Add New Documentation to An Existing Part
We will artificially synthesize the codon-optimized HQT gene and assemble it with a constitutive promoter and GluD-1 promoter. GluD-1 is a specific and highly expressed promoter in rice seed cells. We are going to transfer the two recombinant-plasmids into rice protoplasts. We hope to achieve high expression of exogenous HQT only in rice seeds. However, due to technical constraints, we can only use rice leaves to collect protoplasts. Therefore, we also constructed a plasmid containing a constitutive promoter to test whether exogenous HQT can be expressed in rice cells. The ideal result is that the group transferred into the constitutive promoter has a higher expression level of HQT, while the group transferred into GluD-1 does not express.
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Add New Parts
In our 2020 project, we provide 5 new parts:
1.HQT(BBa_K3458001)
Hydroxycinnamoyl-CoA quinate hydroxycinnamoyl transferase (HQT) gene encodes a protein of 439 amino acids from L. japonica. It can catalyze the reaction of caffeoyl-Coenzyme-A and quinic acid to produce chlorogenic acid.
http://parts.igem.org/Part:BBa_K3458001
2.GluD-1 Promoter()
The promoter of the Oryza sativa L. glutelin gene (GluD-1), due to the deviation in the GCN4 motif, this pomoter has the characteristics of being specifically expressed in the endosperm of Oryza sativa L.
http://parts.igem.org/Part:BBa_K3458002_BBa_K3458002
3.GluD-1 Promoter+HQT( )
This part is the L. japonica. hydroxycinnamoyl-CoA quinate hydroxycinnamoyl transferase (HQT) coding region, with a composite GluD-1 promoter element. Since our goal is to increase the content of chlorogenic acid in rice seeds specifically, we chose the 1.2kb GluD-1 promoter.
http://parts.igem.org/Part:BBa_K3458004_BBa_K3458004
4.35s Promoter+HQT(Part:BBa_K3458003)
The GluD-1 promoter cannot express the gene in rice protoplasts due to its specific expression in Oryza sativa L. endosperm. To verify this, we designed the composite part that contains HQT and constitutive promoter 35s as a control and used western blot to compare GluD-1 promoter and 35S constitutive promoter.
http://parts.igem.org/Part:BBa_K3458003
5.Apis Mellifera Silk Fibroin 3 With Codon Optimization( Part:BBa_K3458005)
We also improve part BBa_K1763000 (2015 UCLA), to let Apis mellifera Silk Fibroin 3 express in Arabidopsis thaliana better.