  3. Transfer the mixture to the SV Minicolumn assembly and incubate for 1 minute at room temperature

  4. Centrifuge the SV Minicolumn assembly in a microcentrifuge at max speed for 1 minute. Remove the SV Minicolumn from the Spin Column assembly and discard the liquid in the Collection Tube. Return the SV Minicolumn to the Collection Tube afterwards

  5. Wash the column by adding 700 µL of Membrane Wash Solution, previously diluted with 95% ethanol to the SV Minicolumn. Centrifuge the SV Minicolumn assembly for 1 minute at maximum speed

  6. Empty the Collection Tube as before, and place the SV Minicolumn back in the Collection Tube. Repeat the wash with 500 µL of Membrane Wash Solution, and centrifuge the SV Minicolumn assembly for 5 minutes at maximum speed

  7. Remove the SV Minicolumn assembly from the centrifuge (not wetting the bottom of the column with the supernatant). Empty the Collection Tube and centrifuge the assembly for 1 minute with the microcentrifuge lid open (or off) to allow ethanol evaporation

  8. Carefully transfer the SV Minicolumn to a clean 1.5 mL tube. Apply 50 µL of Nuclease-Free Water (at 50ºC) directly to the center of the column, without touching the membrane with the pipette. Incubate at room temperature for 5 minutes

  9. Centrifuge for 1 minute at 14000 rpm. Discard the SV Minicolumn, and store the tube containing the eluted DNA at 4ºC or -20ºC

Contact Details

Address:

Faculty of Applied Sciences

Room F109

TU Delft

Lorentzweg 1

2628 CJ Delft

The Netherlands

Phone:

+31 15 278 18 62

Email:

tudelft.igem@gmail.com