Part:BBa_K1037003
ygfH
succinate CoA transferase
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1208
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
1: we firstly send our plasmid to company for gene sequence. And do sequence alignment with data from NCBI to confirm that there is no other mutant and ORF is right.
data link of NCBI:
http://www.ncbi.nlm.nih.gov/nuccore/NC_007779.1?report=genbank&from=3063235&to=3065157
2. We than induce the cell transformed with plasmid to see ygfD expression. Follow is the photo of SDS-PAGE gel analysis.
3.To prove the function of the biobrick further! We do fermentation and use HPLC to measure the increase of propionate.Follow is the results.
Conclusion : with all these result, we proved that our biobrick is well constructed . We can see both the protein expressed and prove the function of the protein.
//chassis/prokaryote/ecoli
biology | E.coli K12 |
n/a | ygfH |
protein | ygfH |