Difference between revisions of "Part:BBa K3140005:Design"
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===Design Notes=== | ===Design Notes=== | ||
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+ | This part was intended for use in pK18 as a test of our codon harmonisation model. o achieve this, the part was ordered in a gBlock flanked by EcoRI and HindIII sites to enable traditional restriction cloning into pK18. A RBS sequence was added to the gBlock upstream of the part. The RBS sequence used was the consensus Shine-Dalgarno sequence. | ||
===Source=== | ===Source=== |
Revision as of 10:47, 21 October 2019
VVD36-C73A - Truncated VIVID fluoroprotein derived from Neurospora crassa
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 434
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
This part was intended for use in pK18 as a test of our codon harmonisation model. o achieve this, the part was ordered in a gBlock flanked by EcoRI and HindIII sites to enable traditional restriction cloning into pK18. A RBS sequence was added to the gBlock upstream of the part. The RBS sequence used was the consensus Shine-Dalgarno sequence.
Source
The native sequence for VVD (Neurospora crassa) was obtained from NCBI (GenBank accession AF338412.1) and a coding sequence was generated by removing the first 36 amino acid residues and appending a start codon to the start of this truncated sequence. The cystine residue at position 73 (TGC) was then changed to alanine by changing the codon to GCC to yield VVD36-C73A.