Difference between revisions of "Part:BBa K2020002"
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For the varification of the function of this part, a skim milk assay on agar plates was performed. Therefore, LB skim milk agar plates containing IPTG and the needed antibiotic were poured and the ''E. coli'' BL21 cells containing the plasmid with the expression system were streaked out. | For the varification of the function of this part, a skim milk assay on agar plates was performed. Therefore, LB skim milk agar plates containing IPTG and the needed antibiotic were poured and the ''E. coli'' BL21 cells containing the plasmid with the expression system were streaked out. | ||
| − | [[File:T--Aachen--labbook_ecoli_skim_milk_native.png|600px | + | [[File:T--Aachen--labbook_ecoli_skim_milk_native.png|600px| Skim milk plates assay. Cells containing the empty backbone (left) and cells containing the expression system for native subtilisin E (right) after incubation for 3 days at 30°C.]] |
Revision as of 23:06, 19 October 2016
expression system for subtilisin E in E. coli
Once introduced into Escherichia coli, this BioBrick is able to produce subtilisin E and simultaneously secret the enzyme into the periplasm of the cell.
Usage and Biology
Subtilisin E is an alkaline serine protease which non-specifically digests proteins. It is naturally produced by Bacillus subtilis.
This composite part consists of the promoter BBa_R0010, the ribosome binding site BBa_B0034, the newly created BioBrick part BBa_K2020001 and the terminator BBa_B0010. BioBrick BBa_K2020001 is a composite part itself and includes the secretion tag pelB (BBa_J32015) and a subtilisin E gene optimized for E. coli codon usage (BBa_K2020000).
For the varification of the function of this part, a skim milk assay on agar plates was performed. Therefore, LB skim milk agar plates containing IPTG and the needed antibiotic were poured and the E. coli BL21 cells containing the plasmid with the expression system were streaked out.
Comparing the clearance of the skim milk plates, a proteolytic activity could be proven for the cells containing the expression system for native subtilisin E. As a result, these cells growed three days and afterwards, they were able to produce the native protease, which will then digest the skim milk in the agar plates, resulting in a clearance.
In conclusion, subtilisin E in E. coli was sucessfully expressed and its proteolytic activity were proved via skim milk assay.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 280
- 1000COMPATIBLE WITH RFC[1000]