Team:UC Davis/Adding secretion
From 2009.igem.org
The purpose of the secretion system is to introduce a method of secreting target proteins we wish to synthesize in the marvelous host: E.coli. For our secretion system we have taken the idea from (15). Park et. al showed that construct containing the truncated from of ice nucleation protein (INPNC) where found to complete coding region of phaZ1, including its signal sequence could lead to stable secretion of the enzyme (15). We have decided to see if we could co-opt this system to make a more generalized inducible system for protein secretion in which the INPNC and phaZ1 signal sequence serve as carries for a target protein.
Possible challenges:
1. Efficient recognition of
the change site may ()
some of the phaZ1 protein we have only cloned the signal sequence up to
the
cleavage site.
2. The system may only work
for protein in a narrow site range.
3. The expression levels of the system may be low.
Advantages:
- In our secretion system, we are using two genes with different sizes as our target secretion genes, GFP being short in length and Luciferase being comparably long, would test our secretion system and its ability to secrete small and large proteins.
- Testing multiple different combinations, Signal Sequence plus ompA/INPNC would help us find the best combination for our secretion system based on their secretion ability and rank them from strongest to weakest in strength (in this specific system).
- Also, we have submitted the BioBricks to the parts regisitry, therefore they can be used in future studies (for different purposes).
Secretion Models:
Click on a specific model for more information:
There
is wide range of genes present in our environment. Therefore, it is
important
to measure our secretion system’s ability to secrete genes of various
sizes.
Name |
Molecular
Weight (kD) |
Myosin |
200.0 |
-Galactosidase |
116.3 |
Phosphorylase
b |
97.4 |
Ovalbumin |
45.0 |
Carbonic
anhydrase |
31.0 |
Aprotinin |
6.5 |
Insulin,
B chain, oxidized |
3.5 |