Part:BBa_K2014007
AraC-pBAD->sfGFP_8R
Usage and Biology
We have tested and slightly improved Ba_K1481003 biobrick provided to iGEM in 2014 by Poznan_Bioinf team, named "sfGFP with R4-tag under arabinose promoter" Firstly we have checked if four rare arginine codons added to the 3' end of GFP reading frame will influence its translation compared to sfGFP reading frame under identical promoter with an identical 5’UTR - biobrick: Ba_K1481002 provided by Poznan_Bioinf as well. Surprisingly we have found that there is no obvious difference in expression of both genes. It was difficult to believe this because many people optimize reading frames to be expressed in E. coli by removal rare codons especially those for arginine, namely AGG and AGA. There are also available special E. coli strains like BL21 Codon Plus [Rosano GL, Ceccarelli, 2009], which encode additional tRNAs and recognize these codons, constructed to enhance the expression of “difficult” ORFs containing rare codons. To be sure that this what we see is not something obtained just by chance, we have extended this tag to eight consecutive arginine residues.
Our construct contains the synthetic sequence coding for sfGFP [Pedelacq JD, 2006] to which we added poly-histidine tag at N-terminus of coding sequence and eight arginine residues at its C-terminus, encoded by rare AGA and AGG codons (Fig. 1.). The expression of this gene is regulated by arabinose promoter (AraC-pBAD)- a tightly controlled and adjustable promoter used in pBAD expression vectors (Invitrogen, Thermo-Fischer).
In order to check to what extent eight rare arginine codons (AGA, AGG) at the 3’-end of a coding sequence influence the translation we measured the fluorescence of sfGFP_8R reporter during 6h culture of E. coli DH5α in three different media (SB/PKB, LB and M9 minimal medium, see methods section) supplemented with 0,4% of arabinose (Fig. 2, 3, 4). The results were referred to sfGFP (Ba_K1481002) and to sfGFP_Worst (BBa_K2014006). We also decided to compare the fluorescence of sfGFP_8R with another construct sfGFP_TagX. Instead of arginine residues, sfGFP_TagX has degradation tag (a decapeptide sequence: ANDENYALAA), which is added to defective mRNAs devoid of stop codons, by translation of tmRNA which binds to the vacant A-site on a stalled ribosome and directs the truncated protein to proteolysis [Hayes et al, 2001]. The results we obtained indicate that either the 8-arginine tag or degradation tag on C-terminus of coding sequence seems not to be detrimental for recombinant protein production in our system.
After bacteria lysis (See [http://2016.igem.org/Team:UAM_Poznan/Experiments Methods]) we observed a substantial fraction of sfGFP_8R still remained in the pellet (Fig. 5). We presume that the added arginine residues at the C-terminus of coding sequence promotes permanent bonding with other structures in cell due to charge–charge interactions [Vondrášek J et al, 2009]. That can be the reason why graphs show a slight decrease in biosynthesis from sfGFP_8R ORF.
Names’ abbreviations:
sfGFP- Ba_K1481002
sfGFP_W- BBaK2014006
sfGFP_8R- BBa_K2014007
REFERENCES
1. GL Rosano and EA Ceccarelli. (2009) Rare codon content affects the solubility of recombinant proteins in a codon bias-adjusted Escherichia coli strain. Microbial Cell Factories 2009, 8:41.
2. Pédelacq JD, Cabantous S, Tran T, Terwilliger TC, Waldo GS. (2006) Engineering and characterization of a superfolder green fluorescent protein. Nat Biotechnol. 2006 Sep;24(9):1170.
3. Hayes CS, Bose B and Sauer RT. (2001) Stop codons preceded by rare arginine codons are efficient determinants of SsrA tagging in Escherichia coli. Proc Natl Acad Sci U S A. 19; 99(6):3440-5.
4. Vondrášek J, Mason PE, Heyda J, Collins KD and Jungwirth P. (2009) The Molecular Origin of Like-Charge Arginine−Arginine Pairing in Water. J. Phys. Chem. B, 2009, 113 (27), pp 9041–9045
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 1144
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 979
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 961
Illegal SapI.rc site found at 1260
None |