Difference between revisions of "Part:BBa K2010005:Design"
Williamcho (Talk | contribs) (→Design Notes) |
|||
Line 7: | Line 7: | ||
===Design Notes=== | ===Design Notes=== | ||
− | + | This sequence was optimized for E. coli K12 using the Codon Optimization Tool from the IDT website. | |
+ | The T7 promoter was used in order to have strong, inducible transcription, in conjunction with NEB’s T7 Express lysY/Iq Competent E. coli. | ||
+ | RBS 34 was used for standard efficiency. | ||
+ | |||
+ | The GGS linker was used to prevent the His-tag from interfering with the folding of PETase. | ||
+ | |||
+ | The His-tag was included for His-tag purification. | ||
+ | |||
+ | sfGFP was included as a reporter protein. | ||
+ | |||
+ | The ompT tag was included for excretion of PETase. | ||
===Source=== | ===Source=== |
Revision as of 07:19, 8 October 2016
ompT + sfGFP + PETase (PET-degrading enzyme, origin I. sakaiensis)
Assembly Compatibility:
- 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 809
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 1227
Design Notes
This sequence was optimized for E. coli K12 using the Codon Optimization Tool from the IDT website.
The T7 promoter was used in order to have strong, inducible transcription, in conjunction with NEB’s T7 Express lysY/Iq Competent E. coli.
RBS 34 was used for standard efficiency.
The GGS linker was used to prevent the His-tag from interfering with the folding of PETase.
The His-tag was included for His-tag purification.
sfGFP was included as a reporter protein.
The ompT tag was included for excretion of PETase.
Source
This sequence is publicly known and was privately modified.