Golden Gate Assembly protocol
Protocol to insert new promoter made into pSB1A2 that contains BBa_J119044
From Oligos
Go to the Loligator web page to determine how to prepare your oligos to add to the solution described below. br>
OR
From Promoter already cloned in a Plasmid
You can start with BBa_J119022 which contains a promoter that is flanked by BsaI sites. Use 50 ng of this plasmid for your "insert" DNA to be added to the ligation mixture listed below.
Get two new, small microfuge tubes designed to fit into the PCR machine.
One tube will be labeled "ligation", the other "plasmid only". Also put your initials on the tubes.
1 µL diluted oligos cooled overnight (use water instead for "plasmid only" tube). If you are using BBa_J119022, use 50 ng in 1 µL volume.
9 µL ligations mixture provided by your instructor.
use the promoter DNA for the ligation tube but use only water for the plasmid only tube.
Ligation mixture contains:
1 µL (50 ng) plasmid containing part J119044
5 µL dH2O
1 µL 10X Promega Ligase Buffer
1 µL 500 mM KOAc
0.5 µL Bsa I high fidelity (HF) restriction enzyme
0.5 µL T4 DNA Ligase
9 µL final volume
Turn on the PCR machine. Put both of your tubes into the machine.
Program it for the following cylces:
30 cycles of 37C for 1 minute/16C for 1 minute
1 cycle of 37C for 15 minutes
22C holding temperature
This DNA ligation is ready for transformation.
Transformations
You want to do 3 transformations:
a positive control
your experimental ligation
and your negative control ligation
Use all 10 µL of the ligations for a transformation.
You will want to perform a transformation positive control using K315008 which contains pLacI+RBS+RFP in plasmid pSB1A2.
Take one tube of 100 µL competent cells and put 30 µL of cells into each of three 1.5 mL tubes labeled appropriately for each of the three transformations listed above. Plate all three transformations on LB amp plates.
This protocols was developed at MWSU by Dr. Todd Eckdahl, and modified at Davidson College by students in Biology 111 and Romina Clemente.
