Team:SUSTC-Shenzhen/Notebook/Biobricks Characterization
From 2014.igem.org
Notebook
Biobricks Characterization
Contents |
Scheme
At first, we want to characterize plasmid assembled by 3 promoters, 3 RBSs, and 4 chromoprotein (36). Because time limits, we choose 2 promoter, 2 RBSs and 4 chromoprotein (16). In carrying out experiments, we cannot easily differ new constructed plasmid with BBa_E1010 with the self-assembly one. We abandoned BBa_E1010 and do experiments on other chromoproteins.
Results
We successfully constructed 8 parts, and they all are characterized. And 6 parts were sent to Registry of Standard Biological Parts. See them | HERE.
Procedures
- Amplification of Biobricks
- Add RBS
- Add promoter
- Add terminator
Plasmid Construction
9.29 After RBS added, all seven plasmid were cut and ligated with two promoter, J23101 and J23106 respectively.
Enzyme digestion
For plan A
J00 | J06 | B31E10 | B31K916 | B31K09 | B34E10 | B34K916 | B34K09 | B34K11 | ||
---|---|---|---|---|---|---|---|---|---|---|
EcoRI-HF(μL) | 1.0 | |||||||||
XbaI(μL) | 1.0 | |||||||||
PstI | 1.0 | |||||||||
NcoI | 1.0 | 1.0 | ||||||||
Linearized backbone(μL) | 1.0 | |||||||||
DNA(μL) | 3.0 | 4.0 | 8.0 | 7.0 | 4.0 | 5.0 | ||||
10x NEB Buffer 2.1(μL) | 5.0 | |||||||||
ddH2O(μL) | 39 | 38 | 34 | 35 | 38 | 37 | ||||
Total(μL) | 40 |
} LigationTo complete construction quickly, we use 3A assembly to achieve plasmid with resistant to chloramphenicol (A) and standard assembly with resistant to Ampicillin (B). Ligation: In PCR system, 16 to ligate, 65℃ to inactive, and store at 4℃. Transformation
Incubate at 37 CharacterizationReferences
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