Part:BBa_K3868075
pYLXP-2
Promoter of glucose-6-phosphate isomerase gene.This part will go through PCR, accounting gel electrophoresis and gel recovery, and then be used as the functional module of the pYLXP- 2-Nluc plasmid.
Usage
By codon optimization and adding a 6His-tag, the sequence suitable for expression in E. coli was constructed, and we hoped that it could reduce glyoxylic acid in E. coli to get fluorescence signal in the next processes we design.
The coding sequence of target gene was inserted into an expression vectors with BBa_K880005(BBa_J23100 & BBa_B0034) to obtain BBa_K3332056. We transformed the constructed plasmid into E. coli BL21 (DE3) to verify its successful heterologous expression.
- Fig 2. Gene circuit of GRHPR.
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 701
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 994
Illegal BsaI.rc site found at 887
Illegal SapI.rc site found at 1178
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