Lidstrom:Building with DNA

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Obtain Parts

• Perhaps you have them already. Perhaps you will make BioBrick or BglBrick parts via PCR.
• If you make parts via PCR, column purify the product to remove salts, oligos, etc.

Digest with Restriction Enzymes

• Use 500+ ng of each part, 5 uL of 10X buffer, 0.5 uL of BSA (stabilizes enzymes) and 1uL of each restriction enzyme, and water to 50uL.
• 37oC 1.5 hrs, 80oC 20 min (if heat inactivation works with your enzymes), then 4oC forever works in Janet's limited experience.

• Decide if/how to purify:
  • Gel purification removes salts and restriction enzymes, which can increase success with subsequent ligation.
    • If you are cutting an insert out of a plasmid, you need to remove the piece of the plasmid you don't want to ligate. Gel purify in this case so you can select the band with the appropriate size.
    • If you are cutting off small fragments from a PCR product, you can usually column purify because the fragments you cut off are small enough that they don't bind to the column. Recall that column purification has ~90% yield whereas gel purification has ~90% loss. If you are only going to column purify (or skip purification all together) consider running a few uL on a gel to make sure you only have 1 band.
    • Betsy always gel purifies. Amanda usually does but forgot once and it worked.5

Ligate

• add 1 uL of ligase (kit allows 0.1 to 1 uL) to a 50 uL rxn
• Incubate on counter (~2 hours) or at 16oC overnight. The BioBricks/Ginkgo manual suggests only 15 minutes of incubation at 37oC; I have not tried this because it is much shorter than the New England Biolabs suggested times.

Transform

• transform ~10 uL of the product. There is some left over in case you need to try again.

Screen with Colony PCR

• See our colony PCR page for details.

Verify with Sequencing

• See "Sequencing with GeneWiz" page.