Team:NYU Shanghai/Protocols

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Protocols

We built our constructs from pre-made biobrick parts. Our overall conclusion is that 3A assembly is generally inefficient, and an insufficient method for adding small parts (such as a terminator) to a larger construction within pSB1C3. We learned that ratios were extremely important in the process of 3A Assembly, and we made a summary sheet of the equations we used in pre-digest and pre-ligation that accounts for digest dilution and amount needed to ensure results are seen on a gel, not just ligation ratios. We wished we used gibson assembly.

Making Color

Luciferase

Overview

1. Luciferin substrate must be added.
2. D-Luciferin is too large of a chemical to cross the plasma membrane of E. Coli so cell lysis is required to extract luciferase.
3. After cell lysis, the reagent solution can be added to the lysis buffer. Light should be emitted within 5 to 10 seconds of adding the reagent solution.
4. The luciferase/luciferin reaction at 22.5 ºC theoretically offers the greatest light intensity.
5. Solutions of D-Luciferin should be aliquotted and stored in darkness at -80 ºC

Materials

D-Luciferin free acid

ATP

MgSO4 · 7H2O

1M HEPES Buffer

Lysozyme

10 mM Tris-HCl

Lysis Buffer
For E. coli cell lysis, use a freshly prepared lysozyme solution (10 mg/ml) in 10 mM Tris-HCl, pH 8.0.

Reagent Solution
Prepare using ATP free water. Combine 1 mM luciferin or luciferin salt, 3 mM ATP and 15 mM MgSO4 in 30mM HEPES buffer, pH 7.8. Store substrate solution at -20ºC in polypropylene or glass.

Preparing 1mM D-Luciferin
Directions for a 5 mg sample: Dissolve 0.034 gr dithiothreitol in 22 mL of QH2O. Add 0.2 mL of this DTT solution to the 5 mg d-luciferin. Add 4μl of 10M NaOH to dissolve the luciferin. Dilute this into the remaining 21.8 mL of DTT solution and store as aliquots at - 80 ºC in darkness until use.

Procedure
Bacterial lysis:

1. After 12-18 hours of inoculation of bacteria expressing luciferase plasmid, pipette 2 mL of cell culture into a clean 2 mL tube. Centrifuge at 10,000 rpm for 1 minute. Pour out liquid into a collection beaker. Continue this process until all of the cell culture (in the inoculation tube) is gone.
2. Resuspend the pellets in 350 ml of STET buffer (10 mM Tris-HCl with 1 mM EDTA)
3. Add 25μl - 30μl of lysozyme buffer to the resuspended pellet.
4. Mix by vortexing for 3 seconds.
5. Incubate for 2 hours at room temperature.
6. If the reagent is not added immediately, store the lysed bacteria in the -20 ºC freezer until use.

Addition of Reagent Solution:

1. Following the above instructions, prepare a 1mM sample of D-Luciferin.
2. Following the above recipe, prepare the reagent solution.
3. In a dark room, add about 250-350μl of reagent solution to each sample of lysis product.
4. Light should be emitted within two-three seconds.

Example Calculations
Lysis Buffer (Desired Total Volume: 15mL)

Chemical Name	Tris-HCl	EDTA	NaCl
Molecular Weight	N/A	292.23 g/mol	58.44 g/mol
Molarity Desired	10 mM	1mM	0.1M
Calculation	Dilute 1M Tris-HCl:
Final Amount	150μl (+14.85 mL ddH2O)	0.00438 g	0.08766 g

Lysozyme Solution (Desired Total Volume: 15mL)

Lysozyme Solubility	10 mg lysozyme in 1 mL of 10 mM Tris-HCl
Desired Amount of Lysozyme Solution to Make	15 mL
Amount of Lysozyme Needed	10 mg x 15 = 150 mg
Amount of 10 mM Tris-HCl Needed	15 mL

Reagent Solution (Desired total volume: 22 mL)

Chemical Name	ATP disodium salt trihydrate	MgSO4•7H2O	HEPES Buffer	D-Luciferin free acid
Molecular Weight	605.24 g/mol	246.5 g/mol	238.3 g/mol	280.33 g/mol
Molarity Desired	3 mM	15 mM	30 mM	1 mM
Calculation				Use the 1 mM stock solution created earlier
Final Amount	0.039945 g	0.081345 g	0.1573 g	22 mL

Chromoproteins

Building our Construct

Expressing XJTLU's Construct

Recipes

LB-Agar Plates

1. Calculate total amount of volume of LB agar you would need to use. You need about 25mL for every 10cm plate and 10mL for every 6cm plate.
2. For every 100mL of LB agar needed, measure out 4g of LB Agar Powder.
3. Put the agar powder in a flask. Use a much bigger flask to prevent overflow when autoclaiving.
4. Put deionized water into the flask up to the desired volume. Do not mix. LB Agar is not supposed to dissolve in room temperature. If you mix the powder it will get stuck on the walls of the flask
5. Autoclave.
6. After autoclave, move to the hood. Let the LB agar cool until it’s less than 60ºC or until you can touch the flask. While waiting, you can start labeling the plates. DO NOT LET THE AGAR SOLIDIFY
7. Insert any antibiotics/sugars needed. If you are not sure about the ratio, you can follow this simple example:

   50mL LB + 500µL Arabinose* + 50µL Ampicillin**
   *2mg/mL of Arabinose Stock Solution
   **100mg/mL of Ampicillin Stock Solution

8. Swirl the antibiotics/sugars that you just added for a minute.
9. Plate the LB agar into the petri dishes until it is about ⅓ of the level. Do not forget to keep the lid on before and after you plate.
10. Let it cool for about 5 minutes.
11. Invert each plate so that it is upside down
12. Store in the 4ºC freezer

LB Broth

Total Amount of Reagent	100mL	250mL
Deionized Water	100mL	250mL
Yeast	1g	2.5g
Tryptone	0.5g	1.25g
NaCl	1g	2.5g

SOC Media

Materials

0.5% (w/v) yeast extract

2% (w/v) tryptone

10 mM NaCl

2.5 mM KCl

20 mM MgSO4

Per liter:

5 g yeast extract

20 g tryptone

0.584 g NaCl

0.186 g KCl

2.4 g MgSO4

Note: Some formulations of SOB use 10 mM MgCl2 and 10 mM MgSO4 instead of 20 mM MgSO4. SOB medium is also available dry premixed from Difco, 0443-17.
Adjust to pH 7.5 prior to use. This requires approximately 25 ml of 1M NaOH per liter.

15/10 medium

Growth of competent TOP10 cells in Example 2 of the Bloom05 patent is performed in 15/10 broth, which is similar to SOB:

1.5% yeast extract

1% Bacto-Tryptone

10mM NaCl

2mM KCl

10 mM MgCl2

10 mM MgSO4

Reagent	50 mL (in Mols)	100 mL (in M)	100 mL (in Grams)
Tryptone	(2% w/v) 1 g	2 g	2 g
Yeast Extract	(0.5% w/v) 0.25 g	0.5 g	0.5 g
NaCl	0.0005 M	0.01 mol	0.0584g
KCl	0.000125 M	0.0025 M	0.0186 g
MgCl2	0.0005 M	0.01 M	0.09521 g
Glucose	0.001 M	0.02 M	0.36032 g

3A Assembly

Calculations (pdf)

Transformation

Estimated time: 3 hours (plus 14-18 hour incubation)

Materials

2µl resuspended DNA

Competent cells (50μl per transformation)

Ice

2ml tube

42ºC water bath

SOC or LB media

1 LB plate and 1 LB+antibiotic per transformation

Spreader

37ºC incubator

Shaker

Procedure

1. Thaw competent cells on ice.
2. Add 50µL of thawed competent cells into pre-chilled 2ml tube.
3. Add 2µL of resuspended DNA to the 2ml tube. Pipet up and down a few times, gently. Keep the competent cells on ice.
4. Close tubes and incubate the cells on ice for 30 minutes.
5. Heat shock the cells by immersion in a pre-heated water bath at 42ºC for 60 seconds.
6. Incubate the cells on ice for 5 minutes.
7. Add 200 μl of SOC or LB media to each transformation
8. Incubate the cells at 37ºC for 2 hours at 260rpm in the shaker.
9. Label petri dishes with the appropriate antibiotic with the part number, plasmid backbone, antibiotic resistance, and date. Plate 200 µl of the transformation onto the labeled antibiotic dishes, and spread. This helps ensure that you will be able to pick out a single colony.
10. Spread remaining transformation onto labeled LB agar plate and spread, approx 50µl.
11. Incubate the plates at 37ºC for 12-18 hours, making sure the agar side of the plate is up. If incubated for too long the antibiotics start to break down and un-transformed cells will begin to grow. This is especially true for ampicillin - because the resistance enzyme is excreted by the bacteria, and inactivates the antibiotic outside of the bacteria.
12. You can pick a single colony, make a glycerol stock, grow up a cell culture and miniprep.

Controls

Competent cells on LB plate

Competent cells on LB + antibiotic plate

Competent cells + plasmid on LB plate

Miniprep

Estimated time: 40 minutes

Materials

Biomiga Miniprep Kit

Procedure

1. Harvest the bacterial culture by centrifugation for 1 min at 10,000 rpm. Pour off the supernatant and blot the inverted tube on a paper towel to remove residue medium. Remove the residue medium completely.
2. Add 250 µL Buffer A1 (Add RNase A to Buffer A1 before use) and completely resuspend bacterial pellet by vortexing or pipetting
3. Add 250 µL Buffer B1, mix gently by inverting the tube 10 times (do not vortex), and incubate at room temperature for 5 minutes.
4. Add 350 µL Buffer N1, mix completely by inverting/shaking the vial for 5 times and sharp hand shaking for 2 times.
   Note: Incubating the lysate in ice for 1 min will improve the yield.
5. Centrifuge the lysate at 13,000 rpm for 10 minutes at room temperature. If the lysate doesn’t appear clean, reverse the tube angle, centrifuge for 5 more minutes and then transfer the clear lysate to DNA column.
6. Carefully transfer the clear lysate into a DNA column with a collection tube, avoid the precipitations, spin at 13,000 rpm for 1 minute, discard the flow-through and put the column back to the collection tube.
7. Add 500 µL Buffer KB into the spin column, centrifuge at 13,000 rpm for 1 minute. Remove the spin column from the tube and discard the flow-through. Put the column back to the collection tube.
8. Add 650 µL DNA Wash Buffer (Add ethanol to DNA wash buffer before use) into the spin column, centrifuge at 13,000 rpm for 1 minute at room temperature. Remove the spin column from the tube and discard the flowthrough.
9. Reinsert the spin column, with the lid open, into the collection tube and centrifuge for 2 minutes at 13,000 rpm.
10. Carefully transfer the spin column into a sterile 1.5 mL tube and add 50-100 µL (> 50 µL) Sterile ddH20 or Elution Buffer into the center of the column and let it stand for 2 minutes. Elute the DNA by centrifugation at 13,000 rpm for 1 minute. Reload the eluate into the column and elute again.
11. Check results on Nanodrop.

Restriction Digest

Link to NEB Protocol

To determine buffer for double digests

Guide to heat inactivation

General reaction set-up:

Restriction enzyme	10units, generally 1uL
DNA	1ug
10X NEB Buffer	5μl (1X)
Total Reaction Volume	50uL
Incubation Time	1hr
Incubation Temperature	Enzyme Dependent

Controls

DNA with known sites for the enzyme

If control DNA cleaved and experimental DNA resists cleavage, the two DNAs can be mixed to determine if an inhibitor is present in the experimental sample

Ligation

Link to NEB Protocol

1. Make Reaction mixture

Components	20μl Reaction
10X T4 DNA Ligase Buffer*	2μl
Vector DNA (4 kb)	50ng (0.020 pmol)
Insert DNA (1 kb)	37.5ng (0.060 pmol)
Nuclease-free water	to 20μl
T4 DNA Ligase	1μl

2. Ligation temperature and times vary

For inserting a part into backbone (no 3A assembly), the suggested NEB protocol worked	16C overnight or room temperature 10min
For 3A Assembly	Room temperature for an hour, then overnight in 4degree

3. Heat inactivate at 65°C for 10 minutes.


4. Chill on ice and transform 1-5 μl of the reaction into 50 μl competent cells.

Controls

Reaction mixture with no insert DNA

Reaction mixture with no insert DNA and no ligase

Gel Electrophoresis

Reagents and Materials:

1X TAE buffer

Graduated cylinder

125 mL flask

Agarose

Gel pouring tray

Tape

Gel rig

Red Safe

MW ruler

Procedures

1. To prepare 0.4% agarose gel for electrophoresis, add 0.4 g of agarose powder into a suitable container with plenty of room to allow the liquid to boil and be swirled.
2. Add 100 ml of 1x TAE electrophoresis buffer and swirl to suspend the powder in the buffer.
3. Place the flask or the bottle into the microwave and place on a medium setting for 3 mins. Stop the microwave every 30 seconds and swirl the flask or bottle to suspend any undissolved agarose. Boil and swirl until all of the agarose gel particles are dissolved.
4. Cool the agarose solution to 55-60ºC. Add 5 µl of 10,000x DuRed and swirl to mix.
5. Prepare the gel casting apparatus and pour the molten agarose into the gel casting tray containing the comb. Allow the agarose to solidify at room temperature for 15-20 minutes.
6. Carefully remove the comb from the solidified gel.
7. Label a microcentrifuge tube for each miniprep sample.
8. DO NOT add loading dye directly to DNA minipreps collection tube. In a separate tube add 1 µl of 6x loading dye and add 5 µl of DNA minipreps sample and pipet up and down to mix.
9. Run the prepared agarose gel under water to saturate the wells. Then place the gel in the electrophoresis chamber and pour electrophoresis buffer into the chamber until it completely covers the gel by 5mm.
10. Load 5 µl of the 1 kb molecular weight ruler into lane one of the gel.
11. Load 6 µl of miniprep sample with loading dye into the wells of the gel.
12. Connect the electrophoresis chamber to the power supply and turn on the power. Make sure that the wells are closest to the black, or negative side.
13. Run the gel at 100V for 30 min, or until the molecular weight ruler is clearly separated. If you need to leave the gel for a longer time (i.e. if you need to go for lunch), you can decrease the voltage to 80V or 90V and run for an hour or 45 minutes, respectively.
    • Note: The voltage and times apply for a 1% agarose gel. For a lower concentration of gel (e.g. 0.7%) it will take less time for the gel to run to completion. We suggest to run the gel at 80V for 30 minutes. For longer times, run the gel at 60V for an hour or at 70V for 45 minutes.
14. Make sure the dye does not run off the gel.
15. Visualize the gel and record the results.

Controls

Uncut plasmid

Uncut insert DNA

Ladder DNA

Gel Extraction

Estimated time: 45 minutes

Materials
MinElute Midi Gel Extraction Kit

Procedure

1. Pre-weigh a 2.0mL microcentrifuge tube
2. Excise DNA fragment from agarose gel with clean, sharp scalpel. Place in the pre-weighed microcentrifuge tube. Minimize the exposure of the DNA samples under UV and amount of gel cut with DNA.
3. Weigh the tube and calculate the weight of the gel. For every 1 volume of gel (100mg = 100µl) add 3 times the volume of Buffer QG. The maximum amount of gel slice per spin column is 400mg.For >2% agarose gels, add 6 volumes of Buffer QG.
4. Incubate at 50ºC for 10 minutes (or until the gel has completely dissolved). Vortex the tube every 2-3 minutes during incubation to help dissolve the gel. If color is orange or violet after gel slice has dissolved, add 10µl 3M sodium acetate, pH 5.0. The color of the mixture will turn to yellow.
5. Add 1 gel volume of isopropanol to the sample and mix by inverting.
6. Place a MinElute spin column in a provided 2mL collection tube. Apply the sample in the 2.0mL microcentrifuge tube to the MinElute column and centrifuge for 1 min at 13,000 rpm. Discard the flow-through and place the MinElute column back into the same collection tube. If the sample volume exceeds 800µl, simply reload and spin again.
7. Add 500µl Buffer QG to the MinElute column and centrifuge for 1 minute at 13,000 rpm. Discard flow-through and place the MinElute column back into the same collection tube.
8. Add 750µl Buffer PE to MinElute column and centrifuge for 1 minute at 13,000 rpm. Discard flow-through and place the MinElute column back into the same collection tube. If the DNA will be used for salt-sensitive applications, such as direct sequencing and blunt-ended ligation, let the column stand 2-5 minute after addition of Buffer PE.
9. Centrifuge the column in the 2mL collection tube for 1 minute at 13,000 rpm again to remove residual ethanol.
10. Place each MinElute column into a clean 1.5mL microcentrifuge tube. To elute DNA, add 10µl Buffer EB or water to the center of the MinElute membrane. Let the column stand for 1 minute, and centrifuge the column for 1 minute at 13,000rpm.
11. Repeat step 12 but this time load the flow-through back to the membrane. Let the column stand for 1 minute, and centrifuge the column for 1 minute at 13,000rpm.
12. Check Gel extraction product with Nanodrop

Controls

"Digest empty vector cut with a single enzyme, perform the gel extraction, and re-ligate it. A vector cut with one enzyme should re-ligate very easily and provide plenty of colonies on the plate. If it does, then the inability to clone the DNA may be related to some other factor, such as secondary structure of the DNA, repeat sequences causing instability in E.coli, or the DNA cloned codes for a protein that may be toxic in bacteria." Bitesize Bio

PCR

These are the conditions we used to PCR the gBlocks received from IDT. We used Snapgene to design the primers. We used Q5 High-Fideltiy Polymerasefrom New England Biolabs.

Component	50μl Reaction	Concentration
5X Q5 Reaction Mix	25uL	1X
10X NEB Buffer	5uL	1X
10uM Forward primer	2.5uL	0.5uM
10uM Forward primer	2.5uL	0.5uM
Template DNA	10uL	100ng
Nuclease-free water	10μl or none

Controls

No template control

No enzyme control

PCR Cleanup

We used TIANquick Mini Purification Kit.

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