Team:Wash U/Protocol

BioBrick Assembly is a standard protocol for combining two BioBrick parts and positioning them in a destination plasmid. Specific cut sites for standard restriction enzymes are utilized to simplify the protocol and include EcoR1-HF, Xba1, Spe1 and Pst1. The assembly consists of two major parts: digestion and ligation. Note that BioBrick assembly requires purified, isolated DNA for all parts involved (upstream, downstream and destination plasmid). To view the full Biobrick Assembly manual, please click [http://ginkgobioworks.com/support/ here].

Materials

• NEBuffer 2
• BSA
• Restriction Enzymes (EcoR1-HF, Xba1, Spe1, Pst1)
• dI H20
• 10X T4 DNA Ligase Reaction Buffer
• 10X T4 DNA Ligase
• purified upstream BioBrick part
• purified downstream BioBrick part
• purified destination plasmid

Procedures

1. Begin by thawing all DNA along with NEBuffer 2 and BSA.
2. Label three separate PCR tubes upstream, downstream, and destination plasmid. To each tube 500ng of respective DNA and dilute to 42.5uL. Add 5uL of NEBuffer 2 and 0.5uL of BSA to each tube.
3. Add 1uL of the first appropriate enzyme to each tube (see [http://ginkgobioworks.com/support/BioBrick_Assembly_Manual.jpg chart] for correct enzyme). Then add 1uL of second appropriate enzyme to each tube.
4. Flick the tubes to mix contents and microcentrifuge for a few seconds to collect liquid in bottom of tube.
5. Incubate the three digests at 80C for 20 minutes to deactivate the restriction enzymes. The digestion portion of the procedure is now completed. You may wish to store the products at -20C or proceed directly to the ligation step.
6. Begin ligation by thawing 10X T4 DNA Ligase Reaction Buffer and enzyme. Agitate the buffer until all precipitate goes into solution.
7. Add 11uL of H20 to a 200uL PCr tube.
8. Add 2uL of each digest product to the new PCR tube.
9. Add 2uL of 10X T4 DNA Ligase Reaction Buffer to the PCR tube, then add 1uL of the T4 DNA Ligase to the tube.
10. Flick the tube to mix contents and spin the tube in a microcentrifuge for a few second to collect the liquid.
11. Incubate at room temperature for 10 minutes followed by 80C for 20 minutes. This will deactivate enzymes and improve transformation efficiency.
12. The ligation step is now completed. You may wish to store the products at -20C or begin a transformation immediately.

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Digestion

Digestion cuts the DNA at very specific sites with restriction enzymes. This procedure is required for various DNA manipulation techniques including gel electrophoresis and BioBrick assembly. Note: The procedures from this point forward assume that DNA has been amplified and purified. If this is not the case, please read the Polymerase Chain Reaction procedure for amplification and the Mini-Prep procedure for purification.

Materials

• NEBuffer 2
• BSA
• dI H20
• Upstream, Downstream, and Destination Plasmid parts
• Restriction Enzymes (varies depending on digestion)

Procedures

1. Begin by thawing the upstream, downstream, and destination plasmid parts along with the NEBuffer 2 and BSA.
2. In three separate PCR microcentrifuge tubes labeled upstream, downstream, and destination, add 500ng of the respective dried DNA and dilute with dH20 to 42.5 uL.
3. Add 5 uL of NEBuffer 2 and 0.5 uL of BSA to each tube.
4. Add 1 uL of the first appropriate enzyme to each tube. Then add 1 uL of the second appropriate enzyme.
5. Flick each tube to mix reagents and incubate at 37C for 15 minutes.
6. Transfer the tubes to an incubator set at 80C for another 20 minutes. This step will deactivate the restriction enzymes.
7. Digestion is now finished and products should be stored at -20C or proceed to Ligation.

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Ligation

Ligation formally joins two or more pieces of DNA together that are already annealed. Note: this procedure requires the products of a successful digestion.

Materials

• DNA Ligase
• 10X T4 DNA Ligase Buffer
• dI H20
• Upstream, Downstream, and Destination Plasmid parts

Procedures

1. Thaw the 10X T4 DNA Ligase Reaction Buffer and mix to dissolve the precipitate.
2. Add 11 uL of dH2O to a 200 uL PCR tube. Then add 2 uL of each of the digestion products (upstream, downstream and destination) together into this new tube.
3. Add 2 uL of 10X T4 DNA Ligase Reaction Buffer to the 200 uL PCR tube.
4. Add 1 uL DNA Ligase to the PCR tube and flick to ensure the contents are mized.
5. Let the mix stand for 10 minutes at room temperature before incubating at 80C for 20 minutes (deactivates enzymes).
6. Store the products at -20C until they are needed for a transformation.

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Gel Electrophoresis

Gel Electrophoresis is a technique used to separate out DNA according to its length. DNA is loaded into a well, or hole in an agarose gel, and is then pulled through the gel via electric current (DNA has a negative charge). Smaller DNA fragments travel faster through the gel matrix while larger fragments travel slower. To better determine the length of DNA a ladder is often run parallel to an unknown piece of DNA. The ladder consists of several pieces of DNA of known length which serve as a reference point to the unknown fragment. Note that dyes are important in this procedure since DNA alone is invisible. Specific Dyes are needed to adhered to and travel with the DNA through the gel.

Materials

• Agarose
• 1X TAE Buffer
• Ethidium Bromide
• DNA Ladder
• DNA Samples
• Gel Pouring Dock
• Gel Tray
• Gel Box
• Power Supply

Procedures

1. Scale out agarose for gel (0.8% - 2.0%)
2. Add agarose powder to appropriately sized glassware
3. Add 1X TAE Buffer
4. Microwave until boiling
5. Allow solution to cool until glassware is comfortable in hand
6. Add 2ul ethidium bromide and swirl
7. Pour gel solution into level gel tray mounted on the gel pouring dock
8. Insert gel comb with appropriate number of wells
9. Allow gel to set up for approximately 20 minutes
10. Remove gel from pouring dock and submerge just below surface of 1X TAE buffer in gel box
11. Carefully remove gel comb
12. Load DNA ladder and samples
13. Add 3ul of ethidium bromide to the buffer near the positive electrode
14. Attach gel box electrodes to power supply and apply desired voltage
15. Add another 3ul of ethidium bromide to the buffer near the positive electrode when halfway to completion
16. Switch power supply off when gel has run to completion

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PCB Extraction

Phycocyanobilin (PCB) is a blue phycobilin and is essential for the final testing of our project once implanted into Rhodobacter sphaeroides. It is most easily obtained from Spirulina, a cyanobacteria and popular dietary supplement.

Materials

• Spirulina Powder
• dI water
• Methanol
• HgCl2
• Trifluoroacetic acid (TFA)
• Trichloroacetic acid (TCA)
• Acetonitrile

Procedures

1. Rehydrate Spirulina powder in dI water (30ml/g dry weight) for 10 min.
2. Centrifuge at 30,000xg for 20 min, decant and save supernatant.
3. Precipitate phycocyanin from supernatant with 1% (w/v) TCA by incubation for 1h at 4oC in the dark.
4. Collect by centrifugation at 30,000xg for 20 min.
5. Wash with methanol (2x 20ml/g Spirulina powder).
6. Resuspend blue pellet in methanol (2ml/g powder) containing 1mg/ml HgCl2.
7. Incubate for 20h at 42oC in the dark.
8. Remove protein by centrifugation at 10,000xg for 10 min.
9. Precipitate mercuric ion with 2-Mercaptoethanol (1ul/ml), remove by centrifugation at 30,000xg for 10 min.
10. Dilute bilin mixture 10-fold with 0.1% (v/v) TFA.
11. Apply to C18 Sep-Pak cartridge.
12. Wash cartridge with 0.1% (v/v)TFA (2x 3ml) and acetonitrile/0.1% TFA (20:80; 2x 2ml).
13. Elute bilin with 3ml acetonitriel/0.1% TFA (60:40) and dry in vacuo.

Note:Expected yields are 4 umol PCB per 6g Spirulina

Thanks to Dr. Clark Lagarias for providing this protocol. ref

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Glycerol Stock Solution

Glycerol Stock Solutions are excellent for preserving and freezing cell cultures. It is very important that cells not be damaged or continue to grow too fast for various parts of our project.

Materials

• Centrifuge/screw top tubes
• 50% glycerol sol
• LB Cultures

Procedures

1. Label centrifuge/screw top tubes
2. Pipet 300 µl of 50% glycerol solution into each tube
3. Pipet 700 µl of LB culture into each tube
4. Close & vortex to mix.
5. Put in -80 C.

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Designing Primers

We found the Registry's protocol extremely helpful for designing primers and constructed most of our primers from this template. To visit the website, please click [http://partsregistry.org/Help:Primers/Design here].

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Colony PCR

Colony PCR is similar to regular PCR in that it is used to amplify DNA. We have used colony PCR to verify successful transformations by adding grown up cells into the PCR mix, lysing the cells, and then amplifying the DNA. The amplified DNA can then be run through a gel and the number of base pairs can then be compared to an expected result.

Materials

• 0.5uL AccuTaq LA DNA Polymerase
• 5uL 10x Buffer
• 2.5uL dNTP mix
• 1 uL DMSO
• 0.5 uL BioBrick forward Primer
• 0.5 uL BioBrick reverse Primer
• 0.5 uL Enzyme
• 40 uL dI H20
• LB agar plate
• E. coli colony to amplify.

Procedures

1. Create the PCR mix by combining the first 8 ingredients.
2. Touch the colony of E. coli with a sterile plastic loop and do a small streak across a new plate. Swirl this tip in the PCR mix.
3. Begin process of thermocycling with a heat shock of 98C for 30.
4. Next begin the cycling steps with 94C for 15 seconds, then 71C for 20 seconds, then 68C for 5 minutes. Repeat these three steps thirty times.
5. Move solution to 68C for 20 minutes.
6. PCR is now complete and should be held at 4C.

Note: any further streaking should be done with a sterile tip.
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Genomic DNA Purification

Characterization and modeling of individuals parts of our system will require the isolation and purification of genomic DNA from Rhodobacter sphaeroides. One of the main goals of the project is to make BioBricks out of ompR, ompF, pucB/A and the puc promoter coding regions. This DNA however is in chromosomal, not plasmid, form and will require a separate protocol to obtain. Note: This protocol and materials were obtained in a kit called DNeasy from Qiagen. To obtain exact recipes and formulas please contact them.

Materials

• Overnight cultures
• Buffered ATL
• Proteinase K
• Buffered AL
• Ethanol
• DNeasy mini column
• Buffer AW1
• Buffer AW2
• Buffer AE

Procedures

1. Harvest cells by taking 1.5mL from overnight cultures and spinning them down to a pellet.
2. Resuspend pellets in Buffered ATL
3. Add 20uL Proteinase K, mix by vortexing and incubate at 55C for 3 hours shaking every 20-30 minutes
4. Vortex 15 seconds and then add 20uL Buffer AL to the samples mixing thoroughly and incubate at 70C for 10 minutes
5. Add 200uL ethanol to the sample and mix by vortexing
6. Pipet mixture from step 4 into DNeasy mini column sitting in a collection tube. Centrifuge at 12,000RPM for 1 minute and discard the flow through in the collection tube.
7. Place the mini column in a new collection tube and add 500 uL of Buffer AW1. Centrifuge at 12,000RPM for 1 minute and discard the flow through and collection tube.
8. Place the mini column in a new collection tube and add 500 uL of Buffer AW2. Centrifuge at 12,000RPM for 3 minutes and discard the flow through and collection tube.
9. Place the mini column in a clean collection tube and pipet 200 uL Buffer AE on the DNeasy membrane. Incubate at room temperature for 1 minute and then centrifuge for 1 minute at 12,000RPM.
10. Repeat elution as described in step 9 with same collection tube to combine both elutes.

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Gel Extraction

Gel Extraction is intended to recover and reuse DNA that has been purified by gel electrophoresis. The process re-isolates DNA and removes all primers, dyes, and ethidium bromide that may still by present in the band of DNA in the gel, leaving up to 95% of the original DNA. We will be using the GenElute Gel Extraction Kit from Sigma-Aldrich so individual formulas and solutions may be unattainable. Please contact them for more details.

Materials

• gel with desired DNA band
• Column preparation solution
• Gel Solubilization Solution
• Wash Solution Concentrate G
• Elution Solution
• GenElute Binding Column G
• spin columns
• Ethanol
• Isopropanol
• 3M Sodium Acetate Buffer (pH 5.2)

Procedures

1. Dilute the Wash Solution Concentrate G with 48mL of ethanol.
2. Cut out the desired band of DNA from the gel leaving as little excess gel as possible.
3. Weight the excised gel and place into a microcentrifuge tube. Add 3 gel volumes of Gel Solubilization Solution to the tube (for every 100mg of gel, add 300uL of solution). Incubate tube at 60C for 10 minutes or until gel is completely dissolved. Vortex occasionally to ensure gel is evenly dissolved.
4. Prepare the binding column by adding 500uL of Column Preparation Solution to the column and centrifuging for 1 minute. Discard the flow through.
5. Check the color of the tube containing the dissolved gel. If the solution is red, add 10uL of 3M Sodium Acetate to the mix until the solution turns yellow.
6. Add 1 gel volume of 100% isopropanol and mix (may need slightly more isopropanol for gels greater than 2%).
7. Load the gel solution into the binding column and centrifuge for 1 minute and discard the flow through.
8. Add 700uL of Wash Solution to the column and cetrifuge for 1 minute and discard the flow through. Centrifuge the column again for 1 minute to remove excess ethanol.
9. Transfer the column to a new collection tube. Add 50uL of preheated Elution solution (65C) to the column and centrifuge for 1 minute. The desired DNA is now in the collection tube.

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Making Competent Cells

description

Materials

• bulleted list

Procedures

1. numbered steps

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Recipes

Luria Broth (LB) Media

• 10g Tryptone
• 5g Yeast Extract
• 10g NaCl
• 15g Agar
• up to 1 Liter H20
• adjust pH to 7.5

ATCC medium: Van Niel's yeast agar

• 1.0 g K2HPO4
• 0.5 g MgSO4
• 10.0 g yeast extract
• 20.0 g agar
• 1.0 L tap water
• Adjust pH to 7.0-7.2

Super Optimal Broth (SOB)

• 2% w/v bacto-tryptone (20g)
• 0.5% w/v bacto-yeast extract (5g)
• 8.56mM NaCl (0.5g) or 10mM NaCl (0.584g)
• 2.5mM KCl (0.186g)
• ddH2O to 1L

Super Optimal Broth with Catabolite repression (SOC)

• In addition to all of the SOB components,
• 10mM MgCl2 (0.952g)
• 20mM glucose (3.603g)

50X TAE Buffer

• 242 g Tris base (2-amino-2-hydroxymethyl-propane-1,3-diol) (= 2 mole)
• 57.1 ml glacial acetic acid (= 100% acetic acid) (57.19 ml = 1 mole)
• 100 ml 0.5 M Na2 EDTA (pH 8.0)
• ddH2O to 1L

5X TBE Buffer

• 53 g of Tris base (CAS# 37186)
• 27.5 g of boric acid (CAS# 11280)
• 20 ml of 0.5 M EDTA (CAS# 60004) (pH 8.0)
• ddH2O to 1L

Tris EDTA (TE) buffer 5X 1L

• 750 mL d-H20
• 242 g Tris base
• 57.1 mL glacial acetic acid
• 100 mL 0.5M EDTA (93.05 g EDTA in 500 mL d-H20, pH ~8.0)
• fill to 1 L
• adjust pH to 8.5

Agarose Gel (for electrophoresis of DNA >100bp)

• 50 mL 1X TAE buffer
• 0.8 g agarose
• 2.5 microliters EtBr (Caution: EtBr is a known carcinogen)
• Note: Jacob suggested adding 1.0 microliter EtBr to gel and 3.0 microliters to TAE buffer in rig.

CCMB80 Buffer

• 10 mM KOAc pH 7.0 (10 ml of a 1M stock/L)
• 80 mM CaCl2.2H2O (11.8 g/L)
• 20 mM MnCl2.4H2O (4.0 g/L)
• 10 mM MgCl2.6H2O (2.0 g/L)
• 10% glycerol (100 ml/L)
• adjust pH DOWN to 6.4 with 0.1N HCl if necessary
  

  Note:adjusting pH up will precipitate manganese dioxide from Mn containing solutions. 

• sterile filter and store at 4°C
• slight dark precipitate appears not to affect its function

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