Team:Dundee/Parts/Ourbiobricks
From 2013.igem.org
(Difference between revisions)
Line 24: | Line 24: | ||
<h2><a href=”http://parts.igem.org/Part:BBa_K1012002” target="_blank">BBa_K1012002</a> The TorA (Tat-targeting) signal sequence</h2> | <h2><a href=”http://parts.igem.org/Part:BBa_K1012002” target="_blank">BBa_K1012002</a> The TorA (Tat-targeting) signal sequence</h2> | ||
- | This BioBrick contains DNA coding for the TorA (TMAO reductase) signal peptide. This part can be added upstream of a protein of interest, thus targeting it for export across the bacterial cytoplasmic membrane by the twin arginine transport system (Tat) which transports folded proteins. We used this part to export pre-folded PP1 from the cytoplasm to the periplasm of <i>E. coli</i>. | + | This BioBrick contains DNA coding for the TorA (TMAO reductase) signal peptide. This part can be added upstream of a protein of interest, thus targeting it for export across the bacterial cytoplasmic membrane by the twin arginine transport system (Tat) which transports folded proteins. We used this part to export pre-folded PP1 from the cytoplasm to the periplasm of <i>E. coli</i>.<br><br> |
<h2><a href=”http://parts.igem.org/Part:BBa_K1012004” target="_blank>BBa_K1012004</a> The MalE (Sec-targeting) signal sequence</h2> | <h2><a href=”http://parts.igem.org/Part:BBa_K1012004” target="_blank>BBa_K1012004</a> The MalE (Sec-targeting) signal sequence</h2> |
Revision as of 15:15, 26 October 2013
Biobricks
We have submitted two BioBricks to the Registry of Standard Biological Parts that will hopefully be of use to future teams and projects.
1. BBa_K1012001 Protein Phosphatase 1
Human Protein Phosphatase 1 (PP1) is a protein from the family of serine/threonine phosphatases, we have used it as a microcystin binding protein however it regulates many processes in the body therefore it may be used in many other ways.2. BBa_K1012005 ompC-GFP reporter construct.
This is an improved version of >BBa_R0083. BBa_R0083 comprises the ompC promoter, containing OmpR-binding sites. To improve this brick we added a strong Ribosome Binding Site (RBS; from BBa_B0034) followed by Green Fluorescent Protein (BBa_E0040). This was achieved by digesting BBa_R0083 with SpeI + PstI . The RBS from BBa_B0034 was excised with XbaI / PstI, and ligated into the BBa_R0083. The resultant plasmid was digested with SpeI + PstI , and was ligated with the GFP-encoding gene which had been excised from BBa_E0040 by digestion with XbaI / PstI. The resultant plasmid, Bba_ K1012005 responds to the osmotic activation of the EnvZ by producing green fluorescence. This part has been verified to work in this way.In between the European and World Jamborees, we have successfully constructed the following BioBricks we ran out of preparing for the European Jamboree.