Julius B. Lucks/Protocols

Phusion PCR

Ingredients:

• 37 uL H20
• 10 uL Phusion Buffer 5x
• 1 uL dNTP mix
• 0.5 uL Phusion
• 0.5 uL Template DNA
• 0.5 uL Primer F
• 0.5 uL Primer R

1. Combine ingredients in PCR tube, perform following PCR program
   • 1 = 98 C for 0:30
   • 2 = 98 C for 0:15
   • 3 = 55 C for 0:30
   • 4 = 72 C for target_length_kB*20s (20s/kB)
   • 5 = GOTO 2 30 TIMES
   • 6 = 72 C for 2:00 (or larger if step 4 > 2:00)
   • 7 = 4 C for ever
   • 8 = END

Pre-Cut Oligo Phosphorylation

Ingredients:

• 1 uL primer
• 1 uL 10x ligase buffer (black striped aliquat in freezer)
• 7.5 uL water
• 0.5 uL PNK (enzyme freezer - modifying enzyme T4 PNK)

1. Combine ingredients (one tube for each primer) in a tube and incubate at 37 C for 1 hr.
2. Combine the 2 tubes, and add 180 uL water
3. Take this tube and boil for 5 min on a hot plate in a beaker of water (boil water in a beaker and put the tube in the boiling water)
4. Take beaker off hot plate and put on bench to ramp down to room temperature

Use this solution as you would for an insert in a ligation.

Glucose Minimal Media

• Ammonium Sulfate (NH4)2SO4 - 0.502g (0.0038 mol)
  • MW 132.14 g/mol
  • CAS 7783-20-2
• Dibasic Potassium Phosphate KH2PO4*3H2O - 2.244g (0.01 mol)
  • MW 228.23
  • CAS
• Monobasic Potassium Phosphate K2HPO4 - 5.226g (0.038 mol)
  • MW 136.09
  • CAS 7778-77-0
• Sodium Citrate - Na3C6H5O7 - 0.25g (0.00085 mol)
  • HOC(COONa)(CH2COONa)2*2H2O
  • MW 294.10
  • CAS
• Dextrose Anhydrous (glucose) - 1.0g (0.0056 mol)
  • CH2OH(CHOH)4CHO
  • MW 180.16
  • CAS 50-99-7
• Thiamine (0.1% stock) - 0.25ml (xxx mol)
  • MW
  • CAS
• Magnesium Sulfate MgSO4*7H2O (1M stock) - 0.5ml (0.0005 mol)
  • MW 246.48
  • CAS 10034-99-8
• H2O - up to 0.5L

Glycerol Minimal Media

Same as Glucose Minimal Media except substitute for Dextrose Anhydrous

• Glycerol C3H8O3 (50% stock) - 1.04 ml (0.52 g = 0.0056 mol)
  • MW 92.09
  • CAS 56-81-5

SLIC

Reference : Li and Elledge, Nature Methods (2007)

1. Design primers to amplify pieces of interest so that the extremities contain 20-40 bp of holomoly with the target region
2. Amplify pieces with Phusion PCR. Note: gel purify or DpnI digest your products if you used a template with the same antibiotic resistance as your target molecule; otherwise, PCR purification columns are fine. Pieces (e.g.vector backbone) can also be prepared by digestion.
3. Quantify your products using a nanodrop.
4. Aliquot 50-100ng of your backbone in a new tube. Put the other pieces in separate tubes, equivalent to a 1:1 molecular ratio relative to the backbone (volume dosen't matter).
5. Add 1/10 of the volume of 10X T4 DNA ligase buffer in each tube
6. Dilute T4 DNA polymerase to 0.5 U/ul and add 1 ul per tube.
7. Incubate 30 minutes at room temp.
8. Add 1/10 volume of 10 mM dCTP to each tube.
9. Mix the content of the tubes. Incubate 30 minutes at 37C.
10. Transform E. coli competent cells.